GMP Analytical Chemist at Eurofins

Andover, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Sep, 26

Salary

26.0

Posted On

03 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Compliance, Analytical Testing, Pharmaceutical Analysis, Instrumentation Calibration, Data Integrity, SOP Adherence, Troubleshooting, Microsoft Office, Data Analysis Software, Quality Control

Industry

Medical and Diagnostic Laboratories

Description

Company Description 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! Job Description 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. Key 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. Qualifications 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 Additional Information What to Expect in the Hiring Process: 10-15 Minute Phone Interview with Region Recruiter 45-60 Minute Virtual Interview with Manager and/or Group Leader 45-60 Meeting In-Person. on-site to meet with the Team The position is on-site, full-time, first shift, Monday through Friday. Candidates must be flexible to adapt to schedule changes that may require shift changes and/or weekend work, and overtime may be required as needed. Candidates living within a commutable distance of Andover, MA, are encouraged to apply. Excellent full-time benefits including: Comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Hourly rate is between $23.00-$26.00, depending on education and experience Ready to join our team? Apply today! Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. Compensation: USD 23.00 - USD 26.00 - hourly

Responsibilities

Perform routine analytical testing on pharmaceutical samples using validated methods and ensure strict compliance with GMP standards. Maintain laboratory instrumentation and accurately document all work to ensure data integrity.