CareerPlan

Head of QA (w/m/d) GMP Compliance

Hildesheim, NIEDERSACHSENFull-time2026-10-08 → 2026-11-08

Core

Ensuring GMP compliance and data integrity, leading the QA team, and managing quality processes in a pharmaceutical environment.

Role type

Senior leadership quality assurance manager (pharmaceuticals)

Builds

Quality management systems, regulatory compliance, and audit readiness for pharmaceutical clients

Domain

Pharmaceuticals / Regulatory Quality Assurance

Required skills

GMP compliance, CAPA management, audit management, quality documentation, complaint management, quality reporting, SOP development, risk analysis, team leadership, resource planning

Preferred skills

Technical understanding, strategic optimization, cross-functional collaboration, regulatory knowledge

Technologies

GMP systems, validation tools, quality management software

Responsibilities

Ensure GMP compliance and data integrity; Approve and monitor CAPA, change control, and deviation processes; Plan and follow up on regulatory inspections and customer audits; Maintain and update quality documents (e.g., Site Master File, Validation Master Plan); Manage complaints; Conduct self-inspections; Ensure timely creation of Product Quality Reviews; Create, analyze, and evaluate quality reports; Develop site-specific QM systems; Escalate quality-critical issues; Lead and develop the QA team; Coordinate with Production, QC, Engineering, Logistics, and Supply Chain; Communicate with authorities, customers, and suppliers; Travel readiness

Seniority

Senior, hands-on IC with leadership responsibilities