Process Unit Operator

Novartis UK

İstanbul, Turkey
Gmp guidelines compliance
Safety guidelines compliance
Environmental guidelines compliance
Execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of product with the quality and quantity in compliance with the relevant GMP, safety and environmental guidelines

Job Summary

  • Execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of product with the quality and quantity in compliance with the relevant GMP, safety and environmental guidelines.
  • 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.
  • 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.

Matching Summary

Execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of product with the quality and quantity in compliance with the relevant GMP, safety and environmental guidelines.

Skills & Requirements

Must-have

  • GMP guidelines compliance
  • Safety guidelines compliance
  • Environmental guidelines compliance
  • Manufacturing tasks execution
  • Production schedule adherence

Nice-to-have

  • Reimagine medicine mission
  • Valued and trusted medicines company vision
  • Inclusive work environment commitment

Key Requirements

  • Operations Management and Execution experience
  • General HSE Knowledge
  • GMP Knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter