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.

Group 10
Responsibilities:

You will be responsible for:

  • 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.

Group 12
Experience:

We’re looking for someone with:

    • Experience Level: Confirmed (5–7 years) or Expert (10+ years).
    • Technical Knowledge:
      • 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.
    • Soft Skills:
      • Project management, autonomy, adaptability, and strong communication.

CQV Engineer / Consultant - VAF 387

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