Analytical Validation Officer M/F
Il y a 2 mois
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.
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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