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.
On-site · Toronto
The Analyst II performs complex analytical testing using GC-MS/MS and GC-FID instrumentation while ensuring compliance with GMP/GLP and SOPs. They are also responsible for method development, instrument maintenance, and mentoring junior staff members.
On-site · Toronto
The Analyst is responsible for performing analytical testing on API, raw materials, and finished products using various chromatographic instruments while ensuring compliance with GMP and SOPs. They also assist in laboratory investigations, method transfers, and the training of junior staff members.
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.
On-site · Mississauga
The Analytical Chemist will develop, optimize, and validate analytical test methods to support process development and GMP manufacturing. They are also responsible for conducting scientific investigations, performing stability testing, and maintaining laboratory instrumentation in compliance with cGMP standards.
On-site · Toronto
The QC Reviewer is responsible for reviewing laboratory documentation, including finished products and stability studies, to ensure compliance with GMP requirements. They also participate in OOS investigations, CAPA processes, and provide guidance to the Quality Control team during audits.
On-site · Ottawa
The Night Shuttle Driver is responsible for the efficient collection and transportation of environmental and medical samples between client sites and Eurofins laboratories. Additionally, the role involves supporting sample reception operations, maintaining the company vehicle, and performing light administrative duties.
On-site · Mississauga
The Human Resources Generalist supports daily HR operations including onboarding, payroll, benefits administration, and employee records management. The role also assists with recruitment, workplace safety compliance, and employee engagement initiatives to support organizational goals.
On-site · Toronto
The Sample Reception Supervisor oversees daily operations, including the accurate processing of samples through the LIMS and the coordination of sample distribution. This role also provides leadership to staff, manages performance, and ensures compliance with quality and safety standards.
On-site · Toronto
The supervisor is responsible for managing depot operations, including receiving and logging environmental samples into the LIMS system. They also coordinate daily pick-ups and drop-offs while providing direct support to clients via phone and in-person interactions.
On-site · Toronto
The incumbent will manage customer relations, project scheduling, and client account creation for the Biopharmaceutical Product Testing laboratory. They are also responsible for performing various administrative tasks and ensuring regulatory compliance while maintaining a professional image.
On-site · Ottawa
The technician is responsible for performing sample preparation and membrane filtration analysis on water and soil samples using established SOPs. They must also maintain laboratory equipment, manage inventory, and ensure accurate data entry into the LIMS system.
On-site · Toronto
The QA Reviewer is responsible for ensuring compliance with regulatory standards such as ISO 17025 and GMP by reviewing laboratory data and quality documentation. They also manage internal audits, conduct investigations for deviations and CAPA, and support the maintenance of quality systems.
On-site · Toronto
The position is responsible for managing all sample logistics from entry to distribution, including eLIMS template creation and stability study support. The role also involves ensuring GMP compliance, auditing samples, and assisting the Quality Assurance department with training procedures.
On-site · Toronto
The Cash Application Clerk will manage daily cash application activities, including processing cheques, credit cards, and EFTs across multiple business lines. Additionally, the role involves preparing bank deposits, generating aging reports, and responding to business unit inquiries.
On-site · Toronto
The QA Associate is responsible for reviewing GMP documentation, reconciling product lots, and ensuring compliance with regulatory standards. They also assist with investigations, change controls, and the maintenance of quality systems to support client needs.
On-site · Mississauga
The manager will lead drug product manufacturing operations, overseeing production suites, warehouse activities, and technical engineering teams to ensure cGMP compliance. They will also serve as a commercial lead, managing client relationships, revenue forecasting, and the implementation of process improvements.
On-site · Mississauga
The QA Associate provides quality oversight for GMP activities, including batch manufacturing, fill-finish operations, and analytical testing. They are responsible for reviewing batch records, managing deviations, and ensuring compliance with regulatory standards.
On-site · 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.
On-site · 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.
On-site · 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.
