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Job Description THE TEAM: You'll join a team of innovative thinkers who love to experiment, collaborate, and win together. We are passionate about pushing the boundaries of automation, biology, computing, robotics, design, and user experience to benefit our customers and the world. Qualifications • High School Diploma or GED required. Associates Degree or other 2-year technical diploma preferred OR 5+ years of military training and experience testing, and troubleshooting of large military platforms to be considered in lieu of technical diploma., • 1-2+ years experience in a manufacturing environment that involves assembling products with any combination of electronics, robotics, or mechanical components, • Physical Requirement: Must be able to lift up to 50 pounds, work while standing for extended periods and be comfortable bending, leaning, reaching, and working in and around machinery as part of daily job duties., • Experience debugging and repairing electrical components using soldering irons and multimeters., • Must be proficient with electrical reworks such as cable repairs, and surface mount and through hole PCB reworks., • Must use and understand the application of common hand tools, various industry nomenclatures, and have strong assembly skills., • Must be a self-starter who looks for ways to improve the job and related processes and shows initiative in execution., • Working knowledge of spreadsheets, creating, manipulating, and using for data analysis., • Demonstrated proficiency developing work instructions, documenting testing procedures and processes., • Ability to Self-manage your day-to-day areas with minimal supervision, while completing tasks with high quality output and timely delivery, • Familiarity with ERP and PLM software is a nice-to-have that supports future projects this role will own.\nCompany Description BlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers. BlackTree Technical Group is a full-service staffing and recruitment firm. Our team consists of an experienced group of Senior Technical Recruiters and Account Managers with over 40 years of industry experience. Our firm prides itself on our technical knowledge, innovative sourcing strategies, and most importantly, a long-standing record of proven results for both clients and job-seekers.

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 DescriptionScholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the 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 at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: The Human Resource Business Partner (HRBP) provides HR leadership and support to our Research & Development and Tech Ops & Quality organizations. The HRBP is a trusted advisor to leaders, providing expert HR advice and advanced solutions that enable the achievement of business strategies by leveraging effective people processes. This role drives talent, culture, change management and operational excellence for the US & Global organizations, overseeing the delivery of HR programs and services such as leadership, talent acquisition & talent management including employee development, coaching, compensation processes, performance management, organization and change management. This role will also lead Employee Relations processes and procedures to enable effective management, conflict resolution, and problem solving across these organizations. Position Responsibilities: Provides strategic HR leadership and expert guidance to our R&D and TOQ organization for all people processes, delivering HR programs and services to achieve key business objectives. Proactively defines, builds and implements value-added HR strategies and solutions based on the needs of the organization; advising functional leaders in solving complex issues related to organization design, development, and change leadership. Partner with Talent teams to establish strategies and tactics to deliver the people and talent strategy for the R&D and TOQ organizations including the attraction, development, and retention of high-quality talent aligned with growth objectives, long-term capability needs, and corporate strategy. Builds strong partnerships with the HR specialist functions to provide HR solutions to key business needs and to roll out programs that enhance overall employee engagement and organization change initiatives. Implement and manage key HR processes, such as the year-end performance management process (performance assessment, calibration, and compensation planning). Manage employee relation issues to understand employee concerns, identify and implement appropriate employee action and accountability practices. Provides guidance and coaching to managers of all levels to address employee behavior and performance and assisting with the development and delivery of appropriate performance feedback or action plans including corrective/disciplinary actions. Candidate Requirements: 10 years of experience or equivalent combination of education with experience in HR business partnering or related discipline with deep understanding of biotech/pharma industry. Experience developing and implementing HR plans and strategies supporting R&D functions is a must. Highly experienced in talent management, succession planning, leadership and employee development, employee relations, and employee engagement. Strong experience managing and/or leading culture and change management or organizational effectiveness initiatives. Demonstrated employee relations expertise, excellent judgment, and highly developed analytical, interpersonal, problem-solving and communication skills. Ability to distill complex information into key messages, clearly and simply communicating in a compelling way to all levels of an organization Experience in leading large-scale projects, comfortable driving change and embracing innovation in the face of ambiguity and complexity. A leader who is values-driven and able and willing to work at all levels. Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description Job Title: Molecular & Cell Biologist Location: Boston, MA Contractor Work Model: Onsite Hours: M-F 8am-5pm Compensation: $50.00 - $54.95/hr Type: Contract, Potential for extension or conversion to permanent Overview Come join a rapidly expanding Gene Therapy team at a global pharmaceutical company that is responsible for inventing, characterizing, and advancing novel genetic therapeutics for a myriad of clinical applications. Responsibilities • Work with team members to drive forward new gene therapy programs, • Perform cell culture and molecular biology experiments and establish new functional assays to measure gene therapy outcomes both in vitro and in vivo., • Establish and characterize novel assays for endpoint analysis to in vivo studies, • Work cross functionally to deliver data to the project team within expected timelines., • Maintain detailed documentation of scientific work in an electronic notebook. Requirements, • B.S. and/or M.S. in biology or a closely related field with 3+ years of relevant laboratory experience, • Significant aseptic cell culture experience, including gene therapy (e.g. AAV or LNP) experiments, • Experience isolating nucleic acids and proteins from tissues, • Experience planning and implementing experiments independently, • Experience in molecular endpoints, including, PCR, qPCR, ddPCR, and protein analysis (Simple Western Jess, ELISA, MSD, Octet), • Familiarity with primer design, sequencing preparation, and analysis, • Mouse and NHP Tissue processing is a plus, • Experience using automation in workflows is a plus (i.e., liquid handling), • Excellent problem-solving skills and ability to troubleshoot complex issues, • Strong organization, communication, and collaboration skills, • This role may require up to 10% travel for conferences or training. 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: 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 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 Description Job Title: Biochemist/Molecular Biologist Location: Cambridge, MA Type: Contract Compensation: $35-$41.82 Work Model: Onsite – onsite Hours: 40.0 hours/week Overview Our clients BioMedicine Design (BMD) is seeking a highly motivated Biochemist/Molecular Biologist to join Biotherapeutic Expression and Purification group (BEP) in Cambridge, MA. Ideal candidates should have a strong background in molecular biology techniques and experience with nucleic acid production and analysis. Responsibilities • Independently execute high-throughput plasmid DNA production workflows including bacterial culture, plasmid purification, and downstream sample handling • Operate and troubleshoot automated instrumentation including Biotage, Opentrons, and related liquid handling platforms • Perform DNA quality control testing including gel electrophoresis, nucleic acid quantification, purity assessment, and endotoxin testing • Prepare and submit samples for next-generation sequencing (NGS) and support basic data review of sequencing results • Manage plasmid DNA inventory, sample storage, and tracking within electronic databases and sample management systems • Maintain accurate records in an electronic lab notebook and ensure documentation compliance • Collaborate with expression and purification scientists to ensure timely DNA delivery for downstream workflows • Contribute to process improvements to enhance throughput, reproducibility, and cycle time • Communicate progress, priorities, and risks to meet production schedules and deadlines Requirements • B.S. in Biological Sciences, Molecular Biology, Biotechnology, Biochemistry, or a related life sciences discipline • 2+ years experience with molecular biology techniques including plasmid preparation, nucleic acid purification, and quantitative DNA analysis • 2+ years experience with bacterial cell culture systems • Proficiency in DNA QC methods including gel electrophoresis and sample preparation for sequencing • Experience operating automated or semi-automated lab instrumentation • Strong organizational skills with the ability to manage multiple projects in a high-throughput setting • Proficiency with electronic lab notebooks and sample tracking systems • Attention to detail during repetitive, high-volume tasks • Strong communication and teamwork skills • Commitment to laboratory safety and compliance Preferred • Experience with NGS library preparation or sequencing workflows • Familiarity with Python scripting for data analysis or workflow automation • Experience with plate-based (96/384-well) high-throughput workflows • Familiarity with LIMS or sample management platforms (e.g., FreezerPro, Genedata) 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

chemistry expertisescientific document analysisanalytical reasoningdata interpretationresearch skillsquestion and assessment creationenglish written and verbal communicationcollaborationattention to detailindependent workmicro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform. Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI. Job Title: Chemistry Expert Job Type: Contractor Location: Remote Rate: 20$-50$ per task Job Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. Key Responsibilities: • Analyze and interpret complex scientific documents, datasets, and research papers related to chemistry., • Develop, review, and refine high-quality questions and answers that challenge and expand AI understanding., • Apply analytical techniques to assess and extract key insights from provided materials., • Collaborate with cross-functional teams to ensure scientific rigor and clarity in content., • Interface with documentation and contribute to continuous process improvement., • Provide feedback and domain expertise on model outputs and system performance., • Ensure the accuracy, relevance, and integrity of all chemistry-related data and input. Required Skills and Qualifications: • Bachelor’s degree or higher in Chemistry or a closely related field., • 2+ years of professional experience in academia, laboratory, or industry settings., • Proven ability to read, comprehend, and analyze technical documents and research studies., • Excellent English proficiency, with strong written and verbal communication skills., • Demonstrated experience in data retrieval, computation, and analytical reasoning., • Ability to work independently with minimal supervision, delivering high-quality results., • Strong attention to detail and scientific accuracy. Preferred Qualifications: • Advanced degree (MS, PhD) in Chemistry or related discipline., • Experience in creating educational or assessment materials., • Familiarity with interdisciplinary collaborations (e.g., physics, biology).

mechanical engineeringtechnical document analysisproblem-solvingwritten and verbal communicationdata analysisattention to detailself-managementinterdisciplinary collaborationtechnical content creationdata quality assurancemicro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform. Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI. Job Title: Mechanical Engineer Job Type: Contractor Location: Remote Rate: 20$-50$ per task Job Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. Key Responsibilities: • Analyze technical documents and extract key information relevant to your domain expertise, • Generate, review, and refine questions and solutions based on real-world mechanical engineering scenarios, • Collaborate with multidisciplinary teams to ensure accuracy and depth of data and analysis, • Provide detailed written and verbal feedback on document clarity, technical accuracy, and effectiveness, • Apply advanced subject matter knowledge to evaluate and solve complex engineering problems, • Work independently, managing your time to deliver high-quality outputs with minimal supervision, • Contribute to the continuous improvement of data quality and project processes Required Skills and Qualifications: • 2-6 years of professional or academic experience in mechanical engineering or a closely related field (lab, workplace, or academia), • Strong reading comprehension skills, with proven ability to analyze and interpret technical documents, • Exceptional English communication skills, both written and verbal, • Demonstrated experience in creating or evaluating technical content, such as reports, studies, or problem sets, • Ability to work independently and efficiently, with excellent self-management, • High attention to detail and commitment to data accuracy, • Experience interfacing with technical documentation and performing analytical tasks Preferred Qualifications: • Advanced degree (Master’s or PhD) in Mechanical Engineering, Chemistry, Physics, or Biology, • Previous experience contributing to interdisciplinary or research-driven projects, • Familiarity with data-driven analysis or training data preparation

Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Why? Protein dysfunctions directly cause many diseases, such as Alzheimer’s disease. Yet, proteins remain understudied because of technological hurdles. How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org. Who? PTI’s new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists and mass spectrometrists. Alzheimer’s disease and aging will be among the first focuses of this technology-driven research organization. New career opportunitiesMembers of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals. Qualifications we are generally interested in for different roles: • Master’s or PhD in Computational Biology, Bioinformatics, Bioengineering, Molecular Biology, Neurobiology, or related field. BS degree with at least 3 years of experience are also welcome to apply., • Experience with LC-MS/MS, particularly for proteomics., • Able to develop highly-sensitive workflows for data acquisition by LC-MS/MS pipelines., • Experience collaborating with biologists, chemists, research associates, computational scientists, and mass spectrometrists to leverage PTI's multiplexing platform., • Experience in large-scale analyses that involve many samples, such as thousands of single cells or bulk tissues, and then visualizing datasets with Python and/or R as well as the command line., • Reproducible research using tools such as git, Jupyter notebooks, etc., • Experience with cloud environments such as AWS or Google Cloud., • Preparation and analysis of brain samples, or equivalent working experience. In particular, preparing human brain tissue for downstream protein analyses., • Mentoring scientists and research associates. Preparing internal reports and manuscripts, and presenting results at internal or external scientific meetings as appropriate., • Demonstrable commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others.We offer:, • An opportunity to change the world and work with some of the smartest and the most talented experts from different fields., • Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from., • Company-paid group life, AD&D, long- and short-term disability insurance, • 15 days PTO + 10 sick days per year, • 18 company holidays + your birthday off, • $5,000 per year educational reimbursement, • Up to 16 weeks paid parental leave We aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind. 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 DescriptionAbout Us Deep Genomics is at the forefront of using artificial intelligence to transform drug discovery. Our proprietary AI platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms, and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, bioinformatics, data science, engineering, and drug development, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how new medicines are created. Opportunity This role based in Cambridge, MA is focused on the analytical characterization and formulation of oligonucleotides in support of the research efforts at Deep Genomics. The individual in this role will assure the identity and purity levels of oligonucleotides as they are obtained from external CROs as well as from pre-clinical in vitro and in vivo metabolism experiments. The person in this role will also be responsible for the formulation of oligonucleotides for in vitro and in vivo experimentation. Further, responsibility for the management of research samples falls within the remit of this role. The person in this role will also lead the strategy formulation and implementation of an internal build of oligonucleotide analytics lab at Deep Genomics. Key Responsibilities • Maintain efficient workflows for analytical characterization of DG oligos at CROs., • Working with the leader of Molecular Design Chemistry, develop and implement a potential, future plan for the installation of an LCMS system for analysis of oligonucleotides., • Act as DG KOL for characterization of oligonucleotides in terms of identify, purity, and stability., • Develop analytical methods for the future LCMS system to characterize research oligonucleotide samples including characterization of chemical and metabolic stability., • Generate Certificate of Analysis reports from such data., • Perform formulation processes to provide research samples ready for in vitro and in vivo experimentation including endotoxin analysis., • Develop and maintain a sample tracking system for the compounds that come into Deep Genomics at Cambridge., • Future responsibilities may include bioanalysis of PK samples.Basic Qualifications, • PhD in analytical, pharmaceutical sciences, or bio-organic chemistry including expertise in HPLC (high pressure liquid chromatography) and mass spectrometry with 2 years experience; MS in similar fields with +5 years experience., • Excellent communication skills coupled with good collaboration style., • Experience in the laboratory techniques for oligonucleotides., • Experience in designing and implementing new processes for oligonucleotide samples.Preferred Qualifications, • Experience with oligonucleotide therapeutics, analytics, and formulation., • Understanding of in vitro assays and/or in vivo experiment involved in ADAR, siRNA and ASO-modality therapeutics., • Experience in bioanalysis and GxP methods and laboratory operations would be a benefit.What We Offer, • A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery., • Highly competitive compensation, including meaningful stock ownership., • Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program., • Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days., • Maternity and parental leave top-up coverage, as well as new parent paid time off., • Focus on learning and growth for all employees - learning and development budget & lunch and learns., • Facilities located in the heart of Toronto - the epicenter of machine learning and AI research and development, and in Kendall Square, Cambridge, Mass. - a global center of biotechnology and life sciences. Deep Genomics encourages applications from all backgrounds who seek the opportunity to build the world's leading AI-driven genetic medicine company. If you have a disability or special need, accommodation is available on request for candidates taking part in all aspects of the selection process. *This posting reflects a current vacancy. We offer competitive compensation aligned with local market benchmarks. The salary range for this role is $150,000 - $180,000, and reflects Cambridge, USA-based roles; compensation may differ for Canada-based candidates. 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 DescriptionNanobiosym is on the cusp of rewriting the rules of personalized medicine, novel technologies, and healthcare delivery. Founded by a renowned MIT and Harvard trained Physician and Physicist, Nanobiosym's innovative pipeline of products leverage novel advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple other prestigious peer-reviewed funding awards, Nanobiosym is currently adding to its talented team as it expands into a global commercial enterprise.Nanobiosym is currently seeking a talented research associate with molecular biology experience, to help test our new novel technologies. This role will include a combination of data acquisition, data analysis, statistics and troubleshooting, and the development of testing procedures.DUTIESPerform novel technology testing, maintain laboratory records, and prepare reports.Define strategy for testing and optimization.Create and champion new internal processes of testing, data collection, data acquisition, and data analysisExpertise with excel and statisticsExercise technical judgment on test requirements, developing recommendations and translating into course of actionQUALIFICATIONSBS degree in Biology, MS in Molecular Biology Preferred, bioinformatics, biostatistics Prefer 2-5 years of academic or industry experience in molecular biologyExperience in qPCR or PCR preferred but not requiredExperience working in a BSL-2 or BSL-2+ facility preferred but not requiredExperience working in an ISO 13485 environment, and a working knowledge of ISO documentation & QSR requirements preferred but not requiredExperience testing and/or developing life sciences products, including meticulous laboratory notebook skillsMust have an understanding of principles of statistics relevant to product testingMust have an understanding of failure mode and root cause analysisPrefer experience working in fast-paced startup environmentsPrefer experience with automation tools (i.e., run automation scripts, analyze reports and issues, report bugs)Personal QualitiesYou are passionate about testing, quality assurance, healthcare, and technologyYou are highly organizedYou are methodical, detail oriented and effective at time managementYou are a self-starterYou have good interpersonal, verbal communication, and documentation skillsYou can function well in a challenging and fast-paced environmentYou are enthusiastic and positive, with strong skills in the areas of dependability, flexibility, and maturity Job Posted by ApplicantPro

