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CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Overview: Regulatory leaders who leverage regional regulatory experience to actively contribute to an innovative, scientifically sound, global, integrated regulatory vision/strategies for assigned product/s with a patient-centric focus, leveraging regional commercial insights and applying prudent risk-taking to ensure timely delivery of successful regulatory outcomes. Effectively partner with assigned product/s Global Regulatory Affairs Strategy Team (GRAST) GRL plus other regional, labeling and CMC GRAST members to ensure ‘One GRA Voice’, appropriate inputs into risk assessment and decision making. Ensures bi-directional communication with stationed region commercial operations and GRA. With support, engaging with health authority (HA) in stationed country (FDA or EMA), maintaining productive relationship with HA contacts and driving positive regulatory outcomes with respective HA for assigned product/s in conjunction with GRL. Contributes to product health authority interaction with support GRL or Regulatory TA Head. Partner with GRAST members to achieve regulatory deliverables (including leading assigned tasks) while fostering individual accountability, ‘team spirit’, actively contribute and executing on decisions expeditiously resulting in positive regulatory outcomes. * This is a hybrid position based in Waltham, MA or King of Prussia, PA with a minimum of 3 days onsite in the designated work location weekly. Relocation and mobility assistance are not provided. Key Responsibilities: With support, accountable for assigned product relationship with a health authority (FDA or EMA), ensuring alignment with product GRL and as needed, support from Head, Regulatory TA if escalation is required. May negotiate on behalf of CSL with health authority to achieve desired regulatory outcome. Developing regional knowledge regarding health authority requirements, regulatory filing pathway/categories, processes, and ways of working and thus, can provide relevant guidance / assessment to internal stakeholders (e.g., GRAST, GRL & Commercial) on means to address project challenges, leverage regulatory opportunities and advise on risk for developmental, new, and marketed products. Under the product GRL, supports regional regulatory activities as assigned, inclusive of potential to contribute to core document preparation (e.g., core briefing book, pediatric plans, etc.), product filing preparation activities (investigational, new, and marketed) and health authority engagements. Responsible for Module 1 documentation required for submission and supports response to health authority comments activities with guidance from GRL. Actively contribute to the GRAST activities, strategy development, document reviews and competitive regulatory intelligence. Ensures on-time execution of regulatory activities at the regional level, achieving positive regulatory outcomes. Partners with GRL to develop internal communications and distributes GRAS communications to regional commercial stakeholders. Actively connects and maintains relationships with GRAST members, including GRAS Regions and Regulatory CMC. Proactively fosters and promotes effective relationships across Global Regulatory Strategy. Updates and maintains applicable regulatory systems (e.g., Veeva) to ensure tracking and compliance deliverables. Applies the CSL Leadership Capabilities – Build Bridges, Think Beyond, Unleash Outcomes, Ignite Agility, Inspire the Future and Cultivate Talent – to oneself. Minimum Qualifications: Bachelor’s degree in Pharmacy, Biology, Chemistry, Pharmacology, Clinical Medicine, or related life science field. Advanced degree in a related field (MS, PhD, or MD, DVM) or MBA is preferred Minimum of 5+ years of regulatory/submission experience in the biotech or pharmaceutical industry 3+ years of experience working on developmental products Knowledge and understanding of pharmaceutical/biological product development and regulatory requirements for product development and approval in one or more key regions (EU, US, Japan) Experience working in Regulatory Affairs with agency interaction responsibility with at least one health authority is preferred. Relevant experience working in a complex and matrix environment. Ideal candidates will have clinical or device foundation Demonstrated ability to think strategically, assesses prudent risks and develop bold, agile, innovative approaches to complex challenges Proven effective verbal and written communication skills and ability to successfully work across all levels of the organization Foster productive, working relationships within CSL (e.g., R&D and Commercial). The expected base salary range for this position at hiring is $129,000 - $153,000/yr. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the Waltham, MA USA work location at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #LI-HYBRID

Job Description Job Title: Environmental Specialist Job Description The Environmental Specialist plays a hands-on role in the field managing hazardous waste at a variety of client sites. This position focuses on lab pack services, including chemical segregation, packing, and disposal, as well as conducting chemical inventories, audits, and inspections of facilities and laboratories. The role offers significant exposure to environmental health and safety practices, extensive field experience, and daily customer interaction, with strong opportunities for growth and advancement within a rapidly expanding organization. Responsibilities • Work in the field handling hazardous waste, ensuring safe and compliant practices at all times., • Perform lab pack services, including chemical segregation, packing, labeling, and coordinating disposal activities., • Conduct detailed chemical inventories at client sites to document and track hazardous materials., • Carry out audits and inspections of facilities and laboratories to assess environmental, health, and safety compliance., • Collaborate with team members to deliver high-quality field service to a variety of clients in the Greater Boston area., • Assist leadership in developing key accounts and contribute to the creation and refinement of standard operating procedures., • Demonstrate supervisory and leadership potential through positive, professional interactions with team members in the field., • Engage with clients on a daily basis, providing clear communication, answering questions, and delivering excellent customer service., • Follow health and safety guidelines, including OSHA and internal protocols, to maintain a safe working environment., • Perform the physical tasks required for packing, moving, and disposing of chemicals and related materials., • Drive or ride in company vehicles to multiple sites per day, adapting to changing tasks and client needs., • Support continuous improvement by providing feedback from the field on processes, safety practices, and client requirements. Essential Skills • Strong interest in working in the field with hazardous waste and environmental services., • Bachelors degree in a science-related field, such as Environmental Science, Biology, Chemistry, Ecology, Geology, Marine Science, or a closely related discipline., • Prior work experience, ideally in a hands-on role or in customer service (rather than purely research-focused experience)., • Ability to be personable and professional, with strong interpersonal skills to interact with clients daily., • Comfort with the physical aspects of the role, including packing, lifting, and disposing of chemicals and related materials., • Health and safety awareness, with a focus on environmental and hazardous materials handling., • Customer service skills, including clear communication and responsiveness to client needs., • Willingness and ability to work in the field full-time, traveling to various sites throughout the Greater Boston area., • Understanding or practical knowledge of OSHA and general safety practices related to hazardous materials., • Capability to work effectively in small teams and follow guidance from a team lead while contributing to team success. Additional Skills & Qualifications • Environmental Science degree is preferred, though other science-related degrees are also valued., • Experience or coursework in environmental science, field surveying, or related environmental disciplines., • Experience in field service or field-based work is beneficial., • Familiarity with hazardous materials management and lab pack processes is a plus., • Knowledge of health and safety regulations, including OSHA standards, is advantageous., • Demonstrated interest in building a career in environmental services and hazardous waste management., • Ability to grow into supervisory or leadership responsibilities over time., • Motivation to take advantage of structured advancement programs that provide promotions and raises over a 22.5 year period., • Appreciation for working in a growing company with significant internal promotion opportunities, where most leadership has advanced from within.Job Type & Location This is a Contract to Hire position based out of Somerville, MA. Pay and Benefits The pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & Location This is a Contract to Hire position based out of Somerville, MA. Application Deadline This position is anticipated to close on Nov 13, 2026. Workplace Type This is a fully onsite position in Somerville,MA. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionPayrate: $40.00 - $40.00/hr. Responsibilities: • Developing and implementing pioneering and fit-for-purpose analytical methods for: impurity release testing., • Generating, analyzing, and interpreting analytical data to support: product development investigations, and regulatory submissions, • Keeps current in analytical development field including literature and technology development for groundbreaking and regulatory activities, • Supporting analytical projects involving method development, qualification, and transfer, • Provides critical evaluation of analytical data and results to support: product development (for Process Development, Quality, etc.), investigations and regulatory submissions, • Participates in and contributes to critical analytical development teams (e.g., Product and process development teams, Product quality teams) by providing analytical updates and documentation. Basic Qualifications: • Master’s degree & 2 years of Scientific experience OR, • Bachelor’s degree & 4 years of Scientific experience Preferred Qualifications: • Experience and expertise with protein assays, particularly ELISA as well as most common formats for measuring protein-protein interactions., • Experience and expertise with molecular biology, particularly qPCR and DNA isolation., • Experience with GDP documentation and Electronic Laboratory Notebook systems., • Experience and expertise with Microsoft Office software, particularly Word, PowerPoint and Excel., • Experience with ICH Guidelines, • Innovation – positive approach to challenges; champions new insights and initiatives; brings out and applies others’ creativity to improve unit performance, • Communication – establishes and maintains effective communication mechanisms to keep staff appropriately advised; bridges communication between individuals, units and other organizations as necessary, • Social skills – communicates optimally, using appropriate tact and sensitivity; makes others feel respected, valued and understood Pay Transparency: The typical base pay for this role across the U.S. is: $40.00 - $40.00 /hr. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match, life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law. Consent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary. You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC’s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions. Calls may be recorded. Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying “STOP” to :messages or by contacting privacy@aditiconsulting.com. For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy #AditiConsulting #26-05989

Job Description About Aura Biosciences Aura Biosciences is a clinical-stage biotechnology company developing bel-sar, a potentially transformative, first-in-class therapy for patients living with ocular cancers. Bel-sar represents an entirely novel approach to treating ocular cancers via its dual mechanisms of action of acute tumor necrosis and secondary anti-tumor immune activation. The Phase 3 registration study of Bel-sar in early choroidal melanoma, the largest patient segment of uveal melanoma, is fully enrolled, and earlier stage studies in metastases to the choroid and cancers of the ocular surface are ongoing. Aura's mission is to improve outcomes for patients living with ocular cancers by delivering a therapy that not only arrests tumor growth but also preserves vision and quality of life. For more information, visit aurabiosciences.com. Follow us on X, @AuraBiosciences, and visit us on LinkedIn. Position Summary The (Sr) Associate Scientist, Analytical Development will support analytical development and characterization activities for complex biologics, with a focus on virus-like particles (VLPs) and dye-conjugated VLPs. This is a primarily laboratory-based role requiring hands-on experience with molecular biology, electrophoresis, and bioanalytical techniques supporting late-stage clinical drug substance and drug product development. The successful candidate will work closely with Analytical Development scientists to execute analytical testing, support method development, qualification, and transfer activities, maintain high-quality documentation, and ensure laboratory instruments are ready for use. The role also involves collaboration with internal cross-functional teams and external partners, including contract development and manufacturing organizations (CDMOs) and contract research organizations (CROs). Responsibilities Responsibilities include, but are not limited to: • Perform laboratory experiments independently following established protocols to support inter-departmental teams, analytical method development, qualification, transfer, and product characterization., • Independently culture, maintain, expand, and cryopreserve cell lines in accordance with established protocols and quality standards. Maintain cell banks and accurately document passage history and inventory records., • Perform cell-based cytotoxicity, molecular biology, and immunoassays to support product release, characterization, development, stability, and forced degradation studies, including DNA/RNA extraction, qPCR quantification, ELISA, and Gel electrophoresis (SDS-PAGE, Western blotting)., • Collaborate effectively with cross-functional teams to meet project timelines., • Identify, investigate, and resolve technical challenges, experimental deviations, and assay performance issues as needed. Communicate findings to appropriate scientific team members., • Serve as a subject domain lead for assigned techniques to identify atypical trends and providing technical guidance, as applicable, • Operate, maintain, and troubleshoot routine laboratory instruments used for molecular biology, bioassay, and analytical testing., • Maintain accurate, timely, and compliant records in electronic laboratory notebooks in accordance with good documentation practices and data-integrity requirements., • Prepare and review technical documentation, including data packets, standard operating procedures, test methods, and method development reports., • Participate in data review and scientific discussions related to analytical development and product characterization studies and present experimental results and scientific findings to internal and external stakeholders, as appropriate. Education and Experience • Bachelor’s degree in Molecular Biology, Cell Biology, Biochemistry, Biotechnology, Chemistry, Chemical Engineering, or a related scientific discipline., • 2-4 years of relevant laboratory experience demonstrating hands-on experience with molecular biology techniques, including DNA/RNA extraction, nucleic acid quantification, PCR or qPCR, and agarose gel electrophoresis., • Experience in aseptic techniques is required with proven experience in regular cell maintenance techniques. And performance of cell-based cytotoxicity assays., • Motivation to learn and grow and ability for problem solving is highly desirable., • Demonstrated ability to independently execute, document, analyze, and troubleshoot electrophoresis and qPCR experiments. Preferred Qualifications • Experience with one or more additional analytical techniques, such as SDS-PAGE, Western blotting, capillary electrophoresis, ELISA, UV/Vis spectroscopy, or HPLC/UPLC is preferred., • Understanding of analytical method development, qualification, validation, and technology transfer principles., • Experience working in a regulated laboratory environment and applying good documentation and data-integrity practices., • Experience supporting the analytical development or characterization of biologics, including drug substance and drug product., • Familiarity with scientific data analysis, graphing software, and basic statistical concepts., • Some travelling maybe required to assist with assay establishment, troubleshooting at CDMOs Skills and Capabilities • Ability to follow detailed protocols, prepare reagents and samples accurately, and independently troubleshoot routine experimental and instrument-related issues., • Strong attention to detail, scientific curiosity, and problem-solving ability., • Ability to manage multiple assignments, prioritize laboratory activities, and meet established timelines., • Effective written and verbal communication skills., • Ability to work independently while collaborating effectively within cross-functional teams. Salary & Benefit Information Salary Range: $70,000/yr - $115,000/yr (Placement within the listed range depends on many factors including, but not limited to: geographic location, degree, years of experience, and internal company equity) Health insurance with FULL premium coverage 401K with company match Employee Stock Purchase Program (ESPP) Unlimited paid time off (PTO) Company-paid short & long-term disability insurance and life insurance

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description *Hybrid 3x per week in Lake County IL, Florham Park NJ, Waltham MA, or San Francisco CA. Purpose: • Lead global pipeline medical affairs strategy and develop compelling differentiation across the lifecycle, leveraging distinctive insights from the market to shape AbbVie TA pipeline, • Shape initial value and evidence strategy and initiate Ev Gen plans, leveraging insights from payors, patients, and physicians. Direct pipeline execution team, ensuring pull through of strategy to Enterprise Research MSLs, • Collaborate with counterparts in International TAs, Global Therapeutic Area BU and Development, • Represent TA in pipeline governance, where aligned with TA BU Head, • Interface with Operations and Medical Engagement teams to operationalize pipeline strategy Responsibilities: • Lead and oversee pipeline (including BD) medical, value and evidence strategy development across all disease areas within TA to serve both US and International markets for all indications/ brands up to 24-36 months pre-launch (in any geography), • Drive compelling differentiation of medical, value and evidence strategy from discovery, leveraging distinctive insights from US and International markets, • Coordinate across TAs to ensure that TA-level pipeline strategies coalesce into a coherent AbbVie pipeline strategy, • Ensure HCP, Patients and Payor insights are incorporated into the developments programs to accelerate and differentiate clinical and commercialization strategies (e.g., streamlined patient data collection, patient finding), • Co-create the Brand strategy for all assets and ensure US and International market insights are embedded in the brand strategy, • Represent medical affairs in pipeline-related governance, serving as the single point of contact for commercial and development counterparts, • Serve as final decision maker (pre-BU head) for all pipeline-related strategy and decisions, • Manage pipeline resources effectively, redirecting pipeline team to enterprise critical assets along the lifecycle as needed, starting as early as discovery, • Ensure effective handover to US and International inline/ launch teams, onboarding with relevant TAs to share insights/ approach/ etc. from pipeline strategy efforts and minimizing duplication of effort across pipeline and inline teams, • Lead cross-functional gap assessment and Integrated Evidence Planning (IEP) and collaborate with Value and Evidence, • Define strategy for enterprise research MSLs in US and affiliates, leveraging pipeline insights to develop priorities and shape tactical plans, • Coordinate with pipeline execution group in US Medical Engagement to drive execution, • Collaborate with US Medical Engagement to track impact-focused KPIs and re-shape pipeline strategy based on impact or best practicesQualifications, • M.D., or equivalent advanced degree in a relevant scientific discipline (e.g., oncology/hematology), • 15+ years of experience in the pharmaceutical or biotechnology industry, with a focus on oncology, specifically hematology, • Demonstrated expertise in clinical development, regulatory requirements, and commercialization of oncology therapies, • Proven leadership experience in medical affairs, including managing direct and indirect reports, cross-functional teams and influencing strategic direction at the senior executive level, • Strong scientific knowledge of solid tumor biology, clinical trial design, biomarker development, and emerging treatment modalities (e.g., immuno-oncology, targeted therapies, precision medicine), • Proven ability to work cross-functionally and collaborate effectively with clinical development, regulatory, commercial, and other business functions, • Exceptional communication skills, with experience presenting complex scientific information to both technical and non-technical stakeholders Preferred Qualifications: • Familiarity with advanced cancer treatment modalities such as CAR-T therapies, combination therapies, and immuno-oncology, • Strong publication and scientific communication track record in oncohematology, including contributions to peer-reviewed journals and major oncology conferences, • Experience in managing global medical affairs activities across multiple geographic regions (focus on Global strategy and US region) Physical Requirements: • Ability to travel domestically and internationally (up to 25-30%). Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description Job Description We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services. We are seeking entry-level experienced personnel or fresh graduate students willing to be trained as per our client's requirement and able to relocate. Most of our openings require 3-4 days' onsite presence at the client site. Minimum Qualification: 0-3 years of experience in life science (pharmaceutical, biology, chemistry, bioinformatics) or engineering industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or supply chain. Minimum bachelor’s degree in the above concentration. Valid US work authorization. Virtually able to participate in our training program. Able to relocate anywhere in the US. About White Collar Technologies Inc. is one of the fastest-growing pharmaceutical and life science consulting companies. We specialize in providing Information Technology, Engineering, Quality Assurance, and Project Management services. Our clients range from small Biotech and Gene Therapy companies to Large Biopharmaceutical companies. Our white-glove project placement includes the following benefits • State-of-the-art client interview preparations with industry experts, • Relocation Package including airfare and hotel stay, • Competitive salary packages with full benefits package that includes PTO, Sick Time Off, Health Insurance (Medical, Dental, Vision), • 1x1 supervision and support during client project delivery, • No-stress immigration visa processing with reputed attorney firms (CPT, OPT, H1B, H4 EAD, TN, L1, Green Card)\nCompany Description White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector. Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals. We offer our workers Medical Dental and Vision healthcare benefits. White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector. Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals.\r\nWe offer our workers Medical Dental and Vision healthcare benefits.

