
Cqv Lead-pharma/gmp
2 weeks ago
PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.
With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for **CQV Lead **to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.
Key Attributes/Responsibilities:
- Leading the commissioning and validation of pharmaceutical process equipment.
- Using the process automation system for the commissioning and validation of process equipment.
- Protocol Development (IQ,OQ, PQ) / protocol review for process equipment.
- Interface with client personnel and with outside vendors when necessary while performing the above.
- Managing validation projects
- process equipment
- Individual will manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.
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