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Job DescriptionRepertoire Immune Medicines is a clinical-stage biotechnology company harnessing the power of the human immune system to develop transformative therapies for cancer and autoimmune disease. Using its proprietary DECODETM platform—which maps the immune synapse between T cell receptors (TCRs) and their antigen targets—Repertoire translates unique biological insights into potent and targeted off-the shelf immune medicines. The company integrates deep protein engineering expertise with artificial intelligence, powered by a proprietary DECODE database of over one billion TCR-antigen interactions, to accelerate discovery and optimize drug candidates. From its sites in Cambridge, Massachusetts and Zurich, Switzerland, Repertoire is advancing a pipeline of T cell-targeted immunotherapies with the potential to address a broad range of cancers and autoimmune disorders. The company’s lead oncology program, RPTR-1-201, a TCR bispecific, has initiated a Phase 1/2 clinical trial across multiple solid tumor indications. Repertoire plans to advance additional TCR bispecific therapies into clinical trials over the next 12-18 months. In autoimmune disease, Repertoire is partnering with leading pharmaceutical companies to develop mRNA tolerizing therapies designed to selectively expand regulatory T cells and reset the immune system. Repertoire was founded in 2019 by Flagship Pioneering and is supported by a strong investor base. The DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. Role Overview Repertoire Immune Medicines is seeking an accomplished and strategic Vice President, Head of CMC to lead all Chemistry, Manufacturing, and Controls activities across the company’s growing pipeline of protein biologics. This senior leader will be responsible for establishing and executing CMC strategy from development candidate nomination through clinical development. The successful candidate will bring deep expertise in biologics CMC development, demonstrated success building teams and processes in both early‑stage and mature organizations, and a strong track record of technology transfer and management of external manufacturing organizations. This leader will work cross‑functionally with research, preclinical, clinical, regulatory, quality, and finance teams to ensure successful execution of CMC activities related to regulatory filings, cGMP manufacturing and clinical supply. Key Responsibilities CMC Strategy and Leadership • Define and execute end‑to‑end CMC strategy aligned with corporate and clinical development objectives., • Lead and develop a high‑performing Technical Development Team encompassing upstream, downstream, analytical, and formulation development., • Serve as the primary CMC leader for development candidate selection and progression decisions.Manufacturing and External Partnerships, • Identify, select, and manage CDMOs and CROs; negotiate manufacturing, quality, and supply agreements in partnership with executive leadership and finance., • Lead seamless technology transfer of manufacturing and analytical processes to external partners for non‑GMP and GMP production., • Oversee drug substance and drug product manufacturing from development candidate nomination through clinical supply, ensuring on‑time delivery for regulatory submissions and clinical trials., • Monitor manufacturing timelines, budgets, and performance; proactively identify opportunities to accelerate development and control costs.Technical and Quality Oversight, • Establish critical quality attributes (CQAs), process controls, and fit‑for‑purpose control strategies to ensure product consistency and robustness., • Oversee analytical method transfer, method qualification, stability programs, and product shelf‑life assignments., • Provide leadership and oversight of QA activities with external QA consultants and quality systems appropriate for company stage., • Oversee clinical labeling, packaging, and supply logistics through supervision of clinical supply partners.Regulatory Support, • Review technical documentation and reports from CDMOs and CROs., • Author and oversee CMC sections of regulatory submissions and amendments., • Partner closely with Regulatory Affairs to support health authority interactions related to CMC.Organizational Leadership, • Develop CMC operating plans, milestones, and short‑ and long‑term objectives across all pipeline programs., • Build scalable systems and processes appropriate for company growth., • Influence company culture through collaborative leadership, mentorship, and cross‑functional partnership.Qualifications and Experience, • PhD in Biochemistry, Biology, Biotechnology, Chemical Engineering, Biological Engineering, or a related discipline., • 15+ years of experience in the pharmaceutical or biotechnology industry, with substantial leadership responsibility in biologics CMC, process development, and manufacturing., • Recognized expert in biologics CMC process, development, and strategy, including application of Quality by Design (QbD) approaches to support robust manufacturing processes and consistent product quality across development stages., • Proven experience building and leading teams and developing talent in matrixed and outsourced environments., • Extensive experience with technology transfer to CDMOs, including cell line development, upstream and downstream process development, analytical method development, scale‑up, and GMP manufacturing., • Hands‑on experience with formulation development and stability studies for drug substance and drug product to support regulatory submissions and clinical trials., • Strong working knowledge of drug development across research, preclinical, clinical, and regulatory functions., • Experience with bispecific proteins, Fc‑fusion proteins, or other complex biologics preferred., • Demonstrated ability to author high‑quality technical documentation for regulatory submissions., • Exceptional leadership, communication, and stakeholder management skills, with the ability to drive strategic discussions with senior management and external partners., • Proven ability to build consensus and solve complex problems across diverse, cross‑functional teams., • Willingness to travel domestically and internationally as needed to support CDMO oversight.The base salary for this role ranges from $204,000 to $292,000 and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future. Repertoire is committed towards social responsibility and developing an inclusive culture. Much as the power of the immune system lies in the diversity of T and B cells, our work requires the creativity and ingenuity of a diverse workforce. We believe in actively pursuing equity in all facets of the work experience at Repertoire. We will continue to educate ourselves about the inequities and barriers present in our society and take action as a company where we can make a difference. Repertoire is proud to be an Equal Opportunity Employer. Recruitment & Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto. Powered by JazzHR QsN01trgCo

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 DescriptionRole Summary • Responsibilities: You will be responsible for a variety of administrative, coordination and scientific tasks related to client projects, as well as working on company and team initiatives, • Salary: A starting salary of $58,000 per annum. This increases to $60,000 for successful candidates who hold a master’s qualification (please note this is a standardized, non-negotiable salary), • Benefits: Hybrid working options that allow you to work from home up to 50% of your time, generous holiday allowance, flexible working hours, private medical and dental insurance, 401K plan, life insurance, full funding for external training, comprehensive travel insurance and more, • Role Type: Full-time, permanent, • Start Date: We currently recruiting for start dates in early 2026, • Location: This role is available in our Boston office About the Role Project Coordinators are based in each of our scientific team s and support with a wide range of administrative, project coordination, and scientific tasks. These teams are broadly described as Medical Communications, Market Access, Evidence Development, and Rare Diseases. Your interest in the different areas of our work will be explored at the various recruitment stages and you will be assigned to a team when you join. Many Project Coordinators also work across teams, giving them the opportunity to explore a wide variety of project types and responsibilities. The responsibilities of the Project Coordinator role are varied, and, in a typical week, the majority of your time will be spent overseeing the delivery of scientific work to our clients in the healthcare sector, with responsibility for the smooth running of projects. This will include identifying and suggesting improvements to processes, as well as implementation of these changes, with the aim of enhancing quality and efficiency within the team and, where appropriate, across the wider company. You may also work on internal projects that contribute to the successful operation of your team. Key responsibilities may include: • Formatting, consistency and general quality control review of scientific documents, including reimbursement submissions, reports, slide sets, manuscripts, abstracts and posters, • Assisting Project Managers with client and healthcare professional communication on multi-component projects, and the production of progress reports and summaries that enhance the level of customer service delivered, • Coordinating logistics and providing project support for both in-person and virtual events and meetings, for example congresses, symposiums and advisory boards, • Day-to-day co-ordination of the project team and monitoring of project timelines, in collaboration with the project manager, • Scheduling meetings, recording minutes and coordinating their distribution, • Assisting the team with the development of planning tools to optimize the productivity of the team and cross-collaboration between the team and other teams, • Supporting the accurate referencing of scientific materials, including preparing reference packs, • Screening records for relevance to research questions and extracting data from relevant publications, • Liaising with our Creative team on the development of figures and other visuals to be included in reports, • Supporting the development of client proposals and tracking those sent and responded to, • Management of project compliance, which includes completing compliance training, preparation of project compliance documentation, liaising with client compliance teams, and acting as the internal point of contact for all compliance-related queries, • Liaising with external suppliers, including translation agencies, as well as digital and marketing agencies and other consultancies, to ensure smooth delivery of projects, • Ownership of tasks in our project management system to support the correct budgeting and invoicing of projects, • Supporting Analysts and Medical Writers with the write up of methods and results of projects into engaging reports and slide sets, • Reformatting of scientific documents to ensure adherence to client requirements and/or relevant submission guidelines, • Helping project teams to keep abreast of the latest potentially relevant sources of information and industry guidelines to inform their project work, and keeping all team resources up to date, • Organizing team monthly meetings and other internal activities Hybrid Working Policy: We recognize that home-working can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. At the same time, we believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. Therefore, we offer flexible working arrangements that allow our colleagues to work from home for up to half of the time, measured across a 2-week rolling period. Please note that as part of our wider flexible working policy, employees may work outside of Massachusetts for up to 4 weeks annually. Career Profile We offer many opportunities for personal and professional development at Costello Medical. Please click below to read firsthand accounts from our colleagues about their time with the company: https://www.costellomedical.com/careers/working-at-costello-medical/ A Day in the Life of a Project Coordinator To learn more about a typical day for a Project Coordinator at Costello Medical, please click here: https://www.costellomedical.com/day-in-the-life/project-assistant.html Requirements About You The ideal candidate will be proactive, innovative and eager to take on new challenges and responsibilities with an ambition to develop in the role. You will receive close training and mentorship from experienced colleagues, so no prior industry experience is required. This role will suit those who have excellent attention-to-detail and organizational skills, a talent for communication and a passion for improving healthcare outcomes. Essential requirements for the role are: • A degree level or equivalent qualification in a scientific discipline (minimum GPA 3.3). Postgraduate qualifications (minimum GPA 3.3) would be an advantage, but they are not a requirement for the role. We welcome applications from candidates with a diverse range of specialisms, including but not limited to; biology, chemistry, pharmacy, biomedical sciences, global health, epidemiology, biochemistry, and medicine, • A flair for, and attention to, detail, • Exceptional written English, which you will use in client work, email communication and internal messaging, • Effective verbal communication skills, which you will use when working with colleagues and clients, • The ability to tailor your communication style to a variety of audiences, including healthcare professionals, patient groups, suppliers, clients, non-scientific colleagues and governmental bodies, • Being self-motivated and enthusiastic, with a genuine interest in healthcare and an eagerness to learn about new areas of science, • Excellent organizational skills and a passion for maintaining high levels of organization across tasks and processes, • The ability to respond to conflicting deadlines, work independently and self-manage your time, • The self-awareness to reflect on your own performance, alongside a willingness to take ownership of your work and the development of your career, • A commitment to delivering excellent customer service, • A desire and aptitude for collaborative working across project teams, where you share knowledge with others in your team to promote the attainment of a common objective, and work together to overcome obstacles to success, • A “can do” approach, and the initiative, positivity and creativity required to continually improve the service we offer, • Embodying Costello Medical’s values, which includes being committed to delivering quality work, championing innovation in healthcare, acting with integrity, and supporting your colleagues as they would support you, • Good knowledge of Microsoft Office Benefits About Costello Medical Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access, and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies, and charitable organisations. We have been listed in the Top 100 Best Companies to Work For list since 2017, the Boston Globe’s Top Places to Work list in 2025, and were proud to receive B Corporation accreditation in 2022. Learn more about us, our work, and our mission on our website: https://www.costellomedical.com/ The Recruitment Process Our recruitment process includes a short assessment, involving two tasks, for you to complete remotely, followed by a telephone interview with a member of our Talent Acquisition team. If successful, you will be invited to an interview. Our standard recruitment process lasts around 1 month however, this can be adapted if necessary. As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please click here to read more about this and contact the People Team via recruitment@costellomedical.com should you require reasonable adjustments at any stage. We currently have start dates throughout 2025, which occur on a monthly basis. You will be asked to state your availability on your application form. Whilst there are no set application deadlines, we strongly recommend applying as early as possible so that we can begin processing your application. Please note that this role is available in our Boston office. What We Offer • A starting salary of $58,000 per annum. This increases to $60,000 for successful candidates who hold a master’s qualification. Please note that this salary is standardized and non-negotiable”, • Private medical insurance with a company contribution, • Dental and vision cover, • 23 days’ vacation leave increasing by 1 day to a maximum of 27 days. 6 public holidays plus 1 floating holiday, • The chance to work from home for up to half of your working time, • Retirement savings via a 401k plan with up to a 5% employer match, • Paid funding for external education and study leave, • Life insurance, • Comprehensive travel insurance, • Flexible and reasonable working hours, • Regular company-funded social activities Please click here to learn about our reward package and the other benefits of working for Costello Medical: https://www.costellomedical.com/careers/benefits-package-in-the-us/ How to Apply You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable. While we embrace Artificial Intelligence (AI) technologies to innovate and improve processes, we want to understand your unique skills and experiences throughout the recruitment process. Therefore, if you use AI to assist with your application, we recommend that you do not rely solely on this technology to generate your application materials. As your role may involve developing new written content from scratch and handling confidential data that cannot be uploaded to AI technology, it is important for us to assess your own skills and abilities. Please contact the Talent Acquisition team at recruitment@costellomedical.com if you have any questions about the role or application process. Visa Sponsorship We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa.

