Third-Party QA Lead: Biotech Compliance & SCN
$45 - $51 per hourThe Fountain Group
A leading staffing agency is seeking a Third-Party QA Management Specialist in Framingham, MA. The ideal candidate will oversee Third Party Quality operations, ensuring compliance with regulatory standards. This role requires 4+ years in biotech or pharmaceutical environments and proficiency in Veeva quality management systems. The position has a pay rate of $45-51 hourly and offers the potential for extension or conversion after a 6-month contract. #J-18808-Ljbffr The Fountain Group
- A leading company specializing in strategic workforce solutions is seeking a Quality Assurance professional in Marlborough, Massachusetts. The role involves developing quality systems, ensuring compliance with FDA regulations, and supporting the quality assurance processes...Suggested
- ...seeking a Quality Assurance Specialist to oversee QA standards across programs for adults with... ...and intellectual disabilities. You will ensure compliance with DDS, MassHealth, CARF and other accrediting bodies, and lead continuous quality improvement initiatives. The...Suggested
- ...Supervisor provides leadership for all Quality Assurance processes in compliance with the medical device regulatory requirements, supervises... ...Qualifications Experience supervising employees or leading team members. Minimum of 5 years working in a Quality Assurance...SuggestedHourly payContract workWork at officeMonday to FridayShift workNight shiftAfternoon shift
- ...collaborate with informatics engineers to benefit the internal analytic process. You will drive the generation and testing of hypothesis leading to new biological insights.Expected to effectively communicate analytical results with internal project collaborators through both...SuggestedImmediate start
- ...Pharma sponsors and the biotech community, supported by over... ...role responsible for leading quality assurance strategy, compliance oversight, and audit execution... ...Serve as the primary QA liaison for Biometrics functions... ...EDC vendors, and other third-party providers supporting...SuggestedWork at office
$267k - $327k
...Summary: The Executive Director, Quality Compliance is a senior Quality leader responsible... ...the Quality Master Plan.Responsibilities:Lead and develop the Quality Compliance team... ...including internal, external, and vendor/third-party auditsOversee audit strategy, execution,...Full timeFlexible hours2 days per week3 days per week$220k - $300k
...biopharmaceutical and clinical markets. Job Summary: Nova Biomedical is seeking a Senior Quality Director , to lead corporate-level quality and compliance activities across Nova Biomedical’s global manufacturing sites. This role is responsible for assuring company...Hourly payWork at officeFlexible hours- ...have extensive experience with the Manhattan product suite, particularly in warehouse management systems. Responsibilities include leading projects, overseeing quality assurance and managing integration discussions. This is an excellent opportunity for candidates with a...
- ...Executive Director, Quality Compliance About the Company Innovative pharmaceutical company specializing in oral therapeutics for... ...the company's global GxP compliance framework. This includes leading and developing the Quality Compliance team, establishing and maintaining...
$161.25k - $232.92k
...Bewerbung)job requisition id: R2864341**Job Title**: Head of Quality Compliance* Location: Framingham, MA**About the Job**The Quality... ...enhance the site compliance fostering a culture of compliance* Leading and managing the compliance team, including hiring, training,...Local areaWorldwide$188k - $230k
...Position Summary: The Associate Director, Quality Auditing & Compliance is responsible for leading and executing the company’s risk-based internal Quality... ...onsite audits of internal, external, and vendor/third-party auditsEvaluate compliance with applicable FDA regulations...Full timeWork at officeFlexible hours2 days per week3 days per week$252k - $269k
...Alkermes GLP/GCP/GVP quality programs to ensure compliance across global clinical trials. This... ...role requires an experienced Clinical QA Senior leader who can build high‑performing... ...improvement of Alkermes QMS and compliance, and leads the Alkermes strategy and GXP compliance...Contract workWork at officeLocal areaWorldwideFlexible hours3 days per week- Boston Scientific in Marlborough, MA, seeks a Principal Clinical Quality Assurance Specialist to lead the internal clinical QA program for assigned areas, partnering with cross-functional teams to ensure investigations comply with GCP, ISO 14155, ISO 13485 and company policies...
- ...Principal Clinical Quality Assurance Specialist to support the internal QA program across assigned business areas. You will partner with... ..., while serving as QA representative on project teams and leading audit activities. You will drive inspection readiness, CAPA implementation...
