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Cqv Engineer / Consultant

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Product Life Group

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Location:
France

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

As a CQV Engineer / Consultant at ProductLife Group, you will ensure that pharmaceutical manufacturing systems—equipment, utilities, cleanrooms, and processes—are properly installed, tested, and validated in compliance with international standards. You’ll be deployed on-site to support our clients in delivering safe, compliant, and efficient production environments.

Job Responsibility:

  • Commissioning & Qualification of equipment and systems (FAT, SAT, IQ, OQ, PQ)
  • Validation Activities including cleaning validation, process validation, and environmental monitoring
  • Document Preparation: Draft and review validation master plans, protocols, SOPs, risk analyses, and reports
  • Design Reviews & Walkdowns: Conduct P&ID walkdowns, design qualification, and troubleshooting
  • Audit Support: Participate in internal and external audits and inspections
  • Cross-functional Coordination: Collaborate with production, QA, and engineering teams

Requirements:

  • Confirmed (5–7 years) or Expert (10+ years) experience level
  • Technical knowledge of GMP, FDA, ICH Q8–Q10, ASTM E2500, EU Annex 15
  • Validation of HVAC, clean utilities, process equipment, and computerized systems
  • Familiarity with Kneat, VAL-ENT-IN, SAP, Qualiac
  • Project management, autonomy, adaptability, and strong communication skills

Additional Information:

Job Posted:
January 10, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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