Job DescriptionScholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the 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 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 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 DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute developing technologies, reagents, and computational tools to increase the sensitivity and throughput of protein analysis, with a specific focus on single-cell proteomics. We are applying these innovations to societally-relevant areas of biomedical research. As part of these efforts, we are developing new approaches to study protein dysfunctions in Alzheimer’s and related neurodegenerative diseases. Summary of PositionWe are seeking scientist and senior scientist candidates to help drive our efforts to use single-cell proteomics to understand the causes of Alzheimer’s and related neurodegenerative diseases. Ideal candidates will have expertise in the molecular mechanisms of neurodegeneration and direct, hand-on experience in single-cell analysis, computational biology, and brain tissue handling. Candidates will have the opportunity to work as part of an interdisciplinary team in multiple areas, including on NIH-funded projects, using proteomic technologies developed at PTI to discover new molecular mechanisms of neurodegeneration in Alzheimer’s and related disorders. Day-to-day responsibilities include designing and carrying out experiments to isolate and profile single cells from brain tissue, computationally analyzing large-scale single-cell proteomics datasets, preparing manuscripts and presentations, mentoring junior scientists, and regular meetings with collaborators in and outside of PTI. Candidates will initially work on ongoing projects but will have the opportunity to design and lead their own projects as well. Candidates with less than 1 year of postdoctoral experience will be considered for the scientist position and those with more than 1 year of experience will be considered for the senior scientist position. About PTIPTI is a nonprofit, focused research organization (FRO) established through Convergent Research. FROs aim to accelerate progress across science and technology by tackling large-scale problems with the potential to unlock existing bottlenecks in specific research areas. PTI aims to achieve a 100-1000x increase in the scale of proteomic analysis. To do so, we are developing new technologies and approaches for mass spectrometric proteomics. This includes molecular barcodes, termed “mass tags” that enable sample multiplexing, as well as computational approaches for increasing the sensitivity of protein analysis. We aim to apply these advances in societally-relevant areas, with a specific focus on neurodegenerative disease. To do so, we are collaborating with leaders in neurodegenerative disease from around the world. To learn more about PTI’s approach for studying neurodegenerative disease, please visit this page. To learn more about our technology for increasing the throughput of protein analysis, please visit here. Researchers at PTI have the opportunity to work within an interdisciplinary team of mass spectrometrists, chemists, computational analysts, and biologists to push the boundaries of protein analysis. PTI supports professional development through educational opportunities such as travel to conferences workshops. Members of PTI receive industry-level resources to lead research projects and have the opportunity to disseminate their discoveries and innovations through high-visibility publications, presentations, and submissions to public data portals. Responsibilities: • Design and execute research projects using single-cell proteomics to understand the molecular mechanisms of neurodegeneration in Alzheimer’s and related disease., • Computationally analyze large-scale, single-cell proteomic datasets to identify new molecular mechanisms of disease., • Collaborate with external laboratories, brain banks, and tissue repositories on sample procurement., • Prepare human brain tissue samples for proteomic analysis using methods and technologies developed at PTI., • Help junior scientists gain expertise in experimental techniques used at PTI, analyzing and interpreting experimental results, recording data in laboratory notebooks, and writing up and presenting research results., • Make regular presentations within PTI and to collaborators., • Prepare manuscripts related to project outcomes and grant applications for external funding., • Demonstrate a commitment to diversity, inclusion, and cultural awareness through actions, interactions, and communications with others., • Other duties as assigned.Qualifications:, • PhD Neuroscience or a related field., • Direct, hands-on experience in preparing human brain tissue for downstream analyses., • Direct, hands-on experience with single cell analysis., • Excellent communication and interpersonal skills, record keeping ability, and attention to detail.Preferred Qualifications, • Experience in high throughput or automated tissue sample collection, preparation, and analysis, particularly with human brains., • Experience with mass spectrometry proteomics., • Fluency in R or Python, particularly in the context of single-cell analysis.We offer:, • An opportunity to change the world and work with some of the smartest and the most talented experts from different fields., • Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from., • Company-paid group life, AD&D, long- and short-term disability insurance, • 15 days PTO + 10 sick days per year, • 18 company holidays + your birthday off, • $5,000 per year educational reimbursement, • Up to 16 weeks paid parental leaveWe aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind. 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 Scientist / Senior Scientist, In Vivo Pharmacology & Translational Biology Location: Boston, MA Company: Tevard Biosciences, Inc. Full time: In person Join Tevard Biosciences and help lead our efforts to develop transformative genetic medicines. We are seeking an experienced, independent scientist to help drive the design, execution, and interpretation of studies supporting our engineered suppressor tRNA (sup-tRNA) pipeline in rare cardiac and neuromuscular diseases. In this role, you will take ownership of research questions across multiple biological scales from molecular and biochemical characterization through in vivo efficacy and translational modeling as we advance our lead programs through IND-enabling studies and into the clinic. You will bring both the technical depth to execute complex, multi-modal studies and the judgment to design and troubleshoot experiments with minimal oversight, while working closely and in a collaborative fashion with a small, cross-functional team. What You Will Be Doing • Independently designing, executing, and interpreting in vivo and in vitro studies evaluating AAV-delivered sup-tRNA gene therapy candidates, including dosing, tissue collection, and biodistribution and efficacy assessments., • Leading the characterization of novel disease models through integrated molecular, biochemical, and functional analyses, and using that data to inform go/no-go decisions across pipeline programs., • Applying quantitative molecular techniques (e.g., ddPCR, qPCR/RT-qPCR) to measure vector genomes, transgene and target protein expression, and biodistribution, including assay design and optimization., • Assessing protein-level readouts of therapeutic efficacy via JESS Western blot, ELISA, immunohistochemistry, MSD, or related methods., • Contributing scientific strategy and study design input to IND-enabling packages, target product profiles, and regulatory or partnering documents., • Presenting data and recommendations directly to the leadership team, translating complex datasets into clear conclusions that drive pipeline decision-making., • Collaborating cross-functionally with CMC, analytical development, and external CROs/CDMOs, and mentoring junior scientists as needed., • Maintaining rigorous documentation and experimental records consistent with GLP-adjacent and IND-enabling study expectations. The ideal candidate is expected to have: • A BS, MS or PhD in a biological or chemical discipline, with several years of relevant industry experience., • Prior experience in the Boston-area biotech or pharmaceutical industry, ideally within a gene therapy, rare disease, or drug discovery/development setting., • A demonstrated track record of designing and independently executing experiments and studies, including troubleshooting unexpected results without close supervision., • Hands-on expertise in molecular and protein-based assays (e.g., ddPCR/qPCR, Western blot, ELISA, IHC) and, ideally, AAV biology and workflows, including vector titering., • In vivo experience in rodent models, such as dosing, tissue collection, necropsy/dissection, and behavioral or functional phenotyping., • Strong scientific communication skills, with the ability to synthesize data into clear conclusions for both technical and cross-functional audiences., • A collaborative, team-oriented working style paired with the independent judgment to drive projects forward proactively in a fast-paced, small-company environment., • Strong math skills preferred. To be considered, candidates: • Must be available to work full-time and in person in Boston, MA., • Must be able to demonstrate a proven record of scientific accomplishment (e.g., publications, patents, or program contributions) appropriate to their level of experience.

Job Description Cambridge, MA · In-Person · Contractor-to-Full-Time About Us GT Biosciences is building Deliveromics, the world’s first AI-powered, high-throughput, and multiplexed in vivo data engine for decoding the design rules of drug delivery. Founded by MIT scientists and backed by top-tier investors, we are creating next-generation non-viral, cell-type-specific delivery vehicles for mRNA and siRNA. We are a tightly-knit, fast-moving, and science-driven team dedicated to making routine in vivo cell reprogramming a reality. We value transparency, collaboration, reliability, and scientific rigor, and seek teammates who thrive in an open, cooperative environment and want to grow together with the team and the company. Job Description GT Biosciences is seeking a highly motivated and dependable Research Associate to join our Platform Development Team and support lipid nanoparticle formulation and RNA delivery. This is a hands-on laboratory role designed for someone eager to learn, take some ownership, and grow within a fast-moving, science-obsessed startup environment. Interview Process The interview process includes two virtual interviews and one onsite interview. Selected candidates may then be invited to participate in a paid working trial lasting up to 30 calendar days. Continued employment will depend on performance, reliability, and mutual fit. From day one, you will work directly alongside scientists with world-leading expertise in RNA delivery, LNP engineering, in vivo screening, and translational biotechnology. Our commitment is to teach you new methods and help you build a broad wet-lab skill set. Your job is to learn quickly, execute carefully, and keep going when experiments are difficult. We’re looking for someone eager to learn and improve in a fast-paced environment. This is an in-person position based in Cambridge, MA. Responsibilities Prepare and formulate lipid nanoparticles and related non-viral delivery systems for mRNA and siRNA using established and evolving protocols. Support formulation screens by varying lipid composition, component ratios, buffers, mixing conditions, and other process parameters. Perform formulation characterization and quality control measurements (e.g., particle size, PDI, encapsulation efficiency, RNA concentration, pH, and fluorescence-based assays). Prepare high-quality formulations and samples for in vitro and in vivo studies, including dose calculations, labeling, quality control, and sample tracking. Maintain basic cell culture responsibilities and support transfection, expression, and knockdown assays as required. Handle precision liquid-handling tasks with accuracy and care (e.g., multichannel pipetting, reagent pooling, serial dilutions). Keep meticulous laboratory records and documentation, troubleshoot experiments thoughtfully, and repeat work carefully when results do not meet expectations. Qualifications Required B.S. or M.S. in Chemistry, Biochemistry, Bioengineering, Biology, Pharmaceutical Sciences, or a related field. At least 1+ years of meaningful hands-on experience in a wet laboratory setting (academic or industry). Demonstrated reliability, attention to detail, and strong commitment to accurate, thorough record-keeping. Proficiency with basic laboratory techniques (e.g., buffer preparation, serial dilution, accurate pipetting, and nucleic acid handling). A fast learner who is excited to develop unfamiliar wet-lab skills and become progressively more independent. Persistence when experiments fail, with the ability to stay calm, investigate possible causes, and improve the next attempt. A proactive, team-first attitude with strong ownership, clear communication, and consistent follow-through. Ability to work onsite five days per week at our Cambridge, MA location. Preferred Exposure to lipid nanoparticles, liposomes, nanoparticle formulation, drug delivery, or microfluidic mixing. Experience handling RNA, including mRNA, siRNA, or other oligonucleotides. Experience with DLS, plate readers, UV spectroscopy, HPLC/UPLC, LC-MS, pH, osmolality, or endotoxin testing. Experience with mammalian cell culture, sterile technique, transfection, or cell-based assays. Experience with fluorescence microscopy or plate reader operation. Exposure to nucleic acid-based assays (e.g., hybridization, ligation, or amplification workflows). Basic cell culture skills (e.g., mammalian cell passaging, sterile technique). Proficiency with basic molecular biology techniques (e.g., running gels, making buffers, using DNA/RNA extraction kits). Nice to Have Basic coding or data analysis skills (e.g., Python, R, or Excel for data organization). Familiarity with automated liquid handling or high-throughput screening platforms. Experience preparing formulations or samples for animal studies. Mouse intravenous injection, perfusion, or tissue collection experience. Strong interest in RNA medicines, drug delivery, and central nervous system therapeutics. Compensation: Estimated Contractor Rate: $22-$40 per hour (depending on experience) What we offer: Flexible, generous health benefits upon conversion to full-time employment. Work with a small, world-leading team that values rigorous science and candid collaboration. Learn directly from experts. Rapid professional growth through hands-on training and meaningful scientific ownership.