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 Position will be responsible for CMC leadership and project management for existing and new biologics projects from the drug substance perspective. Responsibilities: • Lead cross-functional S&T product teams and represent the CMC team and/or S&T in interface with S&T leadership, other Operations functions, other AbbVie functions and external partners. Participate in or coordinate Governance efforts such as Product Performance Teams or gate reviews., • Develop comprehensive project plans, budgets, timelines and strategy; biologics projects at all stages of development are included, from phase I through commercial., • Must present technical information regarding biologics manufacturing, process development and process characterization to management and to regulatory agencies., • Prepare and review regulatory briefings and submissions to support clinical trials through registration of the product as well as post-approval life-cycle management., • Manage multiple projects at various stages of development., • Represent assigned projects on the multidisciplinary Asset Development Team.Qualifications, • Ph.D. in biochemistry, biochemical engineering, cell biology or related field with 8+ years of industrial experience (or equivalent) or Master degree in above mentioned field with 16 years of relevant experience, is required., • Very strong writing, presentation and communications skills are required., • Significant technical understanding of biologics manufacturing as well as associated quality and analytical issues is required., • Ability to work in a highly matrixed team and to influence scientists and SMEs in other disciplines is required., • Ability to work against tight timeline to meet business goal., • Experience in biologics manufacturing process support and/or development, analytical development, or biologics process validation is needed., • CMC development experience through IND and/or NDA/MAA., • Experience leading multiple CMC project teams through IND and NDA/MAA preferred., • Technical understanding and experience with small molecule products manufacturing, development, quality and analytics is required., • Knowledge and experience with FDA and global regulatory requirements for CMC issues is required. Ability to influence internal and external experts on CMC regulatory issues, independently. • Demonstrated excellence in writing, presentation, and overall communication., • Demonstrated excellence in leading CMC project teams. 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 thisposting 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 anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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

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 At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. The Discovery Neuroscience In Vivo Pharmacology group in Cambridge, Massachusetts, is seeking a highly skilled and self-motivated Senior Scientist to join a dynamic team supporting target identification, validation, and drug transport facilitation over brain barriers. The successful candidate will drive scientific innovation, has experience making tangible contributions to the discovery pipeline, and has people and project management experience. Responsibilities: • Responsible for design and implementation of in vivo testing of multispecific biologics, small molecules, and siRNAs to support projects in the areas of Alzheimer’s and Parkinson’s disease, • Serve as an in vivo representative in cross-functional teams with Discovery Biotherapeutics, DMPK, and Development Sciences colleagues, providing project updates, analysis, and strategic advice, • Proactively translate department/project team scientific questions into well-designed experiments, utilizing internal and external resources, • Identify and solve technical problems independently, implement new assays and workflows, conceive and implement innovative research ideas, • Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions, • Collaborate with cross-functional partners at various AbbVie sites to advance candidates through discovery milestones, • Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor, • Mentor / matrix manage junior scientists, and be accountable for the effective performance of the team, • Ensure consistency and quality of technical reports, • Uphold impeccable research-related & corporate compliance standards, • May author or co-author peer-reviewed scientific papers or patentsQualifications Minimum Qualifications: • Bachelor’s Degree and typically, 12 years of experience, Master’s Degree and typically 10 years of experience, PhD and typically 4 years of experience., • Background in receptor and / or transporter biology and targeted delivery, • Background in brain barriers biology, • Experience with in vivo models of neurodegeneration, particularly with models of Alzheimer’s and Parkinson’s Disease, • Experience in assay development for target identification and validation, mechanism of action studies, biodistribution and biomarker analysis. Proven ability to troubleshoot and refine assays and workflows, • Proven track record in characterizing complex biotherapeutics in vivo (biologics, small molecules, siRNA), • Proven track record of working in multidisciplinary in vivo pharmacology teams, demonstrated ability to collaborate effectively in a dynamic, cross-functional matrix environment, • Experience managing direct reports, including providing performance evaluations and development opportunities, • Excellent organizational skills, strong data analysis and critical thinking skills, and the ability to manage multiple projects simultaneously, • Goal-oriented and highly self-motivated team player with excellent verbal and written communication skills with experience contributing to technical reports and publications Desired Qualifications: • Experience operating effectively in a matrixed, fast-paced discovery organization, • Experience in managing external collaborations, • Experience with ex vivo readouts including immunohistochemistry and biochemistry (e.g., ELISA, WB, qPCR, ddPCR). Experience with image analysis, • Familiarity with CNS-relevant biology and genetic medicine applications Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description Position Overview Psomagen is a global genomics and multi-omics service provider specializing in next-generation or sanger sequencing (NGS, CES), single-cell, and proteomics analysis. We provide advanced research and clinical sequencing services to academic, pharmaceutical, and biotechnology clients. We are seeking Laboratory Technicians, Scientists, and Managers who will contribute to the daily operation, optimization, and leadership of our laboratory facilities in Maryland (MD) or Massachusetts (MA). Depending on the role level, responsibilities include performing laboratory workflows, leading project execution, managing staff, and ensuring compliance with quality standards. Candidates should have hands-on experience in molecular biology, sequencing workflows, or biological sample processing, and a strong interest in multi-omics and high-throughput genomic technologies. Job Profile • Full-time, • Location: Rockville, MD or Cambridge, MA Key Responsibilities 1. Experimental Operations • Perform a range of molecular biology and genomics techniques including:, • Biological tissue and blood sample handling, • DNA/RNA extraction and quantification, • Gel electrophoresis, PCR/qPCR, and NGS library preparation, • Sequencing on Illumina, Ultima, PacBio, or 10x Genomics platforms, • Single-cell assay setup and proteomics sample preparation, • Operate computer-based laboratory systems (e.g., LIMS, instrument software) and record data with accuracy., • Maintain consistent sample tracking, labeling, and data integrity across projects. 1. Laboratory Maintenance & Quality Control • Monitor and maintain laboratory equipment performance; perform calibration, troubleshooting, and minor repairs as needed., • Manage inventory of reagents and consumables, ensuring readiness for high-throughput operations., • Ensure all experimental steps comply with CLIA, CAP, and ISO quality standards., • Prepare and review Standard Operating Procedures (SOPs) and ensure adherence to laboratory safety guidelines. 1. Workflow Optimization & Troubleshooting • Identify and troubleshoot issues with samples, instruments, or reagents to improve workflow efficiency., • Collaborate with cross-functional teams (Project Management, Bioinformatics, and Operations) to streamline experimental pipelines., • Contribute to the development and optimization of new assays, methods, or automation processes for enhanced throughput and data quality. 1. Team Collaboration & Communication • Communicate effectively with internal teams and external clients to clarify sample issues, data discrepancies, or project timelines., • Train and mentor junior staff on laboratory techniques, data recording, and quality control standards., • Participate in inter-departmental meetings to support project execution and continuous improvement initiatives., • Support coordination between MD and MA laboratory teams to maintain consistent SOPs and performance standards. 1. Leadership & Management (Manager-level only) • Supervise daily operations of laboratory teams and assign workload based on project priorities., • Oversee staffing schedules, including weekend or evening shifts when required., • Lead performance evaluations, enforce safety compliance, and manage cross-training to ensure flexibility within the team., • Collaborate with senior management to plan resource allocation, project timelines, and capacity expansion strategies. Qualifications Required • Bachelor’s degree in Molecular Biology, Biochemistry, Biotechnology, or related field., • Practical experience with molecular biology techniques (e.g., PCR, NGS library preparation, nucleic acid purification)., • Strong attention to detail, organizational skills, and data recording accuracy., • Familiarity with laboratory information systems (LIMS) and computer-based instrumentation., • Excellent communication and teamwork skills. Preferred • Prior experience in genomics, sequencing, or multi-omics laboratories., • Knowledge of single-cell, spatial transcriptomics, or proteomics workflows., • Experience operating Illumina, PacBio, or other sequencing platforms., • Understanding of genomics, sequencing technologies, or multi-omics research trends., • Experience working under CLIA/CAP regulatory environments and preparing documentation for audits., • Demonstrated leadership or supervisory experience (for Manager level). Additional Information • Positions are available in both Rockville, MD and Cambridge, MA laboratories., • Occasional weekend or evening shifts may be required to meet project deadlines., • Psomagen offers a collaborative, data-driven environment that encourages continuous learning and technical excellence. Benefits • Medical, Dental, and Vision insurance (100% employer-paid premium), • 401K with immediate participation and company match after 1 year, • Paid time-off with roll over option, • Long-term employment cashable vacation, • 2-hour off for an annual check-up, • Lunch allowance and drinkware reimbursement, • Visa sponsorship is offered when needed, • Money Gifts for congratulatory/condolences, • Free gym facilities near the company Company Overview Psomagen, Inc., founded in 2004 in Rockville, MD, is at the forefront of genetic and genomic testing. The company offers cutting-edge genomic services through next-generation and Sanger sequencing with data analysis services for applications in basic research and clinical diagnostics. The service laboratory has been certified under the Clinical Laboratory Improvement Amendments (CLIA) and accredited by the College of American Pathologists (CAP), which demonstrates the highest level of quality and safety in the market. Listed on the KOSDAQ in July 2020, the company is rapidly expanding its business from B2B to B2C and from Research to Clinical markets. The company has broadened its capabilities in the healthcare space such as at-home kits for analysis of genetic traits and microbiome profiles. With CLIA-certified and CAP-accredited laboratories, the company is looking to further expand service offerings in the clinical laboratory diagnostics market such as a laboratory-developed test (LDT) for COVID-19. As an EEO/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, color, sex, pregnancy, national origin, ancestry, citizenship, sexual orientation, gender identity or expression, protected genetic information, age, disability, marital status, veteran status, religion, height, weight, other protected group status, or any other basis protected by the laws where we employ people. G2025-04207

Job Description Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitableculture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our Commercial team as a Business Development Manager, Northeast.The Business Development Manager is responsible for driving revenue growth and expanding strategic accounts within the assigned territory. Reporting to the Director of Sales, this role develops and executes territory strategy, cultivates high-value OEM, diagnostics, life sciences, and therapeutic partnerships, and advances complex commercial opportunities across the product portfolio. The position combines technical expertise, consultative selling, and market intelligence to expand pipeline, increase market share, and build long-term strategic relationships that support sustained commercial performance. How you will make an impact: • Develop and execute a comprehensive territory strategy aligned with revenue and growth objectives., • Drive new business development while expanding and retaining key strategic accounts., • Lead complex sales cycles, including opportunity qualification, technical consultation, negotiation, and contract execution., • Build executive-level relationships with OEM, diagnostics, biotech, and therapeutic partners., • Maintain accurate pipeline management and forecasting through CRM tools to support data-driven decision-making., • Provide technical and commercial expertise across mRNA, enzymes, oligonucleotides, bioconjugation, and related platforms., • Engage key opinion leaders (KOLs) and industry influencers to enhance brand visibility and accelerate adoption., • Monitor competitive landscape, market trends, and customer needs to inform territory planning and strategy., • Deliver voice-of-customer insights to Marketing and R&D to influence product development and positioning., • Collaborate cross-functionally to resolve customer issues, advance opportunities, and ensure high customer satisfaction., • Perform other functions and duties as required The skills and experience that you will bring: • Bachelor's degree in Biology, Molecular Biology, Biochemistry, Genomics, or related life sciences discipline; 5+ years of B2B commercial sales experience in biotechnology, genomics, biologics/CDMO, or related sectors., • Proven success in strategic account development, complex deal negotiation, and achieving or exceeding territory revenue targets., • Strong technical expertise in mRNA, enzymes, NTPs, oligonucleotides, bioconjugation, or related advanced biologics platforms., • Demonstrated experience managing long, consultative sales cycles with therapeutic, OEM, or diagnostics customers., • Proficiency in CRM platforms (e.g., Salesforce) and business software tools; strong forecasting and pipeline management skills., • Excellent executive-level communication, presentation, and relationship-building skills., • Self-motivated and effective in remote, independent, and cross-functional environments., • Willingness to travel up to 50% to support client engagement, conferences, and internal initiatives. The anticipated salary range for this position is $120,000 - $130,000. In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. #LI-Remote The benefits of being a #MiracleMaker: • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions., • Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/ To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/ Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.

Job Description Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitableculture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our Commercial team as a Business Development Manager, Northeast.The Business Development Manager is responsible for driving revenue growth and expanding strategic accounts within the assigned territory. Reporting to the Director of Sales, this role develops and executes territory strategy, cultivates high-value OEM, diagnostics, life sciences, and therapeutic partnerships, and advances complex commercial opportunities across the product portfolio. The position combines technical expertise, consultative selling, and market intelligence to expand pipeline, increase market share, and build long-term strategic relationships that support sustained commercial performance. How you will make an impact: • Develop and execute a comprehensive territory strategy aligned with revenue and growth objectives., • Drive new business development while expanding and retaining key strategic accounts., • Lead complex sales cycles, including opportunity qualification, technical consultation, negotiation, and contract execution., • Build executive-level relationships with OEM, diagnostics, biotech, and therapeutic partners., • Maintain accurate pipeline management and forecasting through CRM tools to support data-driven decision-making., • Provide technical and commercial expertise across mRNA, enzymes, oligonucleotides, bioconjugation, and related platforms., • Engage key opinion leaders (KOLs) and industry influencers to enhance brand visibility and accelerate adoption., • Monitor competitive landscape, market trends, and customer needs to inform territory planning and strategy., • Deliver voice-of-customer insights to Marketing and R&D to influence product development and positioning., • Collaborate cross-functionally to resolve customer issues, advance opportunities, and ensure high customer satisfaction., • Perform other functions and duties as required The skills and experience that you will bring: • Bachelor's degree in Biology, Molecular Biology, Biochemistry, Genomics, or related life sciences discipline; 5+ years of B2B commercial sales experience in biotechnology, genomics, biologics/CDMO, or related sectors., • Proven success in strategic account development, complex deal negotiation, and achieving or exceeding territory revenue targets., • Strong technical expertise in mRNA, enzymes, NTPs, oligonucleotides, bioconjugation, or related advanced biologics platforms., • Demonstrated experience managing long, consultative sales cycles with therapeutic, OEM, or diagnostics customers., • Proficiency in CRM platforms (e.g., Salesforce) and business software tools; strong forecasting and pipeline management skills., • Excellent executive-level communication, presentation, and relationship-building skills., • Self-motivated and effective in remote, independent, and cross-functional environments., • Willingness to travel up to 50% to support client engagement, conferences, and internal initiatives. The anticipated salary range for this position is $120,000 - $130,000. In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. #LI-Remote The benefits of being a #MiracleMaker: • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions., • Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/ To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/ Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.

