Technicien Support Qualité Production H/f - Cdd

LFB Biomanufacturing

Lille, France
Treatment of deviations
Impact assessment documentation
Action plan development
You will be responsible for treating less complex production deviations, coordinating root cause investigations, and documenting impact assessments

Job Summary

  • You will be responsible for treating less complex production deviations, coordinating root cause investigations, and documenting impact assessments.
  • Key tasks include developing action plans to prevent recurrence, monitoring their progress, and implementing preventive and corrective actions in collaboration with workshop RSA.
  • The role offers benefits such as transport cost participation, group advantages (mutual insurance, provident fund, works council, savings plan), and preferential rates for sports subscriptions.

Matching Summary

You will be responsible for treating less complex production deviations, coordinating root cause investigations, and documenting impact assessments.

Skills & Requirements

Must-have

  • treatment of deviations
  • impact assessment documentation
  • action plan development
  • preventive and corrective actions
  • manufacturing best practices

Nice-to-have

  • scientific background
  • team player
  • proactive problem solver

Key Requirements

  • BAC+2 scientific degree
  • pharmaceutical industry experience
  • good manufacturing practices knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter