Manufacturing Technician - Pharmaceutical Operations

Eurofins USA PSS Insourcing Solutions•Groton, CT

About The Position

Eurofins PSS is seeking a Manufacturing Technician to support pharmaceutical manufacturing operations in a highly regulated environment. The role operates, sets up, troubleshoots, maintains, and optimizes manufacturing equipment and processes that transform raw materials into intermediate and final patient-ready products. The technician completes and maintains GMP-compliant production documentation, supports classified manufacturing environments, tracks operational performance, and participates in continuous improvement. The position is full-time, Monday through Friday, 8:00 a.m. to 5:00 p.m., with overtime as needed and possible weekend or holiday work based on business needs. Candidates must be authorized to work indefinitely in the United States without sponsorship; the employer will not provide sponsorship.

Requirements

High school diploma or associate's degree and at least 2 years of manufacturing experience in a regulated environment such as GMP, ISO, medical device, pharmaceutical, biotechnology, or food manufacturing; alternatively, a bachelor's degree in a scientific or technical field.
Mechanical aptitude, including the ability to troubleshoot, diagnose, and resolve equipment-related issues.
Valid driver's license.
Ability to stand, bend, reach, climb, and lift up to 55 pounds as needed.
Ability to wear required personal protective equipment, including safety glasses, respirators, protective suits, and facility uniforms.
Authorization to work indefinitely in the United States without sponsorship.

Nice To Haves

Experience in industrial manufacturing, automotive maintenance, military technical work, or another mechanically focused field.

Responsibilities

Operate, set up, and support 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 batch records, logbooks, labels, check sheets, protocols, change controls, and Quality Tracking System (QTS) records.
Complete production documentation accurately and on time.
Perform equipment operation, routine maintenance, operator care, and basic troubleshooting.
Diagnose and resolve mechanical and operational issues to minimize downtime and maintain production efficiency.
Support operation and housekeeping of classified manufacturing environments.
Collect, analyze, and report operational performance metrics.
Participate in continuous improvement initiatives to enhance safety, productivity, quality, and compliance.
Adhere to GMP, safety, quality, and regulatory requirements.