Job Description Job Title: Lab Operations Contractor Duration: 12 Months Location: Cambridge, MA Lab Operations Contractor The Neurology Therapeutic Area (TA) is seeking a highly organized and proactive Laboratory Operations Contractor to support our research teams at our Cambridge Crossing (CX) facility. This individual will play a key role in ensuring efficient laboratory operations, enabling scientists to focus on advancing innovative research programs. The successful candidate will serve as a central operational resource across the TA, coordinating laboratory infrastructure, equipment management, vendor interactions, facilities support, bio sample logistics, and research operations. This individual will partner closely with scientists, group leaders, business operations personnel, facilities teams, and external service providers to maintain a safe, compliant, and highly productive research environment. The position reports to a Neurological Diseases TA scientist and works collaboratively across multiple functions to drive operational excellence and continuous improvement. Key Responsibilities Laboratory Operations Serve as a point of contact for day-to-day laboratory operations within the Therapeutic Area, providing concierge or end-to-end level support as needed. Coordinate and lead laboratory startup, ongoing maintenance, and operational support activities. Identify operational bottlenecks and implement process improvements to enhance laboratory efficiency and productivity. Maintain visibility of operational issues, drive resolution, and partner with R&D Operations and Workplace Experience to mitigate risks and ensure business continuity. Laboratory Equipment Management Act as a point contact for laboratory asset management services. Maintain accurate equipment inventories and asset records. Coordinate installation, qualification registration, relocation, and retirement of laboratory equipment. Ensure compliance with metrology, calibration, preventative maintenance, and temperature-monitoring requirements. Coordinate equipment service, repairs, maintenance activities, and vendor interactions. Serve as the primary point of contact for laboratory equipment emergencies, coordinating rapid response, troubleshooting, vendor engagement, and recovery activities to minimize operational downtime and ensure continuity of laboratory operations Coordinate and maintain equipment data infrastructure, partnering with DigitalLiaison with scientists to organize and coordinate equipment training, updates, or other technical advice or support as needed. Facilities and Laboratory Support Partner with Cambridge Crossing facilities teams and support service providers to ensure smooth laboratory operations. Coordinate laboratory consumables, chemical inventories, buffer preparation services, waste management, and shared resource utilization. Facilitate facilities repair requests and monitor issue resolution. Help maintain laboratory organization, safety, and compliance standards. Procurement, Materials Management, and Logistics Serve as a subject matter resource for procurement and materials management processes. Serve as point of contact and expert user to resolve issues and questions regarding procurement workflows. Support scientists in purchasing activities and shipments coordination, including receiving, inventory management, and vendor communications as needed. Facilitate laboratory supply management to ensure uninterrupted research activities. Assist with operational budgeting, purchase order tracking, and invoice reconciliation as needed. Assist with license and contract process support as needed (biological material, digital software, etc) Biosample and Freezer Management Serve as point of contact and knowledge point on best practices for bio sample and cell line management and inventories in partnership with internal teams. Support biosample logistics and ensure adherence to established handling, storage, and shipping procedures. Assist with coordination and compliance of licenses for cell licensing, including tacking usage agreement, material transfer agreements (MTAs), and ensuring adherence to vendor and institutional requirements Assist with management of on-site and off-site freezer capacity, space allocation, maintenance, monitoring, and contingency planning. Daytime primary responder role for monitored units. Animal Research Operations Serve as a liaison with the animal research facility and related operational teams. Coordinate activities related to animal usage tracking, licensing, and operational planning. Support management of animal related licenses and compliance documentation . Cross-Functional Support Act as an "expert user " for key operational systems and processes, including: Procurement and purchasing systems, Source to Pay Materials management Shipping and receiving Facilities services Laboratory asset management IT support services Office and laboratory equipment support Health and Safety Workplace Experience Build strong partnerships across scientific, operational, and administrative functions. Support onboarding and offboarding of new employees, contractors, and interns within the group including lab orientation walkthrough, IT support and other facilities/office equipment needs. Qualifications Required Bachelor's degree in biology, Neuroscience, Life Sciences, or a related scientific discipline. Minimum of 4 years of experience working in a laboratory or research environment. Demonstrated experience supporting laboratory operations, laboratory management, project coordination, or related operational functions. Strong organizational and prioritization skills with exceptional attention to detail. Demonstrate strong interpersonal and communication skills, building effective relationships with scientists and cross-functional teams. Ability to manage multiple competing priorities in a dynamic research environment. Excellent communication, collaboration, and stakeholder management skills. Proficiency with Microsoft Office applications and laboratory management systems. Preferred Industry experience within biotechnology, pharmaceutical, or research organizations. Experience with laboratory startup, space management, equipment asset management, or facilities coordination. Functional knowledge and understanding of laboratory equipment include operation principles, functionality, and applications across standard lab workflow. Familiarity with biosample management, laboratory compliance requirements, and animal research operations. Experience implementing process improvements and driving operational efficiencies. Experience working in a BSL2 or BSL2 wet lab, understanding of health, safety and best practices operations within a laboratory environment. Competencies and Characteristics Highly organized, communicative, and self-motivated Strong problem-solving and analytical skills Customer-service mindset with a collaborative approach Ability to work in a highly matrix environment and build relationships and points of contact across multiple groups and departments Ability to work independently while effectively influencing across teams Comfortable operating in a fast-paced and evolving environment Commitment to operational excellence, compliance, and continuous improvement #TB_PH #ZRHC #Linkd Why TalentBurst? At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth. Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships. We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options. TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce. \nCompany Description Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA Founded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website www.talentburst.com or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA

Job DescriptionBenefits: • Bonus based on performance, • Competitive salary, • Health insurance, • Paid time off, • Stock options plan Scientist/Senior Scientist, Biology Lead – Kidney Experience About the Role We are seeking a highly motivated, hands-on, and scientifically rigorous Scientist/Senior Scientist with deep expertise in both in vitro and in vivo kidney biology, renal disease mechanisms, and translationally relevant kidney disease models to build and lead our kidney biology engine at a venture-backed startup biotech company. This individual will play a foundational role in establishing integrated in vitro and in vivo kidney research platforms that enable target discovery, mechanistic validation, therapeutic screening, and development candidate nomination for next-generation targeted genetic medicines. Our therapeutic focus is on kidney diseases leveraging our novel ligand-guided siRNA delivery platform. The ideal candidate combines extensive bench expertise in renal cellular biology, kidney disease models, in vivo pharmacology/efficacy studies, and translational assay development, with a strong builder mentality suited for a fast-paced, venture-backed startup. This is an unique opportunity to shape core scientific capabilities, work closely with executive leadership, and directly impact therapeutic programs from target discovery through preclinical development. This position is primarily on-site in Boston, MA. Key Responsibilities Kidney Biology Engine Development (Primary Focus) · Build and lead the internal kidney biology platform spanning both in vitro and in vivo capabilities to support discovery and development of renal-targeted therapeutics · Establish, optimize, and scale kidney disease-relevant cellular, molecular, and animal models · Develop robust, scalable bioassays and experimental workflows to support: ü Kidney target biology validation ü Receptor expression, trafficking, and internalization characterization ü Ligand discovery and screening ü Ligand–siRNA conjugate uptake, endosomal escape, and functional knockdown ü In vivo PK/PD, biodistribution, efficacy, and biomarker analyses · Design mechanistic assays and translational studies for kidney disease pathways relevant to therapeutic targets Program Execution · Design, execute, troubleshoot, and interpret complex in vitro, ex vivo, and in vivo studies across multiple kidney disease programs · Generate high-quality data packages to support discovery decisions, target prioritization, and development candidate nomination · Drive scientific rigor in assay reproducibility, translational relevance, and platform scalability In Vivo Biology and Translational Leadership · Lead or significantly contribute to in vivo kidney disease studies, including efficacy, biodistribution, PK/PD, and mechanistic studies · Support selection, management, and interpretation of external CRO or academic in vivo studies · Integrate in vitro and in vivo findings to refine therapeutic hypotheses, delivery strategies, and biomarker plans · Contribute to translational biology strategy supporting future IND-enabling development Cross-functional Leadership · Serve as a scientific leader across biology, platform, and therapeutic program needs · Collaborate closely with chemistry, delivery, translational, regulatory, and external teams · Help define scientific strategy for kidney therapeutic programs and platform evolution Data, Communication, and Documentation · Maintain rigorous industry standard ELN documentation · Present findings to internal research team, leadership & external partners · Contribute to patents, publications, study reports, and data presentations Required Qualifications · PhD in Nephrology, Renal Biology, Cell Biology, Molecular Biology, Pharmacology, or related field with 3–8+ years of relevant postdoctoral and/or industry experience · Deep expertise and extensive hands-on bench experience in both in vitro and in vivo kidney biology, kidney disease mechanisms, and translational renal models · Strong technical expertise in mammalian cell culture (including different kidney cells), qPCR/RT-qPCR, flow cytometry, ELISA/MSD, Western blot, immunostaining, advanced imaging, and functional assay development · Excellent scientific communication, problem-solving, and collaborative skills Preferred Qualifications · Hands-on experience in kidney therapeutics, nephrology, or precision medicine · Direct experience with renal efficacy studies, PK/PD, biodistribution, or translational biomarker programs · Experience with siRNA, ASO, mRNA, or nucleic acid therapeutics · Experience with ligand-mediated or receptor-targeted delivery systems · Prior startup biotech experience What We Are Looking For · Builder mindset with excitement to create new platform · Hands-on leader who enjoys bench work · Strong problem solver comfortable with ambiguity in a startup environment · Collaborative team player

Job DescriptionRole Location: Waltham, MA The Company We are Alloy Therapeutics - a biotechnology ecosystem company 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 biotechnology infrastructure company 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, like this position, to appreciate their colleagues who have less flexibility. We are all one team! The Role We are seeking a hands-on scientist with strong expertise in LC–MS to lead bioanalytical characterization of oligonucleotide therapeutics, focusing on DMPK and biological interpretation. This LC–MS-focused role involves generating and interpreting data on oligonucleotide exposure, stability, metabolism, protein binding, and structural integrity to answer DMPK-relevant questions and link analytical findings with PK/PD and biological activity. Key Responsibilities • LC–MS–Driven Bioanalysis: Develop and execute LC–MS/MS and LC–HRMS methods for quantitative and structural analysis of oligonucleotides in biological matrices. Design and perform stability, degradation, and Metabolite Identification (MetID) studies to support DMPK. Provide a higher throughput or automated protein binding data (LC-MS Proteomics) ., • Exposure & Disposition: Apply LC–MS and other methods to assess oligonucleotide–protein interactions, binding, and disposition, interpreting how stability, metabolism, and chemical modifications influence systemic and tissue exposure., • DMPK & Biological Integration: Interpret LC–MS data within a DMPK context, collaborating with cross-functional teams to link findings with PK, PD, and biological readouts (e.g., target knockdown, gene expression)., • Data Analysis & Communication: Perform quantitative LC–MS data analysis, troubleshoot analytical issues, and clearly communicate analytical and DMPK insights to inform decision-making.Required Qualifications, • Ph.D. or M.S. in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field., • 3+ years (Ph.D) or 10+ years (M.S.) of post-academic experience, • Demonstrated experience with LC–MS and high-resolution MS (HRMS) oligonucleotides bioanalysis, including stability, MetID, and protein binding studies., • Comfort working cross-functionally in a discovery environment.Preferred Qualifications, • Experience with chemically modified oligonucleotides and/or conjugates., • Ability to interpret LC–MS data in a DMPK and biological context., • Exposure to PK/PD concepts and molecular biology-based analytical technologies (e.g., qPCR, ddPCR).Key Skills & Competencies, • LC–MS/MS and LC–HRMS (core expertise), • Oligonucleotide exposure, stability, metabolism, and protein binding, • DMPK-relevant data interpretation, • Strong troubleshooting ability and scientific judgment, • Clear cross-functional communication 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 annual base salary range is $126,000 - $150,000, 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 A1y1zprA3i

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 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 DescriptionScismic is supporting the growth of a Cambridge, MA biotech startup that is pioneering mRNA-modulating therapies to cure a broad range of genetic diseases. The company is exploring the use of its novel platforms in neurological disorders, heart disease, and muscular dystrophies. Position summary: We are looking for Research Associate (RA-I or RA-II) with an innovative mindset, great attention to detail and ability to work collaboratively to solve problems, to help advance therapeutic candidates to the clinic. The successful candidate will have an opportunity to positively impact patients with serious unmet medical needs while working closely with our world-class scientific team, including with company’s scientific co-founders. In this position, you will collaborate with the in vivo pharmacology team to study effects of therapeutic lead candidates. The RA will work with animal models for rare genetic diseases and will be responsible for executing experiments to quantify molecular, cellular, and physiological readouts, in addition to supporting in vivo dosing studies and related research activities within the in vivo pharmacology group. This is an exciting opportunity for a motivated scientist to further develop their skills in neuroscience, physiology and gene therapy while helping to make an impact on lives of patients suffering from rare diseases. Key responsibilities for this position include: • Establish and quantify readouts for in vivo efficacy, biodistribution, and other effects of dosed articles in animal models of rare genetic disorders, • Maintain, genotype and characterize mutant mouse lines and their associated phenotypes, as well as assist with animal husbandry, • Execute and/or troubleshoot diverse assays – physiological, behavioral, or tissue-based - perform relevant analysis, document all experimental details and results, • Assist with experiments using cultured cells, virus vector production and/or titration and execute assays for DNA/RNA and/or protein quantification, • Perform surgical procedures on animal models using multiple dosing routes, • Work with team members to regularly update electronic lab notebook (ELN) prepare high quality reports and scientific presentations, • Be up to date with relevant scientific literature and adapt to changes in priorities. Qualifications: • A BS/MS in Neuroscience, Physiology, Molecular/Cellular Biology, or a related Life Science discipline, with 0-2 years’ experience working in a life science research lab., • Hands-on experience working with rodent animal models (mouse or rat) – including animal handling and husbandry is required, • Candidates with experience in post-hoc procedures including tissue extraction, embedding and processing, immunohistochemistry (IHC), protein/nucleic acid extractions and/or PCR based methods (e.g., qPCR, ddpCR) will be preferred., • Additional experience with one of the following methods will be a plus: in situ Hybridization (ISH), RNAscope, imaging/microscopy, image anaylsis as well protein detection/quantification methods such as Western Blot, ELISA, etc., • Familiarity with various dosing routes in mice – including (but not limited to) Intracerebroventricular (ICV), intrathecal(IT), Intravenous(IV), Intra-muscular (IM), Intraparenchymal routes – is desirable., • Experience with mouse/rat behavior assays (e.g. open field, rotarod) would be good to have but not required., • Ability to work collaboratively with colleagues and effectively handle and prioritize multiple tasks in a fluid, fast-paced work environment, • Ability to master new concepts quickly, highly organized, with excellent oral and written communication skills Title commensurate with level of experience. We are accepting applications to build a pipeline of potential candidates for future opportunities. If your qualifications align with our requirements, we will contact you once the hiring process begins. Thank you for your interest in this role.