- ...Description Manage QMS compliance with the appropriate internal and external regulatory requirements (including but not limited to FDA,... ...Manage the CAPA, Complaints, SCAR, and Audit Findings processes. Lead supplier management, including maintaining the Approved Supplier...
$148k - $180k
...the Executive Director, External Operations Quality, this role serves as a key Quality contact for external partners and ensures compliance with company standards, Quality agreements, and applicable regulatory requirements.The Senior Manager partners with Technical Operations...Full timeContract workFlexible hours2 days per week3 days per week$200k - $220k
...Software (non-product) Validation (CSV), labeling and sterilization compliance, and periodic/ad-hoc risk reviews. Qualifications: Bachelor’s... ...Oracle is a plus Key Responsibilities: Leadership & Culture Lead through company values and reinforce a strong, global Quality Culture...Full time- ...RoslinCT is seeking an Environmental Monitoring QC Manager in Hopkinton, MA to lead cleanroom testing programs, supervise EM analysts, and ensure compliance with cGMP and FDA standards. The role emphasizes data integrity, investigation writing, CAPAs, and timely regulatory...
$267k - $327k
...performance, proactively manages quality and compliance risks, and drives timely resolution of... ...manufacturing network.Responsibilities:Lead Quality oversight and governance of CMOs,... ...readinessEstablish and maintain alliance partner QA governance, responsibilities, and...Full timeContract workFlexible hours2 days per week3 days per week- ...Alkermes GLP/GCP/GVP quality programs to ensure compliance across global clinical trials. This... ...role requires an experienced Clinical QA Senior leader who can build high-performing... ...improvement of Alkermes QMS and compliance, and leads the Alkermes strategy and GXP compliance...Contract work
- ...WE ARE RoslinCT is a world-leading cell and gene therapy contract... ...Operations, is responsible for leading QA plant operations and expertise... ...of QA specific procedures for compliance and identify opportunities for... ...experience in a pharma/biotech company with internal...Full timeContract workWork at officeFlexible hoursWeekend work
- ...seeking an experienced Operations Quality Manager to join a leading medical device manufacturing organization in Eastern Massachusetts... ...manufacturing-related quality activities, ensuring product compliance and high operational standards. Team Management: Direct...Relocation packageFlexible hours
- ...supplements program. The role coordinates sample submissions to 3rd party labs, tracks results, and manages document control for the Pure... ...inspectors, manage the document change process, and help ensure compliance with quality and regulatory requirements. #J-18808-Ljbffr...Monday to Friday
$200k - $260k
...’s vision is to build a world leading oncology company bringing the... ...growing supply demand. Lead QA input into CDMO selection, onboarding... ...(eQMS, DMS, LMS), ensuring compliance with Part 11 / Annex 11 and... ...GMP Quality Assurance within biotech or pharmaceutical development....Contract workTemporary workFlexible hours- ...Director of Quality & Compliance General Gelsight seeks an experienced and versatile Quality professional to lead compliance efforts. This key position will provide company-level leadership of Quality and Defense standard compliance across all products and services...Full time
$107.1k - $150k
...with Product Integrity, Product Development, Engineering, PMO, Compliance, Legal Supply Chain, and Commercial teams, you will translate quality... ...geographic expansion of the medical devices’ portfolio, and lead post-market surveillance activities—ensuring quality is...Temporary workLocal areaFlexible hours$146.22k - $160k
...by creating solutions so advanced, they redefine innovation for the world. It’s an amazing challenge. And it’s waiting for you now. Leading a test team using the latest technologies, the Test Lead will coordinate and execute the test approach and document system...Remote workFlexible hours$139k - $159k
...building plans for tracking and resolving deficiencies (including third party, owner/architect/engineer, and internal items).... ...identification, safetycomplianceand sustainability. Experience leading and directing the work of others. Nice to Have: OSHA-30certification...Full timeFor contractorsFor subcontractor$118.3k - $207.4k
...Partner with clinical, data science, engineering, product, legal, compliance, and customer-facing teams to operationalize AI evaluation... ...process. Please note that use of AI-generated responses or third-party support during interviews will be grounds for disqualification...Full timeWork at office$150k - $170k
...Summary: The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) operations across multiple U.... ...reagents. This role ensures product quality, regulatory compliance, and operational excellence throughout the manufacturing lifecycle...Hourly payWork at officeFlexible hoursShift work
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