Job Description Scholar Rock is delivering muscle-targeted breakthroughs to transform the treatment of spinal muscular atrophy (SMA) and other rare neuromuscular diseases where muscle atrophy remains a critical unmet need. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the biopharmaceutical company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more about our neuromuscular franchise at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: Scholar Rock is looking for an associate director level subject matter expert to build clinical operations compliance while upholding our core values and staying true to our mission. Reporting to the Head of Clinical Operations, the Associate Director/Director, Clinical Operations Compliance will play a key role in oversight of adherence to standard procedures and support of issue management for the clinical programs, and ensuring programs are inspection ready. Position Responsibilities • Ensure consistency in the implementation of clinical project plans by providing reviews and support template development or refinement., • Lead initiatives, create process/ standards, and ensure consistency, communication, and change management across Clinical Operations, specifically related to SOP and work instruction creation and management, outsourcing, and compliance., • Partner with cross-functional team members within Regulatory, Quality, Data Sciences, Clinical Research, Pharmacovigilance, and other key cross-functional groups to support department compliance objectives., • Develop TMF standards and oversight in support of inspection readiness Develop or refine Standard Operating Procedures (SOPs), vendor endorsement team process, and functional builds, e.g. TMF standards., • Support outsourcing partnerships through issue escalation, resolution, and CAPA mediation and documentation as a support to governance oversight., • Provide compliance oversight of clinical operation activities (trial management, site monitoring, vendor management, TMF, data operations, IMP management, and closeout activities, etc.) for clinical trials., • Review key documents in conjunction with other functional area leads (e.g. protocols, SOPs, project plans, and inspection requests, etc.)., • Serve as the Clinical Operations compliance subject matter expert for SOPs, GCP, ICH, FDA, EMA, and other applicable regulatory requirements, ensuring practical application/compliance across study teams and vendors throughput the trial lifecycle., • Issue escalation, documentation, and resolution in partnership with Clinical Operations and Quality Assurance business practices., • Ensure consistent implementation of training and learning, including responsibility for managing functional training matrices and adherence by personnel, as well as oversight of vendor training and learning processes., • Contribute to global clinical / regulatory submissions., • Responsible for assisting in inspection readiness activities, including mock and site inspections., • As a subject matter expert, actively educate, engage with and seek input from key stakeholders to bolster organizational effectiveness and efficiency., • May require travel, including international travel., • Flexible to support in-office days.Candidate Requirements, • Bachelor’s Degree (scientific discipline preferred); advanced degree preferred, • Minimum 8 years of experience in a biotech/pharmaceutical/ CRO setting; minimum 6 years of clinical operations experience; minimum 3 years in a supervisory role, • Proven record of success supporting complex drug development trials, including inspection readiness preparation and experience with positive outcomes from inspections, • Demonstration of effective leadership through vision for her/his team, coaching and mentoring, and organizational development, • Highly organized, outcome oriented, self-motivated performance, • Comfortable in a fast-paced environment with the ability to adapt to change, • In depth knowledge and understanding of all aspects of clinical trials, • Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills, • Ability to analyze complex issues to develop relevant and realistic plans, programs and recommendations, • Excellent knowledge and experience with federal regulatory requirements and guidelines for Good Clinical Practice, • Outstanding oral and written communication skills including authoring and driving the development of SOPs and other key trial documentsScholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description A global and top 200 Am Law firm seeks an associate to join their Life Sciences Patent Group in their Boston office. The ideal candidate must have 1-5 years of patent prosecution experience with strong verbal, written, and interpersonal skills, superior academic credentials, with backgrounds in one of the following fields: biology, immunology, biochemistry or bioinformatics. Advanced degree preferred. Current patent bar membership with previous law firm experience. Candidates are expected to draft and prosecute patent applications, prepare patent opinion letters, provide IP counseling to clients, and conduct patent due diligence studies in connection with business transactions, and working with other practices in the firm to provide full service to life science companies.

Job Description Biocytogen is a comprehensive research and discovery service provider for biotech and pharmaceutical industry and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with the current focus on immuno-oncology and oncology. We are looking for a highly motivated research associate with the ability to work both independently and in a collaborative manner. Biocytogen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Biocytogen is committed to nurturing junior scientists to progress within our organization, providing a supportive environment for career advancement. This opportunity is ideal for individuals who can recognize and seize learning opportunities. Job Responsibilities: ● Perform preclinical pharmacology studies in rodents. Tasks include drug administration via multiple routes (IV, IP, SC, PO etc), blood and tissue collection, and tumor volume measurement. Experience with small animal surgery is a plus. ● Communicate and coordinate with other scientists on a project team to draft, finalize, and implement study protocols. Follow protocols and independently execute tasks. ● Collect and record data. Prepare summaries of experimental procedures and results and present data in team meetings. ● Develop, perform, interpret, and troubleshoot a broad range of in vitro assays including immune cell profiling, cytokine profiling, functional assays using primary cells, as well as cytotoxicity/apoptosis assays using primary and/or cultured cells. ● Innovate and expand our assay portfolio by identifying, evaluating, and implementing new assay technologies through literature research, academic collaborations, and adaptation from other groups within the company. Requirements ● Bachelor’s or Master’s degree with 1-3 years of academic or industry research experience. Demonstrated experience in small animal handling and pharmacology is highly preferred. ● Experience with small animal handling, drug administration, and blood and tissue collection is preferred. ● Experience in cell biology, biochemistry, and/or molecular biology, in particular assay development and execution, is required. This includes cell-based assays, tissue culture, biochemical assay technologies, and protein and RNA expression analysis. ● Experience with cell culture and in vitro assays is desirable. ● Experience in primary immune cell-based assays is strongly preferred. ● Experience in flow cytometry (FACS) analysis is preferred. ● Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment. ● Collaborative team player. Be flexible and prioritize tasks based on team and company goals. ● Communicate effectively at all levels, within teams, with internal and external collaborators. ● Strong organizational skills. Maintain research data and records with the highest integrity. ● Ability to multitask in a fast-paced environment. Benefits • Medical Insurance, • Dental Insurance, • Vision Insurance, • Health Reimbursement Accounts, • Life and AD&D Insurance, • Short & Long Term Disability Insurance, • 401K with Company Match, • Paid Time Off, • Paid Sick Days & Holidays BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one’s qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

Job DescriptionBiology Research Scientist Job Type: Contractor Location: Remote Hours: 10–20 hours/week Duration: 1–2 months minimum, with likely extension Start: Immediate Job Overview We are seeking experienced Biology Research Scientists to support a project focused on validating protein target assignments against primary scientific sources and UniProt records. You will review research papers and patents, identify target assignment errors, propose corrected UniProt accessions, and provide concise, evidence-based scientific reasoning. Key Responsibilities • Review primary research papers and patents to verify protein target assignments., • Compare target assignments against UniProt and identify discrepancies., • Classify target assignment errors using a structured taxonomy., • Propose accurate UniProt accessions where assignments are incorrect., • Document clear, concise, evidence-grounded reasoning for each determination., • Apply expertise in pharmacology, biochemistry, molecular biology, or chemical biology to evaluate target relationships.Required Skills, • Protein Target Identification, • UniProt, • Primary Literature Review, • Protein Biochemistry, • Molecular Biology, • Pharmacology, • Binding & Functional Assays, • Scientific Data Interpretation, • Evidence-Based Reasoning, • Technical DocumentationQualifications, • BA/BS + 5 years, MS + 2 years, or PhD with relevant industry/drug discovery experience., • Background in pharmacology, biochemistry, molecular biology, or chemical biology within biotech, pharma, or CRO environments., • Hands-on experience with assays such as SPR, TR-FRET, radioligand binding, kinase assays, or GPCR functional assays., • Experience interpreting IC50, Ki, and Kd data., • Currently active in a bench-based research, scientist, or associate scientist role., • Working knowledge of UniProt or related workflows such as SAR, HTS, target validation, biochemical profiling, or IND-enabling studies.Nice to Have, • Experience with ChEMBL, BindingDB, or PubChem., • Selectivity profiling or counterscreening experience., • Understanding of agonist/antagonist vs. activator/inhibitor distinctions.Screening Questions, • What is your highest relevant degree and how many years of industry research experience do you have?, • What is your experience with protein target identification and UniProt?, • Which binding or functional assays have you performed hands-on?, • Do you have experience interpreting IC50, Ki, or Kd data?, • Have you worked with ChEMBL, BindingDB, or PubChem?, • Are you currently bench-active in a research or scientist role?, • Are you available for 10–20 hours per week with an immediate start?

Job Description Scholar Rock is delivering muscle-targeted breakthroughs to transform the treatment of spinal muscular atrophy (SMA) and other rare neuromuscular diseases where muscle atrophy remains a critical unmet need. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the biopharmaceutical company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more about our neuromuscular franchise at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: The Sr. Medical Director, Drug Safety & Pharmacovigilance is a key position within the company and safety department, with significant impact on the development and life cycle of drug development projects. Responsible for providing safety strategy, expertise, and guidance, pre- and post-approval for assigned products, the Sr. Medical Director will drive the proactive implementation of risk management initiatives in accordance with global regulatory requirements. Core responsibilities will encompass continuous and efficient evaluation of safety data, perform signal detection, evaluation and assessment and management of the safety profile of the compound. In addition, the position will work closely with cross functional teams and Departments for achieving project goals, within timelines & with high quality. Position Responsibilities: • Lead and support development of pharmacovigilance strategies for products within Therapeutic area, to ensure compliance with corporate clinical development and commercial goals., • Oversight and conducting of signal detection activities include monitoring, evaluation, interpretation, management and communication of safety information., • Responsible for oversight and conduct of Product Safety Committee (PSC) meeting(s) to evaluate risk-benefit for the compounds with support from cross-functional teams. Escalate and present safety issues to the Executive Safety Committee., • Medical safety review including causality assessment of all available safety data generated from various sources (e.g. pre-clinical, clinical trial data, post-marketing and literature) throughout the development process for assigned compounds/projects., • Provides medical expert safety review input into all critical documents for products in clinical development (e.g., INDs/NDA/BLA submissions, protocols and amendments, ICFs, IBs, and clinical research reports (CSR)), • Oversight of aggregate reports and signal evaluation reports for assigned projects., • Responsible for the Clinical content of responses to inquiries from regulatory authorities related to Safety topics., • Provide leadership and support to Contract Research Organization (CRO) staff to ensure overall delivery of services. Ensures vendor oversight of outsourced Medical activities, as applicable., • Oversee and collaborate with internal safety scientists within TA, • Assist with the writing and development of SOPs as required to ensure compliance to regulations and local laws., • Lead high quality planning and execution of external meetings and internal stakeholder meetings (e.g., DMCs, Vendor oversight meetings, etc.), • Demonstrated ability to build effective working relationships, influence, negotiate, and drive organizational engagement. Ability to be flexible and adapt quickly to the changing needs of the organization., • Support process improvement and functional training at departmental & company level, • Ensure that the highest quality, ethical & professional values are demonstrated in all aspects of work., • Ensures compliance with corporate policies and procedures, as well as all related healthcare laws and regulationsCandidate Requirements:, • MD or MBBS or MD-PhD or equivalent medical degree, • 5 or more years of pharmaceutical experience in Drug Safety & Pharmacovigilance., • Strong understanding of pharmacovigilance regulations in the US and EU., • Experience in supporting drug safety activities in registrational clinical studies, • High level of medical competence, with an ability to balance this with industry standards to achieve business goals, • Demonstrated skills in scientific analysis and reasoning., • Sound knowledge of overall drug development process from discovery to registration and post marketing requirements & surveillance., • Prior IND, as well as NDA/BLA (filing/submission) and other regulatory interaction experience is highly desirable, • Strong track record of delivering results through effective team and peer leadership in matrix, • Excellent leadership & organizational skills, analytical skills, presentation skills, and strong experience in translating important data into clinical strategies.Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description About Parabilis Medicines Parabilis Medicines is a clinical-stage biopharmaceutical company dedicated to creating extraordinary medicines for patients with serious diseases by unlocking biologically important targets long considered undruggable. The company has pioneered a new class of alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that have historically been beyond the reach of conventional medicines. The company's lead investigational medicine, zolucatetide, is the first and only direct inhibitor of the β-catenin:TCF interaction, a central node in the Wnt/β-catenin pathway that has eluded drug developers for decades. Zolucatetide is being evaluated in the clinic across multiple Wnt/β-catenin-driven diseases, including desmoid tumors, familial adenomatous polyposis (FAP) and a range of other solid tumor indications. Beyond zolucatetide, Parabilis is advancing additional Helicon-based programs focused on other challenging targets where we believe our medicines could have life-altering impact. For more information, visit www.parabilismed.com or follow us on LinkedIn. What's the opportunity? We are seeking a highly motivated, hands-on Principal Associate Scientist to join our Biology team and support the advancement of pre-clinical oncology programs. This scientist will be a key bench-facing member of the program, designing and executing the cellular and molecular experiments to understand how Helicon candidates engage and interfere with the target; how target interference alters cancer-cell biology, and which pharmacodynamic and response biomarkers may help translate the mechanism toward development. The successful candidate will generate rigorous, decision-enabling data and provide scientifically grounded recommendations to help define translational and clinical opportunities for addressing significant unmet medical needs. Reporting to the program biology lead, the ideal candidate combines excellent experimental skills with strong mechanistic reasoning. This individual will work independently on problems of diverse scope, develop and qualify new assays, adapt published approaches to novel scientific questions, and generate high-impact biology data in a highly collaborative, fast-paced biotechnology environment. Key Responsibilities • Independently design, optimize, execute, and troubleshoot cell-based assays to characterize and assess lead Helicons, including target engagement, potency, selectivity, mechanism of action, and differentiation opportunities., • Develop and apply cellular and molecular assays, including CETSA, AlphaLISA, HTRF, NanoBRET, cell proliferation, qPCR, ELISA/MSD, Co-IP, flow cytometry, and western blot across 2D and 3D cell models., • Develop, optimize, and qualify new assay systems and disease-relevant models—including cancer cell lines, primary cells, and 3D organoid cultures—to address questions that existing platforms cannot answer., • Investigate the biological contexts associated with sensitivity and resistance to lead Helicons and develop testable hypotheses for pharmacodynamic and response biomarkers., • Work with Translational Biology, DMPK and in vivo Pharmacology colleagues to select informative models and translate cellular findings into tissue PK/PD and biomarker studies where appropriate., • Collaborate closely with other functions within the program to generate decision-enabling biology data supporting lead optimization, development-candidate nomination and IND-enabling activities., • Present experimental results, interpretations, and recommendations clearly to project teams, the broader Biology and company organizations., • Maintain complete, timely and traceable experimental records and uphold high standards for data integrity, reproducibility and scientific transparency. What you'll need to be successful: • B.S. in cell biology, molecular biology, cancer biology or a related field with 8+ years of industry experience in biotechnology or pharmaceuticals, or an M.S. with 6+ years., • Substantial hands-on experience with mammalian cell biology, cell culture and quantitative cell-based pharmacology or assay development., • Demonstrated proficiency in cell and molecular biology techniques such as HTRF, AlphaLISA, CETSA, Western, Co-IP, qPCR, CyQUANT, Flow Cytometry, ELISA/MSD, Imaging, etc., • Experience using CRISPR/Cas9, RNAi, viral expression/transduction, or related genetic approaches to investigate biological mechanisms., • Experience studying determinants of drug response or resistance and developing pharmacodynamic or response-biomarker hypotheses is highly desirable., • Demonstrated ability to adapt published methods to novel scientific questions and to build working relationships with collaborators outside your own area of expertise., • Experience in oncology drug discovery is strongly preferred. Familiarity with peptides, targeted protein degradation, or other therapeutic modalities beyond conventional small molecules is a plus., • Strong organizational skills and meticulous attention to detail in experimental documentation., • Collaborative mindset with a high degree of initiative, curiosity, and enthusiasm for developing revolutionary medicines. Core Values Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit. • Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable., • In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options., • Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact., • All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history. The base salary range for this position is $108,000-$128,000, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees' overall well-being. As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law. 30 Acorn Park Drive | Cambridge, MA 02140 | www.parabilismed.com

Job DescriptionPatent Attorney – Life Sciences (Biotech / Pharma) Location: Boston, US Overview A highly regarded, boutique intellectual property firm is seeking a Patent Attorney with a strong life sciences background to join its growing practice. This role offers the opportunity to work on complex and cutting-edge matters in biotechnology, pharmaceuticals, and related fields. Key Responsibilities • Draft and prosecute U.S. and international patent applications, • Work closely with inventors, scientists, and in-house counsel, • Conduct:, • Patentability analyses, • Freedom-to-operate (FTO) analyses, • Validity and infringement assessments, • Support IP due diligence for transactions and licensing matters, • Provide strategic intellectual property guidance to clients, • Collaborate with attorneys and technical specialists on complex patent mattersTechnical Focus, • Biotechnology, • Pharmaceuticals, • Molecular biology, genetics, therapeutics, • Diagnostics, antibodies, gene therapyQualifications, • Ph.D. (or equivalent advanced degree) in biology, molecular biology, genetics, or related field, • USPTO registration required, • ~3–5+ years of patent prosecution experience (more senior candidates also considered), • Strong academic credentials, • Excellent written and verbal communication skillsBenefits, • $170,000 – $250,000 base salary (depending on experience and level), • Potential Bonus, • Comprehensive health, dental, and vision insurance, • 401(k) with employer contribution, • Paid time off + holidays, • Flexible / hybrid work environment, • Professional development and mentorship opportunities

