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.
Quality Control Admin Finish Line Staffing ServicesQuality Control AdminMansfield, MAThis position is ideal for someone who enjoys reviewing documentation, ensuring accuracy, and supporting quality processes that help deliver compliant, high-quality products. In this role, you will review manufacturing documentation, inspect product labeling, verify test data, and ensure all records meet ISO 13485 and FDA regulatory requirements.
Quality Control Analyst Actalent IncQuality Control AnalystCambridge, MA$35–$40 / hourThe Quality Control (QC) department is essential for ensuring compliance with cGMP operations through the inspection of components and raw materials, as well as quality testing of intermediate, stability, and final product samples. 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.
Quality Control Manager (Traveling) Consigli Construction Co IncQuality Control Manager (Traveling)Milford, MADocumentation and Reporting: Maintain detailed documentation of inspection findings, including photographs, data sheets, and non-conformance reports, and generate regular quality reports for project management. Quality Control Planning: Develop and implement comprehensive quality control plans aligned with project requirements, including inspection checklists, sampling procedures, and testing protocols.
NewDirector, Quality Control Contractor Centessa Pharmaceuticals PlcDirector, Quality Control ContractorBoston, MA$95–$120 / hourThe Director, Quality Control (contractor) will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development. Contractors engaged through Centessa are employed through a third-party agency that serves as the employer of record and provides access to a comprehensive benefits package.
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 II Anika Therapeutics IncQuality Control Analyst IIWestborough, MAnClick the button below to submit your application for this position.\n \nApply Now\n \nOther Open Positions\n \nCareer\n \nShift Lead Aseptic Manufacturing\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Shift Lead Aseptic Manufacturing leads day-to-day aseptic manufacturing floor operations for sterile drug and medical device products produced within ISO 5\u2026\n \nView Position\n \nCareer\n \nSenior Warehouse Specialist\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Senior Warehouse Specialist plays a crucial lead role in managing complex warehouse operations, including domestic and international shipments, inventory control, and\u2026\n \nView Position\n \nCareer\n \nQuality Control Microbiologist\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The QC Microbiologist performs microbiological testing and validation activities supporting commercial manufacturing operations under GMP conditions, ensuring compliance with regulatory requirements, product\u2026\n \nView Position\n \nProducts Navigation" data-detect-dark-bg="true">Products\n\n Regenerative Solutions\n OA Pain Management\n Our Technology\n \nResources Navigation" data-detect-dark-bg="true">Resources\n\n Literature & Videos\n News & Blog\n Just For Patients\n Events\n Certifications\n Form 1095-C\n Instructions for Use\n Find a Doctor\n \nCompany Navigation" data-detect-dark-bg="true">Company\n\n About Anika\n Meet Our Team\n Our Story\n Join Us\n \nConnect Navigation" data-detect-dark-bg="true">Connect\n\n Investor Relations\n Contact Us\n Find a Rep\n \nFollow Us\n\n LinkedIn\n Instagram\n Facebook\n X\n* YouTube\n \n3 Media Web Solutions, Inc\n \n2026 Anika Therapeutics, Inc. In this role, you develop subject matter expertise in analytical testing methodologies, laboratory instrumentation, and quality control systems within regulated pharmaceutical and medical device environments.\n \nHow You'll Contribute\n\n Perform analytical testing of incoming raw materials according to USP, EP, ACS Reagent Index, and approved internal methods.\n
Senior Director, Analytical Development and Quality Control Generate Biomedicines IncSenior Director, Analytical Development and Quality ControlMA$210,000–$300,000 / yearThe Senior Director will serve as the senior analytical and QC partner to CMC, Process Development, MS&T, Quality, Regulatory, Supply Chain, and external partners, ensuring protein therapeutics are supported by phase-appropriate, scientifically rigorous, inspection-ready analytical control strategies that advance key company objectives and enable late-stage development and commercialization readiness. Reporting to the Vice President, Technical Operations, this leader will shape the future analytical and QC operating model for Generate's biologics portfolio, including analytical strategy, method lifecycle management, release and stability testing, specifications, comparability, external QC operations, GMP readiness, and commercialization preparation across CDMO and contract testing partners.
Quality Controller (Manufacturing) MOOQuality Controller (Manufacturing)East Providence, RIDiversity Statement We are working hard to create a representative, inclusive and super-friendly team, because we know that different experiences, perspectives and backgrounds make for a better workplace. And we are committed to continuous investment in building an open and inclusive environment, welcoming a diverse audience of candidates who see themselves working and thriving at MOO.
Quality Control I (2Nd Shift) Moo PrintQuality Control I (2Nd Shift)East Providence, RIYour value to the business lies in your ability to identify, contain, and solve quality problems before they impact our customers, directly contributing to MOO's reputation for high-quality, delightful products and supporting our continuous improvement goals. We've got half a million customers, mostly small and medium businesses in North America, the UK, and Europe - businesses that, like us, get all excited about putting something real and beautiful into people's hands.
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 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.
Quality Control Technician Amrize LtdQuality Control TechnicianMASubject to applicable law, employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit tests. Additional Requirements: Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment ("PPE"), including but not limited to respirators.
Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract) Rentschler BiopharmaQuality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)Milford, MassachusettsThe Quality Control Analyst II, Release and Stability Testing is responsible for the cGMP analytical testing of stability samples and evaluation of data to ensure compliance with analytical methods, stability protocols, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (cGMP). SME to support or lead activities related to OOS/OOT investigations, deviations, change controls, corrective actions, and preventive actions to correct and eliminate the potential for non-conformances.
Quality Control Data Reviewer Rentschler BiopharmaQuality Control Data ReviewerMilford, MassachusettsAs part of the Milford site’s Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control laboratory. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law.
Quality Control Systems Manager CharterQuality Control Systems ManagerMassachusettsDocumentation & Reporting Prepare and maintain required QC documentation, including daily QC reports, test results, deficiency logs, and meeting minutes. Types of work include environmental remediation, demolition, excavation, dredging, utility work, and landfill cap/closure projects.
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.
NewDirector, Quality Control (contractor) Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and CompanyDirector, Quality Control (contractor)Boston, MA$95–$120 / hourDescription of Role The Director, Quality Control (contractor) will provide leadership and oversight for analytical testing, stability programs, specification management, and quality control activities supporting clinical and commercial development. Key Responsibilities Analytical Oversight and Tactical Support Develop and Le...
Quality Control Analyst II BioPharma Consulting JAD GroupQuality Control Analyst IINorton, MAThe role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.