Validation Engineer- Facility/Utility/Process Equipment-Pharma

4 days ago


Singapore Pes International Full time

Overview
Validation Engineer- Facility/Utility/Process Equipment-Pharma
Consulting Manager at PES-Providing PMC/Client Side Rep Solutions to the Life Sciences and Mission Critical industry. PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, we focus on delivering high-quality outcomes for multinational clients.
We are currently looking for
Validation Engineers
to join us on a permanent role to help deliver various projects in the Life Sciences Industry. This role is based in Singapore.
Responsibilities
Lead the commissioning, Qualification and Validation of pharmaceutical facilities, utilities and process equipment.
Use the process automation system for the commissioning and validation of process equipment.
Develop (IQ/OQ/PQ) protocols and review protocols for process equipment.
Interface with client personnel and outside vendors as needed while performing the above.
Manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and needed support.
Qualifications
4-7 years of validation/CQV experience.
Experience in validation activities related to facilities, utilities and process equipment in pharma environments.
Details
Employment type: Full-time
Seniority level: Mid-Senior level
Industries: Pharmaceutical Manufacturing
PES International operates as an equal opportunity employer.
No discrimination based on age, race, religion, sexual orientation or any other factor with no bearing to employment skills. We welcome applications from persons of any background for this role.
If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Nelson Anthony ( ).
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