Job Description Job Title: Research Associate - Antibody Discovery Location: Cambridge, MA Type: Contract Work Model: Onsite – onsite Hours: 40.0 Responsibilities • Perform routine and advanced molecular biology laboratory techniques in support of antibody discovery projects., • Conduct PCR, DNA/RNA isolation, restriction digestions, gel electrophoresis, bead-based purification, and related molecular biology workflows., • Support next-generation sequencing (NGS) library preparation and sequencing activities., • Execute experiments requiring precise pipetting and handling of small-volume samples., • Follow established laboratory protocols and standard operating procedures with a high degree of accuracy and consistency., • Generate high-quality experimental data and maintain thorough laboratory documentation., • Troubleshoot laboratory processes and identify opportunities for workflow improvements., • Collaborate closely with scientists across molecular biology, immunization, and antibody discovery functions., • Contribute to technology development initiatives, including automation and process optimization efforts., • Participate in cross-training opportunities across the broader research team. Requirements • Bachelor's degree in Molecular Biology, Biochemistry, Biotechnology, Cell Biology, Biological Sciences, or a related discipline., • Research experience gained through industry, academic, or laboratory-based environments., • Hands-on experience with core molecular biology techniques, including:, • PCR, • DNA/RNA isolation, • Gel electrophoresis, • Pipetting and sample preparation, • General laboratory procedures, • Strong organizational skills and exceptional attention to detail., • Ability to follow protocols precisely while maintaining high-quality standards., • Excellent communication and teamwork skills., • Demonstrated eagerness to learn new techniques and technologies. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X. We are seeking an experienced corporate development leader to build and maintain a comprehensive view of the solid tumor oncology landscape, translate scientific and competitive intelligence into clear portfolio priorities, and identify external opportunities that can strengthen Crescent’s pipeline. You will partner cross-functionally with Research, Clinical Development, Business Development, and Executive leadership to evaluate assets, inform strategic decision-making, and prepare decision-oriented recommendations for the executive team and Board. Responsibilities • Landscape intelligence: Build and continuously maintain a comprehensive view of existing and emerging therapies across solid tumor oncology, spanning approved agents, late- and early-stage clinical assets, and preclinical modalities., • Portfolio matrix: Develop and own a matrix / portfolio view mapping our own therapies, partner therapies, and prospective in-licensing targets against tumor types, lines of therapy, mechanisms of action, and combination potential., • Search & evaluation: Proactively search for, identify, and evaluate potential opportunities (research collaboration, in-licensing preclinical and clinical assets, platform technologies and research tools) that are consistent with external BD strategies for the advancement of Crescent's Oncology pipeline, and driving sustainable growth for the Company. Review external opportunities for scientific merit and feasibility., • Prioritization & gap analysis: Identify and prioritize where partnering, collaboration, or asset in-licensing can complete or strengthen the portfolio and articulate the strategic case for each opportunity., • Data sourcing: Source, validate, and synthesize intelligence from clinical, competitive, and commercial databases to support decision-making (e.g., ClinicalTrials.gov, primary literature)., • Cross-functional partnership: Partner closely with Research, Clinical Development, Business Development, and Executive leadership to translate portfolio strategy into actionable prioritization and resource allocation., • Executive communication: Prepare clear, decision-oriented materials for the executive team and Board that communicate portfolio positioning, trade-offs, and recommendations. Education & Experience, • Advanced scientific degree strongly preferred — PhD and/or MD in a relevant discipline (oncology, immunology, molecular/cancer biology, pharmacology). Exceptional candidates with equivalent depth of expertise and experience will be considered., • Demonstrated ability to understand and critically evaluate the mechanisms of action for oncology therapeutics, • Minimum 12 years of experience in oncology portfolio strategy, competitive intelligence, business development, translational research, or a closely related function within biopharma., • Hands-on fluency with clinical-trial, pipeline, and competitive-intelligence databases, and the ability to structure disparate sources into a coherent analytical framework., • Proven ability to build structured frameworks (matrices, prioritization models) that turn complex scientific and competitive information into clear strategic recommendations., • Strong written and verbal communication; able to translate dense science into decisions for scientific and non-scientific stakeholders alike., • Strong analytical, strategic thinking, and problem-solving skills., • Excellent communication and leadership abilities; able to influence across all levels of the organization., • Ability to thrive in a fast-paced, ambiguous environment while managing competing priorities., • Commitment to fostering a diverse and inclusive workplace. What We Offer • Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment, • Competitive compensation, including base salary, performance bonus, and equity, • 100% employer-paid benefits package, • Flexible PTO., • Two, one-week company-wide shutdowns each year, • A commitment to your professional development, with access to resources, mentorship, and growth opportunitiesSalary Range The salary range for this position is $290,000 to $320,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Additional Description for Pay Transparency: The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation – Unlimited PTO; Sick time – 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave – 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - https://www.crescentbiopharma.com/careers/#benefits Please note: Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status. Please note, Crescent does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between Crescent and the agency. Crescent will not pay any fees related to unsolicited resumes. #LI-CBIO

Job Description Job Title: Biologist Location: Boston, MA Contractor Work Model: Onsite – onsite Hours: M-F 9am-5pm Compensation: $48.69 - $57.28/hr Type: Contract, Potential for extension or conversion to permanent Overview As a Scientist in Cell Engineering and Assay Development, you will engineer novel cell lines and develop the in vitro assays used to characterize them in support of our allogeneic cell therapy programs. You will design genetic constructs and mRNA, generate engineered cell lines using viral vectors and transient mRNA-based expression, and build cell-based assays to evaluate the function of engineered cells. You will work closely with cross-functional teams to advance cell therapy programs from discovery through preclinical development. Responsibilities • Design and engineer novel cell lines in iPSCs, tumor cell lines, and other immortalized and primary cell types to support allogeneic cell therapy programs, • Generate stable engineered cell lines using lentiviral transduction and other viral vector systems, • Design genetic constructs and mRNA for stable and transient gene expression, including knock-in, knockout, and reporter strategies, • Perform transient mRNA-based expression to rapidly prototype and validate cell engineering strategies, • Establish clonal engineered cell lines through cell sorting (FACS) and single-cell cloning, • Develop, optimize, and execute cell-based assays to characterize engineered cells, including live-cell analysis on the Incucyte platform, • Design and run in-depth, multi-parameter flow cytometry panels to phenotype engineered cells and assess immune checkpoint receptor expression, • Evaluate the functional impact of genetic modifications on engineered cell phenotype and function, • Design and execute experiments, analyze data, and interpret results to evaluate the performance of engineered cells in vitro, • Communicate experimental data effectively through written reports and oral presentations., • Demonstrate flexibility and motivation to learn and apply new technologies for cell engineering and assay development. Qualifications Required:, • Bachelor’s degree in Cell Biology, Molecular Biology, Immunology, or a related field plus 5 years of relevant experience in biotechnology, pharmaceutical industry, or academic research., • Master’s degree in Cell Biology, Molecular Biology, Immunology, or a related field plus 2 years of relevant experience in biotechnology, pharmaceutical industry, or academic research., • Hands-on experience with lentiviral cell line generation is required. Additional Skills/Preferences:, • Experience engineering iPSCs and tumor cell lines, • Proficiency in construct design and mRNA design, • Experience with cell engineering using viral vectors and transient mRNA-based expression, • In-depth flow cytometry expertise, including panel design, cell sorting (FACS), and multi-parameter data analysis, • Working knowledge of immune checkpoint receptor biology, • Experience with live-cell analysis platforms such as Incucyte and xCELLigence, • Proficient in developing in vitro cell-based assays, including work with human cell lines and primary cells, • Strong analytical, problem-solving, and decision-making skills., • Excellent interpersonal and communication skills., • Ability to work independently and collaboratively within a team environment. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M- #LI- Ref: #558-Scientific

Job Description Job Title: Bench Scientist II Location: Cambridge, MA Type: Contract Compensation: $35-$41.82 Work Model: Onsite – onsite Hours: 40.0 hours per week Overview Leading pharmaceutical company looking for an entry level Bench Scientist II. Ideal candidates should have a Bachelors degree in biology, immunology, molecular biology, biochemistry, or a related scientific discipline, with at least 2 years of full-time laboratory experience in an academic or industry setting. Responsibilities • Provide laboratory support for discovery research activities, including cell culture, molecular biology, and immunology-related laboratory work., • Execute established workflows supporting rodent immunization, serum titer screening, B cell sorting, molecular cloning, and related sample processing activities., • Maintain reagent inventories, prepare laboratory materials, and ensure operational readiness for discovery activities., • Document experimental procedures, results, and observations accurately in laboratory records and internal data systems., • Summarize data and communicate key findings, experimental progress, and campaign outcomes to project teams. Requirements • Bachelors degree in biology, immunology, molecular biology, biochemistry, or a related scientific discipline, with at least 2 years of full-time laboratory experience in an academic or industry setting., • Experience in a laboratory setting with cell culture, molecular biology techniques, immunology-related research, and antibody-related assays/testing., • Comfortable working with laboratory animals (primarily mice), tissue collection/dissection, and open to learning animal handling procedures., • Strong laboratory organization skills, including reagent handling, inventory support, and maintaining materials needed for experimental workflows., • Background in immunology, cell biology, molecular biology, translational research, or antibody research is preferred. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Clinical Laboratory Team Leader – Blood Bank Location: Boston, MA Schedule: Monday–Friday, 3:00 PM – 11:30 PM, rotating weekends Compensation: $39.00 – $48.02/hour + Sign-On Bonus Available About the Opportunity A leading healthcare organization is seeking an experienced Blood Bank Team Leader to join its laboratory leadership team in Boston, Massachusetts. This role offers the opportunity to lead laboratory operations in a fast-paced hospital environment while supporting high-quality patient care and mentoring laboratory staff. The ideal candidate will have strong technical laboratory expertise, proven problem-solving skills, and previous experience working in a clinical laboratory setting. Key Responsibilities • Perform routine and complex laboratory testing in accordance with established procedures and regulatory requirements., • Evaluate specimen acceptability and ensure proper handling throughout the testing process., • Monitor, operate, maintain, and troubleshoot laboratory instrumentation., • Review and verify test results to ensure accuracy and timely reporting., • Assist with technical oversight, workflow coordination, and staff support within the department., • Perform and document quality control, quality assurance, and preventative maintenance activities., • Prepare, evaluate, and implement new reagents, controls, and testing procedures as needed., • Maintain adequate inventory of laboratory supplies and reagents., • Support specimen processing activities when necessary., • Ensure compliance with laboratory safety standards and regulatory guidelines., • Serve as a technical resource for laboratory staff and assist with problem resolution. Qualifications • Bachelor's degree in Clinical Laboratory Science, Medical Technology, Biology, Chemistry, or a related life science field., • Minimum of four (4) years of clinical laboratory testing experience., • ASCP or AMT certification preferred., • Strong technical knowledge of clinical laboratory operations and instrumentation., • Ability to work independently and effectively within a team environment., • Experience with laboratory information systems (LIS) is preferred., • Excellent communication, organizational, and critical-thinking skills., • Must be able to pass a color vision screening., • Flexibility to work overtime and alternate shifts as needed. Compensation & Benefits • Competitive hourly compensation based on experience and qualifications., • Sign-on bonus available for qualified external candidates., • Comprehensive benefits package including:, • Medical, Dental, and Vision Insurance, • Life Insurance, • Short-Term and Long-Term Disability Coverage, • 401(k) Retirement Plan, • Paid Time Off, • Tuition Reimbursement, • Employee Stock Purchase Program About us: At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 19 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories. It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities. If at any time during the application process, you need an accommodation, please contact recruiting@lighthouselabservices.com for assistance. Lighthouse Lab Services | 844-974-1929 | lighthouselabservices.com #LLS2

Job DescriptionRole Location: Waltham, MA The Company We are Alloy Therapeutics — a biotechnology ecosystem and Product Development Organization (PDO) empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. May the Best Drug Win. Alloy has evolved from a startup into a global product development organization operating 11 divisions across 5 research sites in 4 countries on 3 continents. Our model - Integrated Independence - combines centralized capabilities with entrepreneurial operating divisions. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. At Alloy, we have an ethos of "Mentorship-By-Apprenticeship" in all of our positions. We strive to have workers in the office when needed to interact organically and face-to-face. Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year. We respect and value our colleagues for their hard work that requires them to be in the lab every day. We ask our people who have more flexible accommodations to appreciate their colleagues who have less flexibility. We are all one team! About the Role at Alloy Therapeutics As Director of Protein Science, you will lead a team responsible for high-throughput mammalian protein production and mg-scale expression in support of therapeutic programs. In this role you will leverage antibody building blocks to create multi-specific antibody formats that custom fit the needs of our mechanistically-diverse partner base, from large pharma companies to emerging biotech companies and academic collaborators. You will work closely with the discovery, analytics and pharmacology teams to review data in real time and make the necessary scientific adjustments to ensure a successful campaign. In addition, you will serve as a project leader overseeing the on-time completion of project activities, accomplishing shared objectives, and meeting rigorous partner timelines. Strong communication skills are essential for this role, as you will interact with a diverse group of stakeholders both within and outside the company. You will also be accountable for high-quality partner communication throughout the project life cycles, including drafting research proposals, updating project status and timelines, and presenting final deliveries. In parallel, you will provide regular project updates and presentations to internal stakeholders to ensure alignment with project goals and timelines and addressing any potential issues or concerns promptly. This role will report directly to the site head Antibody-Powered Division Waltham, MA, with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. How You’ll Drive Impact • Drive: Scientific direction and execution of monoclonal discovery and multispecific engineering campaigns., • Innovate: Ensure the application of cutting-edge technologies and methodologies in protein expression., • Collaborate: Integrate protein engineering and cutting-edge efforts efficiently into product offerings and engage with external collaborators in discovery of biologics., • Deliver: Efficient execution of partner projects balancing quality, timelines, and costs, while ensuring successful completion of therapeutic discovery that meet our partners’ objectives., • Lead: Marshal, inspire, and mentor a cross-functional team of scientists. Lead by example by going the extra mile to ensure we are successful delivering on projects., • Communicate: Communicate effectively with key stakeholders externally and internally, fostering productive interactions both upward and downward, and across teams at different sites. Key Responsibilities • Lead and grow a team of protein scientists, • Own molecular biology, antibody expression, purification, and quality control workflows, • Engage prospective customers to articulate multispecific antibody production strategies, • Deliver high-throughput and mg-scale antibody production runs successfully and on time, • Drive major decisions, balance tradeoffs and resolve technical issues with projects, • Lead process improvement initiatives across the antibody-powered division, • Ensure rigorous data capture in ELN/LIMS systems, • Bring innovative scientific and technological solutions to increase business competitiveness of bispecific service offerings Qualifications • You have a PhD in a relevant scientific field (e.g. Biochemistry, Biophysics, Molecular Biology, etc) with a minimum of 8 years of industry experience in antibody or protein engineering, or a master’s degree with 12+ years of relevant industry experience., • You have a track record leading protein expression, purification, and characterization functions supporting drug discovery, • You have hands-on depth in recombinant mammalian protein expression systems, • You have broad and deep experience with complex purification techniques and process/method development for bi- and multi-specific antibodies., • You have a proven track record of successful execution and delivery of projects within scope, budget, and timeline., • You have demonstrated the ability to work in a fast-paced, dynamic environment and adapt to changing priorities and deadlines., • You have excellent communication skills, both written and verbal, with the ability to effectively communicate with stakeholders at all levels., • You have excellent leadership and team management skills, with the ability to motivate and mentor team members., • Ability to work across various US and international time zones., • Accommodate occasional travel as needed (10%). Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation • Competitive base and equity compensation commensurate with level of experience and independence, • 401(k) company matchHealth & Family, • Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered, • Company-paid disability (STD, LTD) and life insurance, • Paid parental leave, • Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)Unique Perks, • Unlimited PTO (paid time off) and flexible schedules, • Annual stipend for continuing education with commitment to your career through individualized professional development plan, • Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated range is $170,000 - $200,000, with the final offer based on factors like your experience, skills, and alignment with our needs. Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines. We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help. Alloy Therapeutics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status. If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at recruiting@alloytx.com. We will make every effort to respond to your request for disability assistance as soon as possible. Powered by JazzHR JgrN8wivKV

Job Description Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. Job Summary The Technical Product Specialist – PAT Bio is a critical commercial support role responsible for driving growth of Nova Biomedical’s BioProfile FAST CDV Analyzer across North America. This position works in close partnership with North American Key Account Managers (KAMs) to develop new opportunities, manage complex sales processes, and ensure a high-quality customer journey from initial engagement through evaluation and close. The ideal candidate combines strong scientific expertise with hands-on experience in automated cell counting technologies and excels in cross-functional collaboration, technical selling, and opportunity management. If you’re passionate about technical sales and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! Responsibilities Serve as the technical and commercial specialist for the BioProfile FAST CDV Analyzer across North America Partner closely with North American Key Account Managers to grow the FAST CDV business Proactively prospect, identify, and develop new FAST CDV leads and sales opportunities Own and manage the sales process and customer journey for all FAST CDV opportunities, from qualification through close Develop a deep understanding of the U.S. key account landscape and drive consistent FAST CDV messaging across territories Coordinate closely with Field Applications to ensure successful product demonstrations, evaluations, and customer trials Lead technical sales presentations and deliver compelling, value-based messaging to scientific and commercial stakeholders Manage complex sales cycles, including objection handling and competitive positioning Generate quotations and support opportunity negotiation in collaboration with KAMs Maintain accurate opportunity tracking, forecasting, and customer records within the CRM system Manage and maintain FAST CDV demonstration and evaluation equipment Act as a central FAST CDV resource for sales, applications, and internal stakeholders Experience Requirements Bachelor’s degree in a scientific discipline (biology, biotechnology, biochemistry, chemistry, or related field required; advanced degree preferred) Strong scientific background with hands-on experience in automated cell counting systems Experience selling, supporting, or using trypan blue dye–based cell counting technologies Prior experience with Beckman Coulter ViCell XR, ViCell BLU, or similar automated cell counters strongly preferred Experience supporting or managing complex sales processes within biotechnology or biopharmaceutical markets preferred Excellent organizational and time management skills Strong presentation, communication, and technical demonstration abilities Ability to manage multiple opportunities across multiple territories simultaneously Proven ability to navigate complex customer organizations and sales objections Strong collaboration skills and a team-first mindset Comfortable working alongside and supporting multiple Key Account Managers (approximately nine) Proficiency with CRM tools and standard business software Willingness to travel as required to support customer engagements and evaluations Physical Requirements & Working Conditions for this role include: • Willingness to travel as required (including air and ground transportation)., • Valid driver’s license and ability to safely operate a motor vehicle as needed for job responsibilities., • Able to store, transport materials, samples, or demonstration equipment (up to ~25 pounds)., • Comfort with standing and engaging with customers for extended periods., • Ability to adapt to varying work environments (e.g., customer sites, laboratories, offices). Why work for Nova Biomedical • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements (job specific), • Professional development, engagement and events, • Company marketplace for lunch and snacks! (location specific), • Company subsidized cafeteria (Waltham) Work Location: North America, Remote, Travel Schedule/Hours: Monday to Friday, 9:00 AM – 5:00 PM Targeted Salary Range: $90,000 - $140,000/year, variable included in pay Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. About the Company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed up drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy Policy https://www.novabiomedical.com/privacy-policy/

