Entry-Level Chemist — HPLC/GC, GLP/GMP Training

Eurofins USA BioPharma Services; Columbia Township (MO); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Columbia, MO is seeking an Entry-Level Chemist to join the Trace Analytical Structural Chemistry (TASC) team. This role offers hands-on laboratory experience in a regulated environment, supporting research and development studies, following SOPs and quality standards.

You will perform testing, operate and maintain analytical instrumentation, and document work in compliance with cGMP/GLP guidelines while collaborating with teammates to meet project timelines and

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or a related scientific discipline.
• Authorization to work in the United States indefinitely without sponsorship.
• Hands-on experience with HPLC and/or GC is preferred.
• Experience with GLP, GMP, or LIMS is a plus.

Responsibilities

• Perform laboratory testing and analysis following SOPs, protocols, and study requirements
• Generate accurate and reliable experimental data
• Operate and maintain analytical instrumentation
• Document work in accordance with cGMP and/or GLP guidelines
• Assist with research and development projects
• Analyze and interpret scientific data
• Work both independently and collaboratively to meet project timelines

Skills

HPLC

GC

Lab experience

Organizational skills

Communication skills

GLP/GMP/LIMS

Education

Bachelor's degree in Chemistry/related field

Job description

Eurofins USA BioPharma Services in Columbia, MO is seeking an Entry-Level Chemist to join the Trace Analytical Structural Chemistry (TASC) team. This role offers hands-on laboratory experience in a regulated environment, supporting research and development studies, following SOPs and quality standards.

You will perform testing, operate and maintain analytical instrumentation, and document work in compliance with cGMP/GLP guidelines while collaborating with teammates to meet project timelines and