Technical Writer (6 months contract)

NO DEVIATION PTE. LTD.

Singapore
Not specified
Cqv lifecycle documentation authoring
Iq oq pq protocol development
Gmp regulatory compliance knowledge
No Deviation Pte. Ltd. is seeking a Technical Writer for a 6-month contract in Singapore to support the development and management of CQV lifecycle documentation in the pharmaceutical sector. The role requires a candidate with strong compliance awareness and experience in authoring validation protocols within a regulated industry

Job Summary

  • The Technical Writer is responsible for developing and managing commissioning, qualification, and validation documentation within a regulated pharmaceutical environment.
  • This role requires ensuring all documentation aligns with GMP requirements, Annex 15, and site-specific quality systems to support audit readiness.
  • Candidates will collaborate with Engineering, QA, and Automation teams to maintain document integrity and meet project timelines.

Matching Summary

Match Score: 85

No Deviation Pte. Ltd. is seeking a Technical Writer for a 6-month contract in Singapore to support the development and management of CQV lifecycle documentation in the pharmaceutical sector. The role requires a candidate with strong compliance awareness and experience in authoring validation protocols within a regulated industry.

Skills & Requirements

Must-have

  • CQV lifecycle documentation authoring
  • IQ OQ PQ protocol development
  • GMP regulatory compliance knowledge
  • Document version control and traceability
  • Cross-functional team collaboration

Nice-to-have

  • Experience with Veeva or TrackWise systems
  • Risk assessment and RTM methodologies
  • Annex 15 and ASTM E2500 familiarity
  • Cleanroom system qualification experience

Key Requirements

  • 3-5 years CQV documentation experience
  • Degree or Diploma in Engineering or Life Sciences
  • Proven experience authoring IQ/OQ/PQ protocols

Work Rights

Not specified

Tailored Resume

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