Are you a GMP Specialist looking for a career change? Is job security as important to you as a responsible position and diverse tasks that you can manage and take ownership of independently thanks to your experience and expertise? Trust our expertise – we have the right position for you in the pharmaceutical industry: We are currently seeking a GMP Review Specialist at our Biberach location. Apply online now! We value equal opportunities and welcome applications from people with disabilities, whose inclusion is of particular importance to us. Your responsibilities will include: GMP review of electronic manufacturing instructions (Master Batch Records) for batch documentation in biopharmaceutical production (upstream and downstream) using BioMES 8 software; independent planning and execution of checks of electronic manufacturing instructions and accompanying electronic documents; maintenance of master data (material, object, etc.) in BioMES 8 and SAP; and administrative tasks such as creating and conducting internal training sessions, collecting key performance indicators, onboarding new colleagues, processing change control requests, and preparing for and supporting audits.
- Completed studies in a natural science field, e.g. in biotechnology, process engineering, chemical engineering or similar.
- Alternatively, completed vocational training in a natural science field, e.g. as a pharmaceutical technician or chemical technician with several years of professional experience (possibly further training as a technician, industrial master craftsman)
- Experience in the pharmaceutical industry or other large-scale manufacturing plants with a good understanding of production processes.
- Experience in a GMP environment
- Strong IT affinity and enjoyment of working with screens
- Good German and English skills, both spoken and written.
- Independent and precise work style
- High level of initiative, communication and teamwork skills