GMP Specialist | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
This role is for a detail-oriented GMP Specialist to join a pharmaceutical company in Biberach. The primary focus will be on the GMP review of electronic manufacturing instructions (Master Batch Records) for batch documentation in biopharmaceutical production, utilizing BioMES 8 software. Key responsibilities include planning and executing controls of electronic manufacturing instructions, maintaining master data in BioMES 8 and SAP, and performing administrative tasks such as training, data collection, and supporting audits. The ideal candidate will have a strong understanding of production processes, excellent IT affinity, and a precise, independent working style. This is an excellent opportunity for professionals with a scientific background and experience in the pharmaceutical industry to contribute to critical quality assurance processes and ensure compliance within a dynamic environment.
Required Skills
Education
Bachelor's degree in a scientific field (e.g., Biotechnology, Process Engineering, Chemical Engineering) or comparable, alternatively a completed scientific vocational training (e.g., Pharmaceutical Technician, Chemical Technician) with several years of professional experience (possibly further training as a Technician, Industrial Master)
Experience
- Experience in the pharmaceutical industry or other large-scale manufacturing operations with a good understanding of production processes
- Experience in a GMP environment
Languages
Additional
- Not specified
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