Pharma Manufacturing Operator: Process & Equipment Expert

Eurofins; New London (CT); On-site; USD 42,000 - 66,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins USA PSS Insourcing Solutions is seeking an on-site Manufacturing Operator to support documentation, batch records, and the conversion of raw materials into patient-ready products. You will operate and troubleshoot manufacturing equipment while maintaining strict GMP/ISO-compliant records.

The role emphasizes hands-on mechanical aptitude, ability to work within a classified environment, and contribution to continuous improvement initiatives that impact patient outcomes.

Qualifications

• Must have 2+ years of manufacturing experience in a regulated environment such as GMP, ISO, etc.
• OR; Bachelor's degree in relevant scientific field
• Valid Driver's license required
• Physical requirements: standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required
• Must be able to wear appropriate PPE when necessary
• Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

• Generate, support, and execute manufacturing documentation, including batch records and logbooks.
• Process materials into intermediate products and final patient-ready presentations.
• Set up manufacturing equipment with accurate documentation.
• Maintain a classified manufacturing environment and perform operator care tasks.
• Generate, manage, and report operational performance data.
• Identify and participate in continuous improvement initiatives to enhance processes.

Skills

Mechanical aptitude

Problem-solving

Electrical troubleshooting

Education

High School Diploma or Associate's Degree

Bachelor's degree in relevant scientific field

Tools

Manufacturing equipment operation

Job description

Eurofins USA PSS Insourcing Solutions is seeking an on-site Manufacturing Operator to support documentation, batch records, and the conversion of raw materials into patient-ready products. You will operate and troubleshoot manufacturing equipment while maintaining strict GMP/ISO-compliant records.

The role emphasizes hands-on mechanical aptitude, ability to work within a classified environment, and contribution to continuous improvement initiatives that impact patient outcomes.