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CQV Engineer

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CQV Engineer - Pharmaceuticals - 12-Month Contract - Limburg, Netherlands 

Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer for their new Capex investment project. As a scientific and technology innovator, this is a superb opportunity to onboard as our client continues to make strides towards a healthier world for all.


Responsibilities:
  • Prepare validation documents including URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
  • Execution of IQ/OQ and PQ for equipment, systems and utilities.
  • Write reports of completed CQV activities
  • Stay informed of industry regulatory changes as it applies to equipment / facility validation.
  • Support in writing and/or revising procedures applicable to the Engineering activities.
  • Support the Engineering group to prepare the validation, requalification and maintenance program.

Required experience:
  • Bachelor degree or equivalent in a relevant subject area.
  • Flexibility and adaptability, able to perform in an ever-changing environment.
  • Demonstrable (3-6 years) experience within a validation role.
  • Experience in GMP environment or similar, familiar with GDocP, Data Integrity and ALCOA++
  • Strong planning skills and self-motivated, able to work autonomously.
  • Business-level fluency in English; other languages are nice to have but not required.

If this role is of interest to you, please apply now! 

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