Job DescriptionParallel Squared Technology Institute (PTI) is a non-profit research institute aiming to catalyze a leap in protein analysis technology and use it to explore new biological frontiers. PTI supports open research and educational opportunities supporting rapid career development for scientists, engineers, and mathematicians. Why? Protein dysfunctions directly cause many diseases, such as Alzheimer’s disease. Yet, proteins remain understudied because of technological hurdles. How? To resolve these limitations, PTI will develop mass tags enabling a new framework for multiplexed protein analysis by mass spectrometry towards achieving 100-fold increase in throughput. Scientists at and collaborating with the institute will use these gains to directly investigate disease mechanisms and resolve problems that have proven intractable for decades. Our proof of principle technology and strategies are outlined at: parallelsq.org. PTI’s new approach requires synergy between a diverse team of chemists, machine learning engineers, biologists, and mass spectrometrists. Alzheimer’s disease and aging will be among the first focuses of this technology-driven research organization. New career opportunities Members of PTI will be supported with industry-level resources to lead research projects and disseminate their discoveries and innovations to the broader biomedical community through frequent publications, presentations, and submissions to public data portals. Summary of Position We are looking for either a Research Associate or Senior Research Associate who is interested in mass spectrometry. This person will be working on maintaining MS instruments for running multitudes of samples for a variety of projects in addition to other responsibilities. In order to be seriously considered for this position, we require a cover letter as part of the candidate's application.Responsibilities • You will learn how to set up, operate and maintain mass spectrometers from multiple major vendors., • Protein sample preparation., • Inventory management for reagents and samples., • Analyze experimental data and interpret results for internal and public presentation., • Preparation of lab reagents and media.Required Qualifications, • Bachelor’s degree in Chemistry, Biology, or related field. Advanced degrees or >2 years of experience will be considered for Senior RA position. Basic proficiency with biochemistry techniques or chemistry techniques., • Demonstrated enthusiasm and interest in analytical chemistry., • High level of initiative and flexibility, excellent communication and teamwork skills., • Attention to detail., • Good time management.Preferred Qualifications, • Familiarity with analytical techniques, mass spectrometry preferred., • Familiarity with liquid chromatography., • Protein and peptide sample preparation and purification methods.Who Will Love This Job, • You are passionate about science and technology and are eager to work in a team environment., • You love learning new techniques, new technologies, and new concepts., • You want an environment that will support your future plans as a scientist or engineer., • You are committed to open science ideas and want to see your work disseminated broadly.We Offer, • An opportunity to change the world and work with some of the smartest and the most talented experts from different fields., • Excellent medical, dental, and vision insurance with many $0 premium options for you and your family with several national and regional providers. Most employees have more than 20 plan options to choose from., • Company-paid group life, AD&D, long- and short-term disability insurance, • 15 days PTO + 10 sick days per year, • 18 company holidays + your birthday off, • $5,000 per year educational reimbursement, • Up to 16 weeks paid parental leave, • Industry competitive salary We aim to help fill a structural gap in today's R&D system. We enable fundamental research that requires unusual levels of scale and coordination yet is not rapidly monetizable by industry. We’re bringing together top talent from academia, industry, and startups to build a new model for innovative R&D. As an incubator within the Schmidt Futures Network, we identify high-impact scientific or technical research and development opportunities, ultimately defining and launching these projects as Focused Research Organizations. We are an Equal Employment Opportunity employer that proudly pursues and hires a diverse workforce. We do not make hiring or employment decisions on the basis of race, color, religion or religious belief, ethnic or national origin, nationality, sex, gender, gender-identity, sexual orientation, disability, age, military or veteran status, or any other characteristic protected by applicable local, state, or federal law or company policy. We strive for a healthy and safe workplace and strictly prohibit harassment of any kind. 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 Biocytogen is seeking highly skilled and motivated scientists to join our antibody discovery team. This role is dedicated to optimizing therapeutic antibody binders from our RenBiologics program, which generates an extensive library of therapeutic antibodies targeting thousands of druggable genes. The successful candidate will utilize advanced antibody engineering techniques to improve binding affinity, specificity, stability, and therapeutic functionality. This work supports the development of antibodies across diverse therapeutic areas, including immuno-oncology, inflammatory and autoimmune diseases, neurology, cardiovascular conditions, and metabolic disorders. Key Responsibilities Target Selection and Program Design -Select and evaluate therapeutic targets with a strong understanding of MOA, druggability, and delivery options. -Design experimental strategies to advance candidates from Biocytogen’s RenBiologics Antibody Binder/Lead Library toward therapeutic development. Project Management -Drive projects by assembling resources, managing timelines, and ensuring alignment with program objectives. Antibody Engineering and Optimization -Engineer antibodies to improve affinity, specificity, stability, and manufacturability. -Optimize antibodies through advanced molecular designs, such as Fc engineering or bispecific formats. Lead Evaluation and Development -Evaluate lead antibodies for binding, function, and developability, ensuring readiness for preclinical development. Collaboration and Reporting -Work with discovery, manufacturing, and BD licensing teams to advance and out-license antibody assets. -Maintain clear documentation and present findings to internal and external stakeholders. Requirements -PhD in Biochemistry, Molecular Biology, Immunology, or a related field with 2+ years of relevant experience, or MS with 5+ years of experience in antibody engineering and project management. -Strong expertise in target biology research, including understanding MOA, druggability, and formulation requirements. -Proven experience in antibody engineering and optimization, including affinity maturation and stability improvement. -Demonstrated ability to independently drive projects, assemble resources, and meet critical milestones. -Excellent collaboration and communication skills for working with cross-functional teams and presenting findings effectively. 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 Description Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics. We are seeking a Senior Scientist to join our Biologics Cell Line Development team in Boston, MA and help push the boundaries of biotherapeutic cell line development. This role is for a scientific innovator and a manager of junior scientists. The successful candidate will conduct & supervise CHO-based cell line development for biologic therapeutics moving into clinical development. Significant effort designing complex experimental approaches to improve expression systems and workflows through innovation and implementation of new technology is also an important part of this role. The successful candidate will also work cross-functionally with Asimov’s synthetic biology, modeling, process development and analytical teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. About the Role: You’ll perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment. You’ll drive innovation through the development of improved genetic components, host cell line engineering and cell line development process optimization. You’ll identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and continued innovation. You’ll represent the cell line development team on cross-functional projects, making decisions for cell line activities and effectively communicating results, progress and plans. You’ll represent Asimov externally, contributing to industry conferences, industry forums, filing patents, and publishing peer-reviewed manuscripts. You’ll manage and mentor a team of 3+ scientists focused on CHO-based biologics CLD, providing technical direction and supporting them in their professional development. About You: 5+ years of experience in CHO-based cell line development is a must, stemming from expressing IgGs and bispecifics in an industrial CLD environment. You have a Ph.D. in Biological Engineering, Cell Biology, Molecular Biology, or a related field. You’re a creative problem solver never satisfied with the status quo and get excited about the opportunity to drive the creation of disruptive technology. Minimum 1 year experience managing direct report(s) and providing technical guidance. Don’t let this stop you from applying, but it’s a plus if you are familiar with any of the following: vector optimization to improve titer and product quality attributes for complex bispecific scaffolds; CLD process optimization; or development of automated high-throughput screening for CLD workflows. Experience working with a global customer base isn’t a requirement for this role but bonus points if you have it. 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 ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives. Compensation Range: $145K - $165K

Job DescriptionDescription: Predicta is building a molecular insights platform for blood cancer care. From a single blood sample, we generate longitudinal genomic and immune insights that help clinicians and researchers better understand disease biology, guide treatment decisions, and monitor disease evolution over time. We are seeking a highly motivated R&D Scientist who will lead assay development efforts spanning flow cytometry and NGS technologies, including whole genome sequencing and single-cell RNA-seq. The ideal candidate has a strong technical background in immunology, cell biology, and genomics, with experience developing highly robust and reproducible assays deployed in clinical or research settings. This individual will play a key role in developing assays for the characterization of tumor and immune cells, from multi-color flow cytometry immunophenotyping and FACS-based sorting through to downstream NGS library preparation and sequencing, translating early research concepts into clinical assays. This laboratory-based scientist should be passionate about developing cutting-edge cytometry and genomic assays and will work closely with an inter-disciplinary and cross-functional team of other laboratory-based scientists and computational biologists, focused on improving blood-based cancer diagnostic capabilities in areas including cancer detection, measurable residual disease, and other related applications. Key responsibilities • Design, develop, and optimize molecular assays spanning flow cytometry and NGS for tumor cell and immune characterization, • Lead multi-color and spectral flow cytometry panel design (10–30+ colors), fluorophore selection, antibody titration, and FACS-based cell sorting, • Contribute to development and optimization of NGS workflows, including library preparation, sample processing, and quality control, • Develop and optimize sample processing workflows (whole blood, bone marrow, PBMC isolation) that feed both flow cytometry and NGS/single-cell pipelines, • Use FACS to identify rare cell populations for downstream single-cell RNA-seq and other NGS applications, • Evaluate and implement new technologies, reagents, and platforms spanning cytometry (e.g., spectral flow) and sequencing to improve assay performance, robustness, and scalability, • Establish and maintain QC metrics, instrument standardization, and assay validation practices across both cytometry and sequencing workflows, • Plan and execute experiments independently, analyze data (FlowJo for flow; and standard NGS QC pipelines), and clearly communicate results to internal stakeholders, • Collaborate closely with the R&D and computational biology teams to ensure seamless integration of wet-lab and analytical workflows across modalities, • Develop and document standard operating procedures (SOPs), protocols, and technical reports suitable for regulated environments, • Maintain meticulous, reproducible records and contribute to shared protocols, • Follow, document, and adapt experimental protocols with care and precision, • Mentor junior scientists and contribute to building best practices within the R&D organization, • Support technology transfer from R&D into product development and clinical operations as needed Requirements: • PhD (or BS/MSc with significant industry experience) in immunology, molecular biology, cell biology, genetics, bioengineering, or a related field, • 5+ years of hands-on laboratory experience spanning flow cytometry/immunophenotyping and molecular biology assay development, preferably in a cutting-edge research/R&D environment, • Deep expertise in multi-parameter and spectral flow cytometry, including panel design, instrument operation and FACS-based cell sorting, • Deep expertise in NGS technologies, including library prep, sequencing platforms, and workflow optimization; experience with single-cell RNA-seq or related single-cell technologies (scWGS, scATAC-seq, scMultiomics) is a strong plus, • Strong understanding of immune cell subsets and immunophenotyping, particularly in the context of hematologic malignancies, • Hands-on experience with compensation, fluorescence-minus-one (FMO) controls, and gating strategy development, • Strong experimental design, troubleshooting, and data interpretation skills, • Demonstrated success working in cross-functional, fast-moving research or startup environments and collaborating with computational scientists, • Outstanding written and verbal communication skills, • Ability to handle several fast-paced projects concurrently, • Demonstrated curiosity and scientific rigor with excellent problem-solving skills, • Ability to engage in crucial conversations – providing and receiving feedback Preferred qualifications • Hands-on experience linking flow cytometry-sorted populations directly into NGS or single-cell library preparation workflows, • Experience developing assays intended for clinical or regulated use (e.g., CLIA, CAP, or FDA-regulated environments), • Familiarity with computational methods and software for analysis of flow cytometry and/or NGS data, especially for quality control, • Prior experience bringing assays from early research through to product development, • Experience with automation of cell and molecular biology assays, especially sample extraction, cell staining/sorting, and NGS library preparation, • Background in immunology, immuno-oncology, or immune-mediated diseases Work Location • This role is based in Cambridge, MA and is a full time in-office role. Travel may be required in the future. Why Join Predicta Biosciences? This is a unique opportunity to be part of a mission-driven team advancing precision diagnostics for hematologic cancers. You’ll play a key role in shaping the quality and performance of our clinical testing efforts and contribute directly to patient-impactful innovations. The annual salary range for this position is $120,000 - $180,000 plus a 10% bonus opportunity. Predicta considers a variety of factors when determining base compensation, including experience, skills, education, qualifications, and geographic location. Actual compensation will vary, and it is not typical to be hired at or near the top of the range for the role. Additional rewards include equity, flexible time off, 401k Plan, medical, dental and vision plans that are 90% paid by Predicta and a partially company-funded HSA.

