Pharma Manufacturing Technician — GMP Operator

Eurofins; Groton (CT); On-site; USD 57,308,000 - 70,202,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions in Groton, CT is seeking a manufacturing technician to support pharmaceutical production. You will operate, troubleshoot, and maintain complex equipment while ensuring product quality and safety documentation.

You will generate and manage batch records, logbooks, labels, check sheets, protocols, change controls, and quality systems, contributing to continuous improvement efforts. Weekend or overtime may be required.

Qualifications

• 2+ years of manufacturing experience in a regulated environment such as GMP, ISO, etc.
• High School Diploma or Associate's Degree
• Valid Driver's license
• Authorized to work in the United States indefinitely without restriction or sponsorship
• Must be able to wear appropriate PPE when necessary

Responsibilities

• Generate, support, and execute manufacturing documentation (batch records, logbooks, labels, check sheets, protocols, change controls, quality tracking systems)
• Perform manufacturing activities to convert raw materials into intermediate products
• Process intermediate materials into final patient-ready product presentations
• Set up manufacturing equipment and ensure documentation is completed accurately
• Support operation and upkeep of a classified manufacturing environment
• Complete operator care tasks for manufacturing equipment
• Generate, manage, and report operational performance data
• Identify and participate in continuous improvement initiatives

Skills

Mechanical aptitude

Troubleshooting

Physical stamina

Education

High School Diploma or Associate's Degree

Job description

Eurofins USA PSS Insourcing Solutions in Groton, CT is seeking a manufacturing technician to support pharmaceutical production. You will operate, troubleshoot, and maintain complex equipment while ensuring product quality and safety documentation.

You will generate and manage batch records, logbooks, labels, check sheets, protocols, change controls, and quality systems, contributing to continuous improvement efforts. Weekend or overtime may be required.