Full Description

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 Senior QA Validation Engineer to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities

• At least 8 years experience in CQV/QA Validation Engineering
• Act as QA representative for DeltaV automation and CSV activities
• Review and approve URS, FRS, SDS, Risk Assessments, and Validation Plans
• QA review/approval of IQ, OQ, PQ protocols and reports
• Ensure data integrity (ALCOA+) and Part 11 compliance for DeltaV systems
• Oversight of automation change controls, deviations, and CAPAs
• Participate in FAT/SAT, testing, and discrepancy resolution
• Support regulatory inspections and audits (FDA, EMA, MHRA, etc.)
• Interface with Automation, CQV, IT, and Quality teamsust have experience in CQV in a pharmaceutical project

If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony (careers@pes-international.com).

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

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.