Job Description Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics. We are seeking a Principal Scientist to join our Biologics Cell Line Development team in Boston, MA and help push the boundaries of biotherapeutic cell line development. This role is for a scientific innovator and a manager of junior scientists. The successful candidate will conduct & supervise CHO-based cell line development for biologic therapeutics moving into clinical development. Significant effort designing complex experimental approaches to improve expression systems and workflows through innovation and implementation of new technology is also an important part of this role. The successful candidate will also work cross-functionally with Asimov’s synthetic biology, modeling, process development and analytical teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering. About the Role: You’ll perform CHO cell line development processes including transfection, cloning, characterization, and cell banking using state-of-the-art equipment. You’ll drive innovation through the development of improved genetic components, host cell line engineering and cell line development process optimization. You’ll identify emerging practices for biologics cell line development and manufacturing to shape scientific strategies and continued innovation. You’ll represent the cell line development team on cross-functional projects, making decisions for cell line activities and effectively communicating results, progress and plans. You’ll represent Asimov externally, contributing to industry conferences, industry forums, filing patents, and publishing peer-reviewed manuscripts. You’ll manage and mentor a team of 3+ scientists focused on CHO-based biologics CLD, providing technical direction and supporting them in their professional development. About You: 8+ years of experience in CHO-based cell line development is a must, stemming from expressing IgGs and bispecifics in an industrial CLD environment. You have a Ph.D. in Biological Engineering, Cell Biology, Molecular Biology, or a related field. You’re a creative problem solver never satisfied with the status quo and get excited about the opportunity to drive the creation of disruptive technology. Minimum 1 year experience managing direct report(s) and providing technical guidance. Don’t let this stop you from applying, but it’s a plus if you are familiar with any of the following: vector optimization to improve titer and product quality attributes for complex bispecific scaffolds; CLD process optimization; or development of automated high-throughput screening for CLD workflows. Experience working with a global customer base isn’t a requirement for this role but bonus points if you have it. 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 ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives. Compensation Range: $170K - $190K

Job Description Senior AI Scientist – Drug Discovery & Computational Biology (Hybrid - Boston, MA, USA) We are looking to hire a candidate with the mentioned skill sets and experience for one of our clients within the Healthcare Industry. This is a 6+ month contracting role, with potential for extension. This is a HYBRID role. Key Responsibilities: We are seeking a highly skilled professional with deep expertise in applying Artificial Intelligence and Machine Learning to drug discovery and development. The ideal candidate will have experience in Drug Discovery & Computational Biology (Must). The candidate should demonstrate a strong track record of leveraging advanced computational approaches to accelerate therapeutic discovery and possess the ability to collaborate effectively with multidisciplinary research and development teams. Required Skills/Qualifications: • Deep expertise in applying Artificial Intelligence and Machine Learning to drug discovery and development., • Experience in Drug Discovery & Computational Biology (Must)., • AI and machine learning methodologies for drug discovery, including predictive modeling, lead optimization, and translational research applications., • Graph machine learning techniques for biological networks, molecular property prediction, target identification, and knowledge graph-based discovery., • Virtual cell screening and AI-driven target discovery platforms, with particular focus on rare disease research and therapeutic innovation., • AI-driven molecular design for small molecules and biologics (Abs/VHH), including toxicity prediction, off-target assessment, developability analysis, and candidate optimization., • Structural biology, including protein structure analysis, molecular interactions, computational modeling, and integration of structural data into drug discovery workflows., • Healthcare Domain experience (Must)., • Ability to collaborate effectively with multidisciplinary research and development teams. Other Job Details: • Job Type: C2C or W2., • Duration: 6+ months with high possibility of extension., • Pay Rate: $75/hr. on C2C or $65/hr. on W2., • Location: Hybrid - Boston, MA, USA., • Interviews: Video interviews., • Docs required: ID proof will be required.

Job DescriptionScismic is supporting the growth of a Cambridge, MA biotech startup that is pioneering mRNA-modulating therapies to cure a broad range of genetic diseases. The company is exploring the use of its novel platforms in neurological disorders, heart disease, and muscular dystrophies. Position summary: As an expert scientist in cellular neurobiology, you will be responsible for establishing cellular assays to demonstrate in vitro proof of concept for company tRNA therapeutic leads and characterize the cellular activity and downstream disease-relevant biology to help prioritize candidates for in vivo studies. Key responsibilities for this position include: • Establish in vitro disease models in relevant cell types including primary neurons and glia isolated from transgenic animal models and patient-derived iPSC lines., • Design, troubleshoot, and execute cell-based assays in human and rodent cell lines to characterize the efficacy and safety of company's novel tRNA therapeutic leads., • Understand mechanism of action of lead candidates and establish assays and endpoints relevant to downstream target and disease biology. Conduct literature searches; communicate understanding in internal forums and with external collaborators and partners. Minimum qualifications:, • A BS/MS in Neurobiology, Molecular/Cellular Biology, physiology, or a related discipline., • Extensive hands-on experience with a variety of molecular, cellular and/or physiological techniques (isolating rodent neurons and establishing primary neuronal cultures, neurite outgrowth, qPCR, western blotting, microscopy, calcium imaging, synaptic imaging, multi-electrode arrays, human IPS/ES cell culture, etc)., • Prior experience using AAV/lentivirus in primary or iPSC-derived neurons is highly desirable., • Ability to master new concepts and technologies quickly and run experiments independently., • Scientifically rigorous, highly organized, with excellent oral and written communication skills., • Ability to work independently as well as collaborate with colleagues and effectively prioritize and manage multiple tasks in a fluid, fast-paced work environment Title commensurate with level of experience. We are accepting applications to build a pipeline of potential candidates for future opportunities. If your qualifications align with our requirements, we will contact you once the hiring process begins. Thank you for your interest in this role.

Job DescriptionCrescent 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 RangeThe 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 Senior / Principal Research Associate, In Vivo Studies Location: Boston, MA Reports to: Scientist II Job Type: Full time, Onsite About Us We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo gene editing. Job Summary The In Vivo Studies team is hiring a Senior / Principal Research Associate to support the planning, execution, and analysis of in vivo pharmacology and biodistribution studies that advance our preclinical programs. This is a hands-on role for a scientifically rigorous, highly organized researcher who can execute rodent studies, collect high-quality samples, maintain strong study records, and partner closely with Translational Research, Delivery, Editing, and Program teams. The location for this position is expected to be onsite in our Boston lab. Responsibilities • Support the design, planning, and execution of in vivo rodent studies evaluating delivery, biodistribution, editing efficiency, pharmacodynamic activity, tolerability, and related preclinical endpoints., • Perform hands-on in vivo study activities under approved protocols, which may include animal handling, dosing support, clinical observations, body weight tracking, sample collection, necropsy support, and tissue harvest., • Prepare study materials, dosing solutions, collection supplies, labels, chain-of-custody documentation, and sample inventories to ensure studies run smoothly and reproducibly., • Process blood, plasma, serum, bone marrow, spleen, liver, and other tissues for downstream molecular, cellular, and protein-based analyses, including nucleic acid and protein extraction workflows., • Coordinate with internal scientists and external partners or CROs to align study timelines, protocols, sample logistics, data transfers, and documentation requirements., • Maintain accurate electronic and paper study records, including protocols, worksheets, sample maps, deviations, reagent logs, and raw data consistent with data integrity and reproducibility expectations., • Analyze and summarize study observations and sample metadata; contribute to interpretation of in vivo results in the context of program goals., • Contribute to protocol development, study reports, SOPs, and continuous improvement of in vivo operations and sample-processing workflows., • Present study updates, operational risks, and key results in team meetings; collaborate cross-functionally with Translational Research, Delivery, Editing, and broader research teams., • Mentor or train junior team members on study preparation, sample handling, documentation practices, and relevant laboratory workflows as appropriate for level. Qualifications • BS or MS in biology, pharmacology, molecular biology, biomedical sciences, veterinary technology, or a related discipline, with approximately 5-6 years of relevant hands-on research experience in industry or an equivalent research setting., • Direct experience supporting in vivo rodent studies, including study setup, animal handling, dosing support or study procedures, sample collection, tissue harvest, and post-collection processing., • Strong understanding of in vivo study execution, sample traceability, protocol adherence, and the importance of accurate, contemporaneous documentation., • Hands-on experience with downstream tissue and sample processing for molecular, cellular, or protein-based assays such as qPCR / RT-qPCR, ddPCR, ELISA, flow cytometry, Western blot / Jess, sequencing, or related analytical readouts., • Ability to plan daily study activities, anticipate operational needs, troubleshoot issues, and communicate risks or deviations promptly., • Comfort working in a fast-paced, cross-functional research environment with changing program priorities and multiple concurrent studies., • Clear written and verbal communication skills; comfortable summarizing study status, sample inventories, observations, and data for a scientific audience., • Commitment to high-quality animal care, ethical research practices, and compliance with approved study protocols, SOPs, and institutional requirements. Preferred Qualifications • Experience supporting in vivo studies for gene editing, nucleic acid therapeutics, cell or gene therapy, biologics, or targeted delivery platforms., • Experience with LNP-based, antibody-based, receptor-targeted, or other delivery technologies in preclinical models., • Familiarity with biodistribution, pharmacodynamic, toxicology, or translational biomarker study designs., • Experience with common rodent dosing or sampling routes such as IV, IP, SC, PO, retro-orbital, submandibular, tail vein, or terminal cardiac collection, as applicable to approved protocols., • Experience processing hematopoietic tissues or working with bone marrow, spleen, peripheral blood, HSC / HSPC biology, immune-cell phenotyping, or flow cytometry workflows., • Experience coordinating external CRO studies, shipping biological samples, managing sample manifests, or reconciling datasets across internal and external teams., • Familiarity with electronic lab notebooks, study management systems, animal facility systems, or inventory / sample tracking tools., • Prior experience supporting IND-enabling, GLP-like, or regulated preclinical studies. Benefits • Competitive salary, equity, and comprehensive benefits package., • Opportunities for professional growth and leadership development., • Fast-paced, collaborative, and innovative work environment., • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity. How to Apply Interested candidates will click Apply to proceed to our application portal and will need to submit a resume and cover letter detailing relevant experience. To be considered for the role, applicants must be: • Eligible to work in the United States for any employer without current or future sponsorship., • Able to work onsite in the lab, based on the location listed for the position (either San Diego, CA or Boston, MA). Please check the position listing when you Apply for the location of each role., • Direct candidates only and not from a third party, i.e., staffing agency. Equal Opportunity Employer We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Salary Range $90,000 - $120,000

Job DescriptionJob Title: Quality Control AnalystJob Description The Quality Control (QC) department is essential for ensuring compliance with cGMP operations through the inspection of components and raw materials, as well as quality testing of intermediate, stability, and final product samples. Various techniques, such as assay transfers and validation of new instrumentation, are utilized within the Quality Control Laboratory to maintain cGMP compliance. As a Quality Control Analyst, you will perform routine testing of raw materials, in-process, and final products in accordance with SOPs for product release and validation. Responsibilities • Run and execute PCR and PCR techniques., • Perform microbiological assays for in-process and final product samples., • Conduct analytical methods for final bulk material/finished goods., • Test and disposition of raw materials and perform environmental monitoring., • Review QC data for compliance to procedures and specifications., • Calculate and evaluate results., • Participate in lab maintenance and administration duties., • Initiate lab investigations and deviations., • Provide lab support including glass washing and autoclaving., • Demonstrate an understanding of CGMPs and their application to responsibilities., • Follow accurate oral and written procedures for testing of in-process and final product samples.Essential Skills, • Proficiency in PCR techniques and testing., • Experience in microbiology, biology, or similar life sciences., • Understanding of quality control, microbiology, and qPCR., • Familiarity with CGMPs and quality control procedures.Additional Skills & Qualifications, • BS degree with 3+ years or MS degree with 2-4 years of experience in microbiology, biology, or a related field., • Experience with QC bioassays, particularly utilizing PCR., • Experience with microbiological testing, biological assays, or environmental monitoring.Work Environment This position operates on a first shift from Monday to Friday during the training period, which takes place in Cambridge. After 2-3 months of training, the schedule will change to Sunday through Thursday, with work locations in both Cambridge and Burlington. Job Type & Location This is a Contract position based out of Cambridge, MA. Pay and Benefits The pay range for this position is $35.00 - $40.00/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) Workplace Type This is a fully onsite position in Cambridge,MA. Application Deadline This position is anticipated to close on Sep 8, 2026. 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment 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 thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job Description Biocytogen Boston Corp is seeking a highly motivated and versatile Pharmacology Scientist to support both in vivo and in vitro preclinical research services in the fields of immunology, immuno-oncology, metabolic disease and neurology. This role is ideal for candidates with broad expertise in pharmacological studies, disease model development, and cell-based assays, who are passionate about evaluating novel therapeutic agents for clients. The successful candidate will be a critical member of our fast-paced and expanding CRO team, actively engaging in both hands-on experimental work and strategic project management to support biotech and pharmaceutical partners Key Responsibilities In Vivo Pharmacology • Design and develop animal models, execute in vivo experiments to evaluate the biological efficacy of novel therapeutic agents., • Independently lead in vivo service projects and preclinical studies, acting as Project Manager or Study Director., • Perform animal handling, tumor inoculation, drug administration via multiple routes, blood and tissue collection, tumor measurements, and PK/PD studies., • Design and execute internal model-building projects and characterize various humanized mouse models., • Provide troubleshooting support and technical guidance to junior associates., • Collaborate closely with the BD/Sales team for client project planning and technical discussions., • Present project results to clients and internal stakeholders; prepare scientific reports and summaries., • Mentor and facilitate the growth of junior research associates. In Vitro and Ex Vivo Pharmacology • Independently develop, validate, and perform a broad range of in vitro and ex vivo assays including:, • Immune cell profiling from blood and tissues., • Functional assays using primary cells (T cells, NK cells, macrophages)., • Cytokine profiling, cytotoxicity, and apoptosis assays., • Develop new assay technologies by researching scientific literature and adapting methodologies from collaborations and other internal teams., • Perform flow cytometry (FACS), ELISA, Western blot, qRT-PCR, and multiplex cytokine analyses., • Contribute to the design and support of in vivo pharmacology studies from an in vitro perspective., • Present research findings at internal meetings and contribute to external scientific discussions. Requirements • PhD in pharmacology, immunology, cancer biology, or related biomedical field., • Extensive hands-on experience in animal models and preclinical in vivo pharmacology., • Proven skills in cell-based immunological assays including T cell activation, NK cell-mediated cytotoxicity, and macrophage functional assays., • Proficiency in PK/PD model establishment and analysis., • Expertise in flow cytometry, cytokine profiling (ELISA, qRT-PCR, multiplex assays), and immune cell isolation from tissues., • Experience with surgical procedures in rodents is highly desirable, • Cross-functional knowledge across therapeutic areas is a plus., • Strong communication, organizational, and team collaboration skills with the ability to prioritize in a fast-paced environment., • Demonstrated ability to independently manage projects and work with cross-functional teams. 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 Description Reporting to the VP of Regional Sales, EMEA the Field Application Scientist will provide the scientific introduction of Vizgen’s technology to customers with a focus on biological discovery and helping customers efficiently generate their own data using Vizgen’s MERSCOPE platform. The ideal candidate will support customer training and wet lab/analysis support. This exciting position requires complex scientific problem-solving skills, efficient communication, and a passion for helping customers. The Field Application Scientist will be responsible for supporting and coordinating solutions to our customers’ and collaborators’ wide range of needs, focused on both pre-sales and post-sales. The successful candidate will also manage and coordinate all technical aspects of customer demonstration projects and represent Vizgen and engage with scientists and other customers at trade shows and scientific conferences. Key Responsibilities: • Develop expert-level knowledge of Vizgen’s technology, including sample preparation techniques, instrumentation, software, network communications, and full integration of the overall platform, • Develop expert-level knowledge of preparing tissue samples with Vizgen’s reagents and chemistry and how they impact the performance of the platform, • Present product information and scientific applications for customer seminars and trade shows, • On-board, train, and support new customers to ensure protocols are understood and followed properly, • Work with customers to help design custom gene panels, • Support customers in their data workflow to ensure high-quality results are generated efficiently in a broad range of applications, • Provide technical guidance to customers on experimental design for single-cell spatial analysis, • Document customer issues, investigate underlying causes, and work closely with the Vizgen support and R&D teams to implement solutions, • Closely collaborate with the sales team in identifying new customer and market opportunities, • Collect feedback from current customers and communicate to product teams and management to help guide product development, • Represent Vizgen in a professional and friendly way when engaging with both external and internal customers Requirements and Qualifications: • PhD or MS in relevant scientific or engineering disciplines, • 5+ years of customer support in life science genomics or imaging fields, • Single-cell or spatial biology analysis experience preferred, • Highly skilled in managing sample preparation and analysis for RNA detection in tissue, • High sense of urgency for resolving customer issues, • Experience operating in both start-up and large corporate environments preferred, • Solid interpersonal and team management skills, • Excellent communication and presentation skills, • Highly organized, disciplined, and efficient in meeting deliverables, • Highly proficient in the use of business platform tools, including PowerPoint, Excel, Word, documentation control, customer support ticketing, and other relevant software applications, • Ability to independently troubleshoot and resolve customer issues in the lab, applying creative problem-solving in real time., • Willingness to travel 50%+ of the time, primarily within the France, Nordics, UK, • Fluent in both French and English, with the ability to communicate scientific and technical content clearly in both languages Equal Employment Opportunity We are an Equal Opportunity Employer and are committed to creating an inclusive workplace where all employees and applicants are treated with respect and fairness. Employment decisions are made without regard to race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, disability, genetic information, marital status, veteran or military status, or any other characteristic protected by applicable federal, state, or local law. We are dedicated to fostering a workplace that values diversity, equity, inclusion, and belonging, where every employee has the opportunity to contribute and succeed

