cGMP API Manufacturing Technician — Hands-On Production

Eurofins; New London (CT); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, Dental & Vision

Life and Disability Insurance

401(k) with company match

Paid vacation & holidays

Job summary

Eurofins USA PSS Insourcing Solutions seeks a hands-on manufacturing professional to support cGMP production of clinical-scale APIs. You will operate equipment, execute batches, document activities, and drive continuous improvement in a fast-paced pharmaceutical environment.

Join a multidisciplinary team focused on quality, safety, and compliance, with opportunities to contribute across Quality, Process Chemistry, Tech Transfer, and Production teams.

Qualifications

• High School Diploma or GED required.
• 4+ years of experience in pharmaceutical, chemical, biotech, or related manufacturing environments.
• Experience working in a cGMP-regulated setting.
• Working knowledge of production control systems and manufacturing operations.
• Strong troubleshooting, problem-solving, and critical-thinking skills.
• Highly organized with strong attention to detail and the ability to manage multiple priorities.
• Ability to work independently while collaborating with cross-functional teams.
• Willingness to stand for long periods, wear PPE, and lift up to 50 lbs.
• Strong written and verbal communication skills.
• Proficiency in Word and Excel.
• Authorized to work in the United States without sponsorship.

Responsibilities

• Execute process instructions and batch records in a cGMP environment.
• Prepare, operate, monitor, sample, and clean manufacturing equipment.
• Support equipment commissioning, qualification, and troubleshooting activities.
• Complete manufacturing documentation including batch and cleaning records.
• Follow cGMP, safety, environmental, and site procedures.
• Report deviations, safety concerns, and quality observations promptly.
• Manage manufacturing waste according to approved procedures.
• Participate in shift handovers and maintain cross-team communication.
• Collaborate with Quality, Compliance, Process Chemistry, Tech Transfer, and Production teams.
• Support SOP reviews and continuous improvement initiatives.
• Manage priorities independently and assist less-experienced teammates.
• Complete required training and participate in site safety programs.
• Perform routine material handling, lifting up to 50 lbs.

Skills

4+ years experience

cGMP manufacturing

Troubleshooting

Detail-oriented

Independent work

Communication skills

PPE awareness

Microsoft Office

Lifting 50 lbs

Authorization to work in US

Education

High School Diploma or GED

Associate degree (Science/technical)

Tools

Delta V Production Control System

Job description

Eurofins USA PSS Insourcing Solutions seeks a hands-on manufacturing professional to support cGMP production of clinical-scale APIs. You will operate equipment, execute batches, document activities, and drive continuous improvement in a fast-paced pharmaceutical environment.

Join a multidisciplinary team focused on quality, safety, and compliance, with opportunities to contribute across Quality, Process Chemistry, Tech Transfer, and Production teams.