Associate GMP Compliance Auditor | Associate GMP Compliance Auditor (m/w/d)
Abax Personaldienstleistungen GmbH
Job Summary
This role involves supporting the Quality Assurance (QA) management team by executing compliance tasks, primarily focusing on auditing third-party vendors in Ludwigshafen am Rhein. The Associate Auditor will be responsible for planning and scheduling audits, conducting paper-based quality assessments (e.g., reviewing quality questionnaires and history), and maintaining the approved supplier list and global audit plan. Key duties include gathering internal and external audit metrics for trend analysis, assisting senior auditors in developing and updating departmental systems and procedures, and supporting external partner quality management during regulatory or client inspections. Candidates should possess a Bachelor's degree in Biosciences or Engineering and 0-2 years of relevant experience, coupled with a fundamental understanding of cGMP regulatory standards within the pharmaceutical or medical device manufacturing sectors. This is an excellent opportunity to gain foundational experience in global compliance and quality management.
Required Skills
Education
Bachelor's degree in Biosciences or Engineering, or equivalent combination of education and experience
Experience
- 0-2 years of experience in auditing or related areas
- Fundamental understanding of cGMP regulatory standards
- Experience in laboratory and/or pharmaceutical/medical technology manufacturing
- Experience in Quality Assurance/Regulatory Affairs
Languages
Additional
- Located in Ludwigshafen am Rhein, Germany
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