Director GMP QA

Get AI-powered advice on this job and more exclusive features. This role will oversee quality operations, vendor compliance, regulatory readiness, and support for clinical development and manufacturing activities, ensuring alignment with global health authority requirements. Key Responsibilities: Lead QA team and quality systems for GMP/GLP compliance Manage audits, regulatory inspections, and CAPA processes Oversee vendor and contract partner quality performance Contribute to regulatory submissions and inspection preparedness Advise leadership on quality strategy and risk management Qualifications: 10+ years in QA leadership within biopharma, ideally with small molecule experience Strong knowledge of global GMP/GLP regulations (FDA, EMA, ICH, etc.) Experience with CDMOs, regulatory submissions, and quality systems Strong leadership, communication, and problem-solving skills Details: Candidates must be local. Hybrid on-site work model with limited travel. Seniority level

Seniority level Director Employment type

Employment type Full-time Job function

Job function Quality Assurance Industries Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Meet Life Sciences by 2x Sign in to set job alerts for “Director of Quality Assurance” roles.

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