Process CQV Engineer - Biopharma

PES is an international services companyproviding 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 ison consistently delivering high quality outcomes for our multinational clients.

This focus and our people's experience in deliveringconsistent quality results for our clients over the past 20 years have been keyto our success to date.

We are currently looking for a Process CommissioningEngineer to join us on a permanent basis to help us deliver variousprojects in the Life Sciences Industry.
Key Responsibilities:

1. Execute commissioning activities for upstream, downstream, utilities, and process equipment systems.
2. Review P&IDs, process flow diagrams, design specifications, and vendor documentation.
3. Lead system walkdowns, punch listing, and mechanical completion verification.
4. Coordinate SAT, IOQ support, loop checks, functional testing, and start-up activities.
5. Work closely with QA, Validation, Engineering, EHS, and Operations teams to ensure GMP compliance.
6. Support troubleshooting, deviation resolution, and handover to operations.

If you'd like to find out about this opportunity or anyother opportunity, please forward your CV to Sruthi Srikanth ([Confidential Information]).

If you would like to find out about the latest Jobs andProjects we are involved in then do follow us on LinkedIn:https://www.linkedin.com/company/processengineeringspecialists/mycompany/

PES International operates as an equal opportunityemployer. No terminology in this advert is intended to discriminate on thegrounds of age, race, religion, sexual orientation or any other factors with nobearing to employment skills and we confirm that we are happy to acceptapplications from persons of any background for this role.