Alternance En Chimie Analytique - Support Analytique H/f
med-in.at
Igoville, France
Development and validation of analytical methods
Hplc, uplc, gc techniques
Quality rules (bpf, fda)
You will contribute actively to projects aimed at ensuring the reliability, robustness, and performance of analytical methods used for quality control of raw materials and finished products
Job Summary
You will contribute actively to projects aimed at ensuring the reliability, robustness, and performance of analytical methods used for quality control of raw materials and finished products.
You will participate in the development and optimization of new analytical methods (physico-chemistry, HPLC, UPLC, GC...) and contribute to method validation, including writing protocols and reports.
We encourage you to invent for life and offer the opportunity to develop within one of the world's leading pharmaceutical companies.
Matching Summary
You will contribute actively to projects aimed at ensuring the reliability, robustness, and performance of analytical methods used for quality control of raw materials and finished products.
Skills & Requirements
Must-have
Development and validation of analytical methods
HPLC, UPLC, GC techniques
Quality rules (BPF, FDA)
Scientific rigor and analytical mindset
Technical document writing
Nice-to-have
Interfunctional knowledge development
Multinational environment
Diversity, equity, and inclusion culture
Proactivity and autonomy
Key Requirements
Master's or Engineering School in Analytical Chemistry
Ability to write and understand technical documents in English