Additionalinformation

Additional Information

• Position is full-time, schedule is 2nd Shift, Monday - Friday | 2:00 PM - 10:30 PM.

• Base pay is between $22.50-23.50/hr

• LinkedIn: #LI-EB1

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

Companydescription

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.

Jobdescription

Job Description

As part of our Quality Control support team, you’ll play an important role in keeping our lab operations running smoothly and compliantly. This role is a great fit for early talent seeking to develop experience in a regulated laboratory environment.

• Verify and review sample submissions to ensure they meet Quality Control requirements
• Receive, label, organize, and properly store samples according to established procedures
• Deliver samples to Quality Control laboratories for testing in a timely and accurate manner
• Perform routine temperature, environmental, and/or CO₂ monitoring and document results
• Support compliance with regulatory and quality standards (cGMP, SOPs, safety guidelines)
• Communicate and collaborate with internal teams and external customers as needed

Why QC Sample Management?

• Develop real‑world experience in a laboratory and quality‑driven environment
• Build a strong foundation in regulatory compliance and sample handling
• Work alongside experienced scientists and quality professionals
• Develop transferable skills in documentation, accuracy, and cross‑functional communication

Qualifications

• Bachelor’s degree in a life sciences field (biology, chemistry, biochemistry, or related discipline)
• Exposure to or interest in working in a cGMP‑regulated environment (prior experience is a plus but not required)
• Ability to work in the United States on a full‑time basis without current or future sponsorship