Validation Engineer

NO DEVIATION PTE. LTD.

Singapore
Dq iq oq pq validation documentation
Gmp regulated environment experience
Temperature mapping and calibration
The role supports validation lifecycle activities across direct, indirect, and no-impact systems within a regulated pharmaceutical environment

Job Summary

  • The role supports validation lifecycle activities across direct, indirect, and no-impact systems within a regulated pharmaceutical environment.
  • Candidates will generate, review, and approve validation documentation such as DQ, IQ, OQ, and PQ while ensuring GMP compliance.
  • The company offers generous leave policies, comprehensive health coverage, and opportunities for professional development in an inclusive culture.

Matching Summary

Match Score: 85

The role supports validation lifecycle activities across direct, indirect, and no-impact systems within a regulated pharmaceutical environment.

Skills & Requirements

Must-have

  • DQ IQ OQ PQ validation documentation
  • GMP regulated environment experience
  • Temperature mapping and calibration
  • Periodic requalification protocol execution
  • Cross-functional stakeholder coordination

Nice-to-have

  • Strong attention to detail
  • Excellent communication skills
  • Ability to manage multiple tasks
  • Audit readiness support
  • Collaborative team culture

Key Requirements

  • Diploma or Degree in Engineering, Life Sciences, Pharmacy, or related field
  • Experience in validation or qualification within GMP-regulated environments
  • Familiarity with temperature mapping and equipment qualification processes

Work Rights

Not specified

Tailored Resume

Cover Letter