
Validation Engineer- Facility/Utility/Process Equipment-Pharma
4 days ago
Validation Engineer - Facility/Utility/Process Equipment - Pharma
Direct message the job poster from Process Engineering Specialists
Overview
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 the US, our core focus is on delivering high-quality outcomes for multinational clients. Our people’s experience in delivering quality results over the past 20 years has been key to our success.
We are currently looking for
Validation Engineers
to join us on a permanent role to help deliver various projects in the Life Sciences Industry.
Responsibilities
Leading the commissioning, qualification and validation of pharmaceutical facilities, utilities and process equipment.
Using the process automation system for the commissioning and validation of process equipment.
Protocol development (IQ, OQ, PQ) and protocol review for process equipment.
Interface with client personnel and outside vendors as necessary while performing the above.
Manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and needs.
Qualifications
4-7 years of validation/CQV experience.
Location
Singapore
How to apply
If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Nelson Anthony ( ).
About PES and equal opportunity
PES International operates as an equal opportunity employer. We do not discriminate on age, race, religion, sexual orientation or any other factors with regard to employment skills and we welcome applications from persons of any background for this role.
Employment details
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Quality Assurance and Engineering
Industries: Pharmaceutical Manufacturing
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