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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