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As an associate scientist, you will be part of a driven team within pharmaceutical development. You will provide critical analytical support for innovative synthetic therapeutics from early clinical phases up to registration. In this dynamic role, you will contribute directly to the purity and identity of reference standards for GMP testing. You will find ample space to grow, strengthen your analytical skills, and make a tangible impact on the health of patients worldwide.
Job Responsibility
Perform precise analyses for the characterization of reference standards, focusing heavily on liquid chromatography, ion chromatography, and gas chromatography
Develop fit-for-purpose analytical methods that meet strict reporting thresholds for accurate purity determination
Support product and process characterization, method validation, and stability studies using advanced LC techniques
Ensure full compliance with relevant regulatory guidelines, specifications, GMP standards, and safety regulations
Scientifically evaluate and interpret generated analytical results to guarantee the highest quality standards
Requirements
You hold a master's degree in chemistry, pharmaceutical sciences, biochemistry (or a related scientific field), or a bachelor's degree with relevant experience
You demonstrate strong theoretical knowledge and hands-on expertise in liquid chromatography, IC, and/or GC
You are familiar with chromatography data systems such as Empower or OpenLab
You maintain high quality standards for your work, take accountability for your results, and adapt quickly to changing priorities
You work well independently and thrive as a positive, collaborative team player
You are proficient in English, both spoken and written