Are you looking for a flying start in pharma? Become an associate scientist with a world leader in therapeutic innovation and develop your expertise in liquid chromatography!
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jobdetails
overzicht
- strombeek-bever, vlaams-brabant
- vast
- voltijds
gepubliceerd op 29 mei 2026
- referentienummer
- JN -052026-577516
volgende stappen
randstad professional
je bent een krak in finance, life sciences, hr, sales & marketing, engineering, healthcare of office & administration support. en je wil uitblinken in een van deze domeinen? da's helemaal oké. jij kiest hoe je je loopbaan invult.
jobdetails
Job Description
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.
Are you looking for a flying start in pharma? Become an associate scientist with a world leader in therapeutic innovation and develop your expertise in liquid chromatography!
Job Description
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.
belangrijkste verantwoordelijkheden
- 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.
vaardigheden
GXPClinical Trial ProtocolDocumentopmaakOperationele Ondersteuningkwalificatie
- 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.
opleiding
Bachelor