Job DescriptionEssential Functions: Lab Manager " Ensure that the Analytical Development (AD) team adhere to lab safety guidance and waste disposal guidance. " Be the point of contact with EHHS on behalf of the AD team. " Oversee inventory management such as purchasing, storing, and allocating of new laboratory equipment and supplies. " Develop and manage a lab request intake and triage system (e.g., via Microsoft Teams or Smartsheet) to collect non-urgent requests, coordinate prioritization with lab managers and key stakeholders, and ensure timely follow-through while improving workflow efficiency and reducing ad hoc interruptions. Research Associate " Execute functional potency bioassays in support of Analytical Development activities. " Perform potency testing using ELISA, other plate-based platforms, and flow cytometry, as needed. " Support biologics-related AD workstreams through routine assay execution and data collection. " Assist with assay troubleshooting, optimization, and performance trending under manager guidance. " Maintain assay raw-data trackers and perform basic data analysis. " Maintain clear, accurate documentation in electronic lab notebooks and test forms. " Support routine management of assay reagents, consumables, and laboratory materials as needed. Education and Experience:? " Bachelor s or master s degree in Cell & Molecular Biology, Biochemistry, or an equivalent qualification. " At least 2 years of relevant industry or regulated-laboratory experience preferred; candidates with a master s degree and 0 2 years of industry experience may also be considered. " Preferred experience in the cell and gene therapy space. " Experience with sample management and ELN/LIMS systems. Knowledge, Skills, and Abilities: " Experience with a variety of biology lab equipment (e.g., multi-channel pipettes, centrifuge, microscope, plate reader, plate washer, flow cytometer). " Good organizational habits. " Proficient in Microsoft Excel and Word. " Proven problem solving and troubleshooting abilities. " Good written and oral communication skills. " Ability to work in a collaborative environment with a team. EEO: Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

Job DescriptionDetails for the position are as follows: • 6-month contract to start with the strong possibility of extension or conversion depending on performance and business needs, • $60 hr, • Location: Cambridge, MA – 100% onsite, • Interview process: 1-hour virtual interview with a short scientific presentation and panel discussion, • Targeted Start date: November 16.Job Description:, • We are seeking a highly motivated, lab-based Biologist to join a collaborative, cross-functional team supporting small molecule drug discovery programs within Oncology. This 6-month contract position will focus on advancing drug discovery projects from early research concepts toward clinical candidates., • The ideal candidate will have strong hands-on experience with cell-based assays, assay development, and an understanding of compound mechanisms of action (MOA). This individual will be responsible for designing and executing experiments, developing and troubleshooting assays, and generating and interpreting data to better understand oncology target biology, compound activity, and potential biomarkers., • This role offers the opportunity to work across diverse oncology research projects and collaborate with scientists from multiple disciplines to support the identification and advancement of promising drug candidates., • Oncology Target Biology: Validate oncology targets using preclinical models, including cell lines and organoids, and develop derivative models using genetic approaches., • Cell-Based Assay Development: Develop, optimize, and troubleshoot cell-based phenotypic assays, including proliferation, survival, cell cycle, and apoptosis assays using 2D/3D culture systems and clonogenic formats., • Experimental Design & Execution: Design and conduct experiments to investigate compound mechanisms of action (MOA), evaluate biological responses, and identify potential biomarkers., • Laboratory Techniques: Utilize techniques such as Western blotting, ELISA, flow cytometry, RT-PCR, and high-content imaging to support experimental studies and biological characterization., • Data Analysis & Interpretation: Generate, analyze, and interpret experimental data to assess compound behavior, understand biological mechanisms, and support drug discovery decisions., • Scientific Communication & Collaboration: Present experimental findings and communicate results effectively with cross-functional project teams to support ongoing oncology research programs., • Documentation & Record Keeping: Maintain accurate and organized experimental records in accordance with laboratory best practices, including generating high-quality data to support AI applications and deployment.Required Skills:, • Bachelor’s or Master’s degree in biology or a relevant scientific field with 4-6 years post-graduation research experience, or PhD with 2+ years post-graduation research experience., • Strong understanding of compound mechanisms of action (MOA) and cellular responses to drug treatment., • Hands-on experience developing, performing, and troubleshooting cell-based assays., • Experience with experimental design, data analysis, and interpretation in a laboratory research environment., • Familiarity with molecular and cellular biology techniques such as Western blotting, ELISA, flow cytometry, RT-PCR, and high-content imaging., • Experience working with cell lines, 2D/3D cell culture systems, or organoids is highly relevant., • Ability to collaborate effectively with scientists across multiple disciplines and communicate scientific findings clearly., • Experience in oncology research or small molecule drug discovery is highly desirable.By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy

Job Description Direct Counsel is representing a prestigious AmLaw firm seeking a midlevel Intellectual Property Associate (1–5 years) to join its highly regarded Life Sciences Patent Prosecution practice. Locations: • Boston, • Chicago, • Houston, • Orange County (Costa Mesa), • Philadelphia, • San Francisco, • Seattle, • Silicon Valley, • Washington, D.C. This is an exciting opportunity for an attorney or patent agent with a strong scientific background and biotechnology patent prosecution experience to work with cutting-edge life sciences and emerging growth companies. Responsibilities • Handle sophisticated patent prosecution and IP counseling matters for innovative life sciences companies, • Advise clients in areas including:, • Antibodies, • DNA & RNA therapeutics, • Gene-editing technologies, • Chemical biology, • Molecular and cellular therapeutics, • Collaborate closely with emerging companies and scientific innovators on strategic intellectual property protectionQualifications, • 1–5 years of biotechnology patent prosecution experience, • Advanced degree required, preferably a Ph.D., in a life sciences discipline such as:, • Molecular Biology, • Immunology, • Biochemistry, • Cell Biology, • Related scientific fields, • USPTO Registration Number / Patent Bar membership required, • Strong academic credentials and excellent analytical, writing, and communication skillsCompensation Expected salary range in Massachusetts: $225,000 – $435,000, depending on experience, qualifications, and market factors. Comprehensive benefits package includes medical, financial, retirement, and paid leave benefits. If you are interested in this opportunity, please apply through directcounsel.net with your resume, law school transcripts, and cover letter.

Job Description About Avalyn Avalyn aims to transform the treatment paradigm for pulmonary fibrosis and other serious, rare respiratory diseases. The company is advancing optimized inhaled formulations of established antifibrotic medicines designed to deliver drug directly to the lungs, enhance local efficacy, and reduce systemic side effects. Avalyn's AP01 program is an optimized inhaled formulation of pirfenidone currently being evaluated in MIST, a global Phase 2b clinical trial in patients with progressive pulmonary fibrosis (PPF). AP01 has demonstrated encouraging safety and clinical activity across Phase 1b and an ongoing, multi-year open-label extension trial, with long-term data supporting the potential to preserve lung function while improving tolerability relative to historical oral pirfenidone. Avalyn's AP02 program is an optimized inhaled formulation of nintedanib currently being evaluated in AURA, a global Phase 2 clinical trial in patients with idiopathic pulmonary fibrosis (IPF). Avalyn is also advancing AP03, an inhaled fixed-dose combination of pirfenidone and nintedanib, designed to deliver multiple antifibrotic mechanisms through a single lung-targeted platform. By leveraging its proprietary drug-device approach and deep expertise in rare respiratory disease development, Avalyn aims to establish a new standard of care in pulmonary fibrosis through inhaled, lung-targeted therapies. For more information, please visit avalynpharma.com and follow the company on LinkedIn. Position Overview: The Associate Director, Nonclinical Development will serve as a key scientific contributor within the Translational Sciences organization, supporting the advancement of Avalyn's pipeline through pre-clinical and clinical development stages. This individual will contribute to integrated development strategies that leverage pharmacology, translational science, biomarkers, and nonclinical evidence packages to inform candidate progression, dose selection, regulatory submissions, and clinical development plans. Reporting to the VP, Translational Sciences, the role requires strong pharmacology expertise, excellent scientific judgment, and exceptional technical writing skills to effectively synthesize and communicate complex data to cross-functional teams, regulatory agencies, and external stakeholders. The successful candidate will be a highly collaborative partner with a focus on scientific rigor, operational excellence, and advancing program objectives in a dynamic small biotech environment. Key Responsibilities: • Apply pharmacology expertise to evaluate mechanism of action, target engagement, exposure-response relationships, and dose selection strategies across development programs, including inhalation programs and respiratory models., • Design and execute translational research strategies that connect nonclinical findings to clinical hypotheses for inhaled anti-fibrotic therapeutics., • Lead the planning, oversight, and interpretation of nonclinical studies designed internally and conducted through CRO partners, ensuring alignment with program objectives, timelines, and regulatory expectations., • Contribute to the development and oversight of nonclinical and clinical bioanalysis strategies and activities, as appropriate., • Identify and qualify translatable biomarkers that can be deployed in early clinical trials to assess target engagement and disease modification., • Partner with CMC, Clinical Pharmacology, Regulatory, and Biostatistics to integrate translational data into IND-enabling packages and clinical study design., • Author, review, and provide strategic input to regulatory documents, including IND submissions, investigator brochures, briefing documents, nonclinical overviews, and clinical development plans, applying strong scientific writing and communication skills., • Monitor external scientific and competitive landscapes to identify emerging opportunities, technologies, and development strategies relevant to respiratory diseases and broader portfolio objectives., • Evaluate nonclinical and clinical data to identify opportunities, risks, and key development decisions across the portfolio., • Present data and strategies at internal team meetings and external scientific conferences. Qualifications: • Ph.D. (or equivalent degree) in Pharmacology, Physiology, Pulmonary Biology, Biochemistry, or a closely related field is required., • A minimum of 7-10 plus years of relevant industry experience in translational sciences, nonclinical pharmacology, or related functions within biopharmaceutical drug development is required., • Demonstrated experience with inhaled drug delivery and/or respiratory pharmacology is highly preferred., • Deep knowledge of pulmonary fibrosis biology and relevant in vitro, ex vivo, and in vivo disease models is required; familiarity with complex signaling pathways is a plus., • Familiarity with biomarker strategy, including identification, qualification, and application in early-phase clinical trials., • Exceptional scientific writing skills with demonstrated experience serving as a primary author for regulatory submissions, development plans, study reports, investigator brochures, briefing books, and manuscripts., • Strong scientific communication skills; able to distill complex data for cross-functional audiences., • Collaborative and team-oriented with the ability to thrive in a fast-paced, small company environment. Proposed pay range $179,000—$202,000 USD

Job DescriptionRole Location: Waltham, MA The Company We are Alloy Therapeutics — a biotechnology ecosystem and Product Development Organization (PDO) empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. May the Best Drug Win. Alloy has evolved from a startup into a global product development organization operating 11 divisions across 5 research sites in 4 countries on 3 continents. Our model - Integrated Independence - combines centralized capabilities with entrepreneurial operating divisions. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. At Alloy, we have an ethos of "Mentorship-By-Apprenticeship" in all of our positions. We strive to have workers in the office when needed to interact organically and face-to-face. Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year. We respect and value our colleagues for their hard work that requires them to be in the lab every day. We ask our people who have more flexible accommodations to appreciate their colleagues who have less flexibility. We are all one team! About the Role at Alloy Therapeutics As Associate Director of Antibody Discovery Programs, you will play a key role in shaping and leading strategies for our antibody discovery initiatives. This position entails driving the discovery of novel antibody-based therapeutics, with special focus on multispecific antibodies. You will be accountable for scientific oversight of dozens of therapeutic programs every year by working collaboratively with a range of large pharma companies, emerging biotech companies and academic collaborators. A crucial aspect of this role involves providing a deep understanding of drug discovery projects to drive effective project strategies in collaboration with our partners. You will ensure executional excellence by evaluating scientific strategies, reviewing data in real time and making the necessary scientific adjustments to ensure a successful therapeutic discovery campaign. In addition, you will collaborate closely with project leaders overseeing the successful completion of project activities, accomplishing shared objectives, and meeting rigorous partner timelines. Another key accountability of this role is serving as a change agent to drive continuous improvement of ADS service offerings to achieve sustained operational efficiency. Strong communication skills are essential for this role, as you will interact with a diverse group of stakeholders both within and outside the company. You will also be accountable for high quality partner communication throughout the project life cycles, including drafting research proposals, updating project status and timelines, and presenting final deliveries. In parallel, you will provide regular project updates and presentations to internal stakeholders to ensure alignment with project goals and timelines and addressing any potential issues or concerns promptly. This role will report directly to the site head Antibody-Powered Division Waltham, MA, with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. How You’ll Drive Impact • Drive: Scientific direction and execution of multispecific antibody projects., • Innovate: Ensure the application of cutting-edge technologies and methodologies in antibody discovery projects., • Collaborate: Integrate protein engineering and cutting-edge efforts efficiently into product offerings and engage with external collaborators in discovery of biologics., • Deliver: Efficient execution of partner projects balancing quality, timelines, and costs, while ensuring successful completion of therapeutic discovery that meet our partners’ objectives., • Lead: Marshall, inspire, and mentor a cross-functional team of scientists. Lead by example by going the extra mile to ensure we are successful delivering on projects., • Communicate: Communicate effectively with key stakeholders externally and internally, fostering productive interactions both upward and downward, and across teams at different sites. Key Responsibilities • Accountable for scientific success of antibody discovery and multispecific engineering campaigns., • Drive major decisions, balance tradeoffs and resolve technical issues with a campaign., • Coordinate execution and partner relationship with alliance management and project management., • Lead process improvement initiatives across ADS functional areas., • Bring innovative scientific and technological solutions to increase business competitiveness. Qualifications • You have a PhD in a relevant scientific field (e.g. Biochemistry, Biotechnology, Biology) with a minimum of 6 years of industry experience in early drug discovery and development, or a master’s degree with 10+ years of relevant industry experience., • You have broad and deep experience with antibody discovery and engineering, especially yeast-display based methods., • You have a strong background in the design and optimization of antibody-based therapeutics., • You have a proven track record of successful execution and delivery of projects within scope, budget, and timeline., • You have demonstrated the ability to work in a fast-paced, dynamic environment and adapt to changing priorities and deadlines., • You have excellent communication skills, both written and verbal, with the ability to effectively communicate with stakeholders at all levels., • You have excellent leadership and team management skills, with the ability to motivate and mentor team members., • Ability to work across various US and international time zones., • Accommodate occasional travel as needed (10%). Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation • Competitive base and equity compensation commensurate with level of experience and independence, • 401(k) company matchHealth & Family, • Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered, • Company-paid disability (STD, LTD) and life insurance, • Paid parental leave, • Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)Unique Perks, • Unlimited PTO (paid time off) and flexible schedules, • Annual stipend for continuing education with commitment to your career through individualized professional development plan, • Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated range is $150,000 - $200,000, with the final offer based on factors like your experience, skills, and alignment with our needs. Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines. We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help. Alloy Therapeutics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status. If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at recruiting@alloytx.com. We will make every effort to respond to your request for disability assistance as soon as possible. Powered by JazzHR aJvokMMVe9

Job Description Job Title: Bench Scientist I Location: Cambridge, MA Type: Contract Compensation: $31-$36.55 Work Model: Onsite – onsite Hours: 40.0 Overview Leading pharmaceutical company looking for an entry level Bench Scientist I. Ideal candidates should have a bachelors degree with experience handling proteins, biological samples, cell cultures, or related laboratory materials. Responsibilities • Perform routine laboratory activities in support of molecular profiling and bioconjugation projects., • Handle, prepare, and work with proteins, biological samples, and cell culture materials., • Prepare solutions, buffers, and reagents following established protocols., • Execute experimental procedures with accuracy and attention to detail, including pipetting and sample preparation., • Support bioconjugation workflows under the guidance of senior scientists., • Receive, organize, track, and maintain laboratory materials, compounds, and inventory., • Assist with sample allocation, shipping, and general laboratory logistics., • Maintain accurate experimental records using electronic laboratory notebooks (ELNs)., • Analyze, summarize, and communicate experimental data through reports and presentations., • Follow laboratory safety procedures and maintain a clean and organized work environment., • Collaborate effectively with cross-functional team members to support project goals. Requirements, • Bachelor's or Master's degree in:, • Biochemistry, • Biology, • Biotechnology, • Molecular Biology, • Chemical Biology, • Biomedical Sciences, • Or a related scientific discipline, • Hands-on laboratory experience gained through academic research, internships, industry, or other research environments., • Experience handling proteins, biological samples, cell cultures, or related laboratory materials., • Knowledge of fundamental laboratory techniques and scientific principles., • Strong organizational skills and attention to detail., • Excellent verbal and written communication skills., • Demonstrated ability to learn new techniques quickly and work effectively in a fast-paced environment. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

