Senior Compliance Specialist | Compliance Senior Specialist (m/w/d)
Randstad Professional
Job Summary
As a Senior Compliance Specialist in the pharmaceutical industry, you will be responsible for independently managing discrepancies such as deviations, Out of Expectation/Specification (OOX) events, and other quality incidents as a Lead Investigator. This role involves leading cross-departmental compliance projects and independently addressing various GMP (Good Manufacturing Practice) issues, including conducting risk analyses and organizing GMP training sessions. A key part of the role is presenting deviations and OOX findings in English during client meetings, audits, and inspections. The ideal candidate will possess a Master's degree in Biotechnology, Pharmaceutical Technology, Biochemistry, or a related field, coupled with several years of professional experience in biotechnological production and strong GMP knowledge. Excellent communication, presentation, and moderation skills in both German and English are essential for success in this dynamic and responsible position.
Required Skills
Education
Master's degree in Biotechnology, Pharmaceutical Technology, Biochemistry, or comparable qualification
Experience
- • Several years of professional experience in biotechnological production
Languages
Additional
- Not specified
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