About the Position

We are seeking an experienced QC Validation Specialist for a 6-month project in a pharmaceutical manufacturing facility in Tuas, Singapore.

Responsibilities

Equipment Lifecycle Management: Execute end-to-end qualification (IQ/OQ/PQ), requalification, relocation, and decommissioning/retirement protocols for a wide range of QC laboratory analytical and micro equipment.
Hands-on Validation: Lead validation activities for systems including, but not limited to: HPLC, CE, UV-Vis Spectrometers, TOC Analyzers, Microplate Readers, Liquid Particle Counters, Analytical Balances, Incubators, and Particle Counters.
Documentation & Compliance: Author, review, and execute validation master plans, protocols, deviations, and final summary reports in strict accordance with Good Manufacturing Practices (GMP).
Cross-functional Coordination: Collaborate closely with QC Lab Analysts, Quality Assurance, and external vendors to minimize lab downtime during relocation and equipment retirement.
Data Integrity & Archiving: Ensure instrument software, audit trails, and historical data are securely backed up and compliant with data integrity standards prior to equipment decommissioning.

Education: Minimum of a Diploma or Bachelor’s Degree in any Engineering field, Science, or a related technical discipline.
Experience: Minimum of 5 years of hands-on experience in the qualification, requalification, relocation, or decommissioning of GMP laboratory equipment within the pharmaceutical or biopharmaceutical industry.
Technical Expertise: Demonstrated, deep familiarity with analytical and laboratory instrumentation (e.g., Chromatography systems, spectrometers, counters, and controlled temperature units).
Regulatory Compliance: Robust understanding of GMP regulations, data integrity principles, and data lifecycle management.

Salary: Up to SGD 9,500 / month (Base) + SGD 250 Monthly Transport Allowance
Contract Period: July – December 2026
Location: Tuas, Singapore

We are a leading-edge pharmaceutical manufacturing facility in Tuas, committed to ensuring absolute compliance with strict global GMP regulations.

Please click on the 'apply' button to apply online. For more information, please reach out to Wai Ling Tai. (EA: 94C3609 / R1110392)