Eurofins

Global lab testing and analytics network

GMP Analytical Chemist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeGroton, CT, USA$22.25 - $27.25 /hr

About the Job

Requirements

Ability to work in a Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP) environment while following appropriate documentation and safety practices.
Experience with GMP, wet chemistry, high-performance liquid chromatography (HPLC), Raman spectroscopy, and Fourier-transform infrared spectroscopy (FTIR) is required.
A bachelor's degree in science or another related degree concentration, or equivalent directly related experience, is required.
Strong computer, scientific, and organizational skills are required.
Experience with electronic laboratory notebooks (eLN), laboratory information management systems (LIMS), and data trending is a plus.
Excellent oral and written communication and attention to detail are required.
Ability to work independently and as part of a team, be self-motivated and adaptable, and maintain a positive attitude is required.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies is required.
Ability to work Monday through Friday, 8 a.m. to 5 p.m., with overtime as needed, is required.
Candidates may be requested to work weekends, overtime, and holidays based on business needs.
Authorization to work in the United States indefinitely without restriction or sponsorship is required.

Responsibilities

Use analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product throughout all phases of development, including excipient, packaging, and post-packaging support.
Perform analytical testing, including compendial testing for excipients and packaging release, disintegration, dissolution, HPLC/UPLC, supercritical fluid chromatography (SFC), generic testing such as solvents, water, ash, titrations, heavy metals, inductively coupled plasma mass spectrometry (ICP-MS), and ultraviolet (UV) testing, as well as compound-specific methods.
Set up and analyze drug substance and drug product stability samples.
Develop and validate analytical methods for drug substance and drug product.

Desired Qualifications

Experience in a GMP laboratory and analytical chemistry is preferred.
Experience with electronic laboratory notebooks (eLN), laboratory information management systems (LIMS), and data trending is preferred.

Job Description

Ability to work in a GLP or GMP environment with appropriate documentation and safety practices.
Experience with GMP, wet chemistry, HPLC, Raman, FTIR are required
Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post-packaging support.
Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV), and compound-specific methods.
Set up and analysis of drug substance and drug product stability samples.
Method development and validation of analytical methods for drug substance and drug product

Qualifications

Bachelor’s degree in science or other related degree concentration, or equivalent directly related experience.
Strong computer, scientific, and organizational skills.
Experience with eLN, LIMS, and data trending is a plus.
Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivated, adaptable, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

Preferred Qualifications:

Experience in a GMP laboratory, analytical chemistry preferred.
Experience with eLN, LIMS, and data trending.

Additional Information

Position is Monday-Friday, 8-5. Overtime as needed
May be requested to work on weekends, overtime, and holidays based on business needs
Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
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
Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Compensation: 22.25 to 27.25 (USD) (HOURLY)

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

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