GMP Laboratory Analyst

Eurofins•Groton, CT

7d•$25 - $31

About The Position

Eurofins Scientific is seeking a detail-oriented and motivated GMP Laboratory Analyst to support analytical and microbiological testing and laboratory operations in a GMP environment. The role includes water testing for manufacturing facilities, GMP release and stability testing of clinical supplies, and analytical support for drug substances and drug products throughout development. Testing may involve compendial and compound-specific methods, as well as excipient, packaging, and post-packaging support. The analyst will also set up and analyze stability samples and develop and validate analytical methods for drug substances and drug products. The position is Monday through Friday, 8:00 a.m. to 5:00 p.m., with overtime as needed. Weekend and holiday work may be requested based on business needs. Candidates within commuting distance of Groton, Connecticut, are encouraged to apply.

Requirements

Bachelor’s degree in science or a related degree concentration, or equivalent directly related experience.
Strong computer, scientific, and organizational skills.
Experience with electronic laboratory notebooks (eLN), LIMS, and data trending.
Excellent oral and written communication skills and attention to detail.
Ability to work independently and as part of a team; self-motivated, adaptable, and positive.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Authorization to work in the United States indefinitely without restriction or sponsorship.

Nice To Haves

Experience in a GMP laboratory, microbiology, and analytical chemistry.
Experience with eLN, LIMS, and data trending.
Experience with GMP, microbiological testing, wet chemistry, HPLC, Raman, and FTIR.

Responsibilities

Perform total viable count testing, including filtration and pour plate, as well as appearance, coliform, and chlorine testing for manufacturing facility water.
Perform analytical testing to support GMP release and stability testing of clinical supplies for drug substance and drug product throughout development.
Conduct compendial testing, including excipient and packaging release testing, disintegration, dissolution, HPLC/UPLC, SFC, and generic testing such as solvents, water, ash, titrations, heavy metals, ICP/MS, and UV.
Perform compound-specific analytical methods.
Set up and analyze drug substance and drug product stability samples.
Develop and validate analytical methods for drug substances and drug products.
Maintain appropriate documentation and follow safety practices in a GLP or GMP environment.