GMP Analytical Chemist: HPLC, Stability & Release

Eurofins

New London (CT)

On-site

USD 65,000 - 90,000

Full time

11 days ago

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Benefits offered by this job

Medical + dental + vision
Life and disability insurance
401(k) with company match
Paid vacation and holidays
U.S. work authorization

Job summary

Eurofins in Groton, CT is hiring a team member to support GMP release and stability testing of clinical supplies for drug substances and products. The role involves analytical testing across multiple methods including HPLC/UPLC, dissolution, disintegration, UV, and SFC, within a GMP/GLP framework.

You will develop and validate analytical methods, analyze stability samples, and work both independently and as part of a collaborative team, with opportunities for training and growth within a global

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.

Responsibilities

  • Support GMP release and stability testing of clinical supplies for drug substance and drug product.
  • Perform analytical testing including disintegration, dissolution, HPLC/UPLC, SFC, UV, and related methods.
  • Set up and analyze drug substance and drug product stability samples.
  • Method development and validation of analytical methods for drug substance and drug product.

Skills

GMP experience
HPLC
Raman
FTIR
ELN
LIMS
Data trending

Education

Bachelor's degree in science

Tools

LIMS
ELN

Job description

Eurofins in Groton, CT is hiring a team member to support GMP release and stability testing of clinical supplies for drug substances and products. The role involves analytical testing across multiple methods including HPLC/UPLC, dissolution, disintegration, UV, and SFC, within a GMP/GLP framework.

You will develop and validate analytical methods, analyze stability samples, and work both independently and as part of a collaborative team, with opportunities for training and growth within a global

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