Pharmaceutical Manufacturing Technician

Eurofins; New London (CT); On-site; USD 52,000 - 82,000; Full time

Benefits offered by this job

Health benefits

Dental and vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins PSS is hiring for a full‑time pharmaceutical manufacturing role in a controlled clean room environment. You will execute batch records, SOPs, and quality documentation while operating complex equipment and ensuring GMP compliance.

You will participate in process improvements, data reporting, and cross‑functional collaboration to deliver patient‑ready products. Strong mechanical and communication skills are essential.

Qualifications

• Strong mechanical aptitude and hands‑on technical skills in pharma manufacturing.
• Ability to communicate effectively within a multi‑functional manufacturing team.
• Experience with quality systems and documentation in regulated environments.
• Experience using AI to enhance manufacturing operations is a plus.

Responsibilities

• Execute documentation for manufacturing operations: Paper and Electronic Batch Records, Log Books, Protocols, Change control, QTS, etc.
• Operate manufacturing equipment in a controlled clean room; set up, break down, and cleaning; manage documentation.
• Complete complex bulk product manufacturing activities to convert raw materials into intermediate and patient ready products
• Generate, manage and report operational performance data
• Identify, own and lead continuous improvement projects

Skills

Mechanical aptitude

Communication within multi‑functional팀

AI in manufacturing

Computer literacy

Basic math

Organizational skills

Education

Science degree (HS/AS/BSc)

Tools

Quality systems

Operating Instructions

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

• 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

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.

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:
• 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.