GMP Specialist | GMP Spezialist (m/w/d)
Randstad Professional
Job Summary
As a GMP Specialist based in Biberach, you will play a critical role in the biopharmaceutical production cycle by conducting GMP reviews of electronic Master Batch Records (MBR) for both upstream and downstream processes. Your daily responsibilities include the independent planning and execution of documentation controls using BioMES 8 software, as well as maintaining master data within SAP and BioMES systems. Beyond documentation, you will handle administrative duties such as creating internal training materials, processing Change Control requests, and preparing for audits. This position is ideal for professionals with a strong background in biotechnology or chemical engineering who possess a high affinity for IT systems. Joining Randstad Professional offers the stability of a permanent contract within the pharmaceutical industry, complemented by a performance-oriented salary, structured career development, and the opportunity to work in a highly specialized, agile team environment focused on life sciences.
Required Skills
Education
Bachelor's degree in a natural science field (e.g., Biotechnology, Process Engineering, Chemical Engineering) or a completed vocational training as a Pharmacist/Chemical Technician with additional certification as a Technician or Master Craftsman.
Experience
- Professional experience in the pharmaceutical industry or large-scale technical manufacturing plants
- Practical experience working within a regulated GMP environment
- Proven experience in production processes and electronic documentation control
- Experience in administrative tasks including training coordination and KPI tracking
- Several years of professional experience required if applying with a vocational qualification rather than a degree
Languages
Additional
- Location: Biberach; Full-time, permanent contract; Requires high IT affinity and the ability to perform detailed screen-based work for extended periods.
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