Pharma QC Systems Validation Specialist (6-Month Contract)

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD

Singapore

On-site

SGD 54,000 - 89,000

Part time

14 days+
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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

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.

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