Job Description Repertoire Immune Medicines is a clinical-stage biotechnology company harnessing the power of the human immune system to develop transformative therapies for cancer and autoimmune disease. Using its proprietary DECODETM platform—which maps the immune synapse between T cell receptors (TCRs) and their antigen targets—Repertoire translates unique biological insights into potent and targeted off-the shelf immune medicines. The company integrates deep protein engineering expertise with artificial intelligence, powered by a proprietary DECODE database of over one billion TCR-antigen interactions, to accelerate discovery and optimize drug candidates. From its sites in Watertown, Massachusetts and Zurich, Switzerland, Repertoire is advancing a pipeline of T cell-targeted immunotherapies with the potential to address a broad range of cancers and autoimmune disorders. The company’s lead oncology program, RPTR-1-201, a TCR bispecific, has initiated a Phase 1/2 clinical trial across multiple solid tumor indications. Repertoire plans to advance additional TCR bispecific therapies into clinical trials over the next 12-18 months. In autoimmune disease, Repertoire is partnering with leading pharmaceutical companies to develop mRNA tolerizing therapies designed to selectively expand regulatory T cells and reset the immune system. Repertoire was founded in 2019 by Flagship Pioneering and is supported by a strong investor base. The DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. Role Overview Repertoire Immune Medicines is seeking a Senior Bioinformatics Engineer to join our Computational Engineering team and help power the discovery of transformational immune medicines from our growing immune synapse database. As one of a small group of high-impact engineers, you will make extensive proprietary datasets discoverable, trustworthy, and ready for internal analysis at scale. This position offers a rare opportunity to contribute end-to-end across the protein therapeutic pipeline, from target discovery & screening through pre-clinical development and clinical trial analyses. This role is ideal for a self-motivated engineer who takes pride in building systems that are correct, reliable, and built to last. Key Responsibilities • Build and operate bioinformatics pipelines from instrument to data ecosystem using workflow orchestration and containerized execution., • Build durable data platforms that support data discovery by exposing data through clean, well-documented internal APIs, applications, and SQL databases., • Provision and manage cloud infrastructure as code with secure engineering practices that keep systems robust, safe, and maintainable., • Own engineering standards for the team including CI/CD test automation, version control, and design and review practices that keep systems maintainable as the team grows., • Lead incident reviews and preventative improvements to diagnose the root cause of failures and build safeguards that prevent recurrence with verifiable gating mechanisms., • Own end-to-end data processing and delivery to support scientific decision making around the organization., • Develop agentic workflows and harnesses for developing bioinformatics pipelines.Qualifications/Experience, • Bachelor’s or Master’s degree in computer science, software engineering, bioinformatics, or related coding-heavy majors, with 5+ years of work experience within the biology domain., • Proven experience building/operating production data systems or pipelines (bioinformatics, data engineering, platform/SRE, or ML infrastructure; Postgres and S3-backed data storage)., • Hands-on with containers (Docker or Podman) and cloud infrastructure, ideally including infrastructure-as-code (AWS: ECS Fargate, EC2, S3, EFS, Step Functions, IAM, VPC, CDK)., • Exposure to workflow/orchestration (Step Functions and Nextflow/Snakemake) and event‑driven patterns., • Ability to partner with ML/Comp Bio and Lab Platform users; clear written and verbal communication with non-engineers; product/UX instincts for scientific users (FastAPI, React/Typescript)., • Intellectual curiosity, scientific rigor, and enthusiasm for working in a fast‑paced, evolving research environment.Preferred Qualifications, • Bioinformatics breadth spanning sequencing, mass spec and imaging, including NGS formats (FASTQ, BAM/CRAM) and specific pipeline experience (Cell Ranger, RNA-seq tooling, HLA typing)., • Familiarity with protein language models, protein structure prediction, and molecular dynamics simulation., • SSO/OAuth integration; observability tooling (CloudWatch)., • SOC2/ISO27001/GxP exposure., • Agentic coding fluency – the ability to structure and direct AI coding tools effectively., • Exposure to enabling ML scientists (artifact stores/registries, dataset versioning).Compensation and Benefits The base salary for this role ranges from $160,000 to $185,000 and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k)-retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future. Repertoire is committed to building an inclusive culture. Much as the power of the immune system lies in the diversity of T and B cells, we believe our best work comes from a diverse workforce—and we are committed to pursuing that in all facets of the work experience. Repertoire is proud to be an Equal Opportunity Employer. Recruitment & Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto. Powered by JazzHR GWC6p7rbcK

Job Description Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Marine Biologist! A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is looking for Marine Biologists (At-Sea Monitors) to work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Northeast Fisheries Science Center (NEFCS) aboard commercial fishing vessels. The primary goals of Northeast federal fishery observation programs are to provide quantitative biological, vessel, and gear-selectivity information for various New England and Mid-Atlantic fisheries. The At-Sea Monitor program focuses specifically on the groundfish industry, a grouping of fish that includes many commonly consumed fish such as cod, haddock and various flounder species. Each fishery observer or monitor operates on commercial fishing vessels operating in ports throughout New England and the Mid-Atlantic. If you ever wanted to make a difference, this is how. Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between fishermen and fisheries management scientists like yourself. In order to facilitate that cooperation, marine biologists collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen. Commit to the journey! Click to Learn More about Becoming a Fisheries Observer At-Sea Monitors record detailed information on the gear and fishing activity of the vessels. Monitors work on deck on vessels ranging from 20’ to 100’ on trips roughly ranging from 1 to 14 days collecting data on fish catch and discard and incidental takes such as marine mammals, seabirds, and marine turtles. After attending a 3-week paid training in-person training in Falmouth, MA monitors are deployed from ports throughout New England and Mid-Atlantic states. Gear types assessed include, trawl, gillnet, longline and handline. Accommodations and meal reimbursement during in person session of training are provided. Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety. This is a challenging job, and candidates must be mentally prepared to be away from home for multiple days, and must be physically able to handle heavy lifting, working odd hours, and long days in rough seas. Observing provides an excellent career in marine biology, as observers and monitors are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs. Compensation: Monitors’ starting pay is $19.00/hour. Dependent on enrollment in our H&W benefit, biologists may also be eligible for an additional $4.57/hour for the first 40 hours worked on each calendar week for a total of $23.57 hour. This is a full–time position with benefits. Annually, monitors earn between $35K - $55K a year dependent on their availability to deploy offshore and their personal sea day accomplishments. Monitors will be paid a minimum of 12 hours for each calendar day offshore and are also eligible for additional compensable activities while on land. AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits. Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus. Travel is reimbursed at an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate. Minimum Qualifications: • High school diploma is required., • Experience with data entry on computers., • Monitor candidates must be U.S. citizens, or be legally authorized to work in the U.S., • Candidates must be physically able, as determined by a licensed physician’s certification to perform observer duties., • Your own transportation is required., • Candidates are expected to commit to the program for at least one year. Preferred Qualifications: • Bachelor's degree in biology or a related field from an accredited college or university with 30 credits of biology coursework, 6 credits of marine science is preferred., • At least one undergraduate course in math or statistics preferred., • At-sea experience, • Coursework in Dichotomous Keys, • Experience collecting Field Data and entering databases. Locations: • Applicants must be currently living or be willing to live within 50 miles of Boston, Ma. Contact: If you would like to apply for one of these exciting new openings, please click the following link Careers Page to submit the following information. • Resume, • Cover Letter detailing sea and fish experience., • 3 to 5 academic/professional references (name, email address and phone number), • Unofficial copies of your college (or high school if applicable) transcripts. All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to the Talent Team or 774-770-5833 An Equal Opportunity Employer It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law. Must be able to work in the U.S. • VEVRAA Federal Contractor • Request Priority Protected Veteran Referrals • Equal Opportunity Employer

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Our Services and Objectives Human Cells, Tissues, and Cellular and Tissue-Based Products Testing. We all share a concern for the safe and compatible transplant of donor organs and tissues. That concern translates into testing donor specimens using FDA approved screening kits and reporting data that confirms the release to transplant. Eurofins Donor & Product Testing sets itself apart by its commitment to its customers and its quality of performance. By providing an array of service offerings, Eurofins Donor & Product Testing delivers consistent performance that exceeds our clients' expectations. Duties and Responsibilities • Following prescribed procedures, performing any of the tests within any of the laboratory specialties, calculating the results of the tests performed as necessary, • Operating, calibrating, conducting performance checks, and maintaining any laboratory analyzers or equipment, • Recognizing and correcting basic analyzer malfunctions; notifying management personnel when appropriate, • Preparing reagents or media from a prescribed procedure, • Evaluating media, reagents, and calibrators according to established criteria, • Conducting established quality control procedures on analytical tests, equipment, reagents, media, and products; evaluating results of quality control and implements corrective action when indicated, • Determining performance specifications for new methods, • Performs instrument maintenance, QC reagents and kits, • Performs routine testing including assay validations, • Confirming and verifying results through knowledge of techniques, principles, and analyzers, • Monitoring quality assurance/continuous improvement programs, • Monitoring safety programs in compliance with laboratory regulations, • Utilizes laboratory information systems or other methods to accurately and effectively report patient results, • Review and follow Standard Operating Procedures, • Reporting test results conforming to established procedures, • Supports Eurofins DPT’s business philosophy, leadership values, and ethics, • In order to meet Eurofins DPT’s quality policy and objectives, all employees are expected to meet basic expectations of Eurofins DPT’s quality management system including, but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, and accurate recordkeeping.Qualifications Minimum Educational Requirements • Bachelor’s degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution, • If required by the State in which the laboratory is located, the appropriate State License to perform clinical laboratory testing Work Experience Requirements • 0-2 years of related experience, • Knowledge of the principles, methods, materials, equipment, and techniques of medical technology, • Knowledge of the principles of chemistry, biology, and bacteriology as related to medical technology, • Knowledge of recent developments in the field of medical technology, • Ability to perform assigned tasks according to prescribed procedures and to make accurate observations and records of tests results, • Skill in the use of medical laboratory equipment, • Strong communication skills & analytical thinking, • Performs instrument maintenance, • Performs freezer, refrigerator, and incubator maintenance, • Performs QC reagents needed for patient testing, • Competent to perform routine testing for many tests performed within the department Potential Environmental Factors • This laboratory carefully maintains all hazardous materials. All employees must abide by Eurofins DPT’s Safety and Exposure procedures. This includes using the provided safety clothing and equipment., • For a list of potential chemical hazards, see appropriate SDS sheet. Additional Information Compensation: • $26-$28 per hour Schedule: Wednesday – Saturday ~ 10:00pm-8:30am What we offer: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today! Job Description We are seeking a process development scientist to join the messenger-RNA (mRNA) process development team. The successful candidate will be contributing to early and operational tech development. In this role, the successful candidate will be responsible for production and analysis of RNA constructs and carrying out preparative and purification chromatography. • Perform in vitro transcription (IVT) and purification (chromatography, tangential flow filtration) experiments., • Perform analytical methods including but not limited to capillary gel electrophoresis (CGE), Akta chromatography, HPLC, and ELISA., • Process the data and provide data summaries to team members and key stakeholders., • Prepare buffers, reagents, and stock solutions used for process development activities, following established recipes and SOPs., • Maintain an updated lab notebook, order materials, maintain lab equipment, and support equipment troubleshooting as needed., • Uphold lab safety to the highest level of standards.Qualifications Basic Minimum Qualifications: • B.S. degree in chemistry, chemical engineering, or biochemistry (or related field) with 1+ years of relevant laboratory experience, or M.S. degree in chemistry, chemical engineering, or biochemistry (or related field) with at least 6 months of relevant laboratory experience., • Experience with molecular biology and RNA biochemistry methods including IVT, • Experience with tangential flow filtration (TFF), capillary gel electrophoresis (CGE), Akta chromatography, HPLC, and ELISA., • Experience with good documentation practices and electronic lab notebooks such as Benchling., • Unwavering commitment to safety protocols and procedures., • Strong attention to detail, organizational, and time-management skills., • Excellent written and verbal communication, work planning, data analysis, problem-solving, and critical thinking skills., • Ability to learn new techniques, perform multiple tasks simultaneously, follow SOPs, and comply with company policies., • Ability to work independently and as part of a team, inquisitive, self-motivated, and enthusiasm to learn and contribute in a fast-paced environment., • Authorization to work in the United States indefinitely without restriction or sponsorship. Preferred Qualifications: • Experience developing processes for RNA-LNP, protein, mAB, or AAV therapeutics or vaccines (experience with RNA therapeutics is preferred). Additional Information Position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply. Excellent full-time benefits include: • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • Eligibility for yearly goal-based bonus & merit-based increases, • Compensation: $32.00-$41.00 per hour based on education and related experience Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description The Opportunity Precede Biosciences is seeking a hands-on Associate Director of Regulatory Affairs to lead regulatory strategy and execution for our products and companion diagnostic programs developed with biopharma partners. This is a senior individual contributor role with broad influence across the organization. You will own submissions from strategy through approval, serve as the regulatory lead on cross-functional and partner teams, and translate complex analytical, clinical, software, and bioinformatics evidence into clear regulatory positions. The role is well suited to someone who combines sound judgment with the willingness and ability to draft the work directly. About Precede Biosciences We are pioneering an advanced, minimally invasive, comprehensive epigenomics platform with the potential to profoundly impact the research and development of new medicines and the use of approved medicines in clinical practice across a number of conditions, including cancer. More information on our company and platform can be found on our company website and in our seminal publication in Nature Medicine. We care deeply about creating a place where folks can do their best work from the start and have intentionally created an environment that is defined by purpose, teamwork, and excellence. This means nurturing team spirit, facing challenges together, collaboratively solving complex problems, while also ensuring a strong focus on individual initiative, accountability, and delivery. What You Will Do • Lead regulatory strategy. Develop and execute US and global IVD regulatory strategies from early development through commercialization, including pathway, intended use, claims, evidence, and sequencing of agency interactions., • Own submissions end to end. Author, compile, and drive high-quality submissions and responses, including FDA Pre-Submissions, IDEs, 510(k)s, De Novo requests, PMAs and supplements, and relevant international technical documentation (e.g. in support of IVDR CE)., • Represent Precede with regulators. Lead interactions with FDA and other health authorities or notified bodies, prepare teams for meetings, and convert agency feedback into clear decisions and development plans., • Guide companion diagnostic programs. Serve as the regulatory lead for biopharma collaborations, aligning diagnostic and therapeutic development plans, clinical trial assay readiness, evidence generation, filing strategy, and labeling considerations., • Shape development plans. Partner with assay development, computational biology, laboratory operations, quality, and program teams to define analytical and clinical performance studies that support the intended use and proposed claims., • Ensure submission-ready evidence. Critically review protocols, reports, and technical documentation, including pre-analytical variables, specimen stability, analytical validation, software V&V, clinical performance, and bridging studies, to ensure conclusions are accurate and well supported., • Set expectations and regulatory requirements for IVDs, including software and bioinformatics. Define regulatory requirements for IVD product(s), including software, algorithms, and bioinformatics pipelines used in regulated products or in data supporting diagnostic and therapeutic submissions., • Embed regulatory requirements in the quality system. Contribute to design and development controls, risk management, document control, and audit and inspection readiness in alignment with FDA's Quality Management System Regulation, ISO 13485, ISO 14971, and CLIA and CAP requirements as applicable., • Assess changes and communications. Evaluate product, design, software, manufacturing, and labeling changes for regulatory impact, and review product communications and Research Use Only claims for compliance., • Manage regulatory risk. Interpret evolving requirements, identify risks early, and recommend practical, science-based paths that protect patients, program objectives, and business prioritiesWhat You Bring, • Bachelor's degree in life sciences, engineering, or a related field., • At minimum of 8 years of regulatory affairs experience in medical devices, including substantial experience with IVDs and increasing responsibility for regulatory strategy and submissions., • A demonstrated record of leading and authoring substantial portions of FDA IVD submissions. Direct experience with at least one major premarket pathway, such as 510(k), De Novo, or PMA, is required., • Strong knowledge of US and EU IVD requirements, design and development controls, risk management, and quality system expectations, with the ability to apply requirements to complex scientific and technical questions., • Experience with molecular diagnostics, NGS-based assays, or other complex diagnostics that combine laboratory processes, software, algorithms, and bioinformatics., • Ability to interpret analytical and clinical performance data and determine whether the evidence supports an intended use, claim, or regulatory position., • Excellent technical writing and communication skills, including the ability to explain complex issues clearly to regulators, partners, scientists, and senior leaders., • Sound judgment and comfort operating in a growth-stage environment, balancing strategic direction with hands-on execution and managing multiple priorities with limited oversight. Preferred Experience, • Companion diagnostic development, particularly oncology programs and coordination of diagnostic and therapeutic regulatory strategies from clinical development through approval., • Liquid biopsy, epigenomics, oncology diagnostics, or biomarker-driven drug development., • Global IVD registrations, including familiarity with the European Union In Vitro Diagnostic Medical Devices Regulation and technical documentation expectations., • Regulatory oversight of software and bioinformatics lifecycle documentation for complex diagnostic products., • An advanced scientific degree or Regulatory Affairs Certification. The expected salary range for this role is $175,000 to $220,000 per year. Final compensation will reflect the candidate's qualifications, experience, and geographic location. Employees are also eligible for a performance bonus, equity participation, and comprehensive health benefits. We believe in building an inclusive and balanced team, and we know that strong candidates may not meet every qualification listed. If this opportunity interests you, we encourage you to apply. Precede Biosciences is an equal opportunity employer. We do not discriminate based on race, color, religion, national origin, age, sex, sexual orientation, gender identity, marital status, ancestry, physical or mental disability, veteran status, or any other status protected by applicable law. Precede Biosciences does not accept unsolicited resumes from recruitment agencies or external recruiters. No fees will be paid for unsolicited submissions. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description Blood Bank Laboratory Supervisor Location: Boston, MA Schedule: Monday–Friday, 3:00 PM – 11:30 PM, rotating weekends Compensation: $90,000–$120,000 annually + $15,000 Sign-On Bonus About the Opportunity A respected healthcare organization in the Boston area is seeking an experienced Blood Bank Laboratory Supervisor to oversee daily operations within a high-volume transfusion services department. This leadership opportunity is ideal for a skilled laboratory professional who enjoys mentoring staff, optimizing workflows, and ensuring the delivery of high-quality patient testing services. The successful candidate will bring strong technical expertise, prior leadership experience, and a commitment to regulatory compliance and operational excellence. Key Responsibilities • Supervise the daily operations of the Blood Bank department., • Ensure laboratory testing is performed accurately and results are reported in a timely manner., • Train, mentor, and provide ongoing support to laboratory personnel., • Monitor workflow and staffing levels to ensure adequate coverage across all shifts., • Coordinate scheduling and assist with workforce planning., • Investigate and resolve technical, quality, and production-related issues., • Drive continuous improvement initiatives focused on efficiency, quality, and service levels., • Oversee quality control activities and ensure proper instrument maintenance., • Maintain quality assurance documentation and regulatory records., • Evaluate new procedures, technologies, and process improvements., • Conduct regular performance discussions and provide coaching to direct reports., • Perform bench work as needed while maintaining technical competency., • Ensure compliance with all applicable federal, state, accreditation, and laboratory regulations., • Assist with policy implementation, payroll processing, personnel documentation, and other administrative functions. Qualifications • Associate degree in Clinical Laboratory Science, Medical Technology, Biology, Chemistry, or a related scientific discipline required; Bachelor's degree preferred., • Minimum of five (5) years of clinical laboratory experience as a Medical Technologist, Medical Laboratory Scientist, or Laboratory Technician., • Previous Lead, Senior Technologist, or Supervisory experience strongly preferred., • ASCP or AMT certification preferred., • Strong knowledge of Blood Bank operations and regulatory requirements, including CLIA, CAP, and applicable state regulations., • Experience with Laboratory Information Systems (LIS) and Microsoft Office applications., • Excellent leadership, communication, and interpersonal skills., • Strong organizational abilities with exceptional attention to detail., • Ability to make sound decisions in a fast-paced and evolving environment., • Capable of meeting the physical demands associated with a clinical laboratory setting. Compensation & Benefits • Competitive salary based on experience, education, certifications, and market factors., • $15,000 sign-on bonus available for qualified external candidates., • Comprehensive benefits package including:, • Medical, Dental, and Vision Insurance, • Life Insurance, • Short-Term and Long-Term Disability Coverage, • 401(k) Retirement Plan, • Paid Time Off, • Tuition Reimbursement, • Employee Stock Purchase Program About us: At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 19 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories. It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities. If at any time during the application process, you need an accommodation, please contact recruiting@lighthouselabservices.com for assistance. Lighthouse Lab Services | 844-974-1929 | lighthouselabservices.com #LLS3

