GMP Compliance Specialist (Technology & Production) | Referent (m/w/d) GMP-Compliance im Bereich Technik & Produktion

Job Summary

As a GMP Compliance Specialist in the Technology and Production department, you will play a critical role in ensuring the highest quality standards for sterile pharmaceutical products. Your day-to-day responsibilities include managing and implementing the Contamination Control Strategy (CCS) program, conducting GMP risk analyses, and coordinating process improvement measures across various departments. You will act as a key point of contact during regulatory and client audits, ensuring all activities are documented according to strict GMP standards. This position is ideal for a detail-oriented professional who enjoys collaborative project work and process optimization. The role offers a secure position within the growing pharmaceutical industry, characterized by a strong welcome culture and a collaborative team environment. Please note that this is initially a fixed-term position for parental leave coverage, offering an attractive salary based on the chemical industry collective agreement.