Validation Engineer - Pharmaceutical Equiment - Holland

NL  ‐ Onsite
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Description

Biopharmaceutical Contract Manufacturing Organisation based in Holland have a contract requirement for an experienced VALIDATION ENGINEER.

As this is a CMO organisation we are looking for Validation Engineers who has experience of any of the following equipment:

Requirements:
  • Pharmaceutical/Biotech background and experience of - at least - a couple of years in validating biotech process equipment.
Duties:
  • Perform qualifications and re-qualifications supporting biopharmaceutical manufacturing .
  • Write and execute installation and operational (IOQ) protocols and summary reports.
  • Review and approve validation documentation.
Experience with any of the following equipment:
  • Equipment Commissioning
  • Cleanroom Qualification
  • Autoclaves
  • Clean Steam
  • Cleaning In Place (SIP)
  • Water for Injection (WFI)
  • Refrigerators and Freezers (TCU's)
  • HVAC-systems
  • Incubators and Ovens
  • Bio Processing systems (with PCs).
CSV experience would be highly advantageous.
Start date
Within 4 weeks
Duration
8-9 months
From
Quanta Consultancy Services
Published at
11.04.2017
Project ID:
1323795
Contract type
Freelance
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