Associate Director, Quality Systems Stoke Therapeutics, Inc.Associate Director, Quality SystemsBedford, MA$185,000–$209,000 / yearDirector of Corporate Quality and will interface closely with other cross-functional groups such as CMC, commercial manufacturing, Regulatory CMC, Regulatory Operations, Regulatory Development, Clinical Operations, Clinical Development, PV, IT and other functions within Quality. Represent quality on project teams, as needed and provide GMP compliance interpretation, consultation, and other supportive services necessary to maintain and improve compliance and ensure data integrity.
Senior Manager, Quality Control Stoke Therapeutics, Inc.Senior Manager, Quality ControlBedford, MA$172,000–$192,000 / yearManager, Quality Control (QC) is responsible for overseeing all aspects of GMP testing and supporting stability program management for Stoke' IMPs at Stoke's Contract Testing Laboratories (CTLs) / Contract Manufacturing Organizations (CMOs). Oversee day-to-day management of outsourced GMP release testing at various CTLs / CMOs to ensure successful and compliant execution of laboratory operations to meet GMPs, regulatory requirements, guidelines, internal policies, and procedures.
Senior Specialist, Analytical Technical Operations ModernaTXSenior Specialist, Analytical Technical OperationsNorwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. The role combines scientific understanding, project coordination, and data-driven decision-making to support stability programs, accelerate development timelines, and deliver high-quality analytical data that informs critical product development and regulatory decisions.
Sr. Director, Regulatory CMC Genetix BiotherapeuticsSr. Director, Regulatory CMCSomerville, MassachusettsThe Senior Director serves as a key regulatory partner to Technical Operations, Quality, and Supply Chain, and acts as the primary CMC regulatory interface with global health authorities for post-approval activities, including supplements, variations, annual reports, and inspection support. The Senior Director, Regulatory CMC is responsible for defining and executing global CMC regulatory strategy for approved and late-stage gene therapy products, with a strong emphasis on lifecycle management, change management, and sustained regulatory compliance.
Collaboration Scientist - Lcms Shimadzu ScientificCollaboration Scientist - LcmsNewton, MA$110,000–$115,000 / yearThis role is part of the Product Strategy Group and will focus on evaluating new product concepts, testing prototype technologies, generating reliable scientific data, and gathering meaningful feedback through customer and collaborator engagement. All resumes submitted by search firms to any employee at Shimadzu via email, the Internet or in any form and/or method without a valid written search agreement in place for this position (and agency was requested to work the requisition) will be deemed the sole property of Shimadzu.
Biomedical Equipment Engineer Quest Diagnostics IncBiomedical Equipment EngineerMarlborough, MA$85,000–$93,000 / yearThe role requires a high level of expertise in repair, PM, and extensive knowledge of the specific equipment needing support, including, but not limited to: Olympus AU series analyzers, hematology automated lines, automated sorter/aliquoters, mass spectrometers and other similarly highly complex instrumentation. The Biomedical Engineer will: Ensure instrumentation is up and functioning at all times to achieve production goals, work closely with the Lab Operations and Reliability Engineering teams in coordinating departmental priorities, budgeting, and evaluating progress toward achieving department objectives.
Research Technician Diet, Brain and Sensory Systems Tufts UniversityResearch Technician Diet, Brain and Sensory SystemsBoston, MAThe major goals of the Diet and Aging Brain, Sensory Systems research directive are to (1) identify dietary patterns, specific foods or their components through associations with brain- and vision-related outcomes, as measured in multiple, well characterized longitudinal and prospective studies; and (2) identify their mechanisms and processes using in vivo and in vitro models of age-related brain and visual aging that focus on changes in cognition, inflammation, neurogenesis, neuronal connectivity, and microbiome. Under close supervision of the Principal Investigator and other lab members, the Research Technician conducts a variety of routine experiments following established procedures and protocols, which may include monitoring and feeding laboratory animals, performing assays, tissue culture, electrophoresis, tissue dissection and immunohistochemistry, and other laboratory techniques.
Distinguished Scientist, Group Head Biochemistry SanofiDistinguished Scientist, Group Head BiochemistryCambridge, MA$178,500–$257,833.33 / yearDeep expertise in biochemical assay development and characterization across multiple target classes (enzymes, protein-protein interactions, epigenetic targets, etc.). Provide strategic direction and scientific oversight for biochemistry activities supporting multiple drug discovery programs across diverse therapeutic areas.
MSAT Technical Lead - Drug Substance (Sr Manager) Swedish Orphan Biovitrum ABMSAT Technical Lead - Drug Substance (Sr Manager)Waltham, MA$140,000–$165,000 / yearThe SAT team holds the senior scientific and technical knowledge for the manufacturing and analytical testing of Sobi's clinical and commercial products and is responsible for maintaining the internal and external manufacturing/analytical processes at a validated stage. Lead the technical part of a product transfer, scale-up activities, validations, and oversee manufacturing of Small Molecules processes at external manufacturers for Sobi projects in the clinical and commercial phase.
Supplier Quality Senior Specialist Lantheus Holdings IncSupplier Quality Senior SpecialistBedford, MA$111,000–$185,000 / yearDomestic and international suppliers consist of Contract Manufacturing Organizations (CMO), drug substance precursors, active pharmaceutical ingredient (API) providers, raw material and component suppliers, contractors, 3PL and service providers. The Supplier Quality Senior Specialist is responsible for maintaining Lantheus's Supplier Quality Management (SQM) program, ensuring that systems, processes and procedures between Quality, Supply Chain, Technical Operations and R&D are compliant and aligned with business needs.
Postdoctoral Fellow in Applied Physics Harvard UniversityPostdoctoral Fellow in Applied PhysicsCambridge, MA$67,600–$91,826 / yearTitle Postdoctoral Fellow in Applied Physics School Harvard John A. Paulson School of Engineering and Applied Sciences Department/Area Applied Physics Position Description. Pay offered to the selected candidate is dependent on factors such as rank, years of experience, training or qualification, field of scholarship, and accomplishments in the field.
Tax Supervisor - Accounting Methods and Periods RSM US LLPTax Supervisor - Accounting Methods and PeriodsBoston, MA$86,500–$164,500 / yearResponsibilities: Identification, project management, and initial technical review of AMP projects, supported by Washington National Tax office (WNT) AMP specialists, including overall changes, revenue recognition, expense recognition, inventory/UNICAP/LIFO, capitalization/cost recovery, Section 174 R&E expenditures, leasing engagements, strategic method review projects, and impacts of transactions/mergers on methods. These services include accounting method reviews, the filing of accounting method or period changes, participating in M&A structuring and diligence, writing of technical advice memorandums, researching technical filing positions and broadly interacting with both internal tax professionals and external client stakeholders.
NewScientist, Pharmacokinetics Sample Analysis Merck & Co IncScientist, Pharmacokinetics Sample AnalysisBoston, MA$98,000–$154,300 / yearRequired Skills: Bioanalysis, Biochemistry, Data Analysis, Data Visualization, Detail-Oriented, Drug Metabolism, Ethical Compliance, Good Laboratory Practices (GLPs), Liquid Chromatography-Mass Spectrometry (LC-MS), Pharmaceutical Sciences, Pharmacodynamics, Pharmacokinetics, Pharmacology, Pharmacotherapeutics, Sample Preparations, Small Molecules. The Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) group is seeking a dynamic, strategic thinking and collaborative Scientist to contribute to our company drug discovery and early clinical development efforts, with a focus on lab-based bioanalytical efforts for small molecules and peptides.
NewEngineer I, Drug Product Development ModernaTXEngineer I, Drug Product DevelopmentNorwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. We are seeking a highly skilled and motivated Individual, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply.
Pharmaceutical Strategic Account Manager Becton Dickinson Medical DevicesPharmaceutical Strategic Account ManagerBoston, MassachusettsWaters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance. Drive strategic growth within large pharmaceutical and biotech accounts by managing complex enterprise relationships, identifying expansion opportunities, and leading high-value commercial partnerships.
Engineer II, Drug Product Development ModernaTXEngineer II, Drug Product DevelopmentNorwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. We are seeking a highly skilled and motivated Individual, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply.
Field Application Scientist -France, UK & Nordics Vizgen IncField Application Scientist -France, UK & NordicsCambridge, MAReporting to the VP of Regional Sales, EMEA the Field Application Scientist will provide the scientific introduction of Vizgen's technology to customers with a focus on biological discovery and helping customers efficiently generate their own data using Vizgen's MERSCOPE platform. The successful candidate will also manage and coordinate all technical aspects of customer demonstration projects and represent Vizgen and engage with scientists and other customers at trade shows and scientific conferences.
QTSS Administrator, I or II Ocular Therapeutix IncQTSS Administrator, I or IIBedford, MA$62,000–$68,000 / yearUser access and database administration of Empower 3 and various other analytical test equipment software including: OMNIC, Tiamo, DataPro2, MasterSizer 3000, Keyence Vision, Instron Bluehill and others. Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX.
NewExecutive Assistant To An Executive Officer Biogen IdecExecutive Assistant To An Executive OfficerCambridge, MA$104,000–$136,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. Additionally, you will oversee travel arrangements for the Executive Officer and other PO&T leadership members, provide in-person support during international strategic sessions, and lead elements of PO&T engagements as required.
Director, Regulatory CMC bluebird bio, Inc.Director, Regulatory CMCSomerville, MA$204,000–$245,000 / yearThe Director, Regulatory CMC is responsible for leading execution of global CMC regulatory strategies for approved and late-stage gene therapy products, with a primary focus on lifecycle management, change management, and regulatory compliance. This role supports the development and delivery of post-approval regulatory strategies and ensures effective implementation of manufacturing, analytical, and control changes across global markets.