SonicJobs Logo
Left arrow iconBack to search

API Manufacturing Technician

Eurofins
Posted a day ago, valid for 24 days
Location

Groton, CT, US

Salary

$18 - $30 per hour

Contract type

Full Time

Life Insurance
Disability Insurance

By applying, a Eurofins account will be created for you. Eurofins's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • Eurofins PSS is seeking a candidate to join their multi-disciplinary team in the production of clinical-scale Active Pharmaceutical Ingredients (APIs).
  • The role requires a minimum of 4 years of experience in pharmaceutical, chemical, biotech, or related manufacturing environments, with a focus on cGMP regulations.
  • Candidates must have a High School Diploma or GED, strong troubleshooting skills, and the ability to work independently while collaborating with cross-functional teams.
  • The position offers a salary range of USD 18.00 to USD 30.00 per hour, along with excellent full-time benefits including medical coverage and a 401(k) plan.
  • After an initial training period, team members will work on a swing shift schedule, alternating between first and second shifts.

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: #LI-EB1

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

  • Compensation: USD 18.00 - USD 30.00 - hourly



  • Learn more about this Employer on their Career Site

    Apply now in a few quick clicks

    By applying, a Eurofins account will be created for you. Eurofins's Privacy Policy and Terms & Conditions will apply.

    SonicJobs' Terms & Conditions and Privacy Policy also apply.