Reporting to the Quality Control Department, you will be responsible for carrying out physico-chemical analyses of raw materials, work-in-progress products, finished products, and utilities (water, air), in order to guarantee their compliance with regulatory and pharmaceutical requirements (GMP, Pharmacopoeia, ISO).

Main responsibilities

• Perform physico-chemical analyses using validated methods (pH, titration, HPLC, GC, UV-Vis, Karl Fischer, etc.).


• Carry out purified water and environmental controls in accordance with GMP guidelines.


• Participate in the sampling and identification of raw materials.


• Prepare reagents, standard solutions, and ensure equipment calibration.


• Record and ensure the traceability of analytical results (LIMS, quality documentation).


• Apply GMP, report non-conformities, and contribute to OOS/OOT investigations and CAPAs.


• Participate in first-level equipment maintenance and compliance with HSE rules.


• Contribute to internal and external audits and the updating of SOPs.

• Education: Bachelor's degree +3 in chemistry, analytical chemistry, biochemistry, or equivalent.


• Experience: Minimum 3 years in a laboratory (pharmaceutical, cosmetic, or food industry).


• Knowledge: GMP, Pharmacopoeias (European, USP), analytical validation, metrology.


• Technical skills: Proficiency in analytical techniques (HPLC, GC, UV-Vis, IR, titration...).


• Languages: Fluent French


• Personal qualities: rigor, autonomy, organizational skills, team spirit, and integrity.