QC Systems Validation Specialist - Pharma/ Contract

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD; Singapore; On-site; SGD 54,000 - 89,000; Part time

Job summary

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD in Tuas is seeking a QC Systems Validation Specialist for a 6 months contract. You will validate QC equipment and ensure GxP compliance, focusing on critical instruments such as environmental monitoring air samplers and particle counters.

The role requires hands-on IQ/OQ testing, documentation of deviations, and collaboration with QC to maintain data integrity and regulatory standards in a pharmaceutical setting.

Qualifications

• Bachelor’s or Master’s degree in Pharmacy/Pharmaceutical Sciences or related field with 5–7 years in QC.
• Experience in method validation/verification in pharmaceutical or biotech industries.
• Strong knowledge of GLP, GDP and data integrity requirements.
• Start‑up experience is a plus.

Responsibilities

• Support the implementation and maintenance of QC GxP Systems in compliance with company standards and regulatory guidance, including IQ/OQ testing and exception reporting.
• Write and/or execute IQ and OQ protocols for QC Laboratory Computerized systems/equipment and document deviations.
• Author Qualification Summary Report for QC Equipment.
• Draft QC Systems SOPs and configuration specifications as required.
• Partner with QC to conduct data integrity risk assessment.

Skills

IQ/OQ testing

GxP compliance

Data integrity

Documentation practice

Education

Bachelor's or Master’s in Life Sciences

Job description

QC Systems Validation Specialist - Pharma/ Contract

6 Months Contract
Location: Tuas
Up to $8,000 depending on experience
Industry: Pharmaceutical

Job Summary

Expertise in equipment validation, with a focus on qualifying critical QC instruments such as environmental monitoring air samplers and particle counters

Responsibilities

• Support the implementation and maintenance of QC GxP Systems in compliance with company's Standards and Regulatory guidance, which includes:
• Write and/ or execute IQ and OQ test protocols for QC Laboratory Computerized systems/ electronic equipment, including writing of exception reports.
• Author Qualification Summary Report for QC Equipment.
• Author QC Systems associated procedures such as administrative SOPs and configuration specifications, as required.
• Partner with QC to conduct data integrity risk assessment.

Requirements

• Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing.
• Experience in method validation/ verification in the pharmaceutical or biotechnology industry
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in start-ups will be ideal