Pharmaceutical Production Documentation Specialist | Mitarbeiter (m/w/d) für die pharmazeutische Produktionsdokumentation

Job Summary

This full-time, permanent role involves ensuring the quality and compliance of pharmaceutical production documentation for a client in Pfaffenhofen an der Ilm. Day-to-day responsibilities include the meticulous review of batch documentation post-production, verifying data transfers (paper and electronic), completeness, and plausibility. You will be responsible for checking In-Process Control (IPC) results, controlling and evaluating machine, equipment, and process documentation (e.g., protocols and graphics) for correct process flow, and assessing critical metrics like weighings, balances, and yield determinations. A key function is the evaluation and detailed commentary on disturbances, alarms, and quality-relevant diagnoses. The ideal candidate must possess completed vocational training in a pharmaceutical profession (such as Pharmakant or PTA), coupled with professional experience in pharmaceutical documentation review and a strong understanding of drug manufacturing processes and GMP standards. This position offers a stable contract and the opportunity to contribute significantly to quality assurance within a regulated manufacturing environment.