Quality Validation Specialist - SGGK1

Job Title: Quality Validation Specialist (Contract)

Openings: 5 positions Duration: 6–8 months 

Location: Singapore

Industry: Life Sciences Manufacturing 

About the Role

We are hiring Quality Validation Specialists to support validation and compliance activities within the life sciences manufacturing sector. This contract role is critical to ensuring equipment, automation, and facility systems meet global regulatory standards.

Key Responsibilities

• Conduct validation quality review of lifecycle documents and protocols.
• Support Equipment & Utility Qualification (IQ/OQ/PQ).
• Review Automation Computer System Validation (CSV) protocols for MES, DeltaV, PLC, and related systems.
• Perform Facility Qualification reviews and ensure documentation accuracy.
• Ensure compliance with GMP, GxP, FDA, EMA, and other regulatory requirements.
• Collaborate with QA, Engineering, Automation, and Manufacturing teams to resolve validation gaps.
• Provide risk‑based recommendations to strengthen validation processes.

Qualifications & Experience

• Bachelor’s degree in Engineering, Life Sciences, or related discipline.
• 5+ years of validation/quality experience in pharma or medical devices.
• Strong knowledge of GMP/GxP compliance and validation lifecycle.
• Hands‑on experience with equipment, automation, and facility qualification.
• Familiarity with CSV documentation and risk‑based validation approaches.
• Excellent communication and documentation skills.