Process Validation Expert, Basel

Basel-Stadt  ‐ Vor Ort
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Schlagworte

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Beschreibung

Our Client, a Global Pharmaceutical who is currently on an exciting growth curve are seeking a Validation Expert to be based at their Basel site for an initial 11-month contract with a strong likelihood for extension. The workload will be 50%.
Key responsibilities will include:
  • Provides technical expertise (and may facilitate) pre-validation risk assessments using risk management tools.
  • Works collaboratively and cross functionally to help ensure that process risks are analysed, appropriately controlled and appropriately documented.
  • Ensures that all validation activities are compliant current requirements and cGMP.
  • Manages deviations associated with process validation and makes recommendations for deviation resolution as well as prevention of reoccurrence.
  • Provides technical expertise and recommendations for validation of major or complex changes in manufacturing.
  • Authors and reviews process validation protocols (e.g. launches, weak point remediation) and related reports.
  • Reviews MBRs and associated change controls. Supports the execution at the shop floor.
  • Responsible to translate applicable process parameters and the process control strategy into a focused validation plan for process validation.
  • Participates in pre-validation activities to ensure the success of commercial process validation.
  • Provides technical expertise.
  • Owns the Training Curriculum for its Job Description


The successful incumbent will possess:
  • in Chemistry, Pharmacy, Chemical Engineering or Pharmaceutical Technology.
  • Fluent in English and German.
  • 2-3 years experience in manufacturing/ manufacturing science and technology/technical development/quality.
  • Thorough understanding of Biotech (mammalian cell based) manufacturing processes and related process equipment.
  • Expert in reviewing and writing technical reports.
  • Experience in biotech process validation or biotech cleaning validation (plan and Report writing)
  • Fundamental understanding of standard pharmaceutical analytical testing.


Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start
02/2021
Dauer
11 months
Von
Michael Bailey Associates
Eingestellt
19.01.2021
Projekt-ID:
2031856
Vertragsart
Freiberuflich
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