Pharma Manufacturing Technician - Hands-on Ops & Impact

Eurofins; Groton (CT); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions is seeking a manufacturing operator in Groton, CT to join a clean room environment. You will execute batch records, SOP-based tasks, and report operational data while turning raw materials into patient-ready products.

The role requires 1–3 years in pharmaceutical manufacturing or a regulated GMP/ISO setting, strong documentation skills, and the ability to wear PPE as required. Overtime and weekends may be needed based on business needs.

Qualifications

• Hands-on mechanical aptitude with ability to translate into manufacturing tasks.
• Experience with documentation and record-keeping in a controlled environment.
• Familiarity with quality systems and GMP/ISO context preferred.

Responsibilities

• Execute documentation for manufacturing operations: batch records, log books, protocols, change control, QTS, etc.
• Operate in a clean room environment using SOPs and operating instructions.
• Carry out bulk product manufacturing to convert raw materials into intermediate and patient-ready products.
• Set up, operate, break down, and clean complex equipment; verify documentation.
• Perform activities in a cGMP clean room setting and report performance data.
• Identify and lead continuous improvement projects.

Skills

Mechanical aptitude

Team communication

Computer literacy

Math skills

Organizational skills

Education

High school diploma/Associate/Bachelor in sciences

Tools

Quality systems

Operating Instructions

AI in manufacturing

Job description

Eurofins USA PSS Insourcing Solutions is seeking a manufacturing operator in Groton, CT to join a clean room environment. You will execute batch records, SOP-based tasks, and report operational data while turning raw materials into patient-ready products.

The role requires 1–3 years in pharmaceutical manufacturing or a regulated GMP/ISO setting, strong documentation skills, and the ability to wear PPE as required. Overtime and weekends may be needed based on business needs.