GMP Analytical Chemist

10h10 hours ago

Eurofins

Groton, US · Full-time · $72,000 – $95,000

About this role

Eurofins Scientific operates a global network of laboratories delivering analytical testing services to pharmaceutical clients. The GMP Analytical Chemist role supports release and stability testing of drug substances and drug products across all development phases.

Daily work centers on compendial testing, HPLC/UPLC, dissolution, and compound-specific methods in a regulated GMP setting. Analysts also perform stability sample setup and manage documentation aligned with safety and quality standards.

The position sits within a decentralized network of 900 laboratories where teams handle excipient, packaging, and post-packaging support. Collaboration occurs with discovery pharmacology, forensics, and clinical study groups on complex analytical projects.

Team members develop and validate new analytical methods while maintaining accurate records in eLN and LIMS systems. The environment rewards independent problem-solving and precise execution of validated procedures.

Requirements

Bachelor’s degree in science or other related degree concentration, or equivalent directly related experience.
Experience with GMP, wet chemistry, HPLC, Raman, FTIR required.
Strong computer, scientific, and organizational skills.
Experience with eLN, LIMS, and data trending is a plus.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Experience in a GMP laboratory, analytical chemistry preferred.

Responsibilities

Work in a GLP or GMP environment with appropriate documentation and safety practices.
Utilize analytical methodologies to support GMP release and stability testing of clinical supplies for drug substance and drug product.
Perform compendial testing, disintegration, dissolution, HPLC/UPLC, SFC, and generic testing including solvents, water, ash, titrations, heavy metals, ICP/MS, and UV.
Set up and analyze drug substance and drug product stability samples.
Conduct method development and validation of analytical methods for drug substance and drug product.