Job DescriptionRole Location: Waltham, MA The Company We are Alloy Therapeutics—a biotechnology ecosystem company 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 biotechnology infrastructure company 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, like this position, to appreciate their colleagues who have less flexibility. We are all one team! About the Role In this role, you will support Alloy Discovery Services programs by executing protein science workflows central to antibody discovery, including transient transfection, recombinant DNA cloning, and immunogen design. You will contribute to protein expression at both high throughput and large scale as well as purification activities supporting the broader Protein Science team. The ideal candidate will bring hands-on experience with mammalian cell transfection, recombinant DNA techniques, and a working familiarity with downstream protein purification. We are looking for someone with the scientific curiosity to continuously improve our workflows and the organizational rigor to manage multiple projects in a fast-paced environment. Success in this role requires urgency, attention to detail, and a collaborative mindset that supports teammates and drives project goals forward. How You'll Drive Impact • Support: Contribute to all Alloy modalities by enabling immunogen preparation, molecular biology reagent generation, protein production, and the greater antibody discovery pipeline, • Improve: Continuously evaluate and optimize standard protocols for transfection, cloning, and protein science workflows to enhance efficiency, reproducibility, and scalability, • Collaborate: Partner closely with cross-functional, multidisciplinary teams across biologics discovery programs and Alloy sites, • Deliver: Apply rigorous scientific thinking to experimental design and execution while maintaining thorough documentation; communicate results clearly to stakeholders to enable informed decision-making and project advancement Key Responsibilities • Perform small- to large-scale transient transfections in mammalian cell lines (e.g. CHO) to drive high yield biologics production, • Independently manage multiple cell culture lines maintaining proper tissue culture techniques, • Systematically evaluate and optimize transfection efficiency, cell viability, and expression protocols across scales to improve throughput, consistency, and overall yield, • Execute recombinant DNA workflows, including PCR, Gibson assembly, and plasmid scale-up, • Contribute to antibody construct engineering to support the production of multi-specific antibody candidates, • Support protein expression and purification of biologics using AKTA chromatography systems, including affinity, IEX, and SEC, • Conduct regular QC on biologics including aSEC, CE-SDS or SDS-PAGE, and LAL as needed, • Analyze, interpret, and track deliverables in an electronic laboratory notebook in compliance with industry standards, • Coordinate project handoffs across functional teams to ensure seamless workflow continuity, • Present experimental data and findings during team and departmental meetings, • Ensure timely execution of project activities in alignment with priorities, • Maintain laboratory organization and ensure compliance with safety protocols Required Qualifications • MS with 2+ years or BS with 4+ years of hands-on research experience in molecular biology or a related discipline, • Degree in appropriate scientific discipline (molecular biology, cell biology, biochemistry, immunology, or related field), • Extensive experience with transient expression of antibodies using mammalian expression systems from HTP to multi-liter scale, CHO preferred, • Deep technical understanding of various transfection methodologies (e.g., PEI, lipofectamine, or electroporation) and experience optimizing transfection efficiency and cell viability., • Proficiency in high-density suspension cell culture management, including scale-up strategies from deep-well plates and shaking flasks to bioreactors., • Hands-on experience monitoring cell culture health and metabolic profiles using analyzers such as Vi-CELL or equivalent instrumentation., • Proficiency in recombinant DNA techniques including PCR, cloning, restriction digestion, gel analysis, and plasmid purification at small and large scale, • Experience with designing monoclonal, bispecific, and multi-specific constructs, • Strong organizational skills with the ability to manage multiple projects and prioritize independently, • Ability to maintain electronic laboratory notebooks in compliance with industry standards; familiarity with LIMS is a plus. Good communication skills and willingness to learn and adapt as part of a dynamic, team-oriented environment Preferred Qualifications • Experience in stable cell line generation and vector engineering, • Working knowledge of protein purification techniques, including affinity and size-exclusion chromatography, • Familiarity with bioanalytical techniques to assess protein titer, yield, and purityTaking 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 $93,000 - $110,000, 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 YQEOhgZXtl

Job Description Job Description This Research Associate role focuses on hands-on work with human induced pluripotent stem cells (iPSCs) to support stem cell and disease modeling initiatives. You will maintain, culture, and characterize human iPSC lines while contributing to process development and, where applicable, bioreactor-based scale-up activities. This position offers significant laboratory exposure to advanced cell-based assays, flow cytometry, and qPCR in a highly collaborative research environment that values scientific curiosity and continuous learning. This role is 100% onsite and offers either a Thursday-Monday or Friday-Tuesday schedule. The position is 40 hours per week. If there is less work on the weekends, employees may make up those hours during the week to maintain a guaranteed 40-hour work schedule. Responsibilities • Maintain, culture, and expand human induced pluripotent stem cell (iPSC) lines using robust aseptic techniques., • Characterize iPSC lines using cell characterization methods such as flow cytometry and qPCR to assess quality, identity, and phenotype., • Perform routine mammalian cell culture, with a strong emphasis on human stem cell culture, to support ongoing research programs., • Execute and support cell-based assays to evaluate cell function, differentiation status, and experimental outcomes., • Apply sterile processing practices to ensure contamination-free cell culture workflows and maintain high laboratory standards., • Support stem cell and disease modeling initiatives by preparing, analyzing, and documenting experimental data., • Contribute to process development activities for stem cell culture, including optimization of media, culture conditions, and workflow efficiency., • Assist with bioreactor-based workflows and scale-up activities for iPSC culture and differentiation, as needed., • Participate in the differentiation of iPSCs into downstream cell types according to project requirements and protocols., • Support translational research or therapeutic development programs by executing experiments aligned with project objectives., • Follow and promote GMP-like laboratory practices to maintain compliance with internal quality standards., • Collaborate closely with other scientists and research staff, sharing results, troubleshooting issues, and refining experimental approaches., • Take ownership of assigned projects and experiments, ensuring accurate documentation, data integrity, and timely communication of findings., • Contribute ideas for process improvements, experimental design, and new methodologies within the research group.Essential Skills, • Direct, hands-on experience maintaining and culturing human iPSC cell lines in a research setting., • Strong mammalian cell culture skills, with specific expertise in stem cell culture., • Proficiency with cell characterization techniques, including flow cytometry., • Proficiency with qPCR for gene expression or characterization assays., • Demonstrated aseptic technique and sterile processing experience in a laboratory environment., • Ability to perform and support cell-based assays related to stem cell and disease modeling., • Bachelor's or Master's degree in Biology, Cell Biology, Biomedical Engineering, Biotechnology, or a related scientific discipline., • Ability to work effectively in a collaborative research environment and communicate results clearly., • Strong attention to detail and ability to follow complex experimental protocols and documentation requirements.Additional Skills & Qualifications, • Experience with process development (PD) related to stem cell or iPSC culture., • Bioreactor operation or scale-up experience, preferably involving stem cells or iPSCs., • Experience differentiating iPSCs into downstream cell types., • Experience supporting translational research or therapeutic development programs., • Knowledge of GMP-like laboratory practices and quality-focused workflows., • Experience in research and development (R&D) environments., • Interest in contributing to process improvements, new methodologies, and innovative experimental approaches., • Motivation to work with cutting-edge human iPSC technology and advanced cell-based applications.Work Environment This role is 100% onsite in a laboratory-based research setting. The position is full-time at 40 hours per week, with the option to work either a Thursday-Monday or Friday-Tuesday schedule. If weekend workload is lighter, employees may make up hours during the week to maintain a guaranteed 40-hour schedule. You will work with human iPSC cultures, bioreactors, and process development workflows in a highly collaborative and supportive research team. The environment emphasizes scientific curiosity, continuous learning, and professional development, offering high levels of ownership and visibility within the research group, as well as exposure to bioreactor-based stem cell manufacturing technologies and advanced analytical techniques such as flow cytometry and qPCR. Job Type & Location This is a Contract position based out of Cambridge, MA. Pay and Benefits The pay range for this position is $79.00 - $105.00/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) Workplace Type This is a fully onsite position in Cambridge,MA. Application Deadline This position is anticipated to close on Sep 3, 2026. 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment 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 thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job Description *Relocation and sign on bonus up to 20k offered* Job Title: Cardiac Sonographer Job Description The Cardiac Sonographer performs comprehensive cardiac ultrasound examinations for patients ranging from those with normal cardiac anatomy to those with complex congenital heart disease. This role conducts examinations independently across all phases of care, including diagnostic, pre-operative, intraoperative under anesthesia, and post-operative following complex surgical repairs. The position also supports the non-invasive cardiology laboratory through clinical expertise, equipment oversight, and collaboration with multidisciplinary teams. Responsibilities • Perform cardiac ultrasound examinations that encompass normal cardiac anatomy and complex congenital heart disease across diagnostic, pre-operative, intraoperative under anesthesia, and post-operative phases of care., • Supervise the provision of echocardiography examinations within the non-invasive laboratory, monitoring performance and providing assistance to ensure examinations follow established protocols., • Plan case methodology and conduct comprehensive echocardiography examinations in the laboratory or using portable equipment at other locations as needed., • Establish a supportive and professional relationship with patients and families, clearly explaining examination procedures and communicating any scheduling problems or changes., • Maintain and evaluate laboratory equipment to ensure optimal performance and safety., • Monitor and maintain inventory of standard supplies, initiating reorders in accordance with established par levels., • Prepare and maintain required logs and records related to echocardiography procedures, equipment, and supplies., • Provide instruction and guidance on echocardiography procedures and interpretation of results to sonographers, trainees, and fellows., • Assist in clinical research studies by explaining protocols to staff and overseeing the collection of required clinical data., • Collaborate with physicians, nurses, and other healthcare professionals to support accurate diagnosis, treatment planning, and continuity of patient care. Essential Skills • Demonstrated proficiency in cardiac sonography with the ability to perform comprehensive pediatric echocardiography examinations, including complex congenital heart disease., • Registered Diagnostic Cardiac Sonography (RDCS) certification (adult or pediatric) from the American Registry of Diagnostic Medical Sonography (ARDMS)., • Pediatric Echocardiography (RDCS PE) certification., • Current Basic Life Support (BLS) certification in accordance with American Heart Association standards., • Completion of an accredited Cardiac Ultrasound program in pediatric echocardiography., • Minimum of 2 years of clinical experience in pediatric echocardiography; 5 years preferred., • Ability to supervise echocardiography services in a non-invasive laboratory and ensure adherence to established protocols., • Skill in planning and conducting comprehensive echocardiography examinations using both laboratory and portable equipment., • Strong communication skills to explain procedures, address questions, and provide clear information to patients, families, and healthcare staff., • Ability to maintain accurate logs, records, and supply inventories while ensuring proper equipment function., • Competence in supporting clinical research activities, including protocol adherence and clinical data collection. Additional Skills & Qualifications • Completion of high school or equivalent education., • Bachelor’s degree in a related field such as healthcare, nursing, biology, or a similar discipline is preferred., • Pediatric echocardiography specialty training is preferred., • Experience providing education and training to sonographers, trainees, and fellows on echocardiography procedures and interpretation., • Strong organizational skills to manage multiple cases, maintain documentation, and oversee supplies and equipment., • Ability to build rapport with children and families and provide a supportive, compassionate care experience., • Interest in contributing to clinical research and quality improvement initiatives within the echocardiography laboratory. Work Environment This role operates primarily within a non-invasive cardiology laboratory that utilizes advanced cardiac ultrasound equipment and portable echocardiography devices. The schedule follows rotating 10-hour shifts, requiring flexibility to support patient care across various phases, including diagnostic, pre-operative, intraoperative, and post-operative settings. The environment is collaborative and fast-paced, with close interaction among physicians, nurses, sonographers, trainees, and fellows. The Cardiac Sonographer works in clinical areas where attention to detail, adherence to protocols, and a professional appearance are essential, and may move between laboratory and bedside settings to perform examinations and support patient care. Job Type & Location This is a Permanent position based out of Boston, MA. Pay and Benefits The pay range for this position is $95000.00 - $125000.00/yr. 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. full BCH benefits, medicla, vision, dental, Workplace Type This is a fully onsite position in Boston,MA. Application Deadline This position is anticipated to close on Sep 14, 2026. 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment 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 thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job Description General Fluidics is a clinical diagnostics company developing a novel point-of-care platform capable of simultaneously measuring clinical chemistry, hematology, and immunoassays from human and animal blood samples (https://www.generalfluidics.com). We are seeking a highly motivated and broadly skilled Senior Research Associate to support development of our growing diagnostic assay menu across veterinary medicine and the in vitro diagnostics (IVD) market. This individual will play a hands-on role in the development, optimization, and validation of assays powering our next-generation diagnostic platform. This is an opportunity to contribute directly to innovative diagnostic technology within a highly collaborative and fast-moving biotech environment. Essential Duties and Responsibilities • Design, develop, and validate clinical chemistry, hematology, and immunoassays using human and animal blood samples on our point-of-care platform., • Independently design and execute laboratory experiments to optimize assay and instrument performance in collaboration with engineering and cross-functional teams., • Analyze assay and instrument performance data to support analytical validation, regulatory clearance, and commercial launch activities., • Author experimental protocols, standard operating procedures (SOPs), technical reports, and validation documentation., • Support laboratory quality assurance activities including controls, calibration, and proficiency testing., • Maintain safe laboratory practices in compliance with applicable health, safety, and environmental regulations., • Work safely with both human and veterinary specimens in accordance with laboratory safety standards and procedures. Qualifications and Experience • BS, MS, or PhD in biotechnology, biology, chemistry, biomedical engineering, clinical laboratory science, or a related scientific discipline., • 3–5+ years of experience in industrial, hospital, veterinary, or academic laboratory environments., • Experience independently designing and executing laboratory experiments and analyzing scientific data., • Experience supporting assay development, analytical validation, or clinical diagnostic product development preferred., • Experience working at the intersection of engineering, instrumentation, automation, and wet chemistry strongly preferred., • Hands-on experience with clinical instrumentation such as flow cytometry, hematology systems, clinical chemistry analyzers, and/or immunoassay platforms., • Familiarity with regulated laboratory environments and quality systems (e.g., BSL-2, GLP, CLIA, CAP) highly preferred. Veterinary diagnostics experience is a plus., • Strong written and verbal communication skills with the ability to clearly communicate scientific concepts, data interpretation, and technical findings., • Ability to operate with a high degree of technical competence, organization, and attention to detail in a fast-paced startup environment., • Experience with standard laboratory techniques including pipetting, chemistry formulations, biosafety cabinets, quality control procedures, and instrument calibration., • Strong desire to learn, innovate, and contribute to the development of next-generation diagnostic technologies. Why Join General Fluidics • Work on breakthrough point-of-care diagnostic technology, • High-impact role within a growing biotech company, • Collaborative and innovative R&D environment, • Opportunity to help shape next-generation diagnostic products Benefits • 401(k), • Health insurance, • Dental / Vision insurance, • Disability insurance, • Paid time off, • Annual bonus program\nCompany Description General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (https://www.generalfluidics.com). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (https://www.generalfluidics.com). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

