Senior C&Q/Validation Engineers-Gmp/Pharma

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 Senior CQV Engineers to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities:

• Participate in the CQV of process/FUE and cleaning validation.
• Must have execution experience.
• Using the process automation system for the commissioning and validation of process equipment.
• Interface with client personnel and with outside vendors when necessary while performing the above.
• The individual will manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.
• Protocol Development (IQ,OQ, PQ) / protocol review for process equipment/FUE and/or cleaning validation.

If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony ([email protected]).

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PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.