GMP Stability Scientist - HPLC/GC Specialist

Eurofins BioPharma Product Testing North America; Columbia Township (MO); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins BPT-Columbia in Columbia, Missouri, is seeking a Stability Scientist to join our Stability and Batch Release team. This role focuses on analytical testing to support product stability studies and GMP-compliant batch release activities.

You will work with HPLC and GC methods, document data meticulously, and collaborate with colleagues to meet study timelines while growing your expertise in pharmaceutical analytics.

Qualifications

• Experience in GMP/GLP laboratory environment.
• Hands-on analytical chemistry with HPLC/GC.
• Familiarity with LIMS and meticulous documentation.
• Strong attention to detail, organization and time management.
• Excellent communication and willingness to grow in pharmaceutical analytics.
• Authorized to work in the United States without sponsorship.

Responsibilities

• Perform analytical testing to support stability studies and batch release.
• Operate and maintain HPLC, GC, and other analytical systems.
• Prepare samples, reagents, standards, and documentation per SOPs.
• Collect, review, and document data following GMP/GLP requirements.
• Support study execution, data review, troubleshooting, and report generation.
• Maintain lab safety, quality standards, and organized workspace.
• Collaborate with team members to meet project timelines and client expectations.
• Work with increasing independence on assignments while seeking guidance as needed.

Skills

GMP/GLP environment

HPLC

GC

LIMS

Documentation

Attention to detail

Time management

Communication

Tools

HPLC

GC

LIMS

Job description

Eurofins BPT-Columbia in Columbia, Missouri, is seeking a Stability Scientist to join our Stability and Batch Release team. This role focuses on analytical testing to support product stability studies and GMP-compliant batch release activities.

You will work with HPLC and GC methods, document data meticulously, and collaborate with colleagues to meet study timelines while growing your expertise in pharmaceutical analytics.