Associate GMP Compliance Auditor | Associate GMP Compliance Auditor (m/w/d)
Abax Personaldienstleistungen GmbH
Job Summary
This role involves supporting Good Manufacturing Practice (GMP) compliance and quality assurance activities, focusing primarily on third-party vendor audits and quality assessments. The Associate GMP Compliance Auditor will execute tasks under management guidance, including planning and scheduling third-party audits, conducting paper-based quality reviews (like questionnaires), and maintaining the approved supplier list and global audit plan. A key responsibility is collecting internal and external audit metrics for trend analysis by QA management. Candidates should hold a Bachelor's degree, preferably in Life Sciences or Engineering, and possess a foundational understanding of cGMP regulatory standards, ideally with 0-2 years of experience in quality assurance, regulatory affairs, or pharmaceutical/medical device manufacturing. This position offers an opportunity to develop expertise in supplier management processes and regulatory compliance within a professional environment in Ludwigshafen am Rhein.
Required Skills
Education
Bachelor's degree or studies, preferably in Life Sciences or Engineering. Equivalent combination of education and experience may be accepted.
Experience
- 0-2 years of experience in the function or related areas (e.g., Laboratory, Pharma/MedTech Manufacturing, QA/Regulatory Affairs, Pharma/Healthcare)
- Professional experience in planning and scheduling audits
- Professional experience supporting quality assessments of third-party vendors
- Experience solving problems within a project team with minimal supervision
Languages
Additional
- Located in Ludwigshafen am Rhein, Germany.
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