Job Description Cambridge, MA (In-person) About Us: GT Biosciences is a seed-stage techbio startup building Deliveromics, the first AI-powered, high-throughput, multiplexed in vivo data engine for cracking the design rules of drug delivery. Founded by MIT PhDs and an MIT professor, backed by top-tier investors, we’re creating next-generation, non-viral, cell-type-specific delivery vehicles. We’re a small, fast-moving, science-obsessed team on a mission to make routine in vivo cell reprogramming possible. We’re a small, fast-moving, science-obsessed team on a mission to make routine in vivo cell reprogramming possible. We value transparency and collaboration, 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 mission-driven, multidisciplinary LNP Scientist to join our Deliveromics Platform Development team to advance the next generation of non-viral delivery technologies. In this role, you will design and develop novel ionizable lipids, engineer ligand-conjugated lipid nanoparticle formulations, support Deliveromics in vivo screening, and evaluate performance using both in vitro assays and in vivo animal models. You will be responsible for experimental planning and execution, data analysis and interpretation, and the clear communication of results. As one of the earliest scientific hires at an emerging techbio company, you will have the opportunity to shape platform development, collaborate across disciplines, and contribute directly to transformative delivery solutions for genetic medicines. This is a full-time, in-person position based in Cambridge, MA. Responsibilities: Lead the discovery and development of innovative ligand-LNP delivery technologies, with a focus on improving biological performance, biophysical properties, and in vivo targeting. Design and develop novel ionizable lipids, ligand-conjugated LNP formulations, and related chemistries for targeted delivery applications. Develop, optimize, and implement high-throughput assays to evaluate LNP systems, including stability, delivery efficiency, and critical quality attributes, in both in vitro and in vivo models. Design and execute experiments at the intersection of chemistry, molecular biology, and formulation science, including spatial or sequencing-based readouts when appropriate. Independently plan, execute, and analyze experiments while also overseeing work performed by supporting scientists. Stay current with emerging research, technologies, and competitive landscapes across lipid nanoparticles, nucleic acid delivery, targeted therapeutics, automation, and gene editing modalities. Collaborate closely across chemistry, biology, and automation scientists within the Deliveromics Platform group to troubleshoot challenges and integrate new methods into the screening and development pipeline. Analyze and interpret experimental data using rigorous quantitative and statistical frameworks; generate high-quality reports and provide actionable insights that inform design decisions and platform direction. Establish and maintain complete, well-organized documentation, including protocols, SOPs, experimental records, and data summaries to ensure reproducibility and compliance. Drive process and platform innovation, contributing to technology transfer efforts as workflows mature toward automation, scale, and production readiness. Qualifications: Required: PhD in Chemistry, Bioengineering, Biomedical Engineering, Biochemistry, Biophysics, or a related field. Exceptional candidates with substantial relevant experience will also be considered, regardless of degree. Hands-on experience with ionizable lipids, LNP formulation, RNA/LNP nanoparticle preparation, targeted delivery systems, or related technologies, with a strong track record in industry or academia. Deep expertise in the design, synthesis, purification, and characterization of novel ionizable lipids, lipid conjugates, lipid-like compounds, or related molecular platforms. Practical experience with lipid biology, LNP formulation development and optimization, and in vitro and/or in vivo assays assessing delivery performance. Strong problem-solving skills, meticulous attention to detail, and a high level of experimental rigor. Excellent written and verbal communication skills with the ability to collaborate effectively across diverse scientific and technical teams. A resourceful, adaptable, and emotionally intelligent team member who thrives in a fast-paced, cross-functional environment. Ability to work onsite five days per week at our Cambridge, MA location. Nice to have: Prior experience working with non-human primate models will be a strong plus. Experiences with nucleic acid chemistry (mRNA, ASO, and siRNA, etc.). Basic coding skills (e.g., Python, R, or MATLAB). Hands-on experience troubleshooting liquid-handling platforms or automated lab systems. What we offer Competitive salary and equity. Flexible, generous health benefits. Work with a small, world-class team that values rigorous science and candid collaboration. Opportunity to work with experts from diverse scientific backgrounds. Equal Opportunity Employer: GT Biosciences is an Equal Opportunity Employer. We celebrate diversity and are committed to fostering an inclusive, supportive environment for all employees. All qualified applicants will be considered without regard to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation. We don't expect anyone to know everything. We learn together, support each other, and get better every day! If you are ready to make an impact, we would love to hear from you.

Job Description Bioinformatics Scientist (Mid/Senior) Compensation: $170,000 - $190,000 Location: South San Francisco, CA Job Type: Full-time (Hybrid) Equity: Highly Competitive Equity About Our Client TechStaffers has partnered with one of our clients & they are on a mission to accelerate new cures and promote a healthier planet by unlocking a new level of productivity for scientists. Their sequencing services are used daily by thousands of innovators, including Nobel laureates, Fortune 100 pharma, and over 70,000 scientists. They began by revolutionizing plasmid sequencing, making it exponentially cheaper and faster. Now, they are expanding that same disruptive model across all of genomics, including a new RNA-seq service, to provide scientists everywhere with faster and more affordable access to data. Every team member plays a crucial role in driving the future of biotech research, building the world's most efficient sequencing engine that operates overnight and scales globally. Position Overview We are seeking a highly motivated mid- to senior-level Bioinformatics Scientist to work on the bioinformatics engine that powers this impact. This role is heavily bioinformatics-focused, emphasizing deep domain expertise and the building of scalable products over general software platform skills. You will wear many hats, leading projects from concept through production while maintaining strong ownership of your work. Key Responsibilities • Build blazing-fast, production-grade bioinformatics workflows that process thousands of samples per day., • Develop novel algorithms that turn raw sequencing data into fast, intuitive, and accurate insights., • Hunt down bugs and tame the chaos of real-world sequencing data, including biological artifacts and platform quirks., • Translate bioinformatics outputs into a dynamic scientific UX that feels magical to researchers., • Stay on top of cutting-edge tools and find creative ways to integrate them into real-world pipelines., • Mentor teammates and grow your own skills in a fast-moving, collaborative environment. Qualifications & Requirements • Education: PhD in Bioinformatics, Computer Science, Statistics, Biology, Biochemistry, Physics, or a closely related field., • Experience: 3+ years of experience developing production bioinformatics pipelines., • Industry Background: Minimum of 2 years of industry experience; candidates whose only experience is in academia will not be considered., • Domain Expertise: Strong background in microbial ecology or related fields, with a distinct preference for expertise in microbial genomics., • Technical Tools: Significant, hands-on experience with Nextflow and Docker is critical for pipeline development. Proficiency with standard bioinformatics tooling (Python, Linux, Git) is required., • Sequencing Data: Hands-on work with Illumina or Oxford Nanopore sequencing platforms., • Product Impact: Proven experience building scalable bioinformatics products and clear evidence of delivering impactful, independent projects., • Bonus: Contribution of a novel bioinformatics tool or algorithm is highly regarded as a signal of a top-tier candidate. Ideal Candidate Profile • Thrives with high agency and high ownership, leading projects from idea to production., • Exhibits strong leadership qualities, initiative, and a clear motivation to advance their career., • Is curious about the intersection of biology, algorithms, and software engineering., • Gets excited knowing their work directly accelerates the next generation of medicines and biotechnology., • Values clear communication and loves helping others level up., • Is energized by a tight-knit, fast-paced team environment. Visa Requirements • Visa sponsorship is generally not available., • Able to accommodate TN or H-1B1

