GMP Analytical Chemist
About The Position
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! We are seeking a detail-oriented GMP Analyst Chemist to join our Quality Control (QC) laboratory team. In this role, you will perform routine analytical testing on pharmaceutical samples, ensure compliance with GMP standards, and support laboratory operations through accurate documentation and instrumentation maintenance. This is an excellent opportunity for early-career scientists looking to grow within a regulated laboratory environment.
Requirements
- Bachelor’s degree in chemistry or other science related degree concentration
- 0-2 years of QC analytical experience
- Excellent skills for attention to detail and following procedures to generate reproducible data in a controlled laboratory environment
- Excellent skills in Microsoft Office, data analysis software, and other related applications
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
- Ability to think critically and demonstrate troubleshooting/problem solving skills
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
- 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 (e.g., pH, osmolality, assay/concentration, break-loose and extrusion 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 and organization.
- Identify and troubleshoot basic analytical or instrumentation issues as needed.
- Collaborate effectively with peers, supervisors, and cross-functional teams in a GMP environment.
Benefits
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
