GMP Biotech Chemist — qPCR, ELISA & HPLC
Eurofins
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Benefits offered by this job
Job summary
Eurofins Scientific is seeking a biotherapeutic process development analyst to support large molecule analytical work. The role involves applying qPCR, ELISA, UV-Vis spectroscopy, and HPLC/UPLC techniques to drive method development and data generation in a GMP environment.
The candidate should have 1-3 years of GMP industrial experience and hold a Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, or Chemical Engineering, located within commuting
Qualifications
- Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or related fields.
- 1-3 years of relevant GMP industrial experience.
- Experience with Plate-based assays, qPCR and HPLC is required.
- Electronic laboratory notebook systems and GMP documentation practice.
- Commutable distance to Chesterfield, MO.
Responsibilities
- Provide analytical support to biotherapeutic process development teams focusing on large molecules.
- Utilize qPCR, ELISA, UV-Vis spectroscopy, and chromatographic methods (HPLC/UPLC) to generate high-quality analytical data.
Skills
Education
Tools
Job description
Eurofins Scientific is seeking a biotherapeutic process development analyst to support large molecule analytical work. The role involves applying qPCR, ELISA, UV-Vis spectroscopy, and HPLC/UPLC techniques to drive method development and data generation in a GMP environment.
The candidate should have 1-3 years of GMP industrial experience and hold a Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, or Chemical Engineering, located within commuting
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