Ingénieur Qualification/validation H/f

LFB Biomanufacturing

Alès, France
Qualification and validation protocols
Periodic review and reporting
Change impact assessment
Draft protocols and reports according to procedures and ensure timely availability of compliant equipment

Job Summary

  • Draft protocols and reports according to procedures and ensure timely availability of compliant equipment.
  • Participate in the establishment of service procedures and contribute to the evaluation of change impact on validated/qualified processes.
  • Receive RTT days plus 3 additional days of leave, along with health benefits, life insurance, and meal vouchers.

Matching Summary

Draft protocols and reports according to procedures and ensure timely availability of compliant equipment.

Skills & Requirements

Must-have

  • Qualification and validation protocols
  • Periodic review and reporting
  • Change impact assessment
  • Non-conformity analysis
  • Risk analysis for activity
  • Bioproduction environment experience

Nice-to-have

  • Rigorous and organized
  • Synthesis spirit
  • Proactive improvement proposals

Key Requirements

  • Bac +5 technical engineering degree
  • Minimum 5 years in pharmaceutical industry
  • Professional English

Work Rights

Not specified

Tailored Resume

Cover Letter