Manufacturing Technician - Pharmaceutical Operations

Eurofins Scientific

Groton, CTOn-siteFull time
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Location
Groton, CT
Work style
On-site
Job type
Full time
Posted
Oct 4
15 days ago
Career path

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About the company

Eurofins Scientific

Biotechnology · 10,001+ employees

Eurofins Scientific on LinkedIn

What you'll do

  • Operate and support pharmaceutical manufacturing equipment and processes, maintain GMP-compliant production documentation, and perform routine maintenance and troubleshooting.
  • Support classified manufacturing environments, report performance metrics, and participate in continuous improvement.

What you need

  • Requires a high school diploma or associate degree plus 2+ years of regulated-environment manufacturing experience, or a bachelor's degree in a scientific or technical field.
  • Also requires mechanical aptitude, a valid driver's license, and ability to lift up to 55 pounds and wear required PPE.
  • Education: a high school diploma, an associate degree or a bachelor's degree

Key skills

mechanical aptitudetroubleshootdiagnoseresolve equipment-related issuesValid driver's license

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Perks

  • medical coverage
  • dental
  • vision
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation
  • holidays

See full description on company page, apply now

Read the full posting here
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. Key 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. Required 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) 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. Physical Requirements 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. 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. Why Join Us? 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. Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. May be requested to work on weekends, overtime, and holidays based on business needs. 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 LinkedIn: #LI-EB1 Authorization to work in the United States indefinitely without sponsorship. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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