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.
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.
- ✓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
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.