GMP Analytical Chemist – Stability & Method Development

Eurofins PSS Insourcing Solutions; New London (CT); On-site; USD 85,000 - 105,000; Full time

Benefits offered by this job

Healthcare benefits

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins PSS Insourcing Solutions in Groton, CT is seeking a GMP‑documented analytical chemist to support drug substance and drug product stability testing, method development, and validation in a GLP/GMP environment.

The role requires experience with wet chemistry, HPLC, Raman, FTIR, and release testing, plus strong communication and meticulous record keeping; on‑site, Monday–Friday, with occasional overtime and weekend coverage as needed.

Qualifications

• Bachelors degree in science or related field or equivalent experience.
• Strong computer, scientific, and organizational skills.
• Experience with eLN, LIMS, and data trending is a plus.
• Excellent communication and attention to detail.
• Ability to work independently and as part of a team, self-motivated and adaptable.

Responsibilities

• Work in a GLP or GMP environment with documentation and safety practices.
• Support GMP release and stability testing of clinical supplies for drug substance and drug product across development.
• Perform analytical testing including compendial testing, disintegration, dissolution, HPLC/UPLC, SFC, solvent testing, and related methods.
• Set up and analyze drug substance and drug product stability samples.
• Develop and validate analytical methods for drug substances and products.

Skills

GMP environment

Wet chemistry

HPLC

Raman

FTIR

GLP

Analytical testing

eLN

LIMS

Data trending

Communication

Attention to detail

Education

Bachelors degree in science

Tools

eLN

LIMS

Data trending

Job description

Eurofins PSS Insourcing Solutions in Groton, CT is seeking a GMP‑documented analytical chemist to support drug substance and drug product stability testing, method development, and validation in a GLP/GMP environment.

The role requires experience with wet chemistry, HPLC, Raman, FTIR, and release testing, plus strong communication and meticulous record keeping; on‑site, Monday–Friday, with occasional overtime and weekend coverage as needed.