QA Validation Engineer- CQV/CSV-Pharma/BioPharma

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.

We are currently looking for a QA Validation Engineer to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

• Provide Quality Assurance oversight of Commissioning, Qualification and Validation (CQV) activities to ensure compliance with GMP, regulatory requirements, and site quality standards.
• Review and approve validation lifecycle documentation, including risk assessments, protocols, reports, deviations, and change controls.
• Ensure CQV documentation is technically sound, complete, and compliant with Good Document...