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CQV engineer

  1. France
Paris
  1. Contract
Competitive
  1. Compliance / Quality Assurance
36791
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CQV Engineer - France, Paris - 12 Month Contract

Our client, a global pharmaceutical company, are looking for a CQV engineer to join their team. The company has grown to become a world leader in the development, manufacture, and marketing of innovative pharmaceutical products to alleviate some of the world’s biggest health problems.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:
  • Supervise qualification/validation activities for equipment and product validation.
  • Assist in selecting and procuring new equipment for site expansion and QC.
  • Write, execute, revise, and archive qualification/validation documentation (e.g., Validation Plans, User Requirement Specifications).
  • Manage test plans and ensure the maintenance of validated state.
  • Analyze qualification/validation data and resolve deviations.
  • Coordinate equipment qualification and related projects across departments.
  • Lead quality optimisation projects and process improvements.
  • Act as product/process expert when needed.
  • Monitor technological advancements and industry benchmarks.
  • Introduction of New Products, Equipment, and Processes:
  • Organise test packages and corrective actions for deviations.
  • Support During Audits and Inspections.
Desirable Experience:
  • Hold a Bac+5 (or equivalent).
  • Extensive experience in microbiological qualification/validation in the pharmaceutical industry and project management.
  • Experience in transversal collaboration.
  • Microbiology/physico-chemical versatility is a plus.
  • Fluency in English (B2 level required).
If you would like to apply or find out more, get in touch now!
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