Laboratory Informatics Consultant ZifoLaboratory Informatics ConsultantBoston, MAThe ideal candidate understands how laboratories operate day to day and can design LIMS solutions that support compliant, efficient, and traceable laboratory workflows , while also configuring supporting entities such as instruments and inventory as needed. As a consultant on our team, you will work with pharmaceutical, biotech, CRO, and regulated laboratory environments to design, configure, and deploy informatics solutions that improve data integrity, compliance, and operational efficiency.
Contract, Technical Writer, Life Sciences Lila SciencesContract, Technical Writer, Life SciencesCambridge, MassachusettsPartner with the Grants Manager to develop the technical and scientific components of proposal applications (technical narratives, specific aims, method descriptions, preliminary data write-ups, scientific appendices) for NIH, ARPA-H, DARPA BTO, and UK-funded life sciences initiatives, ensuring consistency in tone, format, and compliance throughout. Reporting to the Head of Government Partnerships, you'll serve as the essential bridge between our life sciences researchers and the people who fund, oversee, and act on their work, taking highly technical findings, methods, and data from biology, biochemistry, and translational research and reshaping them into language that is clear, credible, and decision-ready.
Lims Analyst (Labvantage) ZifoLims Analyst (Labvantage)Boston, MAThe ideal candidate understands how laboratories operate day to day and can design LIMS solutions that support compliant, efficient, and traceable laboratory workflows , while also configuring supporting entities such as instruments and inventory as needed. As a consultant on our team, you will work with pharmaceutical, biotech, CRO, and regulated laboratory environments to design, configure, and deploy informatics solutions that improve data integrity, compliance, and operational efficiency.
Senior Director, QSP/ PBPK Modeling Kiniksa Pharmaceuticals CorpSenior Director, QSP/ PBPK ModelingLexington, MA$281,000–$299,000 / yearStrong understanding of drug development, clinical trial design, and regulatory expectations related to pharmacology and pharmacometrics, experience contributing regulatory interactions related to modeling and simulation and proven experience applying modeling approaches to clinical decision making, particularly for early‑stage development programs. The successful candidate will serve as a scientific and strategic leader, partnering cross‑functionally with Research, Translational Medicine, Clinical Pharmacology, Clinical Development, and Regulatory teams to ensure model‑informed decision making across the portfolio.
Consultant - Technical Excellence & Scientific Operations Quanterix CorpConsultant - Technical Excellence & Scientific OperationsBedford, MAThe Consultant will also provide technical oversight of analytical validation activities supporting laboratory-developed tests (LDTs) and FDA submissions, including review of validation strategies, analytical data, validation reports, and technical documentation supporting regulatory submissions. Reporting to the Vice President of Laboratory Services, the Consultant will serve as a technical authority on the Simoa platform, partnering closely with Custom Assay Development, Laboratory Operations, Project Management, Quality, Regulatory, and Commercial teams.
Onsite Endoscopic Specialist, OR1 - Boston KARL STORZ Endovision IncOnsite Endoscopic Specialist, OR1 - BostonBoston, MAIn this hands-on, customer-facing role, you will support advanced surgical technologies directly within a hospital setting, helping ensure that clinical teams have the equipment, instruments, and resources they need to deliver exceptional patient care. As an Onsite Endoscopic Specialist, youll gain hands-on experience with cutting-edge surgical technologies, build meaningful relationships with healthcare professionals, and make a direct impact on patient outcomes every day.
Senior Plastics Process Engineer Nova BiomedicalSenior Plastics Process EngineerBillerica, MA$130,000–$145,000 / yearPlastics Processing Engineer, you will have guidance and oversight on daily operations within the mold shop including supporting production schedules, maintaining equipment within the department, establishing molding process parameters, executing mold process validations, and resolving molding issues. 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.
NewSenior Associate Scientist (Upstream Process Development) PfizerSenior Associate Scientist (Upstream Process Development)MassachusettsSubject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Bachelor’s degree with 2-4 years’ industrial experience or Master’s degree with 0-2 years experience in Chemical / Biochemical Engineering, Cell Biology, Biotechnology, Biomedical Engineering or a relevant field.
Healthcare Informatics Sales Executive - Eastern Region (New England Area) Siemens Healthcare Diagnostics Inc.Healthcare Informatics Sales Executive - Eastern Region (New England Area)Walpole, MassachusettsIdentify information solutions with and provide solutions in partnership with Collaborate cross-functionally with Customer IT Laboratory Informatics System) and technical teams to co-develop Statements of Work (SOWs) for digital integrations within a customer environment through commercial contracts. To be eligible for employment, applicants must hold a valid driver's license in the state they reside and may not have any prior DUI/DWI convictions or pending DUI/DWI charges or other serious moving violations (unless such a restriction is prohibited by state/local law).
Senior Manager, R&D Data, Data Science, And AI - Digital Health For Neuropsychiatry Johnson & JohnsonSenior Manager, R&D Data, Data Science, And AI - Digital Health For NeuropsychiatryCambridge, MARemote$137,000–$235,750 / yearDigital Endpoints & Tools: Execute the neuropsychiatry-focused digital health strategy by applying AI/ML, modeling, and longitudinal analytics to support patient stratification, endpoint development, and clinical trial optimization, in partnership with disease experts, statisticians, and platforms and clinical teams on study design and validation of digital measures, balancing their informativeness with low clinical burden for patients and study teams. All Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America.
