Pharma Manufacturing Technician – Clean Room, Growth

Eurofins; New London (CT); On-site; USD 52,000 - 82,000; Full time

Benefits offered by this job

Health benefits

Dental and vision coverage

401(k) with company match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins PSS is hiring for a full‑time pharmaceutical manufacturing role in a controlled clean room environment. You will execute batch records, SOPs, and quality documentation while operating complex equipment and ensuring GMP compliance.

You will participate in process improvements, data reporting, and cross‑functional collaboration to deliver patient‑ready products. Strong mechanical and communication skills are essential.

Qualifications

• Strong mechanical aptitude and hands‑on technical skills in pharma manufacturing.
• Ability to communicate effectively within a multi‑functional manufacturing team.
• Experience with quality systems and documentation in regulated environments.
• Experience using AI to enhance manufacturing operations is a plus.

Responsibilities

• Execute documentation for manufacturing operations: Paper and Electronic Batch Records, Log Books, Protocols, Change control, QTS, etc.
• Operate manufacturing equipment in a controlled clean room; set up, break down, and cleaning; manage documentation.
• Complete complex bulk product manufacturing activities to convert raw materials into intermediate and patient ready products
• Generate, manage and report operational performance data
• Identify, own and lead continuous improvement projects

Skills

Mechanical aptitude

Communication within multi‑functional팀

AI in manufacturing

Computer literacy

Basic math

Organizational skills

Education

Science degree (HS/AS/BSc)

Tools

Quality systems

Operating Instructions

Job description

Eurofins PSS is hiring for a full‑time pharmaceutical manufacturing role in a controlled clean room environment. You will execute batch records, SOPs, and quality documentation while operating complex equipment and ensuring GMP compliance.

You will participate in process improvements, data reporting, and cross‑functional collaboration to deliver patient‑ready products. Strong mechanical and communication skills are essential.