Manufacturing Technician - Pharmaceutical Operations

Eurofins; New London (CT); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions seeks a hands-on Manufacturing Technician to operate, troubleshoot, and maintain advanced pharmaceutical equipment in a highly regulated setting. You will generate GMP-compliant documentation and support continuous improvement while ensuring safety and quality.

The role is based in Groton, CT, with a typical Monday–Friday schedule and possible overtime. Ideal candidates have a technical background, mechanical aptitude, and strong documentation skills, plus a

Qualifications

• 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)
• 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.

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 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.

Skills

Mechanical aptitude

Troubleshooting

GMP documentation

Education

High School Diploma or equivalent

Bachelor's Degree in scientific/technical field

Job description

Company Description

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.

Job Description

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.

Qualifications

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-pace 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.

Additional Information

• 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:
• Authorization to work in the United States indefinitely without sponsorship.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.