Associate Director - Life Sciences Advisory - Market Access (Global) GuidehouseAssociate Director - Life Sciences Advisory - Market Access (Global)Boston, MA$135,000–$225,000 / yearSpecific responsibilities for the Global Market Access position include: Track record of success developing, leading, and delivering global (e.g., EU, APAC, LATAM) pricing and access / reimbursement projects, with subject matter expertise on HTA assessment frameworks, pricing & reimbursement archetypes, and national / regional pricing & reimbursement mechanisms. Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrows.
Associate Director - Life Sciences Advisory - Market Access (Us) GuidehouseAssociate Director - Life Sciences Advisory - Market Access (Us)Boston, MA$135,000–$225,000 / yearDesigning and managing project teams to execute various pharmaceutical market access and pricing strategy projects, both qualitative and quantitative, including overseeing development of materials and facilitating discussions as required. Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrows.
Director/Senior Director, CMC Operations Beam TherapeuticsDirector/Senior Director, CMC OperationsCambridge, MA$210,000–$320,000 / yearLead the preparation of source documentation and technical review of CMC sections for global regulatory submissions specifically focusing on Module 3. Act as the CMC subject matter expert during regulatory meetings and support information requests from regulatory agencies. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Director - Life Sciences Advisory - Commercial GuidehouseDirector - Life Sciences Advisory - CommercialBoston, MA$206,000–$343,000 / yearGuidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrow's. Proven track record generating revenues with existing clients demonstrating a passion for developing high value client relationships and executing on an account penetration strategy that results in account growth directly or indirectly.
Research Chemist RevBio, Inc.Research ChemistLowell, MAFull timeDegree in Sciences or Engineering (Chemistry, Biomedical Engineering, or Biochemistry); Bachelor's Degree with 2-4 years of experience, or Master's Degree with 1-3 years of experience in medical device, pharmaceutical, or biotechnology is preferred; Experience with drug delivery development, drug release kinetics, and pharmacokinetics is preferred; Wet lab experience is a must with general physical, thermal, and moisture characterization knowledge; Experience with HPLC-UV-MS is a must; and other analytical techniques such as NMR, FTIR, SEM is highly preferred; Experience with characterization and analysis of crystalline phase using XRD or other such techniques is highly preferred. The ability to work in a multi-disciplinary team environment; The ability to support project timelines independently or within a project team; The ability to develop and perform product testing, including, but not limited to, chemical, physical, and material characterization testing; The internal motivation and ability to assist driving a project to completion; The ability to gain support from various resources both within and outside the company; The ability to communicate effectively the status of a project (or projects); The ability and willingness to receive direction for all facets of management as it relates to Compliance Regulations (i.e., FDA 21 CFR Parts 58 and 820 and ISO 13485); and.
Associate Scientist, Formulation, Pilot Lab Sail BiomedicinesAssociate Scientist, Formulation, Pilot LabCambridge, MA$95,000–$120,000 / year4+ years (M.Sc.) or 6+ years (B.Sc.) of relevant industry experience in LNP formulation optimizations and drug delivery with strong background in nucleic acid therapeutics and education in life sciences or engineering (Pharmaceutical Sciences, Biomedical Engineering, Biochemistry, etc). Sail Biomedicines is seeking a highly talented and self-motivated individual to develop and operationalize lipid nanoparticle formulations at pre-clinical and pilot lab scales.
Director/ Senior Director / Executive Director - Translational Pkpd Project Leader Eli Lilly and CompanyDirector/ Senior Director / Executive Director - Translational Pkpd Project LeaderBoston, MA$177,000–$308,000 / yearIn support of this goal, the Pharmacokinetics/ Pharmacodynamics and Pharmacometrics, (PMx) organization provides leadership and technical expertise to support the discovery and development of new medicines from preclinical lead molecule identification to clinical post-drug approval, with the goal of identifying and developing the right drug with the right dose for the right patient using model-informed drug research and development (MIDD) approaches. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Senior Director, Immunology Data & AI Systems Johnson & JohnsonSenior Director, Immunology Data & AI SystemsCambridge, MARemote$196,000–$342,700 / yearAll Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Partner with Knowledge Management, Data Platforms & Governance, and Master Data Management teams to ensure Immunology data products integrate seamlessly into enterprise ontologies, knowledge graphs, and catalogs.
QSP postdoctoral scientist Eli Lilly and CompanyQSP postdoctoral scientistUs, MassachusettsOur current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL). As a hands-on QSP scientist, you will work alongside experienced mentors and cross-functional teams to develop and apply AI-powered QSP models that integrate deep biological knowledge, pharmacology, and preclinical and clinical data to drive pivotal decisions in drug discovery and development.
Vice President, Pharmaceutical Sciences Beam TherapeuticsVice President, Pharmaceutical SciencesCambridge, MA$310,000–$400,000 / yearLead the preparation of source documentation and technical review of CMC sections for global regulatory submissions specifically focusing on Module 3. Act as the subject matter expert during regulatory meetings and support information requests from regulatory agencies. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.