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Urgent! Pharma Lab Validation Engineer Job Opening In Singapore, Singapore – Now Hiring PROCESS ENGINEERING SPECIALISTS PTE. LTD.

Pharma Lab Validation Engineer



Job description

Roles & Responsibilities

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 Computer System Validation (CSV) engineer to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities:

  • Minimum 2 years of experience in CSV within a GxP-regulated industry (pharmaceutical, biotech, or medical devices).

  • Lead and execute CSV activities for Lab Equipment ensuring compliance with regulatory and company requirements.

  • Develop and maintain validation documentation, including User Requirement Specifications (URS), Validation Plans (VP), Risk Assessments, IQ/OQ/PQ protocols, and Validation Summary Reports (VSR).

  • Perform system impact assessments and risk evaluations to determine validation requirements.

  • Ensure 21 CFR Part 11 and Data Integrity (DI) compliance for laboratory systems.

  • Participate in software/system lifecycle activities, including system design, testing, implementation, and periodic reviews.

  • Investigate and resolve validation deviations, issues, and non-conformances related to laboratory equipment.

If you'd like to find out about this opportunity, please forward your CV to Sruthi Srikanth ( ).

If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn:

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.

Tell employers what skills you have
cGMP Manufacturing
Construction Management
cGMP
GMP environment
cGMP Practices
GMP
FDA GMP
GAMP
IGMP
Protocol
System Design
Computer System Validation
Compliance
Project Management
Medical Devices
Life Sciences
c-GMP
Commissioning


Required Skill Profession

Other General



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