Job Description About GrapheneDx: GrapheneDx is a new diagnostics technology company with a mission to transform consumer diagnostics. Our employees gain experience in a multidisciplinary, fast-paced start-up and have ample opportunities to acquire new skills, engage with emerging technologies, and collaborate closely with an accomplished team, all within in a supportive and energetic environment. GrapheneDx offers a competitive compensation package including base salary, performance bonuses, paid time off, health and dental benefits, and excellent growth opportunities. GrapheneDx is seeking a Research Scientist who will apply their expertise to advance our R&D efforts in biosensor development and communicate valuable insights to a highly collaborative and dynamic team. Summary: The Research Scientist in Assay Development will design and execute experiments to functionalize sensors with nucleic acid or antibody probes for biomarker detection, contributing to the development of a groundbreaking, point-of-care diagnostic platform. Collaborating closely with a senior scientist and a cross-functional team of materials scientists, electronics engineers, and data scientists, this role drives forward a disruptive diagnostic technology poised to redefine the field. Key Duties and Responsibilities: • Drive the development of a novel GFET-based point-of-care diagnostic platform., • Design, execute, and optimize experiments for biomarker detection, including feasibility, pilot, and process optimization studies., • Perform data analysis, critically interpret results, and prepare reports and presentations tailored to the needs and expertise of internal and external stakeholders., • Collaborate with a cross-functional team of scientists and engineers to design experiments aligned with R&D objectives, ensuring sensor technology integration into scalable diagnostic solutions., • Document, refine, and optimize protocols, creating actionable plans to improve processes and advance R&D milestones, • Identify and troubleshoot technical challenges, contributing to regulatory documentation, and ensure protocol compliance where relevant. Essential Experience: • Ph.D. in Biochemistry, Biology, Chemistry, Electrochemistry, Biophysics, or a related discipline, or a Master’s degree with 1-5 years of relevant academic or industry experience., • Proven experience in creating and developing biosensor immunoassays and/or nucleic acid detection assays through probe hybridization., • Strong problem-solving skills, with the ability to identify challenges and propose alternative approaches., • Excellent organizational and analytical skills, including the ability to summarize and translate data into actionable plans., • Effective oral and written communication skills to convey technical information to both supervisors and team members. Desirable Experience: • Experience with non-optical-, electrical-, or electrochemical-based sensors, especially graphene-based or carbon nanotube-based sensing platforms., • Experience functionalizing GFETs with biological probes, such as nucleic acids or antibodies, to enable biomarker detection., • Experience defining and improving biosensor performance metrics, such as sensitivity, specificity, limit of detection (LOD), and other industry-standard used to quantify biosensor efficacy and reliability., • Proficiency in coding or data visualization using Python, Origin, and/or Minitab for data analysis and visualization.

Job Description About the Company We are a seed-stage biotech company currently operating in stealth, leveraging cutting-edge AI to transform the discovery, development, and delivery of biologics. We are backed by leading venture capital investors and supported by world-class advisors. We are assembling a team to join us as we tackle the hardest problems in drug design. About the Role We are seeking a motivated and detail-oriented Research Associate to join our team, with a primary focus on recombinant protein expression and purification. This is a fast-paced startup environment where the ability to work efficiently and independently is essential. We are looking for someone who is proactive, resourceful, and comfortable navigating the demands of a dynamic research setting. In this role, you will be integral to our protein production pipeline, supporting the expression, purification, and biochemical characterization of proteins in bacterial systems, and contributing to cutting-edge research alongside a collaborative and driven team. You will work closely with senior scientists to advance research goals, maintain rigorous data records, and contribute to experimental design and troubleshooting. This is a full-time, on-site position based in Cambridge, MA. Responsibilities Support recombinant protein expression and purification efforts in E. coli, including construct design, expression screening, and purification via affinity and other chromatography methods Perform analytical assays to characterize protein quality and binding activity, including Bio-Layer Interferometry (BLI), SDS-PAGE, and spectroscopy Execute standard molecular biology techniques including PCR, cloning, plasmid preparation, and DNA purification Maintain accurate, well-organized records of experimental protocols, results, and data in Benchling or equivalent electronic lab notebook platforms Assist in experimental planning and troubleshooting in collaboration with senior scientists Contribute to the optimization and scale-up of protein production workflows Communicate results clearly to the broader team through written reports and team meetings Required Qualifications Bachelor's degree in biochemistry, biology, biotechnology, biophysics, chemical engineering, or a related field 2+ years of hands-on experience in recombinant protein expression and purification in an academic or industry setting Proficiency with bacterial (E. coli) protein expression systems and downstream purification using affinity chromatography (e.g., Ni-NTA) Familiarity with analytical and biophysical methods for protein characterization, such as SDS-PAGE, FPLC, and spectroscopy Experience managing experimental data in an electronic lab notebook, particularly Benchling Highly organized and detail-oriented, with strong communication skills and the ability to work both independently and collaboratively Preferred Qualifications Hands-on experience with Bio-Layer Interferometry (BLI) for binding kinetics analysis Experience with protein expression in additional systems such as yeast (P. pastoris or S. cerevisiae) or mammalian cell expression platforms Familiarity with Python or other scripting languages for data analysis and automation Experience with high-throughput expression screening in multi-well plate fo We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description About Avalyn: Avalyn aims to transform the treatment paradigm for pulmonary fibrosis and other serious, rare respiratory diseases. The company is advancing optimized inhaled formulations of established antifibrotic medicines designed to deliver drug directly to the lungs, enhance local efficacy, and reduce systemic side effects. Avalyn's AP01 program is an optimized inhaled formulation of pirfenidone currently being evaluated in MIST, a global Phase 2b clinical trial in patients with progressive pulmonary fibrosis (PPF). AP01 has demonstrated encouraging safety and clinical activity across Phase 1b and an ongoing, multi-year open-label extension trial, with long-term data supporting the potential to preserve lung function while improving tolerability relative to historical oral pirfenidone. Avalyn's AP02 program is an optimized inhaled formulation of nintedanib currently being evaluated in AURA, a global Phase 2 clinical trial in patients with idiopathic pulmonary fibrosis (IPF). Avalyn is also advancing AP03, an inhaled fixed-dose combination of pirfenidone and nintedanib, designed to deliver multiple antifibrotic mechanisms through a single lung-targeted platform. By leveraging its proprietary drug-device approach and deep expertise in rare respiratory disease development, Avalyn aims to establish a new standard of care in pulmonary fibrosis through inhaled, lung-targeted therapies. For more information, please visit avalynpharma.com and follow the company on LinkedIn. Position Overview: The Senior Manager, CMC Technical Writing will author, coordinate, and manage high-quality scientific and technical documentation supporting Avalyn's CMC and product development programs. Reporting to the Sr. Director, Product Development, this individual will work closely with internal technical functions, Regulatory Affairs, Quality, and external partners to ensure development activities, data, decisions, and conclusions are documented clearly, accurately, and consistently. This hands-on role is suited for an experienced scientific or technical writer who can translate complex CMC, pharmaceutical development, and drug-device combination product information into concise, traceable, and scientifically defensible documents that support program knowledge management, regulatory readiness, and submission deliverables. The successful candidate will bring a strong scientific foundation, excellent writing discipline, and the ability to work effectively with subject matter experts to convert technical input into well-structured documents. This role requires sound judgment, attention to detail, and the ability to manage multiple documents and timelines in parallel while maintaining high standards for accuracy and completeness. Key Responsibilities: Development & Technical Report Writing • Lead planning, authoring, review coordination, revision, and finalization of CMC technical development reports and source documents for the drug substance, drug product and device components., • Prepare integrated reports covering formulation, analytical, aerosol characterization, device, manufacturing process, technology transfer, and other CMC development activities., • Work with subject matter experts to synthesize data, development rationale, conclusions, and decisions into accurate, cohesive, and scientifically defensible narratives., • Take ownership and drive documents through structured planning, drafting, cross-functional review, quality control, approval, and finalization while maintaining alignment with program timelines., • Develop clear document outlines, tables of contents, data presentation plans, and review strategies to support efficient drafting and alignment with stakeholders., • Ensure technical documents capture the appropriate development history, rationale, critical assumptions, key findings, limitations, conclusions, and recommended next steps. Cross-Functional Documentation Support • Partner with internal functions and external development partners, including CDMOs, contract laboratories, device partners, and consultants, to obtain and integrate information required for technical documentation., • Support consistent document organization, templates, terminology, and standards to improve knowledge transfer and regulatory readiness., • Facilitate document review meetings, reconcile reviewer comments, and help drive resolution of technical questions or inconsistencies that arise during review., • Maintain effective communication with project teams to ensure technical writing deliverables are prioritized, appropriately resourced, and aligned with program milestones. Regulatory Writing Support • Lead and support CMC content development for regulatory submissions and health authority interactions, including INDs, IMPDs, CTAs, briefing packages, regulatory responses, Master Validation Plans, and related submission content, in partnership with Regulatory Affairs and CMC subject matter experts., • Ensure consistency and traceability between development reports, source documentation, and regulatory submission content., • Contribute to preparation of source documentation that supports future regulatory modules, responses to health authority questions, and internal decision-making., • Review CMC and product development content for clarity, consistency, completeness, and alignment with established regulatory strategy and internal standards. Qualifications: • A minimum of a Bachelor's degree in Chemistry, Pharmaceutical Sciences, Engineering, Biology, or a related scientific or technical discipline required; Advanced degree (e.g., MS, PharmD, PhD or equivalent) preferred., • A minimum of 5-7+ years of experience in pharmaceutical, biotechnology, drug-device combination product, or related life sciences development, with significant experience preparing scientific, technical, or CMC documentation., • Demonstrated ability to independently author complex CMC, pharmaceutical development, or combination-product technical reports., • Experience authoring and reviewing Design History File (DHF) documentation for drug-device combination products is considered a strong asset., • Strong understanding of pharmaceutical development, including one or more of the following: formulation, analytical, process, manufacturing, device, or combination-product development., • Experience with inhaled products, drug-device combination products, late-stage clinical development, CDMOs, contract laboratories, or external partners is highly desirable., • Excellent written and verbal communication skills, with strong attention to scientific accuracy, data integrity, consistency, traceability, and detail., • Strong organizational and document management skills, with the ability to manage competing priorities, multiple document workflows, stakeholder input, and collaborative review processes; proficient in Microsoft Word, document templates, reference management, and quality control., • Scientific curiosity, attention to detail, and sound judgment, with the ability to ask effective questions, clarify technical information and assumptions, and balance technical depth, readability, accuracy, and fit-for-purpose documentation., • Collaborative and proactive working style, with the ability to influence without direct authority, effectively engage subject matter experts, and keep contributors aligned on document objectives, timelines, and deliverables., • Ability to work independently and collaboratively in a fast-paced biotechnology environment with changing priorities. Proposed pay range $150,000—$176,000 USD

Job Description Nanopath is developing a first-in-class in vitro diagnostics platform to transform how diseases are diagnosed. We aim to replace lengthy molecular testing workflows by bringing rapid, high-quality diagnostics closer to the patient. Our mission is to improve patient outcomes – starting with women – through a purpose-built platform that delivers actionable results within a single office visit. The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. We are collectively committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social – is at the forefront of our decision making. About the Role • Support and manage a variety of assay development tasks. We are happy to tailor key responsibilities to the candidate ranging from molecular biology, cell culture, biomanufacturing, and bioinformatics., • Participate in critical team discussions, meetings, and presentations. Our co-ops are given critical and important projects!, • Work directly with our tight-knit team of scientists and engineers to drive our product forward., • Learn more about cutting edge biophysics and interdisciplinary medtech development. Qualifications: • Ability to commit to 15+ weeks of full-time and onsite work in Cambridge, MA, • Current enrollment in a relevant academic program – we are open to undergraduate and graduate degree opportunities, • Sophomore or above with demonstrated experience through past internships or research projects, • Excellent communication and presentation skills, highly organized with demonstrated curiosity, scientific rigor and creative problem-solving, • Proactive self-starter with eagerness to adapt to a fast-paced, dynamic startup environment, • Passion for technology translation and willingness to shape Nanopath's future This is a full-time onsite role in Cambridge, MA starting in early January, lasting no less than 5 months. Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles! Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Senior Manager Regulatory Affairs, Global Reg Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. The Senior Manager assures that regulatory strategies defined within the GRPT, are effectively implemented and maintained in line with changing regulatory and business needs.This individual identifies and gathers data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured or distributed to meet relevant US and Canada regulatory requirements. Responsibilities: • Responsible for a product(s) or products with multiple driver indications within a Therapeutic Area and supports the Manager (Global Regulatory Lead (GRL), Associate Director, or Director), in the development & execution of the regulatory strategy. Assigned matters may have a moderate impact on business activities and operations., • Serves as HA liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation and completion of FDA meeting briefing packages and responses. Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial., • Functions independently in negotiation and decision-making for project related issues that have crossfunctional impact. Assists in the development,training of staff members., • Key contributor responsible for the preparation and review of regulatory submissions consistent within US and Canada regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review., • Supports the regulatory submission and approval process. Broadly applies regulatory/technical knowledge of government regulations and skills across therapeutic areas., • Recommends and implements changes to difficult projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidances, as well as corporate policies and management-related considerations., • Presents pertinent regulatory information to appropriate cross-functional areas., • Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP)., • This role will work a hybrid work schedule (3 days in office, 2 days remotely) from our Lake County, IL; Florham Park, NJ, Cambridge, MA; or Irvine, CA AbbVie headquarters. Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required Qualifications • Required Education: Bachelor’s degree (pharmacy, biology, chemistry, pharmacology) or industry related., • Preferred Education: Advanced Degree a plus. Certifications a plus, • Required Experience: Minimum of 6 years of experience in regulatory affairs, research and development, or a related pharmaceutical industry field, including at least 2–3 years of experience performing pharmaceutical regulatory activities., • Demonstrates excellent negotiation skills, problem solving skills and builds consensus., • Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization., • Able to deliver challenging messages effectively without compromising important business relationships., • Proven skill at implementing successful US and Canada regulatory strategies regulatory strategies., • Experience working in a complex and matrix environment., • Global regulatory experience is a plus., • Experience interfacing with government regulatory agencies. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionDescription: PHLEBOTOMY MANAGER, INPATIENT Salary Range: $83,000 - $120,500 | Boston, MA YOUR HEARTLINE STAFFING CONTACT Elizabeth Banzhaf, LPN | Chief Operating Officer Heartline Staffing Call/Text: 272-230-3157 Email: elizabeth@heartlinestaffing.com LinkedIn: Connect with Elizabeth COMPENSATION & BENEFITS Salary Range: $83,000 - $120,500 Signing Bonus: No Relocation Package: None Benefits listed in the requisition: • Medical insurance, • Dental insurance, • Vision insurance, • Life insurance, • Retirement, • Equity, • Paid time off, • Other benefits (not specified) LOCATION & SCHEDULE Location: Boston, Massachusetts 02118 Work Arrangement: In-Person Department: Phlebotomy Inpatient Schedule: 40 hours Call Coverage: 24/7 Travel Required: Up to 20% POSITION SUMMARY Under the general direction of the Administrative Operations Director, and in collaboration with the Chief of Laboratory Medicine and Section Medical Director, the Phlebotomy Manager leads, manages, monitors, implements, and supervises testing quality and compliance standards in the Department of Pathology and Laboratory Medicine. The position manages multiple laboratory sub-specialty sections, including Blood Bank and Transfusion Services, Central Receiving Area, Chemistry, Hematology, Phlebotomy, Point of Care, or Rapid Response Laboratory. The position ensures maintenance of standards required for College of American Pathologists (CAP), The Joint Commission (TJC), and other applicable accrediting and regulatory agencies, and maintains oversight of laboratory emergency preparedness and safety. ESSENTIAL RESPONSIBILITIES Laboratory Leadership & Operations • Provide management oversight and leadership of assigned laboratory sub-specialty sections and staff., • Promote laboratory testing quality, compliance, patient safety, and employee safety., • Provide 24/7 call coverage., • Support departmental strategic planning and operational improvements., • Oversee equipment maintenance and evaluation of new equipment and test assays., • Address customer feedback and laboratory service concerns., • Coordinate with hospital departments regarding specimen transport. Financial Management • Prepare and manage operating and capital budgets., • Manage staffing expenses and overtime., • Review billing codes, charges, collections, and revenue integrity., • Prepare return-on-investment business analyses., • Support cost effectiveness, resource optimization, and revenue improvement., • Coordinate equipment maintenance and service agreements with Supply Chain. Quality, Compliance & Safety • Oversee collection, analysis, review, and reporting of quality and compliance data., • Monitor compliance with applicable laboratory regulations and accreditation standards, including CAP, CLIA, TJC, OSHA, DPH, FDA, and AABB., • Oversee incident safety report follow-up and support quality improvement reviews., • Participate in quality assurance, turnaround-time studies, and assigned improvement projects., • Maintain laboratory policies, procedures, and required documentation., • Oversee proficiency testing, evaluate results, and implement corrective actions., • Ensure compliance with infection control and laboratory safety procedures. Technical Oversight • Provide scientific and technical guidance regarding instrumentation, test systems, clinical correlation, backup systems, and laboratory performance., • Evaluate and implement laboratory methodologies and technology., • Review equipment maintenance documentation and service agreements. Staff Management & Development • Oversee employee selection, orientation, competency assessment, performance evaluation, and disciplinary processes., • Recommend salary rates for new employees., • Support staff education, cross-training, and professional development., • Coordinate staff utilization and document attendance for payroll., • Maintain laboratory job descriptions and competency programs., • Communicate with laboratory staff, leadership, and other hospital departments. COMMUNICATION • Conduct regular staff meetings and document meeting information., • Collaborate with the Operations Director, Medical Chief, Medical Directors, and other managers., • Communicate with medical and nursing staff regarding laboratory services., • Support customer service programs and respond to service feedback. Other duties as needed. Requirements: MANDATORY QUALIFICATIONS • Bachelor's degree from an accredited university or college in Medical Technology or Clinical Laboratory Science, including successful completion of a supervised clinical internship in an approved hospital laboratory, or a bachelor's degree in an applied science such as Chemistry, Biology, or Biochemistry. REQUIRED, • Minimum three years of clinical laboratory experience. REQUIRED, • In-depth familiarity with accreditation requirements, particularly The Joint Commission and College of American Pathologists. REQUIRED, • Outstanding organizational and interpersonal skills and strong leadership qualities. REQUIRED, • In-depth scientific understanding of the area of responsibility and knowledge of, and ability to perform, Medical Technologist II duties. REQUIRED PREFERRED QUALIFICATIONS • Certification by ASCP, NCA, or an equivalent agency as a Medical Technologist, Clinical Laboratory Scientist, Medical Laboratory Technician, or specialty certification., • Supervisory experience in a clinical laboratory., • Ability to work on-site full time., • Ability to travel within Boston, Brockton, and Brighton. READY TO APPLY? Apply through this posting or contact Elizabeth regarding the Phlebotomy Manager, Inpatient position. Elizabeth Banzhaf, LPN Chief Operating Officer | Heartline Staffing Call/Text: 272-230-3157 Email: elizabeth@heartlinestaffing.com LinkedIn: Connect with Elizabeth EQUAL OPPORTUNITY EMPLOYER Heartline Staffing is committed to equal employment opportunity. Qualified applicants are considered without regard to race, color, religion, sex, national origin, age, disability, veteran status, or any other characteristic protected by applicable law.

