Senior Process Advisor, Pharmaceutical Industry | Senior Process Advisor Pharma (m/w/d)

akut... Kompetente Lösungen GmbH

Biberach an der Riß, Baden-Württemberg, Deutschland
Published Oct 27, 2025
Full-time
No information

Job Summary

This is a critical role focused on optimizing processes and maintaining cGMP compliance within the Cell Culture area of an innovative pharmaceutical company. The Senior Process Advisor will be responsible for coordinating work packages, designing and implementing sophisticated solutions, and providing technical leadership for production coordination. Daily activities include setting process specifications, ensuring adherence to quality and safety standards, and actively participating in troubleshooting and process monitoring through detailed data analysis and chart interpretation. Furthermore, the role involves independently planning and executing expert activities for technical projects, conducting error analyses, and implementing new technologies and processes. Candidates must possess a strong background in Biopharmacy or related engineering fields, coupled with multi-year experience operating large-scale manufacturing systems under GMP conditions. Expertise in specialized systems like GBS, LIMS, SAP, and BioMES is mandatory, along with strong written and verbal communication skills in both German and English.

Required Skills

Education

Completed degree (Bachelor, Diploma, Master) in Biopharmacy, Biotechnology, or Bioengineering; OR completed natural science education combined with certification as a Master Craftsman or Technician.

Experience

  • Multi-year professional experience.
  • Experience in a GMP-regulated environment.
  • Experience handling large-scale manufacturing systems under GMP conditions (ideal).

Languages

German (Intermediate)English (Intermediate)

Additional

  • Fixed-term contract from September 1, 2025, to December 15, 2026. Full-time employment (37.5 hours per week).