Quality Assurance Specialist | Mitarbeiter Qualitätssicherung (m/w/d)

Job Summary

This role involves ensuring the highest quality standards within a pharmaceutical environment, focusing on GMP compliance. The specialist will be responsible for monitoring and tracking GMP status, creating and maintaining Standard Operating Procedures (SOPs) and Batch Production Records (BPRs), and participating in GMP inspections. Key tasks also include process validation, preparing for batch release, handling deviation reports, and reviewing batch-related documentation. The ideal candidate will have a scientific background, preferably with experience in the pharmaceutical sector, and possess strong analytical and problem-solving skills, coupled with a hands-on approach to work. This is an excellent opportunity for a CTA, BTA, or PTA looking for a new challenge in a dynamic pharma setting.