Job DescriptionPhlebotomy Lab Manager, InpatientOverview Emerge is looking for an experienced Phlebotomy Manager, Inpatient to join a prominent Medical Center in Boston, Massachusetts. This role leads inpatient phlebotomy operations and supports broader laboratory quality, compliance, staffing, safety and operational performance. The position works closely with pathology and laboratory medicine leadership and carries responsibility for staff management, regulatory compliance, budgeting, equipment, process improvement and patient service. Location: Boston, MA Schedule: Full-time, 40 hours per week Work Arrangement: On-site Travel: Up to 20% within Boston-area locations Salary: $83,000 to $120,500 Reports To: Operations Director, Pathology Visa Sponsorship: Not available Pasted markdown Pasted markdown Our client is looking for a clinical laboratory professional with strong technical knowledge, leadership skills and experience managing people and laboratory operations. The ideal candidate understands clinical lab regulations, quality standards and patient safety requirements and has experience supporting or leading laboratory teams. Job Responsibilities • Lead and manage inpatient phlebotomy and assigned laboratory operations., • Provide oversight and leadership to laboratory staff., • Maintain quality, compliance and patient safety standards., • Ensure compliance with CAP, Joint Commission, CLIA, OSHA, DPH and other applicable regulations., • Provide 24/7 call coverage., • Manage staffing levels, overtime and employee performance., • Participate in hiring, candidate selection, onboarding and employee development., • Manage operating and capital budgets., • Monitor laboratory billing, expenses and revenue integrity., • Oversee laboratory equipment, maintenance and service agreements., • Review quality-control data and implement corrective action when needed., • Support process improvement and laboratory efficiency initiatives., • Work closely with medical directors, nursing teams, operations leadership and other hospital departments., • Maintain laboratory policies, procedures and regulatory documentation. Qualifications, • Bachelor’s degree in Medical Technology, Clinical Laboratory Science or an applied science such as Chemistry, Biology or Biochemistry., • Minimum 3 years of clinical laboratory experience., • Strong understanding of College of American Pathologists, CAP, and Joint Commission requirements., • ASCP, NCA or equivalent clinical laboratory certification preferred., • Clinical laboratory supervisory experience preferred., • Strong leadership, organizational and interpersonal skills., • Strong scientific and technical understanding of clinical laboratory operations., • Ability to work full-time on-site in Boston., • Ability to travel among Boston, Brockton and Brighton locations as needed. Work Environment, • Full-time, hospital-based position., • On-site work required., • Up to 20% local travel., • Competitive medical, dental, vision, life insurance, retirement and paid-time-off benefits., • Must be authorized to work in the United States without visa sponsorship. If you are qualified for this position, please click "apply now”. Thank you in advance for applying, however, only qualified candidates will be contacted. Who is Emerge? We are a global talent solutions company working with clients all over the world. We deliver talent, recruiting expertise, managed sales, marketing, and business operations solutions to our clients. These solutions are an extension of your existing operations. We are committed to your success, working quickly and efficiently to provide tangible, measurable results. Equal Employment Opportunity Statement Emerge is committed to providing equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status or any other protected characteristic. #IND2

Job Description TITLE Sr. Manager, Scientific Product Management WHAT YOU WILL ACHIEVE Plasmids are Addgene’s largest and most established product portfolio. They are also the platform from which everything else grows — viral vectors, antibodies, new formats, new markets. The Senior Manager, Scientific Product Management owns day-to-day execution across this portfolio, which includes segmentation, catalog health, roadmap delivery, and launch execution, in close partnership with the Director of Scientific Product Management. POSITION REPORTS TO Director, Scientific Product Management SALARY $130,000 - 155,000 annually + our amazing benefits! LOCATION & POLICY ON REMOTE WORK This position will work out of our Watertown, Massachusetts Headquarters with an opportunity to work on a hybrid schedule. Our beautiful office space has free, ample parking with a complimentary shuttle from Harvard Square and is on multiple bus lines, with the cost of public transit covered by Addgene for those onsite at least twice a week. The Role: This is a role for someone who wants to grow a business — who leads with outcomes, moves with urgency, and knows how to translate scientific insight into commercial results. The right candidate will inherit a portfolio with strong foundations and significant untapped potential, and will be expected to deliver on both in the near term while building the strategic runway for 2028 and beyond. To Succeed in this Role, You Will Own: Portfolio Performance & Analytics • Track and report on plasmid portfolio performance — including revenue growth, margin optimization, and long-term portfolio health — and deliver on targets set in the Annual Operating Plan (AOP)., • Set and hit clear performance targets for the portfolio: revenue growth, adoption rates, market penetration, and customer retention across academic, biotech, and pharma segments., • Identify performance gaps and recommend pricing, positioning, promotional, or product-mix adjustments to protect and grow commercial outcomes. Product Strategy & Roadmap Execution • Execute the multi-year plasmid product roadmap, balancing near-term revenue delivery with longer-term innovation bets., • Drive the full product lifecycle for the plasmid portfolio — from opportunity identification and concept validation through launch, growth, optimization, and, where appropriate, rationalization., • Support the I2L (Idea-to-Launch) pipeline for plasmid-related innovations, including new formats like Transfection-Ready DNA, defining what comes next on that roadmap, and shepherding line extension projects through gate decisions., • Apply plasmid segmentation outputs to prioritize where Addgene invests, where it defends, and where it rationalizes — making clear, defensible calls with supporting data., • Develop and implement a plasmid intake evaluation framework for large deposits, including accept/decline criteria and cost-benefit analysis, to improve catalog quality and scalability. Market Insight & Commercial Intelligence • Run an ongoing Voice of the Customer (VOC) program, translating researcher needs into product priorities and roadmap recommendations., • Maintain deep knowledge of the plasmid competitive landscape — who the players are, what they offer, how Addgene is positioned, and where the gaps and white space lie., • Monitor market trends, funding shifts, and emerging research applications (e.g., gene therapy, synthetic biology, CRISPR) to anticipate demand and position the portfolio ahead of the curve., • Turn market intelligence into concrete recommendations, pricing moves, product concepts, or go-to-market adjustments. Go-to-Market Execution • Execute annual commercial plans for the plasmid portfolio — launch activities, marketing coordination, channel activation, and partnership initiatives — in partnership with Marketing, Distribution, and Business Development., • Own the commercial launch of Transfection-Ready DNA and any subsequent new formats, from go-to-market strategy through post-launch performance monitoring and optimization., • Define clear value propositions and messaging for each plasmid segment, ensuring Addgene’s positioning is differentiated, credible, and compelling to target customers., • Partner with the Distribution Manager to ensure distributor partners are equipped, motivated, and accountable for plasmid sell-through in their markets. 2027 Planning & Strategic Roadmap • Provide plasmid portfolio analysis and input into the 2027 Operating Plan and 3–5 year commercial roadmap, under the Head of Product Management's direction., • Develop business cases and Market Requirements Documents (MRDs) for new product ideas advancing through the I2L process, ensuring each is grounded in customer evidence and commercial viability., • Surface partnership opportunities that could accelerate plasmid portfolio growth for the Business Development team to evaluate. Cross-Functional Leadership • Lead cross-functional core teams — spanning Operation, R&D, Marketing, Scientific Engagement, Operations, and Digital product— to deliver portfolio objectives on time and to commercial standard., • Hold cross-functional partners accountable to shared milestones and commercial outcomes, escalating blockers quickly and decisively., • Serve as the internal authority on the plasmid portfolio — the person who knows it best, advocates for it most effectively, and can represent it credibly to any audience., • Represent Addgene externally at conferences, partner meetings, and industry events, building market presence and returning with actionable intelligence. What Success Looks Like Skills and Competencies Required • Bachelor’s degree in a life sciences discipline; advanced degree (PhD or master’s in molecular biology, biochemistry, genetics, or related field) strongly preferred and carries significant weight., • 5–7 years of progressive commercial experience in the life sciences sector, including experience in product management, portfolio execution, or a directly adjacent commercial role., • Demonstrated track record of owning a product portfolio P&L and delivering revenue growth and margin improvement, • Deep understanding of discovery researcher needs, workflows, and purchasing behavior in academic and industry settings, with the ability to translate that understanding into commercial strategy., • Proven experience leading products through a structured innovation or stage-gate process (I2L, Phase-Gate, or equivalent) from concept through commercial launch., • Strong analytical and financial acumen: comfortable building business cases, interpreting performance data, and making data-driven recommendations, • Demonstrated ability to lead and influence cross-functional teams without direct authority, and to hold peers accountable to shared commercial goals., • Excellent communication skills — able to present to executive leadership, engage credibly with scientists, and align commercial teams around a clear strategy., • Commercially oriented mindset: you measure success by outcomes, not outputs. Preferred • Direct experience with plasmid biology, molecular cloning, or related reagent formats (viral vectors, CRISPR tools); hands-on laboratory experience is a genuine plus., • Experience in a nonprofit, CRO, or mission-driven life science organisation where commercial goals must be balanced with broader values., • Familiarity with Addgene’s portfolio, repository model, or academic distribution channels., • Experience developing or applying VOC methodologies a

Job Description Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X. The Senior Manager / Associate Director, Clinical Sample Operations will lead the strategic operational planning, logistical execution, and oversight of biosample management across Crescent Biopharma’s global clinical trial portfolio. This role partners across Clinical Operations, Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, and Non-Clinical, and with external laboratory partners, to ensure clinical trial specimens—including biomarker, pharmacokinetic/pharmacodynamic, genomic, and other specialty samples—are collected, processed, tracked, shipped, stored, and analyzed in accordance with protocols, timelines, quality standards, and regulatory requirements. The ideal candidate combines strong program and project management capabilities, deep laboratory vendor-management expertise, and a meticulous understanding of the clinical sample lifecycle. The successful candidate will be a hands-on, collaborative leader who anticipates operational risks and develops practical solutions in a fast-paced biotechnology environment. Responsibilities Strategic Operations & Trial Lifecycle Support Sample strategy execution: Partner with Clinical Operations, Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, and Non-Clinical to translate scientific and development objectives into executable study-level sample management plans. Protocol and informed consent input: Collaborate with Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, Non-Clinical, and Clinical Operations to review clinical protocols, Investigator’s Brochures, informed consent forms, and related study documents and confirm that biological sample collection, processing, testing, storage, future-use, and destruction requirements are scientifically aligned, operationally feasible, and clearly defined. Laboratory manual oversight: Lead the authoring, cross-functional review, approval, and maintenance of study-specific laboratory manuals, sample collection instructions, and associated site materials. Collection kit readiness: Oversee design, production, distribution, inventory, and replenishment of sample collection kits for global investigative sites. Study execution: Represent Clinical Sample Operations on cross-functional study teams comprising Clinical Operations, Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, Non-Clinical, and other relevant functions; proactively identify risks and implement mitigation and escalation plans to protect sample quality and study timelines. Sample Logistics, Tracking & Data Integrity Chain of custody: Maintain oversight of the complete end-to-end lifecycle and chain of custody of clinical samples from site collection through transport, receipt, processing, testing, transfer, long-term biorepository storage, return, or final destruction. Global logistics: Coordinate shipment strategies and resolve time-sensitive issues related to couriers, customs, import/export requirements, temperature excursions, sample integrity, and site compliance. System implementation: Lead the development, implementation, validation support, and optimization of sample tracking systems and laboratory information management systems across clinical studies. Data reconciliation: Oversee routine cleaning and reconciliation of sample metadata across electronic data capture systems, interactive response technologies, laboratory data transfers, and sample tracking platforms to support interim analyses and database lock timelines. Metrics and reporting: Develop portfolio- and study-level dashboards that provide visibility into sample collection, shipment status, assay readiness, discrepancies, and operational risk. Education & Experience • Bachelor’s degree in life sciences, biology, bioengineering, healthcare, or a related scientific discipline is required; an advanced degree is preferred., • Senior Manager level: Typically 6–8+ years of progressive experience in clinical operations, clinical sample management, biomarker operations, laboratory operations, or a related function within biotechnology, pharmaceutical, or contract research organizations., • Associate Director level: Typically 8–10+ years of relevant experience, including at least 2–3 years of direct people management or leadership of matrixed project teams., • Direct experience supporting oncology clinical trials involving complex, multi-assay biomarker strategies is strongly preferred, • Demonstrated knowledge of the clinical sample lifecycle, laboratory operations, chain of custody, sample logistics, assay workflows, data transfers, and sample data reconciliation, with the ability to integrate requirements across Clinical Operations, Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, and Non-Clinical., • Proven experience selecting, contracting with, budgeting for, and overseeing central laboratories, specialty laboratories, biorepositories, and logistics vendors., • Working knowledge of ICH-GCP, GxP principles, global regulatory expectations, informed consent requirements, data privacy, and biospecimen-related ethical considerations., • Proficiency with eTMF platforms, clinical trial management systems, electronic data capture platforms such as Medidata Rave, and sample tracking or LIMS solutions.Core Competencies, • Exceptional cross-functional stakeholder-management skills, with the ability to build alignment across Clinical Operations, Clinical Science, Clinical Development, Translational Medicine, Clinical Pharmacology, Non-Clinical, and external partners., • Strong strategic planning, project management, prioritization, and vendor-governance capabilities., • Acute attention to detail and a consistent commitment to data integrity, quality, and compliance., • Excellent written and verbal communication skills, including the ability to translate complex scientific and operational requirements into clear plans and decisions., • Proactive, solutions-oriented, “roll-up-your-sleeves” mindset with the judgment and composure to resolve logistics issues in real time., • Ability to thrive in a fast-paced, highly collaborative, and evolving biotechnology environment while managing multiple studies and priorities. What We Offer, • Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment., • Competitive compensation, including base salary, performance bonus, and equity., • 100% employer-paid benefits package., • Flexible PTO., • Two, one-week company-wide shutdowns each year., • A commitment to your professional development, with access to resources, mentorship, and growth opportunities. Salary Range The salary range for this position is $170,000 to $200,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Additional Description for Pay Transparency: The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation – Unlimited PTO; Sick time – 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave – 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - https://www.crescentbiopharma.com/careers/#benefits Please note: Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status. Please note, Crescent does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between Crescent and the agency. Crescent will not pay any fees related to unsolicited resumes.

