Eurofins

Global lab testing and analytics network

Pharmaceutical Manufacturing Technician

Machine & Process OperationConfirmed live in the last 24 hours

Full-timeGroton, CT, USA$18 - $30 /hr

About the Job

Requirements

A high school diploma, Associate's degree, or Bachelor's degree in the sciences.
A valid driver's license.
One to three years of pharmaceutical manufacturing experience, which may be substituted with experience in a regulated environment such as Good Manufacturing Practice or International Organization for Standardization environments.
Experience with quality systems.
Experience completing complex manufacturing operational documents.
Experience using artificial intelligence to enhance manufacturing operations.
Experience using Operating Instructions to perform manufacturing tasks.
Ability to stand, bend, climb, reach, and lift up to 55 pounds.
Ability to wear required personal protective equipment, including a daily uniform, gloves, safety glasses, respirators, and full protective suits.
Strong computer, scientific, basic math, and organizational skills.
Ability to communicate effectively within a multifunctional manufacturing team.
Authorization to work indefinitely in the United States without restriction or sponsorship.

Responsibilities

Execute documentation associated with manufacturing operations, including Paper and Electronic Batch Records, Log Books, Protocols, Change Control, and Quality Tracking System records.
Use Standard Operating Procedures and Operating Instructions to manufacture drug products in a controlled clean-room environment.
Complete complex bulk-product manufacturing activities that convert incoming raw materials into intermediate and patient-ready products.
Set up, operate, break down, and clean complex manufacturing equipment, and manage and check the generated documentation.
Complete activities associated with current Good Manufacturing Practice operations in a clean-room manufacturing space.
Generate, manage, and report operational-performance data.
Identify, own, and lead continuous-improvement projects.

Job Description

This role is a great fit for candidates with strong mechanical aptitude who are looking to translate their hands-on technical skills into a rewarding career in pharmaceutical manufacturing. You'll have opportunities to operate, troubleshoot, and support complex manufacturing equipment while contributing to the production of products that make a meaningful impact on patients' lives.

Execute documentation associated with manufacturing operations: Paper and Electronic Batch Records, Log Books, Protocols, Change control, QTS, etc.
Utilize SOPs and Operating Instructions to manufacture drug product in a controlled clean room environment.
Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate and patient ready products
Set up, operation, break down, and cleaning of complex manufacturing equipment, manage and check documentation generated.
Complete activities associated with cGMP operations in a clean room manufacturing space
Generate, manage and report operational performance associated data
Identify, own and lead continuous improvement based projects

Qualifications

High school diploma, Associate's, or Bachelor degree in the sciences
Must hold a valid driver’s license
1-3 years of Pharmaceutical manufacturing experience; may be substituted with experience in a regulated environment such as GMP, ISO, etc.
Experience with quality systems
Experience completing complex manufacturing operational documents
Experience utilizing AI to enhance manufacturing operations
Experience with utilizing Operating Instructions to perform manufacturing tasks
Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required.
Must be able to wear appropriate PPE (daily uniform, gloves, safety glasses, respirators, and full protective suits)
Strong computer, scientific, basic math, and organizational skills
Ability to communicate effectively within a multi-functional manufacturing team

Additional Information

Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed
May be requested to work on weekends, overtime, and holidays based on business needs.
Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
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 restriction or sponsorship

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

Compensation: 18 to 30 (USD) (HOURLY)

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

Recently Posted Jobs

Explore more opportunities at Eurofins

See more jobs