Additionalinformation

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: #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.

Companydescription

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.

Jobdescription

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-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.