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Manufacturing Technician - Pharmaceutical Operations

Eurofins Scientific Groton, United States
Full-time On-site work

Publication date: 15/09/2026

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Make a Difference Through Advanced Manufacturing

Are you mechanically inclined and passionate about solving technical challenges? Join a leading pharmaceutical manufacturing team where your hands-on skills will directly contribute to producing life-changing therapies for patients around the world. This role offers the opportunity to operate, troubleshoot, maintain, and optimize sophisticated manufacturing equipment in a highly regulated environment while building a rewarding career in the pharmaceutical industry.

OR

- Bachelor's Degree in a scientific or technical field.
- Demonstrated mechanical aptitude with the ability to troubleshoot, diagnose, and resolve equipment-related issues.
- Valid driver's license.

Ideal Candidate

You are a hands-on problem solver who enjoys working with complex equipment, values quality and precision, and thrives in a fast-paced manufacturing environment. Whether you're transitioning from industrial manufacturing, automotive maintenance, military technical experience, or another mechanically focused field, this is an opportunity to apply your skills in a growing pharmaceutical manufacturing career while making a meaningful impact on patients' lives.

Responsibilities

Operate, set up, and support advanced pharmaceutical manufacturing equipment and processes.; Execute manufacturing operations that transform raw materials into intermediate and final patient-ready products.; Generate, complete, and maintain GMP-compliant manufacturing documentation, including:; Batch records; Logbooks; Labels; Check sheets; Protocols; Change controls; Quality Tracking System (QTS) records; Ensure accurate and timely completion of all production documentation.; Perform equipment operation, routine maintenance, operator care, and basic troubleshooting activities.; Diagnose and resolve mechanical and operational issues to minimize downtime and maintain production efficiency.; Support the operation and housekeeping of classified manufacturing environments.; Collect, analyze, and report operational performance metrics.; Participate in continuous improvement initiatives that enhance safety, productivity, quality, and compliance.; Adhere to GMP, safety, quality, and regulatory requirements at all times.

Requirements

High School Diploma or Associate's Degree with 2+ years of manufacturing experience in a regulated environment (GMP, ISO, medical device, pharmaceutical, biotechnology, food manufacturing, or similar); Ability to stand, bend, reach, climb, and lift up to 55 pounds as needed.; Ability to wear required personal protective equipment (PPE), including safety glasses, respirators, protective suits, and facility uniforms.

Benefits

Work with cutting-edge pharmaceutical manufacturing technology.; Develop valuable technical and troubleshooting expertise.; Gain experience in a highly regulated, quality-focused environment.; Contribute to products that positively impact patient health and well-being.; Build a long-term career with opportunities for advancement and professional growth.
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