Commissioning, Qualification & Validation (CQV) Engineer
12 months contract
About the Company:
Our client is a US healthcare and a leading global biopharmaceutical company. They have a revenue of US $40.1 billion, with more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission.
Job descriptions:
- Perform Commissioning, Qualification, Validation team activities with a direct regard for Safety.
- Generate Commissioning & Qualification (C&Q) Procedures for projects.
- Review/qualify lab equipment – Isolator experience is advantageous.
- Writes, review and revise a variety of Installation, Operation and Performance qualification/verification related documents, including any of all of the following: SOPs, validation/verification master plans, guidelines and execution plans
- Facilitate scoping / planning of commissioning spares and consumables.
- Deliver the C&Q activities as required to meet the schedule
- Track progress of C&Q activities as required.
- Execution of Design reviews, shakedown, commissioning, Factory Acceptance Test (FAT's), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) activities.
- Coordinate with project contractors and equipment vendors to execute required tests.
- Allocate project resources for efficient execution of project deliverables.
- Coordinate support during C&Q execution
Job Requirements:
- Min 6 years of Computer System validation, qualification, and commissioning experience
- Experience with validation of equipment controlled by PLCs, BAS/BMS systems, DeltaV, and other typical automated system platforms preferred.
- Experience in the pharmaceutical industry
Reg No: R22104540
EA License no: 94C3609
