GMP Analytical Chemist

10h10 hours ago

Eurofins

Andover, US · Full-time · $46,000 – $52,000

About this role

Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries. We are seeking a detail-oriented GMP Analytical Chemist to join our Quality Control laboratory team. The role centers on routine analytical testing of pharmaceutical samples under GMP standards.

Daily work includes performing compendial and validated methods such as pH, osmolality, assay, and force measurements. You will prepare standards and reagents according to SOPs while operating and maintaining laboratory instrumentation. Accurate documentation supports data integrity and regulatory compliance at every step.

The position sits within a regulated QC laboratory environment that values attention to detail and adherence to established procedures. You will collaborate with peers and supervisors to execute testing and resolve basic instrumentation issues as they arise.

Eurofins emphasizes professional growth by enabling early-career scientists to enter the biopharmaceutical industry and advance from the bottom up. Supportive teams and tools are available while maintaining work-life balance.

Requirements

Bachelor’s degree in chemistry or other science related degree concentration
0-2 years of QC analytical experience
Excellent attention to detail and ability to follow procedures to generate reproducible data in a controlled laboratory environment
Proficiency in Microsoft Office, data analysis software, and related applications
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, and comply with company policies
Critical thinking and troubleshooting skills for analytical or instrumentation issues
Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

Perform routine testing of pharmaceutical samples using compendial and validated analytical methods such as pH, osmolality, assay, and break-loose force.
Prepare standards, reagents, and samples for analysis in accordance with SOPs.
Operate, maintain, and assist with calibration of laboratory instrumentation.
Accurately document all work to ensure compliance with GMP and data integrity requirements.
Execute testing following established procedures with strong attention to detail.
Identify and troubleshoot basic analytical or instrumentation issues as needed.
Collaborate effectively with peers, supervisors, and cross-functional teams in a GMP environment.

Benefits

Professional growth opportunities to enter and advance within the biopharmaceutical industry
Supportive teams and tools for skill development
Work-life balance