Job offer

20201929

GMP Expert (m/f/x)

Developing manufacturing processes and Tech Transfers with focus on GMP compliance

Company

Main tasks

  • An existing facility should be set up as GMP facility and GMP processes should be established.
  • Counsel and contribution to the establishment and implementation of measures within the scope of generating a GMP environment for biotech manufacturing
  • Counsel concerning risk analysis, quality assurance and hygiene measures
  • Develope and implement working instructions (SOPs)
  • Counsel in qualification and validation processes

Requirements profile

  • Project experience in the pharmaceutical industry
  • Intense project experience in a GMP environment
  • Knowledge in quality management
  • Deep knowledge and experience with biotechnological manufacturing processes (e.g. cell banking, fermentation, purification‚…)
  • Experience in auditing
  • Knowledge regarding qualification and validation
  • Proficient german skills and advanced-fluent english skills written and spoken

Contractual conditions

  • Fulltime
  • Remote work is possible, depending on current project status may vary between 2-3 days remote/week
  • Travellingnot planned but could possibly be necessary during the project, seperate travel budget
  • Period: 18.1.2021-18.1.2022

Contact

Is this position interesting? I am looking forward to hearing from you!

Doris Ehrmann

Fon: +49 281 3008424
Mobil: +49 173 700 49 44
Mail: doris.ehrmann@consigen.de