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Laboratory Sample Technician - Entry Level - Second-Shift

Eurofins

Skills

Required

  • biochemistry
  • cGMP‑regulated

Preferred

  • cGMP
  • procedures
  • document results
  • SOPs

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.

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.

About Eurofins

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.

Responsibilities

  • 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?

Requirements

  • 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
  • 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