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Validation Engineer

Location: Hoofddorp
Start: November/December 2021


Job Description:

• Create and execute qualification protocols (IOQ / PQ), including identification and resolution of non-conformances/deviations

• Provide equipment, system and facility qualification guidance and strategy during project planning and development phases

• Oversee and manage validation instrument inventory including calibrations

• Review technical documentation including protocols & summary reports for IOQ / PQ testing, and validation SOPs

• Perform temperature mapping and other miscellaneous validation activities

• Manage contractors performing equipment and system qualifications

• Report status and progress of qualification activities or projects to the Leadership team

• Perform investigations and implement corrective actions related to CAPAs and deviations

• Develop technical specifications

• Support the execution of engineering projects

• Other duties as assigned

 

Required Experience:

  • MBO, BSc or equivalent degree required
  • Similar experience as a Validation Engineer
  • GMP experience in pharmaceutical or relevant industries required
  • Validation experience required
  • Clean room and / or cell therapy experience is preferred
  • Chemical engineering experience will be required for 1 of 3 roles

Are you interested or do you have questions about this specific role? Do not hesitate to contact me by applying to this vacancy!

SIRE® STAFFING SOLUTIONS B.V.

Keizersgracht 440A
1016 GD Amsterdam
The Netherlands
+31 (0) 20 658 9804