Quality Assurance Manager (GMP Environment) | QA-Manager (m/w/d) GMP-Umfeld

Job Summary

This role involves overseeing and optimizing quality assurance systems within a pharmaceutical environment, ensuring strict adherence to Good Manufacturing Practice (GMP) standards. As a QA Manager, you will be responsible for coordinating quality-related inquiries, planning laboratory activities, and managing the analytical lifecycle of pharmaceutical products. A significant portion of the day-to-day work includes the creation, review, and approval of Standard Operating Procedures (SOPs), master documents, and production documentation such as logbooks and checklists. You will also play a key role in preparing for and supporting external audits and regulatory inspections. This position is ideal for professionals who enjoy a mix of administrative oversight and technical documentation. It offers the unique opportunity to work with a renowned engineering service provider, granting access to high-profile projects at prestigious clients while providing long-term career stability through a permanent contract and comprehensive benefits like company pension schemes.