GMP Chemist
Posted 13 Oct 2026
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 1–3 yrs
- Management level
- Individual contributor
- Employment
- On-Site
- Contract
- Full-time
- Visa sponsorship
- Not offered
No salary listed for this role.
Field of studyAnalytical Chemistry, Biochemical Engineering, Biotechnology, Chemical Engineering (or related)
Study levelBachelor's or higher
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
Job Responsibilities and Requirements:
The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.).
Candidates should have familiarity with several of the below laboratory techniques; they should also possess expertise/knowledge with:
· Good Manufacutring Practices
· Quantitative polymerase chain reaction (qPCR)
· Enzyme linked Immunosorbent Assay (ELISA)
· Ultraviolet and visual light spectroscopy (UV-Vis)
· Analytical chromatographic separations using HPLCs or UPLCs
Qualifications
Authorization to work in the United States indefinitely without restriction or sponsorship
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Candidates within a commutable distance of Chesterfield, MO are encouraged to apply
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Electronic laboratory notebook systems and/or GMP documentation practice