Pharma Manufacturing Technician – GMP Operations

Eurofins USA PSS Insourcing Solutions

Groton (CT)

On-site

USD 23,000 - 32,000

Full time

7 days ago
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Benefits offered by this job

Medical, dental, vision benefits
Life and disability insurance
401(k) with company match
Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a hands-on Manufacturing Operator in Groton, CT. The role focuses on operating, troubleshooting, and supporting complex manufacturing equipment to produce patient-ready products.

Responsibilities include generating manufacturing documentation, setting up equipment, and maintaining a compliant, safe production environment with opportunities for continuous improvement.

Qualifications

  • High School Diploma or Associate's Degree.
  • Valid Driver's license required.
  • 2+ years of manufacturing experience in a regulated environment (GMP/ISO).
  • Physical requirements: standing, bending, climbing, reaching, and lifting up to 55 pounds.

Responsibilities

  • Generate, support, and execute manufacturing documentation (Batch records, Logbooks, Labels, Check sheets, Protocols, Change controls, QTS).
  • 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 operation and maintenance of equipment.
  • Generate, manage, and report operational performance data.
  • Identify and participate in continuous improvement initiatives to enhance processes.

Skills

Mechanical aptitude
Troubleshooting
Documentation

Education

High School Diploma or Associate's Degree

Job description

Eurofins USA PSS Insourcing Solutions is seeking a hands-on Manufacturing Operator in Groton, CT. The role focuses on operating, troubleshooting, and supporting complex manufacturing equipment to produce patient-ready products.

Responsibilities include generating manufacturing documentation, setting up equipment, and maintaining a compliant, safe production environment with opportunities for continuous improvement.

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