QC Validation Specialist

LEGATUS FORMWORKS PTE LTD

Singapore
Not specified
Gmp laboratory equipment qualification
Iq oq pq protocol execution
Hplc uv-vis spectrometer experience
The job posting is for a QC Validation Specialist at Legatus Formworks Pte Ltd in Singapore, focused on ensuring compliance with GMP and regulatory requirements in the pharmaceutical industry. The role involves qualification and validation activities for GMP laboratory equipment, requiring significant hands-on experience and strong analytical skills

Job Summary

  • The role is responsible for the full lifecycle of GMP laboratory equipment including qualification, requalification, and retirement.
  • Candidates must execute and support IQ, OQ, and PQ protocols while ensuring strict regulatory compliance.
  • The position requires hands-on experience with specific analytical instruments such as HPLC, TOC Analyzers, and Particle Counters.

Matching Summary

Match Score: 85

The job posting is for a QC Validation Specialist at Legatus Formworks Pte Ltd in Singapore, focused on ensuring compliance with GMP and regulatory requirements in the pharmaceutical industry. The role involves qualification and validation activities for GMP laboratory equipment, requiring significant hands-on experience and strong analytical skills.

Skills & Requirements

Must-have

  • GMP laboratory equipment qualification
  • IQ OQ PQ protocol execution
  • HPLC UV-Vis Spectrometer experience
  • Data integrity compliance knowledge
  • Equipment relocation and decommissioning

Nice-to-have

  • Strong analytical documentation skills
  • Effective communication abilities
  • Team commitment to quality standards

Key Requirements

  • Diploma or Bachelor's Degree in Engineering
  • Minimum 5 years GMP validation experience
  • Experience in pharmaceutical GMP environment

Work Rights

Not specified

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