Junior Analytical Chemist: GMP Lab & Method Development

Eurofins PSS Insourcing Solutions; New London (CT); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a qualified chemist to support drug substance and drug product development by applying analytical methods across all phases. You will prepare, analyze samples, and perform method qualification, validation, and transfer activities in a GMP environment.

Your role will involve degradation and stability studies, data analysis, and maintaining documentation in electronic lab systems, with a focus on quality, safety, and client service.

Qualifications

• Bachelor's degree in chemistry, biochemistry, or related field or equivalent experience.
• Strong GMP knowledge and ability to follow written procedures accurately.
• Experience with analytical chemistry techniques and data documentation.
• Proficient chromatographic techniques including HPLC/UPLC and related methods.
• Ability to analyze data, maintain accurate records, and work in a GMP environment.
• Excellent communication and teamwork skills.

Responsibilities

• Support drug substance and drug product development using analytical methods across all phases.
• Prepare, set up, and analyze samples using chromatography, spectroscopy, dissolution, and related techniques.
• Assist method development, qualification, validation, and transfer activities.
• Conduct degradation, stability, and investigational studies to support product decisions.
• Maintain documentation and data integrity within electronic laboratory systems.
• Operate, calibrate, and troubleshoot analytical instrumentation under guidance.

Skills

Analytical chemistry

GMP knowledge

Data analysis

Documentation

Chromatography

HPLC/UPLC

Teamwork

Education

Bachelor's degree in chemistry/biochemistry

Tools

ELN

Job description

Eurofins USA PSS Insourcing Solutions is seeking a qualified chemist to support drug substance and drug product development by applying analytical methods across all phases. You will prepare, analyze samples, and perform method qualification, validation, and transfer activities in a GMP environment.

Your role will involve degradation and stability studies, data analysis, and maintaining documentation in electronic lab systems, with a focus on quality, safety, and client service.