Job DescriptionTitle: Scientist Location: Cambridge, MA Duration: 07 Months Job Summary Key Responsibilities • Develop, qualify, and troubleshoot chromatographic (GC, HPLC/UPLC) and LCMS based methods for the identification, characterization, and impurity profiling of oligonucleotides, siRNAs, and their formulations, as well as raw material related analytical methods and other methods as needed., • Understand and apply advanced scientific principles, theories, concepts, practices and standards to process and analytical development. Provide analytical support for investigations leading by quality, manufacturing, supply chain., • Perform testing of late development siRNA candidates and their formulations for their characterization. Author method development and qualification reports and SOPs for test methods., • Evaluate suitability of new methods and oversee method qualification and validation in the external contract testing labs., • Author and review analytical sections in regulatory submission documents., • Apply strong technical knowledge of organic and analytical chemistry to support laboratory investigations (deviations/OOS/OOT), as needed., • May serve as a primary contact person for cross-departmental needs or projects and be accountable for key deliverables., • Contribute to the development and/or improvement of technical capabilities as well as initiatives to improve department efficiency. Qualifications • PhD in Chemistry, Biochemistry or related disciplines with 0-4 years industry experience, Master's degree with > 5 years related industry experience or Bachelor's degree with > 8 years related industry experience respectively, with demonstrated chromatographic separation, method development / qualification and structure elucidation expertise., • Experience with HPLC/UPLC and LCMS-based analytical method development desired., • Hands-on experience with oligonucleotides, proteins, or peptides is a plus., • Familiarity with instrument troubleshooting and software including Empower, MassHunter, and UNIFI preferred. Knowledge of GxP requirements and application of statistical methods in the analytical laboratory is a plus., • Strong interpersonal skills, communication, and collaboration.#TB_PH #ZR #RESCIE1 #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. Company DescriptionFounded 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, CAFounded 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 DescriptionAbout UsDeep 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 The Senior/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 support novel target validation by utilizing a variety of genome engineering approaches in both pooled and arrayed formats. The ideal candidate will have strong gene editing, cell biology and molecular biology experience in an industrial setting. Prior experience with oligonucleotide therapeutics such as ADAR, ASO, and/or siRNAs is also highly beneficial. The successful candidate should demonstrate initiative and be able to thrive in a dynamic work environment with cross-functional teams working together to achieve company goals. *Title will be commensurate with prior experience. This position is onsite at our Cambridge, MA site. Key Responsibilities • Plan and execute genome engineering experiments to generate models for target validation., • Execute barcoded pooled screening assays, including NGS library preparation., • Support the development of novel biochemical, cellular and functional assays for our internal therapeutic pipeline., • Maintain and transfect a variety of mammalian cell lines, such as immortalized cell lines., • Perform standard molecular biology techniques (e.g. PCR, qPCR, molecular cloning, etc.)., • Collaborate with a cross-functional team in a dynamic, matrixed environment to achieve shared company deadlines., • Clearly document experiments, standard operating procedures (SOPs) and data in an electronic lab notebook (ELN)., • Communicate and present experimental design and findings with colleagues and project teams.Basic Qualifications, • Bachelor’s or Master’s in Biology, Molecular Biology, Genomics, Biochemistry or a related field with 2-4+ years of relevant pharmaceutical or biotechnology experience., • Gene editing experience in an industrial setting., • Strong understanding of molecular and cell biology., • Experience growing, maintaining and transfecting mammalian cell lines., • Experienced in design and execution of molecular and cellular assays., • Excellent communication, organizational skills and a willingness to learn., • Ability to work independently and manage priorities in a fast-paced technical environment.Preferred Qualifications, • Experience in lentivirus generation, cell line engineering, or flow cytometry is a plus., • Prior therapeutics development experience., • Past experience with RNA editing and/or RNA oligonucleotides., • Next-generation sequencing library preparation, e.g. amplicon sequencing., • 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 $90,000 - $110,000, 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. 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 DescriptionSalary: $121,000 - $172,000 Summary The Scientist, Bioanalytical Development is responsible for performing laboratory activities and experiments related to the development and scientific qualification of bioanalytical methods for preclinical/clinical programs to assess PK. ADA and PD in preclinical and clinical samples. The Scientist, Bioanalytical Development will be responsible for activities related to the bioanalytical method development and qualification for non-regulated/exploratory methods and sample analysis from preclinical studies in support of drug development candidates. Reporting to the Associate Director in Bioanalytical Development, this role will be responsible for the execution of experiments to support IND filings / preclinical development as well as clinical method development. They may also oversee the activities of a research associates and perform project management activities for out-sourced methods including vendor management. Visterra is seeking a flexible candidate with a working knowledge of large molecule/biologics analytical techniques and laboratory skills. The primary focus will be developing and performing bioanalytical methods for programs in preclinical and clinical development, documenting the methods used and summarizing the data collected. This individual will be responsible for the execution and documentation of experiments to develop bioassays and the empirical evaluation of custom reagents to support preclinical/clinical method development. This is a full-time laboratory position based in Visterras facility in Waltham, MA. Responsibilities • Develop ligand binding methods including pharmacokinetic (PK), immunogenicity (ADA) and pharmacodynamic (PD) assays., • Design and independently execute experiments to select/identify appropriate bioanalytical reagents., • Oversee and perform sample analysis from preclinical and clinical studies., • Design and implement specialized in vitro studies designed to enhance mechanistic understanding of drug development candidates as needed on development programs., • Analyze data and trouble shoot assay development activities., • Write reports summarizing data and methods., • Manage and oversee activities of Research Associates., • Implement innovative technologies which offer pragmatic enhancements to the bioanalytical department., • Manage ongoing bioanalysis at external vendors to support large molecule drug candidates., • Negotiate CRO contracts and SOWs; from approval to execution., • Review, edit, and finalize method validation protocols, amendments, and reports, ensuring that documents meet project timelines, expectations, and deliverables, as well as Visterras global regulatory and compliance requirements., • Other duties and responsibilities as required by departmental and business needs., • Travel as needed to attend conferences, events and vendor site visits. Requirements • A minimum of 5 years of working experience, including hands-on laboratory experience in the bioanalysis or biotechnology industry., • An M.S. or Ph.D. in Immunology, Biology, Biochemistry, or related field is preferable, although candidates with a Bachelor of Science (BS) degree with significant research experience are also encouraged to apply, • Experience with ligand binding method development using ELISA and MSD., • Working experiences with biologics., • Proven experience in the development and validation of regulated bioanalytical method assays for pharmacokinetic, pharmacodynamic and immunogenicity evaluation., • Experience with summarizing data in slides and reports., • Experience with vendor management and project management., • Knowledge of regulatory requirements, including GLP, GCP, ICH and other applicable guidelines for Bioanalytical development in support of clinical trials., • Extensive experience with a broad range of bioanalytical platforms including ELISA, MSD and Flow Cytometry and techniques including bridging, direct, indirect, and competitive assays., • Ability to manage a research associate as a direct-report, including assigning and reviewing tasks and mentoring and coaching., • Strong time management and organizational skills, attention to accuracy and detail, and the ability and willingness to multi-task as needed., • This individual will be highly analytical, goal-oriented, and timeline sensitive while maintaining high quality standards. Company Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterras pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab. As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts. Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Job DescriptionSalary: $142,000 - $167,000 The Opportunity We are seeking a highly motivated Scientist to join our team at the forefront of developing a new class of engineered biologics with the potential to transform the treatment of autoimmune diseases. This is an exciting opportunity to work on next-generation therapeutic modalities that combine advanced protein design, high-throughput in vitro and cell-based assays, and in vivo studies to push far beyond what conventional antibodies can achieve. You will work closely with a talented protein design team to push the boundaries of engineered biologics, using cutting-edge computational and experimental approaches to create novel molecules. You will be deeply involved in every stage of the program, with the opportunity to help drive the science from early concept through preclinical proof of concept. Reporting to the Associate Director of Research, the ideal candidate will bring intellectual curiosity, strong fundamentals in cell biology and biochemistry, and a genuine enthusiasm for working in a fast-paced, collaborative environment where the science is truly novel. This is a full-time position located at Visterras offices in Waltham, MA. Responsibilities • Design and execute cell-based and biochemical assays to evaluate the activity, potency, mechanism of action, and selectivity of novel engineered biologic candidates., • Collaborate closely with protein design and engineering colleagues to iterate on molecule design, interpret results in a mechanistic framework, and drive data-informed decisions., • Develop and optimize new in vitro model systems relevant to target biology and therapeutic mechanism, including primary cell assays where appropriate., • Independently analyze and interpret experimental data, troubleshoot methodological challenges, and propose creative solutions., • Contribute to project strategy by building a strong working knowledge of target disease biology and aligning experimental approaches with program goals., • Present experimental findings and strategic perspectives clearly to internal teams and leadership., • Stay current with the scientific literature and contribute emerging insights to the team., • Mentor and provide scientific guidance to junior team members, including research associates and interns. Requirements • PhD in biology, biochemistry, molecular biology, immunology, or a related field; recent graduates are encouraged to apply. Candidates with a B.S. and 8+ years of relevant industry experience will also be considered., • Hands-on experience designing and executing cell-based and biochemical assays, including work with primary and established cell lines., • Strong foundation in protein biology, including expression, purification, and characterization of recombinant proteins., • Prior experience with therapeutic antibodies, biologics screening, or protein engineering is a strong plus., • Curiosity-driven scientific mindset with strong analytical and critical thinking skills., • Excellent written and oral communication skills; comfortable presenting complex data to both scientific and cross-functional audiences., • Collaborative and team-oriented, with the ability to work effectively in an interdisciplinary environment., • Ability to manage and prioritize multiple projects and meet deadlines in a fast-paced setting. Preferred Qualifications • Experience with lysosomal biology, receptor-mediated endocytosis, or intracellular trafficking pathways., • Background in immunology and understanding of relevant autoimmune disease biology., • Familiarity with yeast or phage display, high-throughput screening, or NGS-based methods., • Experience with automation and liquid handling platforms., • Comfort with basic structural biology tools (e.g., PyMOL) to contextualize protein data. Management responsibilities: This position may include supervisory responsibilities Travel: Possible travel to local and national conferences About Visterra Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterras pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab. As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts. Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Job Description Why Join Us? Parabilis Medicines is a clinical-stage biopharmaceutical company dedicated to creating extraordinary medicines that unlock high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that are inaccessible to traditional drug modalities. Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its lead asset, zolucatetide (FOG-001), is a first-in-class, clinically validated direct inhibitor of the interaction between β-catenin and the T-cell factor (TCF) family of transcription factors, implicated in millions of cancer cases annually, including in colorectal cancer, desmoid tumors, hepatocellular carcinoma and a range of other Wnt/β-catenin-driven tumors. In Phase 1 clinical trials, zolucatetide produced the first-ever clinical evidence that it can directly inhibit this interaction, once previously considered "undruggable" despite its role across multiple cancer types. Parabilis is also advancing investigational degraders of ERG and ARON into clinical development for the treatment of prostate cancer, as well as progressing other preclinical programs. Backed by a recent $305 million Series F financing, Parabilis is entering an exciting phase of growth and execution. What's the opportunity? This is a rare opportunity to shape and protect the intellectual foundation of a company redefining what's possible in drug discovery. As Director, Intellectual Property, you will architect and lead the global IP strategy for Parabilis' Helicon™ platform and pipeline—helping unlock the full value of therapies targeting proteins long considered "undruggable." Reporting to the General Counsel, you will operate at the intersection of cutting-edge science and business strategy, partnering closely with Research, Development, CMC, and Business Development to translate breakthrough innovation into durable competitive advantage. In this highly visible role, you will not only build and scale world-class IP for the organization but also serve as a key strategic advisor to senior leadership—guiding critical decisions across pipeline advancement, partnerships, and long-term value creation. Key Responsibilities: • Develop and execute global patent strategies aligned with corporate, R&D, and business objectives., • Design layered IP protection strategies covering composition of matter, methods of treatment, platform technologies, computational methods, and manufacturing., • Lead drafting and prosecution of U.S. and international patent applications., • Conduct invention mining sessions and proactively identify patentable subject matter., • Oversee global prosecution strategy and manage outside counsel., • Lead freedom-to-operate analyses and patent landscape assessments., • Support due diligence for partnerships, collaborations, and financing transactions., • Serve as primary IP advisor to Research, Clinical, Regulatory, CMC, and Business Development teams., • Manage IP budgets and implement scalable portfolio tracking systems., • Present IP strategy updates to senior leadership and Board as needed. What you'll need to be successful: • Ph.D. in chemistry, biochemistry, molecular biology, structural biology, peptide chemistry, protein engineering, or related discipline strongly preferred., • Registered U.S. Patent Agent or admitted U.S. Patent Attorney in good standing., • 5+ years of patent experience in biotechnology, including in-house or law firm experience supporting innovative therapeutic platforms., • Strong familiarity with peptide therapeutics, intracellular delivery systems, oncology drug discovery, and computational drug discovery technologies., • Demonstrated success building patent estates for platform biotech companies., • Deep understanding of U.S. and global patent law relevant to life sciences., • Excellent scientific writing, claim drafting, and strategic communication skills., • Demonstrated ability to utilize AI tools for day-to-day work; baseline proficiency is expected, and advanced or innovative use of AI is a strong plus., • Ability to work hybrid preferred; remote considered. Core Values Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit. • Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable., • In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options., • Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact., • All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history. The base salary range for this position is $220,000-$290,000 per year, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees' overall well-being. As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law. 30 Acorn Park Drive | Cambridge, MA 02140 | www.parabilismed.com

Job Description Title: Scientist I (R&D) Location: Cambridge, MA 02142 Duration: 1+ Year Position Description: The Physical Biochemistry group requests a highly motivated and detail-oriented Senior Associate Scientist to join the group for operational efficiencies. The selected candidate will contribute to a fast-paced, innovative research environment focused on addressing unmet medical needs across immunology, rare disease, and neuroscience therapeutic areas. This position provides opportunities to collaborate within the Therapeutics modalities department; the candidate is expected to execute multi-step processes independently and proactively and communicate progress effectively in oral and written communications. The selected candidate will be expected to: Enable efficient reagent and study organization, documentation, and data reporting, as well as monitoring how protein reagents are stored and distributed across the department. Perform crystallization workflows or straight forward biophysical analysis workflows Enable crystal storage and shipping Demonstrate diligence in equipment maintenance, inventory tracking, and proactive ordering of laboratory supplies, and provide support for day-to-day laboratory management activities. Contribute to effective general laboratory organization and best practices for lab safety. Qualifications: • Bachelor's or Master's degree in Biochemistry or related field, with 1 2 years of relevant experience in an industrial and/or academic laboratory setting., • The candidate must demonstrate strong collaborative skills and excellent communication skills., • Innovative approaches to problem solving and the ability to manage multiple activities in parallel are highly valued. #TB_PH #ZRHC #RESCIE1 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. Company DescriptionFounded 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, CAFounded 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 Description Director of Analytical Development, Biologics REMOTE - East Coast Based Preferred Overview We are partnering with a clinical-stage (late-stage) biopharmaceutical organization seeking a Director of Analytical Development to lead analytical strategy and execution for biologics programs advancing through late-stage development, BLA readiness, and commercialization. This individual will play a critical role in method lifecycle management, regulatory submissions, and commercial readiness, working cross-functionally across CMC, Quality, and Regulatory. This is a fully remote role (U.S.-based). Key Responsibilities • Lead analytical development strategy for late-stage biologics programs, including Phase II/III and commercial readiness, • Oversee method validation, transfer, and lifecycle management in alignment with ICH guidelines (Q2, Q6, Q14), • Drive analytical support for regulatory submissions, including IND amendments, BLA/MAA filings, and responses to health authority questions, • Partner with Drug Substance, Drug Product, and Quality teams to ensure robust control strategies and specifications, • Provide oversight of CDMOs and external testing laboratories, ensuring timelines, data quality, and compliance, • Support comparability, stability, and characterization strategies for process changes and scale-up, • Act as a key contributor during inspections and audits (FDA, EMA, etc.), • Build, mentor, and scale a high-performing analytical team as programs advance toward commercialization Qualifications • PhD (preferred) or MS in Analytical Chemistry, Biochemistry, or related field, • ~10-15+ years of analytical development experience in biologics (monoclonal antibodies, proteins, or related modalities), • Strong expertise in late-stage development, method validation, and regulatory filings (BLA/MAA), • Deep knowledge of analytical techniques (e.g., HPLC/UPLC, CE, MS, bioassays, impurity profiling), • Proven experience managing external partners (CDMOs/CROs), • Familiarity with global regulatory expectations and inspection readiness, • Prior leadership experience with the ability to influence cross-functional stakeholders What Stands Out • Opportunity to shape analytical strategy at a pivotal, late-stage inflection point, • High visibility role with direct impact on regulatory approval and commercialization, • Fully remote flexibility with strong cross-functional exposureCompany DescriptionA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints. Job Responsibilities: -\tConducting Post Market Activities and Post Market Surveillance -\tManaging Customer and Product Complaint Investigation programs Education and Experience: -\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry -\tBachelor's degree -\tComputer proficiencyA top 10 pharmaceutical company with an immense amount of growth after releasing their at home COVID diagnostic tests is looking to bring on 200+ Quality Individuals through a massive hiring campaign. In their search for Quality Specialists, the organization is looking for individuals who will be responsible for reviewing and actioning customer complaints, as well as investigation into said complaints.\r\nJob Responsibilities:\r\n•\tConducting Post Market Activities and Post Market Surveillance\r\n•\tManaging Customer and Product Complaint Investigation programs\r\nEducation and Experience:\r\n•\t1 YR. of experience in a technical role in the medical device/pharma/biotech industry\r\n•\tBachelor's degree\r\n•\tComputer proficiency