Job Description Scholar Rock is delivering muscle-targeted breakthroughs to transform the treatment of spinal muscular atrophy (SMA) and other rare neuromuscular diseases where muscle atrophy remains a critical unmet need. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the biopharmaceutical company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more about our neuromuscular franchise at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: Scholar Rock is seeking a Senior Director, Enterprise Business Applications to develop the IT organization’s future-state integrated team supporting enterprise functions within the company. This leader is responsible for the strategy, governance, and operational excellence of the company's core enterprise business systems, with particular emphasis on Finance and Quality/Regulatory-adjacent platforms (Veeva). This role will establish Centers of Excellence for both Veeva and SAP and lead the company's transformation of core business processes as part of a global SAP implementation. This individual will play a critical role in ensuring the enterprise systems roadmap aligns with the company's commercial launch timelines and long-term growth strategy. This is a hands-on leadership role requiring a blend of strategic vision, deep functional/technical expertise, vendor and program management skill, and the ability to build governance structures from the ground up in a fast-moving environment. Scholar Rock is seeking a Senior Director, Enterprise Business Applications to lead the strategy, delivery, and ongoing evolution of the enterprise systems supporting our growing global organization. This leader will be responsible for the strategy, governance, implementation, and operational excellence of our core enterprise business systems, with initial emphasis on SAP and Veeva. This individual will serve as a strategic technology partner to the business, translating business priorities into scalable processes, capabilities, and technology solutions as Scholar Rock expands its global commercial operations. This is a hands-on leadership role requiring strong business and technical judgment, program and vendor management expertise, and the ability to build scalable capabilities in a fast-moving, regulated environment. Position Responsibilities • Develop and execute a multi-year Enterprise Business Applications Roadmap across Finance, Supply Chain, Manufacturing, Quality, Regulatory, HR, Legal, and other functions, • Serve as a strategic technology partner to business functions, understanding priorities and translating them into enterprise systems capabilities and roadmap priorities, • Establish scalable governance and operating models for SAP, Veeva, and other enterprise applications, including clear ownership, decision rights, standards, and support models, • Lead the global SAP implementation, including systems integrator selection, business process design, implementation, and ongoing optimization, • Partner with business functions to simplify and standardize processes and ensure technology solutions support scalable ways of working, • Oversee the configuration, integration, validation, lifecycle management, and continuous improvement of enterprise applications, • Ensure enterprise applications meet applicable GxP, 21 CFR Part 11, SOX, privacy, validation, and audit-readiness requirements, • Build and lead a high-performing enterprise applications team, leveraging managed services and external partners where appropriate, • Own enterprise application budgets and manage software vendors, systems integrators, and managed service providers, • Drive appropriate adoption of AI, automation, and integration across enterprise business processesCandidate Qualifications, • Bachelor's degree in Information Technology, Computer Science, Finance, Business Administration, or related field; MBA or advanced degree a plus, • 12+ years of progressive experience in enterprise business applications, with at least 5 years in a leadership role, • Direct experience implementing and/or supporting SAP (S/4HANA preferred) in a life sciences environment, • Experience with Veeva Vault applications in a regulated life sciences environment is strongly preferred, • Strong understanding of Finance and enterprise business processes, including R2R, P2P, and O2C, • Experience leading major enterprise system implementations and business transformation, • Experience in a pharmaceutical, biotech, or other regulated industry, particularly during a commercial launch or scaling phase, • Strong business partnership, program management, vendor management, and executive stakeholder capabilitiesScholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We've built a mammalian synthetic biology platform – from cells to software – to enable the design and manufacture of next-generation therapeutics. We are seeking a highly motivated Senior Research Associate or Associate Scientist (Contractor) to join our Analytical Development team for a 6-month contract. In this role, you will run our developability and biophysical screening panel and support routine product-quality (PQ) analytical delivery for our Cell Line Development (CLD) pipeline. You will work hands-on across plate-based and chromatographic assays to characterize antibodies, multispecifics, and other engineered protein formats, generating the data that guides candidate and clone selection. You will be trained and supported by the method owner for each assay, and will grow into independent ownership of routine execution. The ideal candidate is meticulous, enjoys high-throughput laboratory work, and communicates results clearly. About the Role: Execute the developability and biophysical screening panel at plate scale, including hydrophobic interaction chromatography (HIC), self-association by AC-SINS, thermal stability by differential scanning fluorimetry (DSF), ELISA-based non-specific binding, and size-exclusion chromatography (SEC), delivering ranked, decision-ready data on candidate molecules. Execute routine PQ analytical delivery for CLD programs, including sample preparation, small-scale Protein A purification, and HPLC/UPLC- and capillary electrophoresis-based assays, meeting delivery timelines and data-quality benchmarks. Manage high-throughput processing of CLD and screening samples in 96-well format, including system suitability checks, reference standard handling, and use of automated liquid handling where available. Partner with method owners to complete installation and qualification of new assays, then take ownership of their routine execution, troubleshooting, and performance trending. Partner with cross-functional teams to communicate analytical results and insights clearly. Manage multiple projects simultaneously, ensuring timely delivery of results and proactive communication with stakeholders. Drive continuous process and technical improvements, including SOPs and technical reports, while maintaining accurate laboratory notebooks and electronic records, adhering to Good Laboratory Practices (GLP) and safety protocols. This role is a full-time, 6-month contract with the potential for extension or conversion to a permanent position based on business needs and performance. About You: You have a B.S. degree in Chemistry, Biochemistry, Biology, or a closely related field with 3+ years of relevant laboratory experience, or an M.S. degree with 1-2 years of relevant experience. Biopharma industry experience is preferred. You possess hands-on expertise with plate-based assays and microplate readers (e.g., ELISA) and with HPLC/UPLC separations (e.g., SEC, HIC), along with careful small-scale sample preparation for protein analytics. Experience with capillary electrophoresis (CE), UV, and/or MS is a plus. You are comfortable working in 96-well format at high throughput, with a preference for experience in automated liquid handling (e.g., Hamilton) and high-throughput purification. You bring exposure to biophysical or developability characterization (thermal stability by DSF, self-association by AC-SINS, hydrophobicity by HIC, non-specific binding) or to label-free binding assays (e.g., Octet BLI). This is a strong plus rather than a requirement; we will train the right candidate. You have a proven aptitude for troubleshooting analytical instruments and methods with a proactive, solution-oriented approach. You are proficient in data interpretation and the use of statistical tools for trending, supported by strong communication skills to present complex data clearly to diverse audiences. You demonstrate the ability to work effectively in a fast-paced, team-oriented environment with meticulous attention to detail and superior organizational skills. We’re fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.

Job DescriptionPrimary Talent Partners has a new contract opening for a Scientist - II (Associate) to join our pharmaceutical client in Cambridge, MA. This is a 12-month contract to start with the potential for extensions. Pay: $20.50 - $25.52/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship. Description: • Client Research Laboratories (MRL) in Cambridge, MA, is a collaborative research hub focused on discovering innovative medicines that improve human health., • The Retinal and Vascular Biology group is seeking a motivated bench scientist with strong experimental research experience., • This one-year contractor position offers a unique opportunity to contribute to the development of therapeutics for retinal diseases while working closely with multidisciplinary teams across MRL Cambridge, MRL South San Francisco, and the broader Client research network., • The successful candidate will be an experienced and motivated bench scientist with extensive industry experience in in vitro biochemical and cell-based assay development and execution., • Primary Retinal endothelial cells as a previous experience is must have., • Strong hands-on experience with: Mammalian cell culture Primary and immortalized cell culture Primary endothelial cell culture Retinal epithelial cell culture Cellular biology techniques Assay development, optimization, and validation High-throughput or medium-throughput screening Data analysis and interpretation Electronic laboratory notebooks (ELN), PRISMSPECIFIC RESPONSIBILITIES:, • Perform highly complex in vitro assays to evaluate endothelial biology, including barrier function, transport, angiogenesis, differentiation, and specialization., • Culture and maintain primary and immortalized cells used in in vitro assays., • Routinely test compounds represent diverse mechanisms of action and characterize their pharmacological activity., • Analyze, interpret, and present experimental data to project teams., • Optimize and develop in vitro vascular integrity assays., • Participate in team meetings and scientific discussions related to retinal disease and therapeutic target discovery., • Maintain accurate and detailed records in electronic laboratory notebooks and adhere to safe laboratory practices.EDUCATION MINIMUM REQUIREMENT:, • Bachelor's or Master's degree in Biological Sciences, • A minimum of 5 years of industry experience in in vitro biochemical and cell-based assay development and execution, including compound handling and screening workflows.REQUIRED SKILLS:, • Strong hands-on laboratory experience in cell culture and cellular biology techniques., • Industry experience in the development and execution of in vitro assays to support compound screening, validation, optimization, data analysis, and interpretation., • Strong organizational skills and attention to detail., • Strong ability to analyze data and communicate scientific findings effectively., • High level of motivation, curiosity, and passion for scientific research.PREFERRED SKILLS:, • Familiarity with retinal biology, vascular biology, and inflammation., • Experience with primary endothelial or retinal epithelial cell culture. Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws. If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com #PTPJobs #LI-PTP

Job Description Nanopath is developing a first-in-class in vitro diagnostics platform to transform how diseases are diagnosed. We aim to replace lengthy molecular testing workflows by bringing rapid, high-quality diagnostics closer to the patient. Our mission is to improve patient outcomes – starting with women – through a purpose-built platform that delivers actionable results within a single office visit. The company is headquartered at The Engine, the premier tough technology incubator in the Kendall Square ecosystem. We are collectively committed to health equity and the design of solutions for underserved populations and low-resource settings. Corporate sustainability – both environmental and social – is at the forefront of our decision making. About the Role Nanopath is seeking a Process Development Senior Research Associate / Associate Scientist to join our Assay R&D team and help develop, optimize, and scale the workflows that support Nanopath's diagnostic platform. This role will be highly hands-on and will support process development across assay preparation, reagent development, and analytical testing. Responsibilities • Support development of robust, repeatable protocols for reagent manufacturing, array fabrication, and assay execution., • Assist with process characterization, QC, stability, reproducibility, and verification-supporting studies as Nanopath advances toward regulated product development., • Prepare reagents, samples, and materials; maintain lab organization; and support routine equipment use and maintenance., • Collect, analyze, summarize, and present experimental data in a clear and timely manner., • Troubleshoot experimental workflows and collaborate with assay, engineering, product, and operations team members to identify root causes and implement improvements. Qualifications • Bachelor's or Master's degree in bioengineering, biomedical engineering, molecular biology, chemistry, or a related field with 4+ years of relevant industry experience., • Experience with liquid handler automation, automated assay workflows, or programming / operating automated laboratory platforms., • Experience with nucleic acid assays, biosensors, microarrays, or spotting / printing technologies, • Familiarity with design control, quality systems, GLP/GxP principles, or documentation practices for regulated diagnostics., • Extremely well-organized, with a high level of efficiency, attention to detail, and motivation for completing tasks accurately and on time., • Excellent communication and presentation skills., • Experience in cross-functional and highly collaborative work environments., • Passionate about Nanopath's mission for developing a purpose-built solution for women's health. Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At Nanopath we are dedicated to building a diverse and inclusive workplace, so if you're excited about this role but your past experience doesn't align perfectly with every point in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles! Nanopath Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Nanopath does not accept unsolicited resumes from recruiters or agencies and we will not be responsible for any fees related to resumes that are unsolicited. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Nanopath, and Nanopath will not owe any referral or other fees with respect thereto.

Job DescriptionJoin a Global Leader in Workforce Solutions – Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision—Right Talent. Right Time. Right Place. Right Price. Job Title: Scientist - II (Associate) (#MSD1JP00004021) Location: 320 Bent St, Cambridge, MA 02141 (Onsite) Duration: 12 Months Contract Pay Rate: $56.66/Hr on W2 Shift: 8 AM to 5 PM (Monday – Friday) – 40 Hours/Week CONTRACTOR POSITION (ONE YEAR) –RETINAL AND VASCULAR BIOLOGY JOB DESCRIPTION Client Research Laboratories in Cambridge, MA, is a collaborative research hub focused on discovering innovative medicines that improve human health. The Retinal and Vascular Biology group is seeking a motivated bench scientist with strong experimental research experience. This one-year contractor position offers a unique opportunity to contribute to the development of therapeutics for retinal diseases while working closely with multidisciplinary teams across MRL Cambridge, MRL South San Francisco, and the broader client research network. The successful candidate will be an experienced and motivated bench scientist with extensive industry experience in in vitro biochemical and cell-based assay development and execution. EDUCATION MINIMUM REQUIREMENT: • Bachelor's or Master's degree in Biological Sciences, • A minimum of 5 years of industry experience in in vitro biochemical and cell-based assay development and execution, including compound handling and screening workflows. REQUIRED SKILLS • Strong hands-on laboratory experience in cell culture and cellular biology techniques., • Industry experience in the development and execution of in vitro assays to support compound screening, validation, optimization, data analysis, and interpretation., • Strong organizational skills and attention to detail., • Strong ability to analyze data and communicate scientific findings effectively., • High level of motivation, curiosity, and passion for scientific research. PREFERRED SKILLS • Familiarity with retinal biology, vascular biology, and inflammation., • Experience with primary endothelial or retinal epithelial cell culture. SPECIFIC RESPONSIBILITIES • Perform highly complex in vitro assays to evaluate endothelial biology, including barrier function, transport, angiogenesis, differentiation, and specialization., • Culture and maintain primary and immortalized cells used in in vitro assays., • Routinely test compounds represent diverse mechanisms of action and characterize their pharmacological activity., • Analyze, interpret, and present experimental data to project teams., • Optimize and develop in vitro vascular integrity assays., • Participate in team meetings and scientific discussions related to retinal disease and therapeutic target discovery., • Maintain accurate and detailed records in electronic laboratory notebooks and adhere to safe laboratory practices. Why Work With Us? We believe in more than just jobs—we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition • America's Most Honored Businesses (Top 10%), • Fastest-Growing Staffing Firm by Staffing Industry Analysts, • INC 5000 List for Eight Consecutive Years, • Top 100 by Dallas Business Journal, • Spirit of Alliance Award by Agile1 #LS01

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description AbbVie Immunology is expanding its discovery Systems Immunology team in Cambridge, Massachusetts. The team is focused on identifying new targets for the treatment of autoimmune and chronic inflammatory diseases through computational analysis of human disease tissue-derived datasets and validating targets using humanized experimental approaches. We are seeking a highly motivated and skilled individual to join our team as a Computational Immunology Scientist. The successful candidate will develop and implement computational approaches to understand disease biology and drug responses using high-throughput molecular profiling data. This role will involve integrating single-cell RNA-seq, scATAC-seq, TCR/BCR repertoire, bulk RNA-seq, and Olink proteomics data to characterize disease-associated cell states, investigate gene regulatory networks, and identify therapeutic opportunities. The scientist will work in a multidisciplinary team analyzing multiomics datasets to derive insights into immunological diseases and identify novel therapeutic targets relevant to patient cohorts and AbbVie pipeline drugs. The candidate will also contribute to scientific conference presentations, peer-reviewed publications of translational findings, new drug applications, and regulatory filings. If you are passionate about translating complex biological data into actionable insights and advancing personalized medicine, we encourage you to apply. This position will be based in Cambridge, Massachusetts, and requires passion, attention to detail, prior hands-on experience, and teamwork. Key Responsibilities: • Analyze scRNA-seq, and CITE-seq, datasets, including quality control, integration, clustering, and cell-type and cell-state annotation., • Integrate patient cohorts with reference atlases and perform differential expression, abundance, and pathway analyses, accounting for donor variation and study design., • Analyze scATAC-seq data to identify differential accessibility, transcription factor motifs, and candidate regulatory programs; integrate accessibility with gene expression to infer peak-to-gene relationships., • Analyze TCR/BCR repertoires, including clonotype assignment, clonal expansion, diversity, V(D)J usage, and sharing across tissues or time points; link clonotypes to matched single-cell profiles., • Analyze bulk RNA-seq and Olink proteomics data and integrate multiomics findings to support target prioritization and biomarker hypotheses; maintain documented, version-controlled workflows and evaluate methods using cloud or high-performance computing., • Collaborate with internal and external scientists to prioritize hypotheses for validation, communicate findings and limitations, and contribute to presentations and publications. Qualifications, • BS or MS degree in computational biology, bioinformatics, genomics, biostatistics, computer science, or a related quantitative field with typically 5-7+ years (BS) or 2-5+ years (MS) of relevant experience., • Hands-on scRNA-seq analysis experience or experience with scATAC-seq or TCR/BCR analysis, with interest in developing expertise across both., • Proficiency in Python and/or R and experience working in Linux-based computing environments., • Experience with commonly used bioinformatics tools and frameworks such as Scanpy, AnnData, Cell Ranger, scvi-tools, DESeq2, GSEA, WGCNA, or related methods., • Working knowledge of statistical analysis, multiple-testing correction, batch effects, and biological replication in high-dimensional datasets., • Ability to translate biological questions into analyses, interpret and communicate results critically, collaborate effectively, and manage multiple priorities with attention to detail., • Demonstrated ability to work collaboratively, manage multiple priorities, and deliver high-quality analyses with attention to detail. Preferred Qualifications: • Experience analyzing Olink or other high-plex proteomics datasets., • Experience with CITE-seq, ATAC-seq, spatial transcriptomics, or integrative multi-omics analysis., • Experience building or benchmarking machine-learning models, including convolutional neural networks, autoencoders, generative models, transfer learning, or foundation models., • Experience with cloud or high-performance computing, including AWS and/or SLURM., • Understanding of immunology and inflammatory disease biology; experience supporting target discovery with experimental teams and communicating research through presentations, publications, or reports., • Evidence of scientific communication through presentations, posters, publications, technical reports, or related research contributions. Position will be filled at level commensurate with extent of education, experience, and accomplishment— Scientist I or Scientist II Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future., • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees., • This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionCONTRACTOR POSITION (ONE YEAR) RETINAL AND VASCULAR BIOLOGY JOB DESCRIPTION * Research Laboratories (MRL) in Cambridge, MA, is a collaborative research hub focused on discovering innovative medicines that improve human health. The Retinal and Vascular Biology group is seeking a motivated bench scientist with strong experimental research experience. This one-year contractor position offers a unique opportunity to contribute to the development of therapeutics for retinal diseases while working closely with multidisciplinary teams across MRL Cambridge, MRL South San Francisco, and the broader * research network. The successful candidate will be an experienced and motivated bench scientist with extensive industry experience in in vitro biochemical and cell-based assay development and execution. EDUCATION MINIMUM REQUIREMENT: Bachelor s or Master s degree in Biological Sciences A minimum of 5 years of industry experience in in vitro biochemical and cell-based assay development and execution, including compound handling and screening workflows. REQUIRED SKILLS Strong hands-on laboratory experience in cell culture and cellular biology techniques. Industry experience in the development and execution of in vitro assays to support compound screening, validation, optimization, data analysis, and interpretation. Strong organizational skills and attention to detail. Strong ability to analyze data and communicate scientific findings effectively. High level of motivation, curiosity, and passion for scientific research. PREFERRED SKILLS Familiarity with retinal biology, vascular biology, and inflammation. Experience with primary endothelial or retinal epithelial cell culture. SPECIFIC RESPONSIBILITIES Perform highly complex in vitro assays to evaluate endothelial biology, including barrier function, transport, angiogenesis, differentiation, and specialization. Culture and maintain primary and immortalized cells used in in vitro assays. Routinely test compounds represent diverse mechanisms of action and characterize their pharmacological activity. Analyze, interpret, and present experimental data to project teams. Optimize and develop in vitro vascular integrity assays. Participate in team meetings and scientific discussions related to retinal disease and therapeutic target discovery. Maintain accurate and detailed records in electronic laboratory notebooks and adhere to safe laboratory practices.