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 a QC Validation Engineer – CSV to join us on a permanent role to help us deliver various projects in the Life Sciences Industry. 

Key Attributes/Responsibilities 

• Develop and execute validation documents, including URS, IQs, OQs, PQs, QPs, QRs, audit trail reviews, and supplier ERES. 

• Create validation plans aligned with client strategic goals and ensure timely, compliant delivery. 

• Commission and validate new technologies and equipment; including HPLC, GC, etc 

• Experienced in CSV activities for Grade C equipment 

• Participate in investigations of deviations, conduct analyses, and assess changes. 

• Collaborate with multiple functions to organize, plan, and facilitate smooth qualification activities. 

• Lead change control management. 

We are currently looking for candidates in Singapore. 

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Sruthi Srikanth ([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/