Job DescriptionCompany Description The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, a place to call home, apply with us today! Job Description Eurofins is seeking a highly skilled, passionate, and motivated scientist to join our client Analytical Development team to support testing non-GMP samples for development studies such as comparability assessments, process development, stability, product, and process characterization.The Analytical Development team is responsible for developing and implementing new analytical methods, as well as optimizing and improving current methods for the characterization of raw materials, RNA drug substances, and LNP products and programs at various development stages. • Provide testing support for a variety of purposes, including release and stability testing, product characterization, high-throughput analysis, and characterization of complex raw materials., • Collect, process, and analyze experimental data, ensure accurate and timely documentation in electronic laboratory notebook., • Review, interpret, and present data within the analytical team and cross-functionally., • Author, review, and revise technical source documents to support phase-appropriate comparability., • Provide technical oversight to guide analytical/QC investigations, as needed., • Actively collaborate with internal and external process development and quality teams., • Train and mentor junior team members as needed.Qualifications Basic Minimum Qualifications: • B.S. in Analytical Chemistry, Biochemistry, Biophysics, or related field with 3-4 years of biotech industry experience utilizing FTIR, HPLC/UPLC, and LCMS or M.S. degree with 1-2 year of biotech industry experience utilizing FTIR, HPLC/UPLC, and LCMS, • Experience working with various biophysical instrumentation such as HPLC/UPLC (various detectors) and capillary electrophoresis (CE), • Strong technical background on analytical methodologies using IP-RP, IEX, and AEX., • Proficiency with instrumentation such as Waters and Agilent LCs., • Proficiency with software systems such as OpenLab, Empower, and ELN (Benchling is a plus)., • Previous experience developing methods for mRNA (gRNA and LNP are a plus)., • Familiarity with applicable ICH regulations and multi-compendial guidelines related to method validation., • Experience in assay development, qualification, validation, and transfer to GMP environments., • Proven track record of success collaborating effectively with cross-functional teams., • Ability to balance multiple responsibilities, prioritize activities, and navigate ambiguity., • Demonstrated learning agility, scientific problem solving, and strong written and verbal communication skills., • Proactive, creative, and positive attitude., • Unwavering commitment to safety protocols and procedures. Preferred Qualifications: • Experience working with various biophysical instrumentation such as GC, HIAC, and basic particle size characterization fluorescence-based assays., • Strong understanding of SEC-MALS analytical methodology., • Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information The position is full-time, first shift, Monday-Friday with overtime as needed. Candidates living within a commutable distance of Boston, MA are encouraged to apply. Excellent full-time benefits include: • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • Compensation: $37.00-$41.00 per hour based on education and experience, • #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionSalary: $152,000 - $183,000 Summary Visterra, Inc. is seeking to hire a Senior Scientist with strong expertise in immunology and a deep understanding of immune-related diseases, along with broad experience in the discovery and development of antibody-based therapeutics. This individual will play a key role in drug discovery programs by conceiving, developing, and implementing assays to support the discovery and validation of therapeutic antibody candidates. The successful candidate will be a collaborative team player, an effective manager, a critical thinker, and a clear communicator. The ideal candidate will have an advanced degree (Ph.D. or equivalent) in immunology, biology, biochemistry, or a related field, along with a minimum of 3 years of post-graduate research experience in a biotechnology or pharmaceutical setting. Prior experience managing early-career research scientists is required. This is a full-time, on-site position located at Visterras headquarters in Waltham, MA. Responsibilities • Design and execute experiments involving immunization strategies, antibody library generation, antibody engineering, and in vitro/in vivo characterization of antibody-antigen interactions., • Provide scientific leadership on project-based team, advancing therapeutic programs from conception through pre-clinical studies., • Effectively contributes to project strategy development by demonstrating a strong understanding of target biology and aligning experimental approaches with overall program goals., • Independently and critically analyze scientific results, troubleshoot methods, and conceive creative solutions and workflows to address challenges., • Document, analyze and interpret data for internal decision making, publications, presentations, patents and regulatory filings., • Develop research plans and manage multiple workflows and, • Manage activities at contract research organizations (CROs)., • Maintain expertise in the field by staying current to relevant literature and attending relevant conferences. Requirements • A Ph.D. or equivalent advanced degree in Immunology, Biochemistry, Biology, Biotechnology, or a related field, with a minimum of three years of post-graduate research experience in the biotechnology or pharmaceutical industry., • Experience working with immune-related diseases, with a strong understanding of disease biology relevant to therapeutic development., • Expertise in antibody discovery, including protein engineering, expression and purification, and automation of screening and characterization workflows., • Skilled in designing and executing in vitro and in vivo studies to investigate disease biology and assess efficacy, PK, PD, and mechanism of action of drug candidates., • Strong data analysis skills, with the ability to interpret complex experimental results and draw meaningful conclusions., • Excellent scientific communication skills, both written and oral, including the ability to clearly present data and concepts in meetings, reports, and publications., • Self-motivated and capable of independent work in a laboratory setting, while also contributing effectively to collaborative team environments. Other Qualifications • Experience with antibody discovery platforms, such as phage display, yeast display, and next-generation sequencing (NGS), as well as antibody binding characterization techniques such as biolayer interferometry (BLI) and surface plasmon resonance (SPR)., • Experience with flow cytometry (FACS) and a range of immunological techniques, such as ELISA, multiplex cytokine assays, and immune cell profiling., • Experience with high-throughput automation technologies, such as a Tecan liquid handling robot., • A proven track record of working in a dynamic team of scientists, early-career research associates Company Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterras pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab. As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts. Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Job DescriptionDescription: Welcome to an inspired career. At Halozyme Hypercon™, a wholly-owned subsidiary of Halozyme Therapeutics, Inc., we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team – we rise by lifting others up and believe in the power of working together for the collective win. That’s why we need you—to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive. Join us as Senior Research Associate, Analytical Development and you’ll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact people’s lives. How you will make an impact The Senior Research Associate, Analytical Development plays a critical role in generating high-quality analytical data to support the characterization and development of biologic products. This role executes and supports a wide range of analytical methods, including chromatographic and electrophoretic techniques, while ensuring accuracy, compliance, and data integrity in a regulated laboratory environment. Through strong technical execution, attention to detail, and collaboration with cross-functional teams, this position contributes to method development, troubleshooting, and overall advancement of the analytical program. In this role, you’ll have the opportunity to: • Perform routine and non-routine analytical characterization of biologics under established or developing methods, including HPLC/UPLC techniques such as Size Exclusion Chromatography (SEC) to assess aggregation and purity., • Execute capillary isoelectric focusing (cIEF) assays to evaluate charge heterogeneity and assess product consistency, following approved methods or protocols under senior staff guidance., • Execute and support quantitative analytical assays for surfactants and other stabilizing excipients, including sample preparation, data acquisition, and preliminary data processing., • Perform selected microbiological assays (e.g., endotoxin testing) in accordance with approved SOPs to support product characterization and release activities., • Operate, maintain, and perform routine troubleshooting of analytical instrumentation (e.g., HPLC/UPLC systems), including preparation of mobile phases, columns, reagents, and standards., • Accurately document experimental procedures, observations, and results in electronic laboratory notebooks in compliance with Good Laboratory Practice (GLP) and data integrity requirements., • Perform routine laboratory activities such as buffer formulation, reagent preparation, pipetting, and sample handling with a high degree of accuracy and attention to detail., • Support method development, optimization, and qualification activities by executing assigned experiments and providing data and observations to supervising scientists., • Assist with investigations of analytical issues or out?of?specification / out?of?trend results by executing defined experiments and compiling data, under the direction of senior staff., • Collaborate with Analytical Development colleagues and cross?functional partners (e.g., Process Development, Formulation Development, Manufacturing) to support analytical testing needs., • Ensure laboratory safety compliance, proper instrument calibration, and adherence to standard operating procedures (SOPs).Requirements: To succeed in this role, you’ll need: • Bachelor’s degree in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related discipline with 2–4 years of relevant industry experience, or Master’s degree with 0–2 years of relevant experience., • Hands-on experience with analytical techniques such as SEC, cIEF, and chromatographic quantitation assays is preferred., • Experience operating chromatographic systems (HPLC/UPLC) and familiarity with chromatography data systems such as Waters Empower and/or Thermo Chromeleon., • Working knowledge of data analysis and visualization tools, including Microsoft Excel, JMP, and GraphPad Prism., • Demonstrated ability to accurately document experimental work using electronic laboratory notebooks (ELN)., • Knowledge of GLP principles, data integrity expectations, and regulated laboratory practices., • Ability to follow detailed experimental protocols and execute work independently within defined objectives and timelines., • Strong organizational skills, attention to detail, and ability to work effectively in a collaborative laboratory environment., • Effective written and verbal communication skills for reporting data and experimental observations to supervising scientists. Travel: May be required up to 5% of your time. In return, we offer you: • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching., • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement., • A collaborative, innovative team that works as one to amplify your impact—on your career, the work you do and patients’ lives. The most likely base pay range for this position is $68,000-$94,500 per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individual’s exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards. Equal Employment Opportunity Statement Halozyme Hypercon, Inc is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race (including traits historically associated with race, including but not limited to: hair texture and protective hair styles), religion, religious creed (including religious dress and grooming practices), ethnicity, color, national origin, ancestry, age (40 and older), genetic information, disability (mental and physical, including HIV and AIDS), reproductive health decision-making, medical leave or other types of protected leave, domestic violence victim status, political affiliation, medical condition (including cancer/ genetic characteristics and information), sex, gender, gender identity, gender expression, sexual orientation, marital or familial status, citizenship, pregnancy (including perceived pregnancy, childbirth, breastfeeding, or related medical conditions), military or veteran status, or any other status protected by federal, state, or local law. Click here to view the Know Your Rights Poster. Accessibility and Reasonable Accommodations Halozyme Hypercon is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or an accommodation due to a disability, contact Human Resources at talentacquisition@halozyme.com. Halozyme Privacy Notice: Applicant Privacy Notice. To all agencies, please, no phone calls or emails to any employee of Halozyme Hypercon about this requisition. All resumes submitted by search firms/employment agencies to any employee at Halozyme Hypercon via email, the internet, or in any form and method will be deemed the sole property of Halozyme Hypercon unless such search firms/employment agencies were engaged by Halozyme Hypercon for this requisition and a valid agreement with Halozyme Hypercon is in place. If a candidate submitted outside of the Halozyme Hypercon agency engagement process is hired, no fee or payment of any kind will be paid. #LI-Onsite

Job DescriptionAbout UsDeep 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 We are looking for a passionate and detail-oriented Research Associate to become an integral part of our Platform Technology team. This is an opportunity to contribute hands-on to an AI-driven drug discovery platform, generating the experimental data that directly informs the biological models powering our therapeutic pipeline. You will bring scientific curiosity and rigor to the bench, supporting the execution of molecular and sequencing-based assays that our computational and therapeutic teams rely on to advance program goals. This role offers early-career professionals a meaningful foothold in a cross functional discovery environment, with exposure to cutting-edge technologies spanning NGS workflows, liquid handling automation, and diverse RNA therapeutic modalities including ADAR editing, ASOs, siRNAs, and mRNAs. If you are eager to develop technical breadth while contributing to work that has real therapeutic impact, we encourage you to apply.Key Responsibilities • Execute amplicon sequencing workflows, including NGS library preparation and targeted sequencing, under the guidance of senior team members, to support the evaluation of RNA therapeutic candidates., • Carry out library QC using tools such as TapeStation, Qubit and qPCR, flagging workflow bottlenecks to ensure high-quality datasets for downstream computational analysis., • Operate sequencing instruments such as the Illumina NextSeq, including run setup and routine troubleshooting, with increasing independence over time., • Perform routine molecular biology techniques including PCR, qPCR/ddPCR, and nucleic acid extractions from a variety of cell types and tissues., • Assist in running automated workflows on liquid handling platforms (e.g., Hamilton STAR, Agilent Bravo, Beckman Echo) to support scaling of discovery and screening activities., • Maintain accurate and thorough documentation of experimental plans, results, SOPs, and troubleshooting steps within an electronic lab notebook (ELN)., • Contribute to team meetings and share experimental results and assay updates with immediate project collaborators.Basic Qualifications, • BS in Molecular Biology, Genetics, Genomics, Biotechnology, Biochemistry, or a related discipline with 1–3 years of relevant industry or research experience (including internships or postgraduate research)., • Foundational knowledge of molecular and cell biology principles., • Some hands-on exposure to amplicon sequencing or other targeted NGS workflows; broader NGS experience is also welcomed., • Experience with nucleic acid extraction, quantitation, and standard molecular biology techniques such as PCR, qPCR or d(d)PCR, gel electrophoresis., • Strong attention to detail and commitment to rigorous, reproducible lab work., • Ability to work both independently and collaboratively in a team-oriented environment.Preferred Qualifications, • Proficiency with liquid handling platforms such as Hamilton, Beckman, or Bravo., • Working familiarity with RNA therapeutic modalities such as ADAR editing, ASOs, siRNAs, or mRNA., • Experience with mammalian cell culture, including transfection-based assays., • Prior exposure to a biotechnology, pharmaceutical, or platform-driven research environment.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 $75,000 - $90,000, 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. 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 Nanobiosym is an innovative nanotechnology company in Cambridge, MA, 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. Nanobiosym was awarded the 2013 X-PRIZE- the first X-PRIZE ever awarded for healthcare. DUTIES • Lead molecular diagnostic assay development in a hands-on manner through successful FDA submission, • Manage and contribute to regulatory documents, • Project management; personnel management skills preferred, • Design assay performance specifications, • Ensure assay development process meets milestones and timelines, • Troubleshoot and solve technical issues, • Maintain compliant laboratory documents and procedures, • Pro-actively improve efficiency, quality and effectiveness of R & D efforts QUALIFICATIONS • PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field, • Minimum of 7 years of relevant industry experience and IVD assay development, • In depth knowledge and hands on experience with qPCR, sequencing and standard molecular biology techniques, • Demonstrated technical, managerial and leadership expertise in assay development, • Strong understanding of FDA and global regulatory requirements, • Prefer commercial assay experience, • Demonstrated experience and understanding of quality systems (e.g., GLP, ISO, etc.), • Prefer experience working in BSL-2 laboratory facilities, • Strong work ethic and ability to generate high quality work under tight deadlines, • Flexibility in work schedule, • Self-motivated, independent and a driving force of efficient execution, • Strong organizational and project management skills, • Excellent oral and written communication skills Job Posted by ApplicantPro

