Analytical Validation Officer M/F

Il y a 2 mois


ChassesurRhône, Auvergne-Rhône-Alpes, France Novasep Temps plein
Job Description

At Axplora, we are seeking a highly skilled and motivated Analytical Validation Officer to join our team. As a key member of our Methods and Projects Division, you will be responsible for validating and/or transferring analytical methods and analyzing products under development in compliance with Good Manufacturing Practices (GMP) and safety rules.

Main Responsibilities:
  • Validate or transfer analytical methods:
    • Write validation and/or transfer protocols for raw materials, work in progress or finished products
    • Coordinate the execution of tests
    • Process the results and write the validation report
    • Ensure the management of deviations and analytical investigations
    • Check validation protocols and reports and/or analytical transfers
  • Apply the necessary Quality rules (GMP, etc.):
    • Participate in the training of analysts in the various analytical techniques
    • Carry out 1st level maintenance tasks for laboratory equipment
    • Participate in the implementation of improvements in the functioning of the laboratory (e.g. implementation of procedures)
    • Apply the quality documents and procedures in force
    • Write or correct analytical files. Self-verify its analytical data.
Qualifications:

You hold a Bac +5 in analytical chemistry, or BAC +3 with significant experience in a control laboratory in validation and/or analytical transfers. You ideally have solid knowledge of analytical chemistry with particular knowledge of chromatographic techniques (HPLC / UPLC / GC / GC-HS).

Involved, curious, and proactive, you have a spirit of synthesis that allows you to have a sense of priorities in your daily work in compliance with HSE and quality rules (BPF). You are autonomous, rigorous and have a sense of organization. With a team spirit, you demonstrate flexibility and adaptability.

This position is daytime. Technical English desired.



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