Senior Manager, Quality Control Stoke Therapeutics IncSenior 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 Scientist I, Quality Control Candel Therapeutics Inc.Senior Scientist I, Quality ControlNeedham, MA$155,000–$160,000 / yearThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc.
Quality Control Analyst LanceSoft IncQuality Control AnalystLexington, MA$34–$37.29 / hourJob Description Assist in document authoring/ revision and approval (protocols, test methods, SOPs) and other routine laboratory activities supporting the lab as 079 activities are completed by the biochem team. This role supports the daily operations of the QC Raw Materials department, whose primary responsibility is the testing and release of raw materials for GMP use in manufacturing.
Director, Quality Control Dyne TherapeuticsDirector, Quality ControlWaltham, MA$190,000–$230,000 / yearThe Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and commercial stages. Regulatory, Inspection Readiness & Cross-Functional Collaboration Prepares and reviews analytical CMC content for regulatory submissions (INDs, BLAs) and supports interactions with global health authorities.
Environmental Monitoring Associate - Quality Control TandymEnvironmental Monitoring Associate - Quality ControlBedford, Massachusetts$32 / hourThis role supports controlled manufacturing operations by performing environmental monitoring, utility sampling, documentation, and microbial enumeration in a GMP-regulated setting. Perform environmental monitoring tasks for aseptic and controlled areas, as well as plant utility systems, following SOPs and GMP documentation.
Senior Director, Analytical Development & Quality Control Rhythm PharmaceuticalsSenior Director, Analytical Development & Quality ControlBoston, MA$210,000–$370,000 / yearResponsibilities and Duties Strategic Leadership & Analytical Development Define and execute end-to-end analytical strategies across the product lifecycle, including method development, validation, transfer, and lifecycle management from raw materials through drug substance and drug product. Opportunity Overview As the Senior Director, Analytical Development and Quality Control , you will provide strategic and technical leadership for analytical development and quality control across Rhythm’s portfolio, spanning discovery through commercialization and lifecycle management.
Document Control Specialist, Quality The Steely GroupDocument Control Specialist, QualityBedford, MAThis role will work closely with members of the Document Control team and support routine daily operations for Document Management. This position will primarily be responsible for the processing and maintaining of GxP documents throughout their lifecycle with a focus on issuance and reconciliation.
Quality Control Analyst (Contract) 651 Vertex PharmaceuticalsQuality Control Analyst (Contract) 651Boston, Massachusetts$36–$38 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Job Description: Within our Analytical Service team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
Pizza Quality Control Specialist LupoliPizza Quality Control SpecialistLawrence, MAThis role conducts on-site audits, evaluates food preparation and presentation, and partners with restaurant leaders to identify improvement opportunities that enhance the guest experience and protect the Sal's brand. Maintain a proactive presence in the field, fostering accountability and operational excellence.
Head of Quality Control Takeda Pharmaceutical Co LtdHead of Quality ControlLexington, MA$177,000–$278,080 / yearThe actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. Working closely with Manufacturing and Quality partners, you will champion continuous improvement, employee development, and innovation while fostering an inclusive environment where diverse perspectives are valued and everyone is empowered to succeed.
Quality Control Technician II Amrize LtdQuality Control Technician IISaugus, MAWHAT WE'RE LOOKING FOR Education: High school diploma or equivalent Additional Education Preferred: Associates degree Required Work Experience: 3-5 year Required Training/Certifications: State regulated or industry certifications, as required Additional Requirements: Ability to work various hours including weekends and nights. Detailed oriented Able to prioritize work Valid Driver's License, Clean Driving Record Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment, including but not limited to respirators.
NewSenior Quality Control Analyst Actalent IncSenior Quality Control AnalystNorwood, MA$34–$39 / hourThe ideal candidate will have experience in molecular biology techniques, mammalian cell culture, potency assays, and QC testing within a pharmaceutical, biotechnology, or life sciences setting. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Research Associate II, Quality Control Ocular Therapeutix IncResearch Associate II, Quality ControlBedford, MA$98,000–$110,000 / yearOcular 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. This position will support CAPA's, change controls, investigations, and deviations and participate in the development and validation of analytical methods for the Analytical Development group.
Data Review Specialist, Quality Control Ocular TherapeutixData Review Specialist, Quality ControlBedford, MA$98,000–$113,000 / yearPosition Summary: The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding.
Data Review Specialist, Quality Control Ocular Therapeutix IncData Review Specialist, Quality ControlBedford, MA$98,000–$113,000 / yearPosition Summary: The Data Review Specialist will apply strong technical knowledge of laboratory operations, analytical data review, data integrity requirements, and quality systems to perform thorough reviews of analytical chemistry, microbiology, stability, and release testing data for accuracy, completeness, scientific soundness, and compliance with cGMP, GLP, and ALCOA+ expectations. In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging patterns, atypical results, potential OOT signals, and opportunities for improved product understanding.
Quality Control Analyst I, Raw Materials Ocular TherapeutixQuality Control Analyst I, Raw MaterialsBedford, MA$68,000–$75,000 / yearOcular 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. Key Responsibilities: The primary responsibilities of this role will be performing qualitative and quantitative testing of raw materials using techniques such as HPLC, GC, FTIR, UV-Vis, titration, and wet chemistry.
Quality Control Analyst I, Raw Materials Ocular Therapeutix IncQuality Control Analyst I, Raw MaterialsBedford, MA$68,000–$75,000 / yearOcular 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. Key Responsibilities: The primary responsibilities of this role will be performing qualitative and quantitative testing of raw materials using techniques such as HPLC, GC, FTIR, UV-Vis, titration, and wet chemistry.
Associate Director, Analytical Development & Quality Control Alpha-9 Oncology IncAssociate Director, Analytical Development & Quality ControlBoston, MAThe successful candidate will manage relationships with external manufacturing and testing partners while partnering closely with Quality, Regulatory, Technical Operations, and Program Leadership teams to support API development, CMC activities, and timely execution of clinical supply strategies. Alpha-9 Oncology is seeking a highly experienced and motivated Associate Director, Analytical Development & Quality Control, to provide technical and operational leadership for QC activities supporting our clinical-stage radiopharmaceutical programs.
Director, Quality Control Editas MedicineDirector, Quality ControlCambridge, MA$215,000–$235,000 / yearThe successful candidate will collaborate with a high-performing CMC team, coordinating with process and analytical experts cross-functionally in Research and Discovery, Process Development, Analytical Sciences, Manufacturing, and Quality Assurance, to transfer, qualify and oversee in-process and release testing to advance Editas’ in vivo gene medicine portfolio. The Quality team is seeking a highly motivated and experienced technical and organizational leader in gRNA, mRNA, and Lipid Nanoparticle (LNP) analytical methodologies and GMP testing.
NewSenior Director, Biologics Analytical Development and Quality Control Korsana BiosciencesSenior Director, Biologics Analytical Development and Quality ControlBoston, MassachusettsThis leader will oversee the planning and execution of outsourced analytical development and testing activities and will work proactively with external suppliers including CDMOs and contract labs to define project scope, mitigate risks, and ensure successful delivery in relation to technical quality, timelines and budget. Collaborates with internal stakeholders in the areas of Drug Substance Development, Drug Product Development, Combination Product Development, Clinical Supply Chain, Program Management, Preclinical Development, Clinical Development/Operations, Quality, Regulatory Affairs, and external business partners to push project forward.