Biochemistry Scientist — LC/Chromatography & GMP Analysis

LabRulez; Portage (MI); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins USA BioPharma Services in Portage, Michigan, is seeking an Analytical Chemist to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products.

You will operate chromatography systems, prepare samples, set up and validate new analytical processes, and maintain GMP-compliant documentation. Full-time with comprehensive benefits and standard daytime hours.

Qualifications

• Bachelor's degree in chemistry, biology, biochemistry, or related degree concentration.
• Authorization to work in the United States indefinitely without restriction or sponsorship.
• Strong attention to detail and safe, compliant work habits.
• Familiarity with Biochemistry techniques, electrophoresis, chromatography, and aseptic technique.

Responsibilities

• Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products.
• Run the instrumentation independently including chromatographic systems.
• Prepare samples for analysis and run instrumentation with minimal supervision.
• Set up and validate new analytical or related processes used by the department.
• Prepare standards and samples for analysis.
• Execute method transfer protocols.
• Document work as required for GMP compliance.
• Perform monthly maintenance of laboratory equipment.

Skills

Analytical thinking

Instrumentation operation

Documentation

Communication skills

Attention to detail

Safety awareness

Multitasking

Biochemistry familiarity

Education

BSc in Chemistry / related

Tools

Chromatography systems

Analytical instruments

Job description

Eurofins USA BioPharma Services in Portage, Michigan, is seeking an Analytical Chemist to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products.

You will operate chromatography systems, prepare samples, set up and validate new analytical processes, and maintain GMP-compliant documentation. Full-time with comprehensive benefits and standard daytime hours.