Quality Assurance Officer

Merck & Co., Inc.

Wellington, New Zealand
Competitive remuneration + benefits; not specified...
Not specified
Bachelor's degree in science-based discipline
Knowledge of good manufacturing practices gmp
Experience with qa systems and glp requirements
Merck & Co., Inc. is seeking a Quality Assurance Officer for a one-year fixed-term role in Wellington, New Zealand. The position involves ensuring batch documentation compliance and supporting quality assurance systems in a pharmaceutical manufacturing environment

Job Summary

  • The Quality Assurance Officer ensures batch documentation is prepared, reviewed, and released on schedule to meet production and testing schedules.
  • This role offers opportunities for practical development and varied tasks to broaden experience within a collaborative team of like-minded professionals.
  • The position requires maintaining effective document control and ensuring compliance with regulatory and corporate standards in a dynamic environment.

Matching Summary

Match Score: 85

Merck & Co., Inc. is seeking a Quality Assurance Officer for a one-year fixed-term role in Wellington, New Zealand. The position involves ensuring batch documentation compliance and supporting quality assurance systems in a pharmaceutical manufacturing environment.

Salary

Competitive remuneration and benefits; Not specified; Not specified

Skills & Requirements

Must-have

  • Bachelor's degree in science-based discipline
  • Knowledge of Good Manufacturing Practices GMP
  • Experience with QA systems and GLP requirements
  • Batch record review and document control skills
  • SAP transaction experience for batch documentation

Nice-to-have

  • Prior pharmaceutical industry Quality Operations experience
  • Demonstrated leadership and stakeholder alignment skills
  • Collaborative problem-solving in complex teams
  • Continuous improvement initiative participation
  • Strong written and verbal communication abilities

Key Requirements

  • Bachelor's degree or higher in science
  • Prior experience in GMP/GLP manufacturing environment
  • Valid work authorization for New Zealand

Work Rights

Not specified

Tailored Resume

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