Priložnosti V Ms&t Na Oddelku Validacij V Biofarmacevtiki V Lendavi (d/ž/m)

Sandoz

Lendava, Slovenia
Experience in usp and/or dsp bioprocesses
Knowledge of cgmp and regulatory requirements
Ability to prepare validation documentation
Join a high-tech center for the production of biosimilar active substances in Lendava

Job Summary

  • Join a high-tech center for the production of biosimilar active substances in Lendava.
  • Contribute to the validation of biopharmaceutical production processes and ensure compliance with GMP standards.
  • Enjoy flexible working hours and unlimited opportunities for learning and development.

Matching Summary

Join a high-tech center for the production of biosimilar active substances in Lendava.

Skills & Requirements

Must-have

  • Experience in USP and/or DSP bioprocesses
  • Knowledge of cGMP and regulatory requirements
  • Ability to prepare validation documentation

Nice-to-have

  • Strong analytical and communication skills
  • Curiosity and focus on continuous improvement
  • Ability to work independently and manage priorities

Key Requirements

  • Degree in pharmacy or related fields
  • 4-6 years of experience in bioproduction or quality
  • Good knowledge of English and local language

Work Rights

Not specified

Tailored Resume

Cover Letter