Job Description Why Join Us? As a member of the Parabilis Medicines team, you will be a part of an organization dedicated to creating extraordinary medicines for diseases with urgent unmet needs, harnessing our proprietary peptide platform to transform treatment possibilities for patients. Parabilis is a clinical-stage biopharmaceutical company dedicated to unlocking high-impact protein targets long-considered undruggable. The company has developed a new class of stabilized, cell-penetrant alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that are inaccessible to traditional drug modalities. Headquartered in Cambridge, Mass., Parabilis is advancing a focused pipeline of multiple first-in-class therapies across both rare and common cancers. Its lead asset, zolucatetide (FOG-001), is a first-in-class, clinically validated direct inhibitor of the interaction between β-catenin and the T-cell factor (TCF) family of transcription factors, implicated in millions of cancer cases annually, including in colorectal cancer, desmoid tumors, hepatocellular carcinoma and a range of other Wnt/β-catenin-driven tumors. In Phase 1 clinical trials, zolucatetide produced the first-ever clinical evidence that it can directly inhibit this interaction, once previously considered "undruggable" despite its role across multiple cancer types. Parabilis is also advancing investigational degraders of ERG and ARON into clinical development for the treatment of prostate cancer, as well as progressing other preclinical programs. Backed by a recent $305 million Series F financing, Parabilis is entering an exciting phase of growth and execution. What's the opportunity? We are seeking an experienced and motivated Principal Associate Scientist to support cellular biochemistry and cell-based assay development for oncology discovery programs within our Biology team. This is a bench facing role central to building screening cascades, developing target engagement strategies, and contributing to mechanism of action understanding across multiple discovery efforts. Additionally, this scientist would be contributing to workflows at CRO partners, supporting study execution, data review, and troubleshooting in collaboration with project leads The successful candidate will operate within a cross-functional environment working with the biology lead to conceive and develop innovative assay strategies, deepen biological understanding, and generate high-quality, decision-enabling data. This position requires strong scientific judgment, clear communication of complex data, and the ability to independently design, troubleshoot, and execute experiments in a fast-paced research setting. This role is well-suited for a scientist who thrives in a collaborative, growth-oriented environment, demonstrates intellectual curiosity, and a willingness to incorporate feedback to continuously improve both their science and approach. Key responsibilities: • Design and execute target engagement and mechanism-of-action studies to characterize novel therapeutic candidates, • Develop cell-based assays (e.g., NanoBRET, HiBiT, AlphaLISA, HTRF) from conceptualization and proof-of-concept through to validated implementation in collaboration with internal or external cell pharmacology team, • Perform and interpret supporting assays including qPCR, Western blotting, immunoprecipitation, and pulldown assays, • Independently manage experimental workflows, anticipate technical challenges, and drive projects to completion, • Provide technical mentorship and contribute to a collaborative, high-performing team environment, • Maintain high standards of data integrity, documentation, and experimental reproducibility What you'll need to be successful: Education & Experience • B.S. or M.S. in Biology, Molecular Biology, Biochemistry, or a related field with 7–10+ years of relevant industry experience. Required Qualifications • Deep expertise in developing and executing cell-based assays (e.g., NanoBRET, HiBiT, AlphaLISA, HTRF), • Proficiency in molecular and biochemical techniques including qPCR, Western blotting, immunoprecipitation, and pulldown assays, • Experience with cell line engineering (CRISPR/Cas9, viral expression systems), • Demonstrated ability to independently design, execute, and interpret experiments, • Ability to critically evaluate complex datasets, resolve discrepancies, and communicate clear conclusions to cross-functional stakeholders, • Intellectual curiosity, proactively identifying opportunities to deepen expertise or explore new approaches, • Ability to work on-site in bench-facing capacity and actively participate in in-person collaboration Preferred Qualifications • Experience with induced proximity or targeted protein degradation approaches, • Experience in oncology drug discovery Core Values Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit. • Growth-Minded. We're inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable., • In(ter)dependent. We are fiercely independent as a leader in defying the limitations of current therapeutic modalities, and interdependent as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options., • Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact., • All-In. We're All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history. The base salary range for this position is $108,000-$128,000 per year, depending on experience, qualifications, and internal practices. Parabilis's total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees' overall well-being. As an equal opportunity employer, Parabilis Medicines values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law. 30 Acorn Park Drive | Cambridge, MA 02140 | www.parabilismed.com

Job DescriptionCompany Description 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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Our mission is to develop and deliver advanced therapeutics that change lives. We are looking for talented, passionate, and driven individuals to join our Biotherapeutics and Genetic Medicine (BGM) team. As a Senior Scientist in our siRNA group, you will be part of an innovative team focused on advancing RNA-based therapies that have the potential to revolutionize patient care. AbbVie is looking for a Senior Scientist I to join our siRNA group within the Biotherapeutics and Genetic Medicine (BGM) department. This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. Responsibilities • Lead research efforts within a cross-functional team to advance new therapeutic targets for siRNA-based pipeline development., • Design and execute in vitro and in vivo proof-of-concept studies to evaluate novel extrahepatic, targeted siRNA delivery platforms across multiple pipeline programs., • Design and execute receptor expression profiling, ligand–receptor binding, internalization, and trafficking assays., • Evaluate functional delivery and target knockdown in receptor-positive cells and tissues., • Provide scientific leadership and expertise in candidate nomination and pipeline development., • Work independently and maintain a high level of productivity in the laboratory, ensuring efficiency and scientific rigor., • Analyze and interpret multidisciplinary data to generate actionable conclusions and guide future experimental directions., • Collaborate and effectively communicate results with key stakeholders and cross-functional teams throughout the organization., • Contribute as a primary author to scientific publications, presentations, and/or as a primary inventor of patent applications., • Mentor and support junior scientists within the team.Qualifications, • BS, MS, or PhD in chemistry, biology, biochemistry, pharmacology or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of experience., • Demonstrated expertise in siRNA candidate nomination and pipeline development., • Demonstrated experience in drug delivery platforms, receptor biology and targeted delivery., • Hands on experience of uptake, trafficking, and functional delivery assays., • Extensive hands-on experience and techniques for molecular and RNA biology, including cell culture, RNA extraction, RNA quantification (RT-PCR, qPCR, ddPCR), next-generation sequencing (NGS) library preparation, protein assays (ELISA, Western Blot, JESS), flow cytometry and other biomarker quantification., • Experience in assay development and high-throughput screening for siRNA target identification and validation, mechanism of action studies, biodistribution and biomarker analysis is a plus., • Proven ability to develop, troubleshoot and refine assays to enhance sensitivity, reproducibility, and throughput., • Highly self-motivated and capable of thriving in a fast-paced, collaborative team environment., • Strong written and verbal communication skills, with experience contributing to technical reports, publications, or regulatory documentation. Why AbbVie? AbbVie is a global biopharmaceutical company committed to bringing innovative medicines to patients in need. We offer a collaborative work environment, opportunities for professional growth, and the ability to make an impact on the future of healthcare. Join us and be part of a team that is transforming the landscape of genetic medicine. How to Apply If you are passionate about advancing RNA-based therapeutics and have a track record of success in cell and molecular biology, we encourage you to apply! Please submit your resume outlining your relevant experience and why you would be a great fit for this position. 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 ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description 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 Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity. Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore what’s next with us at novabiomedical.com About the role The Technical Product Specialist – PAT Bio is a critical commercial support role responsible for driving growth of Nova Biomedical’s BioProfile FAST CDV Analyzer across North America. This position works in close partnership with North American Key Account Managers (KAMs) to develop new opportunities, manage complex sales processes, and ensure a high-quality customer journey from initial engagement through evaluation and close. The ideal candidate combines strong scientific expertise with hands-on experience in automated cell counting technologies and excels in cross-functional collaboration, technical selling, and opportunity management. If you’re passionate about technical sales and want to be part of a team that is shaping the future of life sciences, we’d love to hear from you, apply today! What you’ll do Serve as the technical and commercial specialist for the BioProfile FAST CDV Analyzer across North America Partner closely with North American Key Account Managers to grow the FAST CDV business Proactively prospect, identify, and develop new FAST CDV leads and sales opportunities Own and manage the sales process and customer journey for all FAST CDV opportunities, from qualification through close Develop a deep understanding of the U.S. key account landscape and drive consistent FAST CDV messaging across territories Coordinate closely with Field Applications to ensure successful product demonstrations, evaluations, and customer trials Lead technical sales presentations and deliver compelling, value-based messaging to scientific and commercial stakeholders Manage complex sales cycles, including objection handling and competitive positioning Generate quotations and support opportunity negotiation in collaboration with KAMs Maintain accurate opportunity tracking, forecasting, and customer records within the CRM system Manage and maintain FAST CDV demonstration and evaluation equipment Act as a central FAST CDV resource for sales, applications, and internal stakeholders What we are looking for in you Bachelor’s degree in a scientific discipline (biology, biotechnology, biochemistry, chemistry, or related field required; advanced degree preferred) Strong scientific background with hands-on experience in automated cell counting systems Experience selling, supporting, or using trypan blue dye–based cell counting technologies Prior experience with Beckman Coulter ViCell XR, ViCell BLU, or similar automated cell counters strongly preferred Experience supporting or managing complex sales processes within biotechnology or biopharmaceutical markets preferred Excellent organizational and time management skills Strong presentation, communication, and technical demonstration abilities Ability to manage multiple opportunities across multiple territories simultaneously Proven ability to navigate complex customer organizations and sales objections Strong collaboration skills and a team-first mindset Comfortable working alongside and supporting multiple Key Account Managers (approximately nine) Proficiency with CRM tools and standard business software Willingness to travel as required to support customer engagements and evaluations Physical Requirements for this role include: Ability to travel within assigned territory. Ability to sit or stand for extended periods and perform repetitive computer-based tasks. Ability to lift and transport materials or equipment up to 66 pounds as required for customer meetings or demonstrations. • The full list of physical requirements for this role is available upon request., • The full list of physical requirements for this role is available upon request. Why work for Nova Biomedical • Flexible Medical, Dental, & Vision Coverage, • Competitive 401k company match, • Bonus Program, Generous PTO and paid holidays, • Generous Tuition reimbursement, • Hybrid and flexible work arrangements (job specific), • Professional development, engagement and events, • Company marketplace for lunch and snacks! (location specific), • Company subsidized cafeteria (Waltham) Work Location: North America, Remote, Travel Schedule/Hours: Monday to Friday, 9:00 AM – 5:00 PM Targeted Salary Range: $90,000 - $140,000/year, variable included in pay Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate’s experience and may vary based on individual factors such as location, skills, and education. EEO Statement: Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Privacy policy https://advancedinstruments.showpad.com/share/DmsEd5QTLlqemTYABlvDW

Job DescriptionYoh presents an excellent long-term mRNA Drug Substance – Senior Research Associate opportunity with a trusted, long-term client located in Waltham, MA. This position is part of a major pharmaceutical company, and requires a Bachelors of Science in Chemistry, Biology, Biochemistry, or related scientific field. Schedule is full-time M-F (7am-8am start time, 8 hour shift) and may require flexibility to work some evenings and overtime due to projects. Key Responsibilities: • Perform routine analytical testing with a strong emphasis on UPLC to assess key quality attributes and characterize mRNA drug substance process development intermediates., • Support assay development and execute mRNA-based assays, including UPLC, ELISA, Capillary Electrophoresis, PCR, and enzymatic assays., • Manage priorities, plan experiments, conduct analyses, and communicate results to project teams., • Contribute to digital transformation initiatives through the implementation of LIMS, ELN, sample testing request systems, and tools for data analysis and visualization., • Contribute to high throughput transformation initiatives by integrating automated workflows, advanced instrumentation (e.g liquid handling systems), and scalable data processing solutions., • Author laboratory standard operation procedures, prepare development reports and deliver presentations for cross-functional team meetings., • Collaborate with internal teams and provide support to various functional groups as needed. Qualifications: • Bachelor’s degree in Chemistry, Biology, Biochemistry, or related scientific field with relevant background and experience is required., • 3-5 years of relevant industry experience is required., • Analytical U/HPLC experience is essential., • Proven ability to follow SOPs and perform routine testing with accuracy and reproducibly., • Prior experience in mRNA analytics and process development is highly desirable., • Proficiency in analytical techniques such as ELISA, qPCR, gel and capillary electrophoresis, UV-Vis spectroscopy, and enzymatic assays., • Experience using chromatography data systems such as Chromeleon and Empower., • Hands on experience with high-throughput automation systems is a plus., • Experience with LC/MS (Q-TOF, QQQ) is a plus., • Experience with data analysis tools such as JMP, Tableau, Power BI, RStudio is a plus., • Strong analytical thinking, statistical data analysis, and problem-solving skills., • Ability to collaborate with internal teams and support cross-functional groups as needed., • Proficiency with Microsoft Word, Excel, and PowerPoint is required., • Good oral and written communication skills are a must. Estimated Min Rate: $30.00 Estimated Max Rate: $36.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs, • Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice Company DescriptionYoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/Yoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/

Job Description Job Title Associate Director / Senior Manager, CMC Project Management Location Boston area preferred (or ability to commute regularly) Company Overview Hongene Biotech is a global leader in nucleic acid manufacturing, supporting RNA therapeutics, mRNA vaccines, and molecular diagnostics. With a vertically integrated platform from raw materials to CDMO services, we enable our partners to accelerate development with efficiency and quality. Position Overview This role will report directly to the VP, Global Head of CMC & Regulatory and is critical in strengthening Hongene’s project management capabilities for its oligonucleotide contract manufacturing services. Level and title will be determined based on experience. We are primarily targeting Senior Manager to Associate Director level. Exceptional candidates may be considered at Director level. The Primary Job Responsibilities 1) Drive project management efforts associated with CMC activities to support oligonucleotide contract manufacturing projects at Hongene Biotech. 2) Support Head of CMC and Oligonucleotide team in developing and executing development and manufacturing strategy and tactical executional plans. 3) Bridge communication between Clients and the internal teams in support of multiple contract manufacturing projects for different clients, including participation in technical calls, tracking of action items and facilitating rapid decision making within the team to drive programs forward. 4) Coordination with AD/PD, manufacture, quality and BD team to build, and manage global clients’ project timelines, work with BD to generating RFP proposals and evaluate necessary resources and ensure RFP proposals are aligned with overall strategy and cost estimation. Proactively identify potential risks, resourcing constraints and conflicts that could impact project timelines; collaborate with the AD/PD, manufacturing, QA/QC teams to develop appropriate solutions. 5) Support projects with strategic partners in US. The candidate must have strong communication skills and be capable of strategically communicating with internal and external stakeholders, as well as effectively communicating across functions and fluent speaking both English and Mandarin. Finally, the candidate must be comfortable with, and thrive in, a fast-paced entrepreneurial environment. Minimal Requirements • B.S or M.S in Pharmaceutical Science, Chemistry, Biochemistry, or related scientific discipline with 8+ years of applicable experience in the biotechnology or pharmaceutical industry., • Demonstrated proficiency in the discipline of project management. Experience with operating in a GMP environment and working in cross functional environments. Demonstrated ability to exercise independent judgement and strategic thinking., • Strong interpersonal skills and experience of managing cross-function projects., • Ability to thrive in a fast-paced, hands-on research and development environment., • Adept at building strong relationships and collaborating with colleagues at all levels., • Ability to discern paths forward within ambiguous environments., • Excellent verbal, written, and presentation skills for communication with internal and external customers is essential. Preferred Qualifications • Minimum of 5 years’ experience in project or program management at a biotechnology or pharmaceutical company with direct involvement in the CMC area, • Experience with project management tools (e.g. MS Project, Smartsheet, Clarizen) and collaboration tools (BOX, SharePoint, MS Teams), • Understanding of the different phases of drug development and cGMP requirements, • Experience in small molecules, oligonucleotides, or biologic drug development, • Located in US EST time zone

Job Description Manus works across industries and value chains to accelerate the transition to BioAlternatives – better performing and more sustainable versions of complex molecules traditionally sourced from plants, animals, or fossil fuels. Our platform is proven to work across scales, bridging the Valley of Death between lab and manufacturing more efficiently and more reliably to deliver the benefits of synthetic biology today. We are seeking a motivated Research Associate in Analytical Chemistry to join our team driving the development of novel biochemical pathways in microbial hosts. In this role, you’ll play a key part in analyzing a diverse range of molecules generated through fermentation and enzyme catalysis, while working closely with a collaborative team of scientists across disciplines. You will also have opportunities to develop new analytical methods that enhance the team’s ability to deconvolute complex metabolic pathways. The ideal candidate brings hands-on experience with HPLC and GC, strong analytical and troubleshooting skills, and a solid foundation in data analysis and laboratory practices. Most importantly, this position offers the chance to grow rapidly as an analytical researcher while learning directly from a highly skilled international team advancing the forefront of biochemical innovation. Why work at Manus: • Opportunity – For motivated, results-oriented team members, our growth creates opportunities for personal and professional advancement., • Accountability – You are given the resources you need to succeed and the freedom to make it happen; in return, we hold each other accountable for our high expectations., • Passion – We love what we do and enjoy working with others who feel the same way. We embrace the challenge and hard work that comes with working on the cutting edge. Responsibilities: • Precisely execute analytical SOPs to quantify small molecules and proteins., • Process and organize analytical data into clear, accessible formats for multiple stakeholders., • Assist in the development and validation of new analytical methods. Required Qualifications: • B.S. or M.S. in Chemistry, Chemical Engineering, Biochemistry, Bioengineering or similar discipline with at least one year of experience in a research lab environment., • Proficiency in basic laboratory techniques (weighing, pipetting, volume measurement) and Microsoft Excel for data organization and reporting., • Hands-on experience operating analytical instruments such as HPLC and GC. Preferred Qualifications: • Experience with LC-MS and GC-MS instrumentation, including method development, optimization, or validation., • Strong analytical skills: data analysis, troubleshooting instrumentation/method issues, interpreting results Preferred Working Style: • Must be very organized and be able to handle multiple projects simultaneously., • Must be a quick learner who is self-motivated and able to ask questions and seek clarity., • Must be flexible with day-to-day duties and able to thrive in a start-up environment., • Must be an excellent, collaborative team member with strong communication skills, • Must hold themselves to the highest professional, scientific and ethical standards. Job Type: Full-Time / on-site

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. 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 Direct Counsel is seeking a Corporate Associate Attorney (Licensing) to join a leading Am Law 100 firm in its San Diego, San Francisco or Boston office. This is an outstanding opportunity for an associate attorney interested in sophisticated licensing, commercial contracting, and technology transactions within the life sciences, biotechnology, pharmaceutical, medical device, and software sectors. About the Role The Licensing & Technology Transactions team works closely with cutting-edge companies developing groundbreaking technologies and therapeutics. As a Corporate Associate Attorney, you will draft and negotiate complex commercial agreements, support strategic corporate transactions, and advise clients on intellectual property, regulatory considerations, and deal structures across all stages of the product and company lifecycle. This role offers substantial client contact, the ability to interact with scientists and business leaders, and meaningful responsibility on impactful transactions. What You’ll Do Draft, review, and negotiate a broad range of commercial agreements, including: Licensing, collaboration, development, and research agreements Clinical trial, manufacturing, supply, and service agreements Patent license agreements and IP assignments Material transfer agreements, NDAs, and distribution agreements Strategic alliance and commercialization arrangements Advise clients on contract interpretation, risk assessment, and compliance issues Conduct due diligence on IP assets and contractual obligations in corporate transactions Review high-volume commercial documents such as confidentiality agreements and terms and conditions Collaborate with scientists, executives, and cross-functional business teams to align legal strategies with operational and commercial goals Stay current on regulatory and legal developments affecting life sciences and technology transactions What We’re Looking For A highly skilled Associate Attorney with 3+ years of experience drafting and negotiating commercial contracts for life sciences or technology clients Strong understanding of intellectual property issues, including patents, trademarks, trade secrets, and copyrights Experience with software licensing, SaaS agreements, and technology transactions preferred Familiarity with data privacy considerations and emerging issues involving AI Excellent negotiation, communication, and problem-solving skills Ability to manage competing priorities, meet deadlines, and maintain exceptional attention to detail A collaborative mindset and professionalism when working with clients, colleagues, and cross-disciplinary teams Qualifications JD or LLM from an ABA-accredited law school Admission to practice in California (or eligibility to sit for/admit via reciprocity) Background in biology, immunology, biochemistry, or a related scientific field strongly preferred Experience supporting biotechnology, pharmaceutical, medical device, digital health, or related technology clients Compensation & Benefits The annualized salary range for this Associate Attorney position is $260,000 – $310,000, depending on experience and other permitted job-related factors. Attorneys are bonus-eligible and receive access to a comprehensive benefits package.

Job DescriptionCompany Summary: Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro is based in Cambridge, Massachusetts. We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health. Korro Bio is seeking a highly motivated Research Associate to join our In Vivo Pharmacology team. This is an exceptional opportunity to work alongside experienced scientists in a collaborative, cross-functional environment as we advance transformative genetic medicines to improve the lives of patients.Key Responsibilities: • Conduct experiments to determine the efficacy of novel oligonucleotides in rodent models across a range of disease indications., • Perform dosing via subcutaneous (SC), intraperitoneal (IP) and intravenous (IV) routes; monitor animal health, collect blood samples, harvest multiple tissues, and coordinate sample storage and analysis., • Provide overall in vivo and ex vivo technical support for projects working to advance one or more experimental therapeutic compounds., • Develop, optimize, and execute ELISA and hELISA assays to quantify target proteins, biomarkers and therapeutic candidates in biological matrices., • Support bioanalytical method development activities for the measurement of drug concentrations and pharmacodynamic endpoints in plasma, serum, and tissue samples., • Generate and analyze in vitro, in vivo pharmacology, and ADME (absorption, distribution, metabolism, and excretion) data to characterize compound exposure and pharmacokinetic/pharmacodynamic (PK/PD) relationships., • Contribute to target engagement assessments by designing and executing appropriate biochemical and cell-based assays to evaluate on-target activity of RNA editing compounds., • Collaborate cross functionally with Discovery Chemistry, Translational Biology, and DMPK teams to support exposure response analyses and inform compound progression decisions., • Maintain meticulous records of all experimental procedures, raw data, and results in electronic laboratory notebooks (ELN)., • Effectively communicate experimental results, observations, and data summaries to team members and cross functional stakeholders through written reports and presentations.Required Qualifications:, • Bachelor’s degree in Biology, Biochemistry, Pharmacology, or a related life sciences discipline with 0-2 years’ experience., • Knowledge of tissue processing and molecular biology methods including RNA purification, PCR, qPCR, sequencing, protein isolation, MSD, western blot., • Hands-on experience with mouse colony management (animal handling, health assessment), dosing techniques (IV, SC, and IP), blood collection (tail vein/submandibular and cardiac puncture), and tissue collection at necropsy for ex vivo analysis., • Proficiency in standard laboratory techniques including cell culture, aseptic technique, and sterile handling of biological samples., • Hands-on experience or strong foundational knowledge in ELISA, hELISA assay design, execution, and troubleshooting for quantification of proteins, antibodies, or small molecules., • Experience with data analysis and visualization software such as Graph Pad Prism, Microsoft Office (including Excel) for summarizing and presenting pharmacology and bioanalytical data., • Familiarity with electronic laboratory notebooks (ELN) for data recording and experiment documentation., • Detail-oriented with strong organizational, problem-solving, and communication skills; meticulous in data recording and documentation., • Thrives in a dynamic environment that requires continuous learning, quick course correction, and flexibility as priorities evolve., • Naturally curious, eager to learn and understand the basic biologic mechanisms underpinning our products and the scientific rationale for RNA editing as a therapeutic modality.Preferred Qualifications:, • Knowledge of cardiometabolic/obesity models or experience with rodent models requiring low-stress handling is highly desirable., • Experience with bioanalytical method development and execution in support of in vivo and in vitro pharmacology or ADME studies is a plus.The range provided is based on what we believe is a reasonable estimate for the base the salary pay range for this job at this time. This does not include annual bonus and equity. The actual salary will be based on a number of factors including skills, competencies, experience, and other job related factors permitted by law.Benefits: Korro offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. 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 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 DescriptionCompany Description 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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description At AbbVie, we are dedicated to solving some of the world’s most complex and serious diseases. Within AbbVie’s Biotherapeutics and Genetic Medicine (BGM) organization, our siRNA team is advancing therapeutic programs from early discovery through development, applying rigorous biology and data-driven decision making to build differentiated RNA medicines. AbbVie is seeking a Senior Scientist I with deep, hands-on expertise in siRNA therapeutic discovery to join the siRNA group within Biotherapeutics and Genetic Medicine (BGM). This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. This role is best suited for candidates with direct, hands-on experience in therapeutic siRNA discovery, where siRNA biology directly informed experimental and program-level decisions. Responsibilities • Independently lead in vitro siRNA discovery biology, including experimental strategy, assay design, execution, data analysis, and interpretation in support of active therapeutic programs., • Design, optimize, and validate fit-for-purpose assays that directly inform siRNA potency, durability, specificity, and mechanism-of-action., • Drive scientific decision making by integrating siRNA knockdown data with orthogonal readouts (protein, functional, and transcriptomic endpoints)., • Identify and resolve key biological and technical risks related to siRNA activity, delivery, and on-target effects., • Work with cross-functional partners (chemistry, delivery, bioinformatics, in vivo biology) to advance siRNA candidates through discovery milestones., • Maintain high experimental rigor and productivity while operating with minimal supervision., • Author internal technical reports and contribute as a primary author on publications and/or inventor on patents.Qualifications, • BS, MS, or PhD in Cell Biology, Molecular Biology, Biochemistry, or related field with typically 10+ years (BS), 8+ years (MS), or 0-3 years (PhD) of relevant experience., • Demonstrated, hands-on experience in siRNA therapeutic discovery is required, including ownership of in vitro siRNA studies that informed go/no-go, lead selection, or optimization decisions., • Extensive experience with mammalian cell culture and molecular biology techniques directly supporting siRNA programs, including RNA isolation, qPCR, ELISA, Western blot, and nucleic acid sequencing (NGS/Sanger)., • Proven ability to independently troubleshoot siRNA-specific challenges (e.g., variability in knockdown, assay sensitivity limits, off-target interpretation)., • Strong data analysis and critical thinking skills, with a track record of translating complex datasets into clear experimental and programmatic recommendations. Desired Qualifications • Strong hands-on experience with stem-loop RT-qPCR, including assay design, optimization, validation, and data interpretation for siRNA and target mRNA quantification., • Direct experience supporting antibody-based or antibody-enabled delivery strategies, including antibody conjugates or biologics-related development., • Hands-on experience analyzing RNA-seq data generated from siRNA perturbation studies, including differential expression analysis and biological interpretation., • Experience with siRNA sequence design and optimization, including target site selection and evaluation of structure–activity relationships., • Familiarity with CNS-relevant biology and genetic medicine applications., • Working knowledge of bioinformatics tools or scripting (e.g., R, Python) to interrogate high-dimensional RNA datasets., • Experience operating effectively in a matrixed, fast-paced discovery organization. Why AbbVie? AbbVie offers a collaborative, science-first environment where discovery scientists play a direct role in shaping therapeutic programs. This position provides the opportunity to work on cutting-edge siRNA medicines with clear line-of-sight from in vitro biology to clinical translation. How to Apply If you have deep, hands-on experience in siRNA therapeutic discovery and are motivated to drive rigorous, data-driven biology in support of RNA medicines, we encourage you to apply. Please submit your resume highlighting your direct contributions to siRNA programs. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job Description Direct Counsel is partnering with a top global law firm seeking a mid-level Patent Prosecution Associate for its premier Life Sciences IP practice. This is an exceptional opportunity for attorneys and scientists passionate about advancing groundbreaking biotechnology innovations through strategic patent protection. About the Role The firm is seeking candidates with 1–5 years of experience in biotechnology-focused patent prosecution, along with an advanced degree (preferably a Ph.D.) in a life sciences discipline such as: Molecular biology Immunology Biochemistry Cell biology Related biotechnology fields You will work on sophisticated patent prosecution and counseling projects involving emerging companies and pioneering technologies, including: Antibodies DNA and RNA therapeutics Chemical biology platforms Gene-editing technologies Other next-generation biotech innovations USPTO registration is required. Candidates must already be registered or be prepared to sit for and pass the patent bar within 12 months of hire. What You’ll Bring Strong scientific foundation in life sciences Hands-on patent prosecution experience Ability to partner with fast-moving biotech clients Clear, precise communication skills (written and oral) Passion for translating scientific advances into strategic IP assets Compensation & Benefits Massachusetts Salary Range: $225,000 – $435,000 Final compensation will be determined during the interview process and may vary based on: Prior experience Relevant technical expertise Business needs Market conditions Total compensation may include: Comprehensive medical and financial benefits 401(k) participation Paid vacation, sick time, and parental leave Additional firmwide benefits and discretionary programs All positions are at-will, and the firm may adjust compensation and benefits based on performance or market factors. About Direct Counsel Direct Counsel partners with leading law firms and in-house legal departments nationwide to connect talented attorneys with outstanding opportunities. We take pride in matching professionals with roles that align with their expertise, values, and long-term career goals. Apply confidentially by sending your resume to sagan@directcounsel.net

