API Manufacturing Technician

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

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Job Description

Join a multi-disciplinary team supporting the cGMP production of clinical-scale Active Pharmaceutical Ingredients (APIs). In this hands-on manufacturing role, you'll support API development through equipment operation, batch execution, documentation, and continuous improvement activities.

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Job Description

Join a multi-disciplinary team supporting the cGMP production of clinical-scale Active Pharmaceutical Ingredients (APIs). In this hands-on manufacturing role, you'll support API development through equipment operation, batch execution, documentation, and continuous improvement activities.

Typical Process Operations Include

• Charging solids and liquids to vessels


• Distillation, extraction, and phase separation


• Crystallization, filtration, and drying


• Equipment cleaning and preparation

Key Responsibilities

• Execute process instructions and batch records in a cGMP environment.


• Prepare, operate, monitor, sample, and clean pharmaceutical manufacturing equipment.


• Support equipment commissioning, qualification, and troubleshooting activities.


• Complete manufacturing documentation, including batch records, cleaning records, and in-process sampling documentation.


• Follow cGMP, safety, environmental, and site procedures at all times.


• Report deviations, safety concerns, and quality observations promptly.


• Manage manufacturing waste according to approved procedures.


• Participate in shift handovers and maintain clear communication across teams.


• 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 team members as needed.


• Complete required training and participate in site safety programs.


• Perform routine material handling activities, including lifting and moving items up to 50 lbs.

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 effectively within cross-functional teams.


• Comfortable working in a manufacturing environment, including standing for extended periods, wearing required PPE, handling hazardous materials, and lifting up to 50 lbs.


• Strong written and verbal communication skills.


• Proficiency in Microsoft Office applications, including Word and Excel.


• Authorization to work in the United States without current or future sponsorship requirements.

Preferred Qualifications

• Associate degree (Science or technical discipline)


• Strong mechanical aptitude and desire to execute hands on manual labor


• Experience with Delta V Production Control System


• Experience in a Pharmaceutical cGMP manufacturing environment


• Experience performing large scale distillations / Filtrations / milling

Additional Information

• After the initial training period of approximately 3 months which will be Monday- Friday from 8am-5pm, team members move to swing shift, which alternates between 1st shift and 2nd shift:
  
  
  
  • 1st Shift is Mon-Fri, 6:00 am to 2 pm
  
  
  • 2nd Shift is Mon – Thurs, 2 pm to 12 pm
  
  
  
  


• May be requested to work on weekends, overtime, and holidays based on business needs.


• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options


• Life and disability insurance


• 401(k) with company match


• Paid vacation and holidays


• LinkedIn:

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.