Lead Compliance Specialist (Part-Time 25%) | Leitender Compliance-Spezialist m/w/d TZ 25% (9,38h/Wo) 34,46€ plus Prämien
apero GmbH Arbeitnehmerüberlassung
Job Summary
This part-time (9.38 hours/week) Lead Compliance Specialist role, based in Biberach an der Riß within the pharmaceutical industry, focuses on ensuring CGMP-compliant operation of pharmaceutical production facilities. The specialist will interpret and implement regulatory requirements, specifically EU-GMP guidelines and FDA regulations, to continuously improve CGMP compliance related to operational procedures, facility design, cleanroom standards, and clothing requirements. Key responsibilities include preparing for and presenting during customer and regulatory audits, managing observations, and implementing corrective and preventive actions (CAPAs). The role involves advising teams on the lifecycle model for facility implementation and changes, and maintaining GMP-compliant documentation for changes, events, and deviations. This position offers a hybrid work model, allowing for 2-3 days of remote work after the initial on-site training period, making it attractive for professionals seeking specialized part-time compliance work.
Required Skills
Education
Master's or Diploma degree in Natural Sciences (e.g., Chemistry, Biochemistry, Biology, Food Technology, or Pharmacy) OR a Master Craftsman qualification with several years of relevant professional experience
Experience
- Several years of professional experience in the pharmaceutical industry
- Experience in functions such as Quality Assurance, Production, Quality Control, or Microbiology
- Extensive knowledge of European and US American cGMP regulations
Languages
Additional
- Part-time position (25% or 9.38 hours per week); Hybrid work model available (2-3 days remote after initial on-site training); Location constraint: Biberach an der Riß
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