Analytical Scientist - HPLC
About The Position
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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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. 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Develop, qualify and validate analytical test methods for drug product, intermediates and excipients Design and execute analytical development studies Write analytical method validation protocols and reports Write and maintain applicable SOPs Provide analytical support to QC, Process Engineering and Manufacturing as applicable Perform externally generated data review Assist in development stability study design and protocol writing Assist management during regulatory inspections and internal audits
Requirements
- Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration
- Authorization to work in the United States indefinitely without restriction or sponsorship
Nice To Haves
- Experience with variety of analytical techniques, method development and validation
- Hands-on experience in HPLC, GC, LCMS, and GCMS is a plus
- Ensure adherence to highest quality and efficiency standards in laboratory operations
- Excellent communication (oral and written) and attention to detail
- Capability to work well on a team and be able to troubleshoot and problem solve in cross functional team setting
- Independently engage and collaborate with coworkers, customers, and management
- 1-5 years of contract laboratory/research or relevant industry experience is a plus
Responsibilities
- Develop, qualify and validate analytical test methods for drug product, intermediates and excipients
- Design and execute analytical development studies
- Write analytical method validation protocols and reports
- Write and maintain applicable SOPs
- Provide analytical support to QC, Process Engineering and Manufacturing as applicable
- Perform externally generated data review
- Assist in development stability study design and protocol writing
- Assist management during regulatory inspections and internal audits
Benefits
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
