Process Transfer And Validation Expert

rezonbio

Duchnice, PL
On-site
Technology transfer activities
Process validation documentation
Gmp and ehs standards
Lead and support end-to-end Technology Transfer activities as a receiving or sending manufacturing site

Job Summary

  • Lead and support end-to-end Technology Transfer activities as a receiving or sending manufacturing site.
  • Prepare, review and oversee key Technology Transfer and process validation documentation (plans, protocols, reports, Master Batch Record inputs).
  • Lead interdisciplinary project teams (10–30 members), manage timelines and ensure compliance with Good Manufacturing Practice (GMP) and Environment, Health & Safety (EHS) standards.

Matching Summary

Lead and support end-to-end Technology Transfer activities as a receiving or sending manufacturing site.

Skills & Requirements

Must-have

  • Technology Transfer activities
  • Process validation documentation
  • GMP and EHS standards
  • cross-functional workstreams
  • recombinant proteins at production scale

Nice-to-have

  • continuous improvement
  • external client meetings
  • Health Authority inspections

Key Requirements

  • Minimum 5 years of experience
  • Higher education in biotechnology, pharmacy, or related fields
  • Strong knowledge of GMP, EMA/FDA guidelines
  • Excellent English skills

Work Rights

Not specified

Tailored Resume

Cover Letter