Pharma Manufacturing Operator — GMP & Process Improvement

Eurofins Group; Groton (CT); Hybrid; USD 52,000 - 68,000; Full time

Benefits offered by this job

Medical coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins Scientific is hiring for a manufacturing-oriented role at the Groton site. The position involves documenting manufacturing steps, converting raw materials into intermediate products, and final patient-ready outputs, with strict adherence to PPE and safety protocols.

The role requires hands-on operation of manufacturing equipment, ability to lift up to 55 pounds, and strong attention to detail within a collaborative team environment.

Qualifications

• High school diploma is required or equivalent.
• Must hold a valid driver’s license.
• Pharmaceutical manufacturing experience is a plus.

Responsibilities

• Generate, assist and execute documentation for manufacture and related records.
• Complete complex bulk product manufacturing activities to convert raw materials into intermediate product.
• Process intermediate bulk into final patient-ready presentation.
• Set up complex manufacturing equipment and manage accompanying documentation.
• Operate and maintain a classified manufacturing space per protocol.
• Perform operator care tasks for maintenance of equipment.
• Generate, manage and report operational performance data.
• Identify and lead continuous improvement projects.

Skills

Communication skills

Computer skills

Teamwork

Education

High school diploma

Job 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

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.movertime 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, CTare 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.

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