Technicien Développement Analytique Et Stabilité (h/f)

Thermo Fisher Scientific UK

Bourgoin-Jallieu, France
Good manufacturing practices gmp adherence
Alcoa plus data integrity principles
Hplc dissolution and kf analytical techniques
The role involves verifying product conformity for clinical trial lots and participating in stability programs

Job Summary

  • The role involves verifying product conformity for clinical trial lots and participating in stability programs.
  • Candidates must strictly adhere to Good Manufacturing Practices and maintain high standards of data integrity using ALCOA plus principles.
  • The position requires managing laboratory resources including reagents, columns, and reference substances while operating HPLC equipment.

Matching Summary

The role involves verifying product conformity for clinical trial lots and participating in stability programs.

Skills & Requirements

Must-have

  • Good Manufacturing Practices GMP adherence
  • ALCOA plus data integrity principles
  • HPLC dissolution and KF analytical techniques

Nice-to-have

  • Team collaboration and mutual support
  • Flexibility with variable shift schedules
  • Experience in method transfer validation

Key Requirements

  • Bac + 2/3 degree in Analytical Chemistry
  • Minimum 2 years experience in pharmaceutical QC
  • Knowledge of pharmacopoeia and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter