Analytical Chemist I

Eurofins•Lancaster, PA

10h•Onsite

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. Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labeling 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. 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. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Requirements

Authorization to work in the United States indefinitely without restriction or sponsorship
Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration
2 years of related pharmaceutical experience in a cGMP environment
HPLC and validation experience

Nice To Haves

Strong computer, scientific, and organizational skills
Experience working with protein chromatography
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Responsibilities

Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
Execute specialized analyses and method transfer and feasibility testing
Document work as required for GMP compliance
Perform tests accurately
Troubleshoot method and instrumentation problems
Use office and instrumentation specific computer software
Produce written reports (e.g., SOP, OMC, client reports)
Develop and execute validation plans
Carry out method transfers and feasibility studies
Train technical staff