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 Quality Control Specialist- GLIMS Implementation to join us on a long term project to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities:

• Review and approve LIMS test scripts (IQ/OQ/PQ) for completeness, accuracy, and compliance
• Ensure test scripts meet GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity requirements
• Verify traceability between URS, risk assessments, and test scripts (RTM)
• Identify gaps, deviations, and non-compliance in validation documentation and testing
• Ensure testing follows approved validation plans and SOPs
• Support resolution and re-review of test deviations and change impacts
• Provide validation approval support for system release and audit readiness
• Collaborate with QA, IT, vendors, and validation teams during review cycles

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

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.