EV

Eurofins Viracor

Verified Job Source

Get results faster, when it matters most.

Lenexa, Kansas

Medical and Diagnostic Laboratories
201–500 people

About

It’s so much more than a specimen. It's a life. With over 30 years of specialized expertise in infectious disease, immunology, transplant, and allergy testing for immunocompromised and critical patients, Eurofins Viracor is committed to helping medical professionals, transplant teams, reference labs and biopharmaceutical companies get results faster, when it matters most. Eurofins Viracor is passionate about providing timely, actionable test results, never losing sight of the connection between the testing we perform and the patients our results ultimately serve. Find out more by visiting us at www.eurofins-viracor.com/clinical Eurofins Viracor is an equal opportunity employer.

Open positions

Laboratory Technician - Eurofins BioPharma Product Testing Toronto Inc.

On-site · Toronto

The Laboratory Technician is responsible for providing technical support, sample preparation, and performing wet chemistry or instrumentation analyses within the Biopharmaceutical Chemistry Testing Laboratory. They must ensure accurate documentation in lab books and maintain compliance with GMP and GLP guidelines.

Warehouse Technician - Eurofins CDMO Alphora, Inc.

On-site · Oakville

Responsible for receiving, sampling, and staging cGMP raw materials while maintaining strict adherence to safety and environmental regulations. The role also involves managing inventory through cycle counts and coordinating logistics between site locations.

Maintenance Technician - Eurofins CDMO Alphora, Inc.

On-site · Mississauga

Install, maintain, and troubleshoot mechanical and electrical equipment and facilities within a GMP-regulated environment. Develop and execute preventative maintenance programs to ensure operational efficiency, safety, and minimal production disruption.

Process Technician (Kilo lab) - Eurofins CDMO Alphora, Inc.

On-site · Oakville

Execute chemical processing operations and production batches for Active Pharmaceutical Ingredients (APIs) following batch record instructions. Maintain strict adherence to cGMP, EHS, and Good Documentation Practices while collaborating across internal departments.