Compliance Specialist | Compliance Specialist (m/w/d) 74.000 €

Job Summary

As a Compliance Specialist in the pharmaceutical industry, you will play a vital role in ensuring the quality and regulatory integrity of drug development processes. Your day-to-day responsibilities involve managing GMP-related tasks, specifically focusing on the qualification and lifecycle management of disposables and packaging materials. You will navigate complex cross-functional change control processes, draft and revise GMP documentation such as specifications and SOPs, and facilitate collaboration between supply chain, quality assurance, and production departments. Furthermore, you will handle investigations, CAPAs, and support audit preparations. This role is unique as it offers the opportunity to work with a top-tier global pharmaceutical company, providing a hybrid working model with significant remote flexibility after an initial on-site training period, all while contributing to meaningful medical advancements.