GMP Analytical Chemist - HPLC, Raman & FTIR Specialist

Eurofins PSS Insourcing Solutions; New London (CT); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Medical/dental/vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a scientist to support GMP release and stability testing of clinical supplies for drug substance and product. The role involves GLP/GMP documentation, analytical testing (HPLC/UPLC, Raman, FTIR), and method development within a fast-paced development setting.

Applicants should hold a Bachelor’s degree in science, with strong organizational and communication skills.

Qualifications

• Bachelor’s 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 (oral and written) and attention to detail.
• Ability to work independently and as part of a team, self-motivated and adaptable.
• Ability to learn new techniques, perform multiple tasks, keep accurate records, follow instructions.

Responsibilities

• Work in a GLP or GMP environment with proper documentation and safety practices.
• Support GMP release and stability testing of clinical supplies for drug substance and drug product across development.
• Analytical testing including compendial testing, disintegration, dissolution, HPLC/UPLC, SFC, 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 & analytical workflows

eLN

LIMS

data trending

communication (oral & written)

independent & team work

Education

Bachelor’s degree in science or related field

Tools

HPLC/UPLC

Raman

FTIR

Job description

Eurofins USA PSS Insourcing Solutions is seeking a scientist to support GMP release and stability testing of clinical supplies for drug substance and product. The role involves GLP/GMP documentation, analytical testing (HPLC/UPLC, Raman, FTIR), and method development within a fast-paced development setting.

Applicants should hold a Bachelor’s degree in science, with strong organizational and communication skills.