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 This role will report to a Scientist in the in vitro discovery and optimization team, 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 • Advance antibody discovery and optimization efforts through innovative in vitro strategies., • Deliver high-quality experimental data supporting lead identification and engineering., • Manage multiple projects with scientific rigor and organizational efficiency., • Support high velocity workflows utilizing multi-disciplinary techniques., • Foster effective cross-functional collaboration and communication., • Contribute to Alloy’s culture of innovation and teamwork. Key Responsibilities • Design, execute, and analyze experiments to support antibody discovery and engineering., • Contribute to the development and optimization of in vitro platforms and workflows., • Collaborate closely with cross-functional teams to align project goals and timelines., • Manage multiple projects simultaneously, maintaining high scientific standards., • Document and communicate experimental findings clearly to stakeholders and teams., • Participate in regular team meetings and contribute to strategic planning., • Provide technical expertise in molecular biology and related techniques., • Support high-throughput screening and assay development efforts., • Stay up to date with emerging technologies and scientific advances in the field., • Maintain an organized and efficient laboratory environment. Qualifications • A minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree., • Hands-on experience in molecular biology techniques (e.g., cloning, PCR, sequencing)., • Hands-on experience with yeast/phage/mammalian display platforms, • Demonstrated ability to manage timelines and contribute to multiple projects in parallel., • Strong organizational and communication skills to work effectively in collaborative settings., • Preferred experience with:, • Flow cytometry, • Cell culture, • NGS sequencing, • High-throughput screening, • Ability to work across various US and international time zones. 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 $93,000 - $110,000, 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 T6BB7elnj3

Job DescriptionScholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the 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 at ScholarRock.com and follow @ScholarRock on X and on LinkedIn. Summary of Position: The Technical Operations Department at Scholar Rock is seeking a scientifically curious and motivated engineer in the Downstream PD & MSAT group. The successful candidate is expected to be proficient in all aspects of the purification process and be comfortable working with a multifunctional team. Experience in late-stage process development and support of external manufacturing is preferred. The selected candidate will work alongside in-house scientists to advance existing projects through the development lifecycle and transfer to CMOs. Proficiency in AKTA operation, TFF, VRF, JMP for data trending and presentation, and design of experiment skills are key traits that will ensure success in this role. Position Responsibilities • Support external manufacturing of clinical and commercial assets, • Own and maintain process monitoring databases (CPV and lot history), • Support manufacturing campaign readiness review process, • Drive batch production record review processes, • Author and drive Downstream change control implementation, • Work closely with CDMO to support tech transfer and manufacturing activities, • Technical presentation to greater TechOps team, • Support process development experiments to develop, optimize, and characterize purification processes for antibodies., • Detailed documentation of all experimental studiesCandidate Requirements, • Educational background in Chemical Engineering, Biochemistry, Biotechnology, or related biological Sciences., • Direct experience working with mAbs is preferred, and MSAT experience is highly desirable, • BS with 6+ years of experience, • MS with 4+ years of experience, • Ph.D. with 0-2 years of experienceScholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Job Description Job Summary This Associate Director, Regulatory Affairs, will work on-site. As a manager, the function of an Associate Director, Regulatory Affairs, is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. Additionally, the individual will develop and supervise regulatory professionals. The individual has department level influence and is generally recognized as an expert resource both within the company and externally. The individual may comment on changing regulations and guidance, interface with outside regulatory agencies and trade associations and provide executive management with regulatory metrics/information. The individual will ensure that data is identified, obtained and effectively presented for the registration of products worldwide. Job Responsibilities • Set strategy and direct preparation of submissions for products to regulatory agencies, and interface with agencies in order to obtain timely approval to produce and market new products., • Provide guidance on regulatory requirements and strategies for product development project teams., • Provide regulatory input for capital equipment and software, including knowledge of IEC standards (e.g., IEC 60601-1)., • Provide regulatory input on cybersecurity and Artificial Intelligence (AI)., • Maintain expert working knowledge of laws, regulations and enforcement decisions related to Quality Assurance (QA), manufacturing and Research & Development (R&D) issues that may impact company operations and decision making; communicate such knowledge to all internal stakeholders., • Consult with and provide advice to senior management of the Company on strategies and plans for regulatory product approvals., • Direct staff in implementing regulatory strategy and preparing regulatory submissions., • Remain current on developments in field(s) of expertise, regulatory requirements, as well as industry trends and train staff regarding changing regulations that affect regulatory submissions., • Maintain knowledge of current and pending regulations through literature, trade journals, professional associations, and by attending conferences., • Resolve and/or facilitate resolution of problems including identifying causes to prevent re-occurrence., • Perform related functions and responsibilities, on occasion, as assigned., • Hire and retain a diverse, highly qualified staff and provide ongoing performance feedback., • Maintain a safe and professional work environment., • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements., • Comply with U.S. Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments., • Maintain positive and cooperative communication. Required Qualifications • Bachelor's Degree or an equivalent combination of education and work experience., • 5-7 years of experience in a regulated industry (e.g., medical products, nutritionals)., • 5-7 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. Note: Higher education may compensate for years of experience. Preferred Qualifications • Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred., • M.S. in a technical area or M.B.A. is preferred. A Ph.D. in a technical area or law is helpful., • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.), • Previous experience with 510k / PMA submissions., • Experience working with hardware/ software devices., • Familiarity with Predetermined Change Control Plans (PCCPs)., • Experience with Medical Devices.

Job Description The Opportunity We are seeking a motivated and detail-oriented Associate Scientist / Scientist I to join our Computational Test Development team at Precede Biosciences. Reporting to our Senior Director, Computational Test Development, this role is focused on the execution and analysis that underpins our diagnostic assay characterization and validation programs. This is a hands-on computational role. You will run analyses, build and maintain quality assessment frameworks, execute in silico simulations, and generate the data-driven outputs that feed directly into our regulatory submissions. If you are energized by rigorous data analysis, take pride in clean and reproducible work, and are excited to contribute to diagnostics that could change how cancer is detected and treated, we want to hear from you. About Us 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, and collaboratively solving complex problems, while also ensuring a strong focus on individual initiative, accountability, and delivery. What You'll Do Assay Characterization & Validation Execute data analyses supporting assay characterization across multiple epigenomic and NGS-based diagnostic tests — from raw data processing through performance metric generation Design and implement quality assessment frameworks to evaluate assay and pipeline performance, including QC metric definition, threshold setting, and failure mode identification Run and interpret validation experiments in close coordination with wet lab and senior computational team members, contributing to study execution against pre-defined protocols Pursue defined research questions semi-independently — taking a scoped problem, designing the analytical approach, executing, and returning well-documented results In Silico Simulation & Thresholding Design and run in silico simulations to model assay behavior under variable conditions — including signal dropout, coverage non-uniformity, and input DNA variability Develop and apply statistical approaches to threshold setting and performance boundary definition, supporting limit of detection and analytical range characterization Systematically explore parameter sensitivity across bioinformatics pipelines to assess model robustness and inform feature selection Regulatory Support & Communication Produce clear, thorough documentation of all analyses code, methods, results, and interpretation to the standard required under design controls Contribute to the authoring of SOPs and analytical summary reports Partner closely with wet lab scientists to ensure computational analyses are grounded in experimental reality and that results are communicated in accessible, actionable terms Present analytical findings clearly in team meetings and cross-functional settings Contribute to a collaborative team environment by sharing code and knowledge openly and proactively Who You Are MSc in computational biology, bioinformatics, biostatistics, or a closely related quantitative field with 3–4 years of industry or post-graduate research experience in a data-intensive biological or biomedical setting, Ph.D. preferred Strong proficiency in R and Python for data analysis, visualization, and reproducible reporting — you write, own, and document your own code Experience with cloud computing environments (AWS) for running scalable analyses Demonstrated ability to execute analytical plans with precision and efficiency, managing multiple tasks without a drop in quality or documentation standards Familiarity with NGS data types and standard processing pipelines — alignment, QC, coverage analysis, or equivalent Clear and organized communicator — written documentation, results presentations, and cross-functional interactions alike Comfortable working in a fast-paced startup environment, following defined protocols while contributing ideas for improvement Nice to have: Exposure to regulated environments — CLIA, CAP, FDA IVD, or design controls in any form Experience with epigenomic data types — methylation, cfDNA, chromatin accessibility, or ChIP-seq Familiarity with statistical thresholding or limit of detection frameworks for diagnostic applications Experience contributing to SOPs, validation reports, or other regulated documentation Associate Scientist: $110,000 - $130,000Scientist I: $125,000 - $145,000 Final compensation will be based on a candidate’s qualifications, experience, and geographic location. Employees are also eligible for performance bonuses, equity participation and comprehensive health benefits.We believe in building an inclusive and balanced team. We also know meeting every single-exact-criteria can get in the way of meeting stellar folks. Please don’t hesitate to apply!Precede Biosciences is an equal opportunity employer. We do not discriminate in regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, marital status, ancestry, physical or mental disability, veteran status, or any other legally protected.Please note that we do not accept unsolicited resumes from recruitment agencies and external recruiters. No fees will be paid for such 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 DescriptionAbout Synolo Therapeutics:Synolo Therapeutics, an early-stage biotechnology company launched by RA Ventures, is pioneering the development of precision-targeted immunotherapies for cancer. Powered by computational protein design and proprietary technologies that yield biological data sets at unprecedented scale and resolution, we are building a pipeline of first-in-class multi-specific biologics with novel functionalities. Synolo was founded by pioneers in the field of protein design and engineering, synthetic biology, DNA sequencing, immunology, and biologics drug discovery and development. About RA Capital:RA Capital Management funds and builds healthcare and life science companies using an evidence-based investment approach informed by TechAtlas, a think tank within RA Capital which analyzes scientific and clinical data from academic literature and industry sources to anticipate how breakthroughs might impact industry stakeholders, physicians, patients, and policymakers. TechAtlas' analyses are captured in a unique collection of competitive landscapes, or ‘maps’, that identify competitive therapeutics, diagnostics, research tools, and/or technological capabilities in a given area. About the Role:Synolo Therapeutics is seeking an experienced Principal Scientist to help establish and advance our analytical and biophysical characterization capabilities within the Protein Science team. This is a unique opportunity to shape a foundational scientific function at an early-stage biotechnology company developing next-generation biologic therapeutics. In this highly collaborative, hands-on role, you will partner closely with Biologics Discovery, Biology, CMC, and external CRO partners to generate the molecular insights that drive protein engineering, candidate selection, and development strategy. By integrating orthogonal analytical and biophysical datasets, you will develop a deep understanding of molecular behavior, identify critical quality attributes, and translate complex data into informed scientific and development decisions. You will play a key role in defining characterization strategies, implementing new technologies, establishing scalable workflows, and strategically leveraging external partnerships to maximize scientific impact and operational efficiency. As the Protein Science organization grows, you will have the opportunity to mentor scientists and contribute to the continued evolution of our capabilities. This role is ideal for a scientist who thrives in a fast-paced, highly collaborative environment, enjoys solving complex scientific problems, and is excited by the opportunity to influence the design, selection, and advancement of innovative biologic therapeutics. Key Responsibilities: • Define and lead analytical and biophysical characterization strategies that address key scientific questions and support therapeutic protein discovery, lead optimization, and development candidate selection., • Design, execute, and interpret analytical, biophysical, mass spectrometry, and stability studies to characterize molecular identity, product quality, critical quality attributes, molecular behavior, and degradation pathways., • Generate molecular insights by integrating analytical and biophysical datasets to establish structure-property relationships and translate findings into protein engineering, candidate selection, and development decisions., • Serve as the analytical and biophysical characterization lead on cross-functional project teams, partnering closely with Biologics Discovery, Biology, CMC, and external CROs to develop characterization strategies, solve complex scientific challenges, and ensure high-quality execution., • Evaluate, implement, and advance analytical and biophysical technologies, workflows, and external partnerships to strengthen internal capabilities and support the advancement of a growing pipeline., • Provide technical leadership and mentorship within the Protein Science organization, fostering scientific rigor, collaboration, innovation, and continuous learning., • Communicate scientific findings, strategic recommendations, and project updates to multidisciplinary teams, senior leadership, and external collaborators.Qualifications & Skills:, • Ph.D. in Biochemistry, Biophysics, Protein Chemistry, Chemical Engineering, or a related scientific discipline, plus 3+/5+ years of relevant industry and/or postdoctoral experience; or M.S. with 8+/10+ years or B.S. with 12+/15+ years of relevant industry experience in therapeutic protein discovery, characterization, or early development, for the Senior Scientist/Principal Scientist levels, respectively. • Deep understanding of protein chemistry, molecular biophysics, therapeutic protein quality attributes, and the analytical and biophysical principles governing protein stability, heterogeneity, and developability., • Demonstrated experience designing, executing, and interpreting analytical, biophysical, developability, and stability characterization studies to support therapeutic protein discovery, lead optimization, and development candidate selection., • Extensive hands-on experience with analytical characterization techniques, including SECHPLC/UHPLC, IEX/CEX, HIC, CE-SDS, icIEF, AC-SINS, and LC-MS (e.g., intact mass, peptide mapping, PTM characterization), as well as biophysical characterization techniques including DLS, DSF/nanoDSF, DSC, and related methodologies., • Experience designing and interpreting developability studies, including the use of orthogonal approaches such as PEG solubility, AC-SINS, self-interaction, viscosity, solubility, and polyspecificity/nonspecific binding assays, or related methodologies., • Experience designing and interpreting accelerated stability, stress, and forced degradation studies, including the investigation of degradation pathways, molecular liabilities, and critical quality attributes., • Demonstrated ability to integrate analytical, biophysical, and biological datasets to establish structure-property relationships and translate findings into protein engineering, candidate selection, and development decisions., • Proven ability to lead scientific initiatives and collaborate effectively across multidisciplinary teams., • Excellent scientific communication, critical thinking, and problem-solving skills, with the ability to communicate complex scientific concepts and influence technical decision-making.Preferred Experience:, • Experience with advanced protein-protein interaction techniques, including SPR, BLI, KinExA, or related technologies., • Experience with therapeutic protein expression, purification, and process development., • Experience with complex biologic modalities (e.g., multispecific antibodies, antibody-drug conjugates, fusion proteins, or other engineered biologics)., • Experience working at the interface of experimental and computational sciences, supporting AI/ML-enabled protein engineering and therapeutic discovery through the generation of highquality analytical and biophysical datasets., • Experience implementing new analytical technologies, establishing laboratory capabilities, and developing scalable scientific workflows., • Experience working with large, multidimensional datasets and leveraging modern computational and AI-enabled tools (e.g., Python, workflow automation, AI coding assistants, interactive scientific applications, and data visualization platforms) to improve scientific productivity, data analysis, and decision-making., • Experience managing external CROs and scientific collaborations., • Experience mentoring scientists and contributing to the growth of a collaborative scientific organization. Title will be commensurate with experience. At Synolo Therapeutics, we are committed to fostering a diverse and inclusive work environment where all individuals are valued and treated with dignity. We believe that diversity drives innovation and strengthens our ability to make a meaningful impact through our work. We are committed to being an equal opportunity employer who ensures that all qualified applicants receive equal consideration for employment without regard to neurodiversity, race/ethnicity, color, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. We kindly ask that recruiting agencies and third-party recruiters do not contact us regarding this position. We are not seeking assistance or accepting unsolicited resumes from agencies at this time. 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 DescriptionNanobiosym is an innovative company in Cambridge, MA that is developing novel technologies to address a broad range of diseases. Nanobiosym was founded by an MIT/Harvard alum to work at the interface of physics, nanotechnology, and biomedicine. This hypergrowth company allows for unique career opportunities with strong long-term incentives. Nanobiosym is currently seeking top notch candidates to help the company scale up its operations.seeking a part-time/full time Laboratory Director to support the establishment, certification, and operation of our CLIA-certified laboratory in Massachusetts. The Laboratory Director will provide clinical, scientific, and regulatory oversight to ensure Nanobiosym delivers accurate, reliable, and high-quality testing services in compliance with applicable regulatory and accreditation requirements, including CLIA, CAP, and other applicable state requirements.The Laboratory Director will be responsible for overseeing laboratory QMS, ensuring appropriate validation and performance of all testing methods, reviewing laboratory procedures, and supporting continuous improvement initiatives. This role provides clinical and technical guidance for test interpretation, quality assurance and regulatory compliance.This is a role intended to support Nanobiosym's CLIA/CAP certification readiness and clinical laboratory operations. The Laboratory Director may delegate specific duties to qualified personnel but retains the ultimate responsibility for ensuring these duties are properly performed and documented.Responsibilities:Serve as the CLIA Laboratory Director for our high-complexity clinical laboratory.Provide overall clinical, scientific, and regulatory oversight of CLIA/CAP-certified laboratory operations.Ensure compliance with all applicable regulatory and accreditation requirements, including CLIA, CAP, and NY State CLEP, as applicable.Oversee quality management program to ensure accurate, reliable, and timely laboratory testing.Review and approve laboratory policies, procedures, test validations, and quality documentation.Monitor laboratory performance and implement continuous quality improvement initiatives.Provide clinical consultation to physicians and other healthcare providers regarding laboratory testing and test results.Support laboratory readiness for regulatory inspections and accreditation surveys.Foster a culture of quality, compliance, and scientific excellence.QualificationsM.D., or Ph.D. in a relevant scientific discipline (e.g., immunology, pathology, clinical chemistry, biochemistry, molecular biology, or a related field).Qualified to serve as Clinical Laboratory Director of a high-complexity CLIA/CAP laboratory under applicable federal and Massachusetts state regulations -- Clinical Laboratory Director License issued by the Massachusetts Department of Public Health (MDPH) is requiredBoard certification in a relevant discipline (e.g., Virology, Molecular Biology, Clinical Chemistry, Clinical Pathology, HCLD, Immunology, or other appropriate specialty) is required.Minimum 8-10 years of experience in high complexity clinical laboratory operations, with at least 5 years in a director-level role overseeing a CAP/CLIA-certified laboratory.Proven track record of successfully establishing or scaling a clinical lab.Demonstrated expertise in molecular diagnostics for assay validation and verification.Strong knowledge of laboratory quality systems, proficiency testing, and inspection readiness.Experience with LIMS platforms, electronic quality management systems (eQMS), and workflow automation in a high-complexity testing environment.Experience working for a fast-paced, growing organization Job Posted by ApplicantPro