Job Description At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. Why Choose Editas? At Editas Medicine, we are a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what is possible in medicine, come join us and become an Editor! Decoding the Role: Editas Medicine is seeking a strong scientific and strategic leader to join our DMPK, Nonclinical Safety and Translational Sciences (DSTS) group. This highly visible role will be accountable for the preclinical bioanalytical strategy, biomarker strategy, data quality, and regulatory readiness, ensuring successful EDIT-401 IND submission and Clinical Trial execution. The role serves as a critical bridge between DSTS/RTO, Clinical Development, and CMC working closely with Clinical Operations, Regulatory Affairs, and Biostatistics to ensure timelines and regulatory expectations are met. Characterizing Your Impact: As the Senior Director, Bioanalytical and Biomarker Development, you will: • Lead assay development, qualification, validation, and execution for measuring drug product components, immunogenicity, biomarkers, and other analytes in biological matrices., • Author BioA/BioM strategies and review nonclinical and clinical protocols to ensure alignment with regulatory expectations., • Design and implement BioA/BioM strategies across discovery, translational, and clinical stages including supporting global trials. Align biomarker plans with program objectives, regulatory expectations, and intended clinical use., • Author, review, and/or approve bioanalytical reports and regulatory and clinical documents including pertinent sections of non-clinical and clinical protocols., • Serve as a subject matter expert in resolving complex analytical challenges and integrating cutting-edge technologies., • Ensure bioanalytical/biomarker studies comply with GXP and other relevant regulatory standards. Partner with compliance teams to identify and qualify CROs and other vendors appropriately., • Serve as BioA/BioM subject matter expert on program teams and sub-teams., • Collaborate with CMC to ensure consistent bioanalytical assays between pre-clinical and clinical development., • Communicate complex scientific concepts effectively to non-expert stakeholders., • Deliver high-quality data within tight timelines, meeting >95% of R&D development expectations., • Apply understanding of disease biology and therapeutic mechanisms to guide biomarker strategy in collaboration with discovery team., • Work closely with Clinical Operations to enable seamless central and specialty laboratory sample analysis for clinical BioA/BioM data., • Ensure team members feel supported, held accountable, and have documented professional development plans with quarterly check-ins., • Develop next-level leaders to support current programs and future pipeline targets., • Develop relationships with external thought leaders to ensure alignment with highest clinical standards and emerging science., • Monitor industry trends, emerging technologies, and evolving regulatory guidance in bioanalysis and biomarkers. Engage with external consortia, working groups, and regulatory bodies to influence industry standards and best practices. Requirements The Ideal Transcript: To thrive in this role, you will need: • PhD or equivalent advanced degree in biochemistry, medicinal chemistry, biology, or related field with 10+ years of relevant industry experience., • Experience in bioanalytical sciences within a regulated drug development environment. Strong knowledge of regulatory requirements and strategic application of bioanalytical and biomarker methods., • Excellent verbal and written communication skills across all levels both within an organization and with external collaborators/companies with the ability to recognize, articulate, and accept calculated risks to make informed decisions., • Demonstrated experience in the appropriate application of various scientific technologies into translational research strategies., • Proven leadership in cross-functional teams and external collaborations; mentor mid-level and junior level scientists., • Experience working on clinical trials., • Experience with LNP and gene therapy is highly desired., • Desirable personal attributes including team player mindset, highly collaborative skills and independence, strong organization, demonstrated ability to work in a fast-paced environment and attention to detail. Benefits Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy. Salary Range: $270,000 - $300,000 Pay Transparency Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices. Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Job Description About us Eli Health is making continuous hormone monitoring possible so users can support their daily and long-term health. No more waiting days to track key biomarkers—get results you can use within minutes. Eli’s flagship product, Hormometer™, is the first instant hormone monitoring platform to deliver results from saliva to mobile app—anytime, anywhere. Developed over six years of R&D, over 2,000 product iterations, and backed by a dozen patent-pending innovations, Eli’s award-winning platform turns hormones into measurable signals you can track and improve. Just as the thermometer and glucometer have transformed health for millions, Eli’s platform is poised to be the next major evolution in tracking changes in stress, endurance, sleep, and more. About the role Eli is looking for an R&D Scientist. You will be a key member of our R&D team, helping to discover new ways to improve current and future iterations of our assay technology. Your primary responsibilities will be to: Contribute to building a novel technology that can shape the next generation of women’s healthcare and at-home testing. Independently design experiments with an exceptional variable control for lateral flow assay development and optimization. Run experiments, record and analyze data, as well as interpret and present results to your team. Find creative and innovative ways to solve R&D challenges. Maintain high-quality work and organization while conducting experiments at a very high rate. Exercise exceptional wet laboratory etiquette, team collaboration skills, and work ethic. This description is not exhaustive. You will have a lot of autonomy over your work as Eli’s technology and research efforts progress. About you You have a Bachelor's or a Master's in Chemical Engineering, Bioengineering, Analytical Chemistry, Biochemistry, or a related field. You have 2+ years of wet lab experience, including 1+ years of laboratory experience beyond the classroom. You have 1+ years of experience leading your own projects in a wet lab environment. You have experience working with and developing assays (keywords include: lateral flow assays (LFA), immunoassays, ELISA, In Vitro Diagnostics (IVD), point-of-care diagnostics, rapid diagnostic tests, paper-based sensors, biosensors, microfluidic, bioconjugation, nanoparticle conjugation, antibody purification). You have experience working with bioconjugation techniques. You are a self-starter who also enjoys collaborating and sharing knowledge and ideas. You think critically and creatively. It is an added asset if some of your experience was at an early-stage startup or related environment (fast-paced, high-growth, innovative, small independent teams, etc.) If you don’t exactly match the description but still believe you are the right person to join the team, please reach out. We value mindset and character. Why you’ll love working at Eli You’ll work with a group of talented and mission-driven people eager to improve lifelong health at scale. You’ll be part of the core team developing and commercializing the first product that monitors hormonal data daily and over a lifetime. You’ll join the early-stage startup phase and have a wide-reaching impact in a constantly evolving, fast-paced environment. You’ll be part of a small (<25 people), high-performing, and diverse team where everything you do results in tangible impact and shapes the company’s trajectory. You’ll be in an environment where people drive their own work, think creatively about open-ended problems, and solve them proactively. You’ll get health insurance (medical, dental, vision, and more) to ensure you and your family stay physically and mentally at your best. You’ll have flexibility over your schedule and vacations. We seek to hire great people, then give them the autonomy and space they need to achieve their goals. Although our office and R&D facilities are in Montreal, we have a distributed team. We prioritize asynchronous workflows and minimize meetings to focus on the work itself. You and your +1 will have unlimited free access to the Bota Bota spa in Montreal to recharge. How to apply Sounds like you? Please apply using this link:https://jobs.ashbyhq.com/eli. Please note that we will not review applications made through other platforms. We look forward to learning about you!

Immediate need for a talented Scientist I. This is a 12 Months Contract opportunity with long-term potential and is located in Waltham, MA (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:26-14552 Pay Range: $40 - $49/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: • Perform characterization testing of gene therapy samples to determine and quantify host cell proteins using solid-phase enhanced sample preparation and LC-MS analytical techniques commonly used in proteomics (i.e. proteomic profiling using DDA or DIA, targeted quantitation using MRM or PRM)., • Assist in analytical method development and execute method qualification experiments to establish accuracy, precision, linearity and sensitivity of quantitative method., • Assist in developing automated liquid handler platforms to increase sample throughput., • Document all method development and testing activities/results accurately in compliance with internal and regulatory standards. Key Requirements and Technology Experience: • Skills-MASS SPECTROMETR, automation liquid handler, Method development and troubleshooting, • Master’s degree in Analytical Chemistry, Biochemistry, or a related discipline with 2-4 years of relevant biotechnology or pharmaceutical industry experience, preferably performing impurity monitoring using LC-MS or proteome/HCP profiling or Doctorate degree with 1-3 years of relevant experience in proteomics., • Effective planning, communication and collaboration skills, • Strong theoretical understanding of macromolecules (e.g., DNA, RNA, proteins) and their chemical properties., • LC-MS systems: Thermo Orbitrap Exploris/Eclipse/Fusion Lumos/Astral; Sciex LCMS Triple Quad 6500., • Software: Skyline, Proteome Discoverer, Byos, Spectronaut., • Practical, hands-on troubleshooting and programming experience with automation equipment, such as Agilent Bravo LT, Hamilton, Andrew or KingFisher., • Gene therapy experience with AAV or LNP is preferred, • HM Notes: 8-person team, working standard 9–5 hours with some schedule flexibility and no planned overtime. The scientist will support protein and LC-MS–based analyses, with a strong focus on mass spectrometry, chromatography, and biological sample preparation., • Daily work includes end-to-end digest workflow execution, optimization experiments, operating nano-LC and mass spectrometry platforms, monitoring instruments, running impurity and enzyme kinetic assays, and utilizing a mix of manual and automated liquid handling systems., • The role also requires data analysis, experiment design based on team feedback, and clear communication of results through summaries and PowerPoint presentations. Ideal candidates hold a Master’s degree in Analytical Chemistry, Biochemistry, or a related field with 2–4 years of relevant biotech or pharma experience (or a PhD with 1–3 years), particularly with LC-MS impurity monitoring or proteomics/HCP profiling, and have experience with software such as Discover, Skyline, or similar peptide mapping tools., • The position starts ASAP (with potential extension after 12 months) Our client is a leading Healthcare Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy _.

Mid-level Patent Litigation Associate - Life Sciences Our client is a global Am law 100 firm, seeking a life science patent litigation associate for its Boston, New York and Washington, DC offices. The salary range for this position is $260k to $365k. Qualifications • 3-5 years of patent litigation experience involving life sciences companies., • Bachelor's degree in a life science discipline [chemistry, biochemistry, biology, chemical engineering or biological engineering or related] is required., • Past experience with litigation involving pharmaceuticals, biotechnology, and/or medical devices preferred., • Trial experience is a plus., • Excellent writing and verbal communication skills., • Bar admission in jurisdiction of practice., • All candidates must be authorized to work in the U.S. About Us Marina Sirras & Associates LLC is a boutique legal recruiting firm committed to connecting exceptional legal talent with top-tier law firms and in-house legal departments nationwide. With decades of experience and a personalized, relationship-driven approach, we take pride in understanding the unique needs of both our clients and candidates. We are a proud member of the National Association of Legal Search Consultants (NALSC) and strictly adhere to the NALSC Code of Ethics. Marina Sirras, our founder, is a former President and Chairperson of the organization, reflecting our longstanding commitment to integrity and professionalism in legal recruiting. To learn more about our team and services, please visit us at _.

The Science Team at Russell Tobin and Associates is hiring a "Senior Associate Scientist - (Physical Biochemistry)" for a top leading pharmaceutical organization.

Job Description Join Beacon Therapeutics (USA) Inc as a Technical Operations & Development Intern and invest in your future while making a tangible impact in the Biotech industry. This hybrid opportunity allows you to collaborate with innovative professionals while gaining hands-on experience supporting gene therapy research and development. You will contribute to meaningful projects that strengthen operational processes and support the advancement of innovative therapies. As a current undergraduate student or recent graduate in a scientific discipline you will bring curiosity and attention to detail to a team that values transparency and accountability. This is your opportunity to build real-world experience while working alongside a diverse and respectful culture based in Cambridge MA. Be bold be curious and apply today to ignite your potential. LET US INTRODUCE OURSELVES If you are passionate about gene therapy and its ability to enhance the lives of patients then Beacon is a great team to join. We are a diverse multinational team working together across the US and the UK both on site and remotely. Everyone plays a role in bringing treatments to patients and every contribution makes a difference. WHAT IT IS LIKE TO BE A TECHNICAL OPERATIONS AND DEVELOPMENT INTERN As a Technical Operations and Development Intern at Beacon Therapeutics USA Inc you will support a key inventory management initiative focused on gene therapy R and D and CMC development materials at an external storage vendor. This internship provides an opportunity to gain exposure to Technical Operations and Development processes including project management technical documentation and study support. You will work on organizing categorizing and streamlining biological materials such as cells plasmids and development samples while partnering with Technical Operations Development and Quality teams to ensure materials are properly labeled and maintained. You will participate in team meetings provide updates on your work and gain insight into how operational discipline supports successful development programs. This is a 12 week internship based on the interns start date. Interns are expected to work Monday through Friday from 8 am to 5 pm with a one hour lunch break not to exceed 40 hours per week. This is a hybrid role based in Cambridge MA with required travel to external storage vendor locations in the Boston north and north shore areas. Reliable transportation is required. WHAT WE ARE LOOKING FOR IN A TECHNICAL OPERATIONS AND DEVELOPMENT INTERN To thrive in this role you will need strong attention to detail and the ability to stay organized while managing multiple tasks. You should be comfortable working independently while also collaborating with cross functional teams. Strong communication skills will be important as you provide updates and engage with team members. Knowledge and skills required for the position are: • Attention to detail and strong planning and organizational skills, • Ability to maintain confidentiality, • Experience with Microsoft Office Suite, • Ability to organize execute and report on an inventory management exercise for biological samples, • Understanding of biological materials such as plasmids cell samples protein samples and cell lines and ability to recognize standard labeling conventions, • Strong written and verbal communication skills, • Ability to manage time effectively and work across multiple priorities, • Previous part time work experience or summer employment Educational qualifications include: Currently enrolled undergraduate student or recent graduate in Biotechnology Biochemistry Chemistry Biology or a related discipline. JOIN OUR TEAM TODAY If you think this role is a fit for what you are looking for we would love to meet you!

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