Manufacturing Technician - Pharmaceutical Operations

Eurofins•Groton, CT

4d•$20 - $25•Onsite

About The Position

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.

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)
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.
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.
Authorization to work in the United States indefinitely without sponsorship.

Nice To Haves

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.