Validation Specialist

Switzerland  ‐ Onsite
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Description

My Client is looking for a Validation Specialist

Tasks:
  • Coordination and oversight of external validation partners
  • Supporting engineering, quality, quality control and production in a campus-wide validation team
  • Define strategy, plan, coordinate aseptic process simulation
  • Define strategy, plan, coordinate and execute all phases for supporting validation activities such as cleaning validation of product contact equipment, cleaning validation of rooms, hold time validation
  • Define strategy, plan, coordinate and execute all phases for performance qualification of rooms
  • Create, review and approve technical and GMP related documentation
    Bridging with cross-functional teams handling and ensuring equipment and process readiness for production


Qualifications
Your profile:
University degree in natural or technical sciences or equivalent by experience
  • Analytical thinking and problem-solving ability
  • Team player, highly proactive and reactive, creative, multitasker and a good time manager
  • Basic Know-how of Qualification/Validation requirements according to cGMP
  • Preferably 3 years of working experience within the pharmaceutical or a biotechnology company
  • Basic Know-how of biotechnology processes
  • Know-how of quality assurance principles
  • Business fluency in German and English.

If interested in this position please do send your CV to my mail: or apply directly.

Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Start date
12/2019
Duration
6 Months
From
Michael Bailey Associates
Published at
07.11.2019
Project ID:
1844840
Contract type
Freelance
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