Senior Compliance Specialist | Compliance Senior Specialist (m/w/d)

Job Summary

As a Senior Compliance Specialist in the pharmaceutical industry, you will be responsible for managing and overseeing complex GMP (Good Manufacturing Practice) documentation, including OOX, CAPA, effectiveness checks, deviations, and risk analyses. Your day-to-day role involves ensuring a constant state of GMP and regulatory compliance within the Quality Control department and actively supporting audits and inspections by preparing relevant documentation and presentations. You will act as a central point of contact between technical departments and quality assurance, coordinating cross-functional compliance topics. This position is ideal for a professional with a strong background in biochemistry or pharmacy who enjoys high-responsibility tasks in an innovative environment. The role offers an attractive salary range of €67,000 to €86,000, a 37.5-hour work week, and the opportunity to work for a global pharmaceutical leader with a clear path for professional development.