Senior Process Advisor, Pharmaceutical | Senior Process Advisor Pharma (m/w/d)
akut... Kompetente Lösungen GmbH
Job Summary
This Senior Process Advisor role, situated within the Cell Culture domain of an innovative pharmaceutical company, focuses on optimizing processes and advancing the Current Good Manufacturing Practice (cGMP) status. The successful candidate will coordinate complex work packages, design and implement sophisticated technical solutions, and provide essential production support and technical leadership. Key responsibilities include ensuring strict adherence to quality and occupational safety standards, conducting in-depth process data analysis (charts, tables, interpretation), monitoring, and troubleshooting. Furthermore, the role involves independently planning and executing expert activities for technical projects, performing error analyses, and creating necessary regulations and risk assessments. Applicants must possess a degree in Biopharmacy, Biotechnology, or a related scientific field, coupled with extensive professional experience in a GMP-regulated environment, ideally managing large-scale manufacturing facilities. Proficiency in systems like GBS, LIMS, SAP, and BioMES, along with strong German and English language skills, is mandatory for success in this challenging and rewarding position.
Required Skills
Education
Completed university degree (Bachelor, Diploma, Master) in Biopharmacy, Biotechnology, or Bioengineering, OR completed scientific training with additional qualification as Master Craftsman (Meister) or Technician.
Experience
- Several years of professional experience
- Experience in a GMP-regulated environment
- Experience in handling large-scale manufacturing facilities under GMP conditions (ideal)
Languages
Additional
- Temporary contract duration (September 1, 2025, to December 15, 2026). Requires proactive and self-motivated working style with high self-initiative and structured approach.
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