Quality Assurance Manager Jobs
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AD, Preclinical & Clinical QA
Associate Director, Clinical, Pre-Clinical & Diagnostic QA 📍 Hybrid or Remote | Southern California HQ | 15-20% TravelJoin a biotech innovator advancing immune-based therapies that aim to reprogram the body's natural defenses to fight cancer and infectious diseases. This company is developing next-gen treatments that go beyond targeting disease.Ab...
Senior Manager, Supplier Quality
Position Summary:The Sr. Supplier Quality Manager is responsible for developing, implementing, and maintaining supplier quality assurance processes to ensure compliance with regulatory requirements and company standards. This role plays a critical part in ensuring that all materials and components sourced from external suppliers meet stringent medi...
AD, Preclinical & Clinical QA
Associate Director, Clinical, Pre-Clinical & Diagnostic QA 📍 Hybrid or Remote | Southern California HQ | 15-20% TravelJoin a biotech innovator advancing immune-based therapies that aim to reprogram the body's natural defenses to fight cancer and infectious diseases. This company is developing next-gen treatments that go beyond targeting disease.Ab...
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Freelance QA Manager
Role OverviewA freelance QA Manager is required to provide interim support at a GMP‑licensed site specializing in sterile and biologics manufacturing. The consultant will ensure compliance with EU GMP and Annex 1, strengthen quality systems, and prepare the site for upcoming regulatory inspections. Key ResponsibilitiesOversee and maintain site qual...
Quality Manager
Hiring: Quality Manager Are you passionate about quality systems and regulatory excellence in laboratory environments? We're looking for a Quality Manager to lead our clients compliance efforts and drive continuous improvement across our operations.Your ImpactAs our Quality Manager, you will:Lead ISO 15189 Quality Management: Maintain and update SO...
Sterilisation Specialist
The Consultant will lead and support sterilisation strategy, validation, and compliance activities across the full lifecycle of medical devices, including implantable Class II/III products. The role requires deep expertise in sterilisation modalities, microbiological testing, and regulatory frameworks under both FDA and EU MDR.The role requires dee...
