Get results faster, when it matters most.
Lenexa, Kansas
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.
Sur place · Ottawa
The technician is responsible for performing sample extractions and analysis using established laboratory methods and SOPs. They must also maintain laboratory equipment, manage consumables inventory, and ensure accurate data entry into the LIMS system.
Sur place · Toronto
The Analyst I provides technical support and analysis of cosmetics products within a microbiology laboratory. Key duties include performing microbial limit testing, environmental monitoring, and maintaining equipment according to Standard Operating Procedures.
Sur place · Toronto
The Analyst II provides technical support and analysis of APIs and finished cosmetic products using HPLC and GC instrumentation. Responsibilities include performing method validations, troubleshooting technical issues, and ensuring compliance with GMP and SOP guidelines.
Sur place · Toronto
The OOS Investigator leads and executes Out-of-Specification, Out-of-Trend, and atypical result investigations within the Analytical Quality Control laboratory. The role focuses on identifying root causes, determining product impact, and implementing effective CAPAs to ensure GMP/GLP compliance.
Sur place · Mississauga
Provide quality oversight for GMP activities including bulk processing, fill-finish operations, and analytical activities for biologics. Responsible for reviewing batch records, managing deviations and investigations, and supporting the Quality Management System.
Sur place · Mississauga
The role focuses on identifying and closing new business opportunities within the Drug Product market to expand the client portfolio. Responsibilities include managing the full sales lifecycle, from prospecting and technical discussions to negotiating commercial agreements and onboarding projects.
Sur place · Toronto
Support the marketing team in executing digital and traditional campaigns and creating content for social media platforms. Conduct market research and analyze competitor activities to inform brand strategies and track campaign performance.
Sur place · Toronto
The specialist manages day-to-day customer billing, accounts receivable collections, and payment applications to ensure timely revenue recovery. They are also responsible for resolving invoicing disputes and maintaining accurate customer records and reports.
Sur place · Edmonton
Conduct sample preparation and analysis of environmental samples using PLM and PCM microscopy. Ensure compliance with QA/QC standards and manage data entry into the LIMS system.
Sur place · Toronto
Responsible for the splitting, grinding, and homogenization of incoming laboratory samples according to standard operating procedures. The role also involves maintaining equipment, managing sample retains, and ensuring turnaround time requirements are met.
Sur place · Toronto
The Accounts Payable Clerk manages day-to-day AP activities, including invoice coding, entry, and payment processing. They are also responsible for maintaining vendor files and handling inquiries within a high-volume corporate environment.
Sur place · Toronto
Ensure the compliance and performance of laboratory instrumentation and software within a GMP-regulated environment. Responsibilities include performing calibrations, executing qualification protocols, and managing metrology operations depending on seniority level.
Sur place · 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.
Sur place · Toronto
The Scientist III will develop and optimize test methods for the characterization and quality control of vaccines and other products. This includes implementing GxP compliant instruments and providing scientific guidance for data interpretation and analysis.
Sur place · Toronto
The role involves managing the receipt, logging, and storage of stability samples while maintaining the stability database and preparing reports. Additionally, the coordinator handles client interactions, project scheduling, and general administrative duties to support lab operations.
Sur place · Toronto
The role serves as the primary liaison between Personal Care clients and laboratory operations to coordinate testing projects and ensure seamless execution. Responsibilities include preparing quotations, managing sample submissions, and supporting account growth through professional client relationship management.
Sur place · Ottawa
Responsible for conducting sample preparation and analysis using inorganic chemistry methods and recording data into the LIMS system. Duties include performing instrument maintenance, calibration, and ensuring compliance with quality assurance manuals.
Sur place · Mississauga
Manage the full accounting cycle with a focus on client billing, invoicing, and accounts receivable collections. Support month-end activities, financial reporting, and audit coordination to ensure operational accuracy.
Sur place · Edmonton
Lead laboratory operations by overseeing purchasing, facility management, and adherence to quality and safety standards. Drive continuous improvement through LEAN initiatives and manage departmental budgets to optimize productivity and profitability.
Sur place · Mississauga
Lead formulation and drug product development activities from early stages through GMP manufacturing for oral dosage products. Provide technical leadership for manufacturing operations, author technical documentation, and manage client engagements.