Compliance Jobs
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Principal Specialist Quality Assurance (Design)
Our client an international life sciences organisation bringing life changing medical diagnostic products to market are looking to add a Principal Specialist Quality Assurance (Design) to an existing team.They are a global leader with a comprehensive portfolio, and you will be joining a team developing diagnostic solutions to aid the acceleration o...
Sr CQV Engineer / Sr Validation Engineer
Senior Validation Engineer / CQV SpecialistLocation: Greenville, NC / Holly Springs, NC Employment Type: Full-Time, On-Site Salary Range: $70,000-$120,000/yearPosition SummaryA leading pharmaceutical manufacturing organization is seeking a few Senior Validation Engineers / CQV Specialists to support commissioning, qualification, and validation acti...
GxP Quality Auditor / Sr Quality Lead
GxP Quality Auditor / Senior Quality LeadLocation: Greenville, NC Employment Type: Full-Time, On-Site Salary Range: $87,780 - $145,307/yearCompany OverviewA leading life sciences organization is seeking a GxP Quality Auditor / Senior Quality Lead to support compliance and quality governance across multiple manufacturing lines. This company partners...
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Regulatory Affairs Consultant (SaMD)
Regulatory Affairs Consultant - Software as a Medical Device (SaMD) Location: Amsterdam, Netherlands (Remote/Hybrid)Length: 12 monthsStart Date: January 2026 About the RoleWe're looking for an experienced consultant to advise on regulatory and quality strategies for software-driven medical technologies. This role is ideal for someone who understand...
QA Engineer
Role: Quality Assurance EngineerLocation: Remote Contract: 6 MonthsOverview: We are seeking an experienced Quality Assurance Engineer to ensure the highest quality standards in new product development projects for our client. This role involves driving quality across design and manufacturing processes, supporting verification and validation activi...
QA Manager Biologics
This is a 6‑month contract position based in Leiden, The Netherlands, requiring a minimum on‑site presence of 4 days per week. The Quality Assurance Manager will play a key role in ensuring compliance with EU GMP standards and supporting biologics production in an aseptic/sterile manufacturing environment. Fluency in Dutch (spoken and written) is ...