Science & Compliance Expert | Expert (m/w/d) Science & Compliance
Simtra Deutschland GmbH
Job Summary
This role is central to the pharmaceutical production operations in Halle, Westphalia, where you will manage critical quality processes for life-saving oncology medications. Your daily responsibilities include overseeing deviations, conducting root cause analyses, and defining CAPA measures to ensure product integrity. You will serve as a vital link between production and quality assurance, drafting technical reports in English and representing the facility during high-stakes customer and regulatory audits. The position offers a unique opportunity to influence compliance standards and handle complex regulatory requirements in a highly regulated environment. It is particularly attractive due to its 37.5-hour work week, competitive collective bargaining salary, and comprehensive benefits package including 30 days of vacation and relocation support.
Required Skills
Education
University degree in natural sciences or technology, preferably in Biology, Biotechnology, or Chemistry.
Experience
- Professional experience in pharmaceutical manufacturing preferred
- Experience in technical writing, specifically for reports, deviations, and audit findings
- Proven experience in managing quality compliance topics such as deviations and complaints
- Experience participating in or presenting during customer and regulatory audits
Languages
Additional
- The role is based in Halle (Westfalen). Candidates must be able to work full-time (37.5 hours/week). Financial support for job-related relocation is available via a relocation allowance.
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