Process Unit Operator

Novartis

İstanbul, Kurtköy, Turkey
Gmp compliance
Manufacturing process execution
Hse knowledge
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world

Job Summary

  • Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world.
  • The Documentation Specialist Admin manages the modification, editing, distribution, review and archiving of GMP manufacturing documents and the edition of the Batch records in order to deliver them to Production in the quality and within the deadlines.
  • Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

Matching Summary

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world.

Skills & Requirements

Must-have

  • GMP compliance
  • Manufacturing process execution
  • HSE knowledge
  • Production schedule adherence
  • Batch record documentation

Nice-to-have

  • Administrative task management
  • Technical complaint reporting
  • Time management for shop floor

Key Requirements

  • Operations management experience
  • General HSE knowledge
  • GMP knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter