Laboratory Sample Technician - Entry Level - Second-Shift
- Rensselaer, United States
- On-site
- Entry Level
- Bachelor's degree
- Posted
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