Job DescriptionAbout Us Deep Genomics is at the forefront of integrating artificial intelligence and complex biology to transform drug discovery. Our proprietary machine learning platform decodes the complexity of RNA biology to identify novel drug targets, mechanisms and therapeutics inaccessible through traditional methods. With expertise spanning machine learning, drug development, bioinformatics, data science, genetics and chemistry, our multidisciplinary team in Toronto and Cambridge, MA is revolutionizing how medicines are created. About the role The Principal Research Associate will join our Platform Biology team and will be a key player in driving our cutting-edge AI RNA therapeutics discovery platform. In this role, you will be responsible for helping characterize our novel compounds, including performing automated high-throughput arrayed screening, as well as downstream characterization of these molecules. Further, you will be instrumental in helping develop, optimise and implement novel cellular and protein assays to advance our internal therapeutics portfolio. The ideal candidate will have strong cell biology expertise, and hands-on experience using primary hepatocyte cells. Relevant knowledge of RNA modalities such as ADAR, ASO, mRNA and/or siRNAs is also highly beneficial. The successful candidate should demonstrate initiative, technical ownership and be able to thrive in a dynamic work environment with cross-functional teams working together to achieve company goals. This position is onsite at our Cambridge, MA site. Key Responsibilities • Design, optimise and execute robust cell-based assays, to support compound screens and lead optimisation., • Culture, maintain and transfect a variety of mammalian cell lines, such as immortalized cell lines, primary cells and co-culture systems, and onboard new cell types and systems to enable drug discovery., • Examine important molecular and functional endpoints in vitro, including RNA and protein readouts, to better understand our molecules in our internal therapeutic pipeline., • Perform standard molecular biology techniques (e.g. PCR, qPCR, Jess/Leo Automated Westerns, ELISA, Western blot, etc.)., • Collaborate with a cross-functional team in a dynamic, matrixed environment to achieve shared company deadlines, and communicate experimental design and findings with colleagues and project teams., • Clearly document experiments, standard operating procedures (SOPs) and data in an electronic lab notebook (ELN).Basic Qualifications, • BS or MS in Biology, Molecular Biology, Genomics, Biochemistry or a related field with 4+ years of relevant pharmaceutical or biotechnology experience., • Strong hands-on experience growing, maintaining and transfecting mammalian cell lines., • Good understanding of molecular and cell biology., • Experienced in design and execution of molecular and cellular assays, including documentation in an electronic lab notebook (ELN)., • Excellent communication, organizational skills and a willingness to learn., • Ability to prioritise and drive work independently in a fast-paced, technical and data-rich environment.Preferred Qualifications, • Hands-on experience using primary hepatocytes is strongly preferred., • Proficiency in automated Western blotting methods, such as the Jess/Leo platforms., • Flow cytometric experience is a plus., • Experience with high-throughput liquid handlers (e.g. Beckman Echo, Agilent Bravo and/or Hamilton STAR/STAR V)., • Next-generation sequencing library preparation, e.g. amplicon sequencing., • Past experience with RNA editing and/or RNA oligonucleotides., • Demonstrated experience working in cross-functional teams.What We Offer, • A collaborative and innovative environment at the frontier of computational biology, machine learning, and drug discovery., • Highly competitive compensation, including meaningful stock ownership., • Comprehensive benefits - including health, vision, and dental coverage for employees and families, employee and family assistance program., • Flexible work environment - including flexible hours, extended long weekends, holiday shutdown, unlimited personal days., • Maternity and parental leave top-up coverage, as well as new parent paid time off., • Focus on learning and growth for all employees - learning and development budget & lunch and learns., • Facilities located in the heart of Toronto - the epicenter of machine learning and AI research and development, and in Kendall Square, Cambridge, Mass. - a global center of biotechnology and life sciences. Deep Genomics encourages applications from all backgrounds who seek the opportunity to build the world's leading AI-driven genetic medicine company. If you have a disability or special need, accommodation is available on request for candidates taking part in all aspects of the selection process. *This posting reflects a current vacancy. We offer competitive compensation aligned with local market benchmarks. The salary range for this role is $115,000 - 135,000, and reflects Cambridge, USA-based roles. 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.

biological data analysisscientific reading comprehensionassessment and question creationwritten and verbal communicationremote team collaborationmicro1 is the leading AI data lab for training frontier models and evaluating AI agents. Experts contribute their diverse subject matter knowledge across domains such as finance, healthcare, STEM engineering, and more. micro1 transforms that real-world expertise into high-quality training data, evaluations, and feedback loops that improve how AI systems learn, reason, and perform. Our platform identifies and vets top talent through an AI recruiter, enabling high-quality expert contributions at scale. We aim to enable 1 billion people to do meaningful work by applying their expertise to AI. As our global expert network grows, micro1 is building the human intelligence layer for frontier AI. Job Title: Biology Expert Job Type: Contractor Location: Remote Rate: 20$-50$ per task Job Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. Key Responsibilities: • Analyze technical documents and extract key information relevant to your domain expertise, • Generate, review, and refine questions and solutions based on real-world mechanical engineering scenarios, • Collaborate with multidisciplinary teams to ensure accuracy and depth of data and analysis, • Provide detailed written and verbal feedback on document clarity, technical accuracy, and effectiveness, • Apply advanced subject matter knowledge to evaluate and solve complex engineering problems, • Work independently, managing your time to deliver high-quality outputs with minimal supervision, • Contribute to the continuous improvement of data quality and project processes Required Skills and Qualifications: • 2-6 years of professional or academic experience in mechanical engineering or a closely related field (lab, workplace, or academia), • Strong reading comprehension skills, with proven ability to analyze and interpret technical documents, • Exceptional English communication skills, both written and verbal, • Demonstrated experience in creating or evaluating technical content, such as reports, studies, or problem sets, • Ability to work independently and efficiently, with excellent self-management, • High attention to detail and commitment to data accuracy, • Experience interfacing with technical documentation and performing analytical tasks Preferred Qualifications: • Advanced degree (Master’s or PhD) in Mechanical Engineering, Chemistry, Physics, or Biology, • Previous experience contributing to interdisciplinary or research-driven projects, • Familiarity with data-driven analysis or training data preparation Job Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. Key Responsibilities: • Analyze, review, and interpret complex biological documents, research papers, and data sets to create high-quality assessment content., • Formulate and vet biology-related questions focused on data retrieval, computation, and critical analysis., • Deliver clear explanations and detailed feedback to enhance AI model understanding., • Collaborate with a remote, interdisciplinary team to ensure ongoing content accuracy and quality., • Contribute domain-specific expertise to support the continuous improvement of AI systems., • Work independently to meet deadlines and achieve high productivity with minimal supervision., • Uphold rigorous standards for written and verbal communication in English. Required Skills and Qualifications: • Minimum 2 years of professional experience in biology, either in academia, laboratory settings, or relevant industry roles., • Demonstrated ability to analyze and synthesize complex biological information from diverse sources., • Strong written and verbal English communication, with an emphasis on clarity and detail., • Excellent reading comprehension, particularly in interpreting research and technical documents., • Experience creating or reviewing problem sets, assessments, or scientific analyses., • Ability to work autonomously and efficiently in a remote environment., • High attention to detail and commitment to quality. Preferred Qualifications: • Advanced degree (Master’s or PhD) in Biology or closely related field., • Experience collaborating with multidisciplinary teams or involvement in cross-functional projects., • Familiarity with computational biology or data analysis tools.

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 Overview We are seeking an experienced and highly motivated neuroscientist with strong drug discovery expertise to join our Discovery Psychiatry team. The successful candidate will apply drug discovery principles into exploratory through late-stage discovery programs and integrate knowledge across in vitro and in vivo electrophysiological approaches. Candidate must have a strong understanding of neural circuits, multimodal neurophysiological methodologies and translational utility. This role is an exciting opportunity to support psychiatry research from target validation, compound profiling, through clinical development in a dynamic, collaborative drug discovery environment. Key Responsibilities Establish Drug Discovery framework in Psychiatry portfolio Contribute to the development and implementation of research workflows that integrate complex multimodal datasets Ensure alignment of development and discovery with broader cross-functional program team goals Support strategic decision-making in psychiatry drug discovery Provide scientific guidance and mentoring to junior scientists and research associates Qualifications Bachelor’s Degree in Science related field with 16 years of related work; Master’s Degree Science or PharmD with 14 years of related work; PhD in Science or related field with 8 years of related work experience. Industry experience within early discovery for Psychiatry Demonstrated experience with neurophysiology and/or functional approaches, including experience in the design and execution of studies investigating synaptic and circuit modulation relevant to psychiatric indications Strong ability to work in cross-functional teams and effectively communicate scientific findings to both technical and non-technical audiences Desired Qualifications Experience building translational frameworks or predictive approaches for functional biology data 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