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 · Ottawa
The Night Shuttle Driver is responsible for the efficient collection and transportation of environmental and medical samples between client sites and Eurofins laboratory locations. Additionally, the role involves supporting sample reception operations, maintaining the company vehicle, and performing light administrative duties.
On-site · Toronto
The Analyst II will perform routine analysis and method validation using HPLC and GC-MS while coordinating research activities for new test methods. They are also responsible for troubleshooting technical issues, supporting OOS/OOT investigations, and providing technical training to staff.
On-site · Toronto
The Analyst II will perform routine analysis and method validation using HPLC and GC-MS while coordinating research activities for new test methods. They are also responsible for troubleshooting technical issues, conducting OOS/OOT investigations, and providing technical training to staff.
On-site · Mississauga
The Human Resources Generalist supports daily HR operations including onboarding, payroll, benefits administration, and employee records management. This role also assists with recruitment, workplace safety compliance, and employee engagement initiatives to support organizational goals.
On-site · Oakville
The Senior Process Technician will lead complex chemical processing operations and mentor junior staff to ensure high-quality production standards. They are responsible for troubleshooting equipment, maintaining safety compliance, and collaborating with team leaders to manage daily manufacturing activities.
On-site · Oakville
Execute chemical processing operations with precision while strictly adhering to batch records, SOPs, and GMP standards. Maintain equipment cleanliness and ensure the safe handling of chemicals and process waste within the manufacturing facility.
On-site · Toronto
The QA Associate is responsible for reviewing GMP documentation, reconciling product lots for QC disposition, and ensuring compliance with regulatory standards. They also assist with investigations, stability programs, and the maintenance of standard operating procedures to support client needs.
On-site · Mississauga
The Drug Product Technician is responsible for executing GMP clinical manufacturing operations, including the operation of automated equipment for oral dosage forms. They also support warehouse operations, maintain facility cleanliness, and ensure compliance with GMP systems and documentation.
On-site · Mississauga
The Senior Research Chemist will lead analytical method development, transfer, and validation activities to support drug product development and GMP operations. They are also responsible for overseeing QC release testing, stability programs, and ensuring full regulatory compliance within the laboratory.
On-site · Mississauga
The Senior Formulation Scientist will lead formulation development activities from early development through GMP manufacturing, including process scale-up and technology transfer. They will also provide technical leadership, oversee GMP operations, and collaborate with clients to ensure project objectives are met.
On-site · Mississauga
The Formulation Chemist will lead the design and execution of formulation studies and manage the scale-up and technology transfer of oral dosage forms to GMP manufacturing. They will also be responsible for drafting GMP documentation and troubleshooting process challenges to ensure continuous improvement.
On-site · Oakville
The Process Specialist will bridge the gap between R&D and manufacturing by designing scalable processes and providing on-the-floor technical support during production campaigns. They are responsible for managing batch records, ensuring operational readiness, and maintaining compliance with cGMP and safety standards.
On-site · Toronto
The coordinator is responsible for receiving, inspecting, and documenting incoming laboratory samples and supplies while maintaining accurate inventory and procurement records. They also coordinate with vendors and internal teams to resolve shipping discrepancies and support overall laboratory operations.
On-site · Mississauga
Develop, optimize, and validate analytical test methods for raw materials and APIs to support process development and GMP manufacturing. Conduct scientific investigations, perform stability testing, and maintain laboratory equipment to ensure compliance with cGMP standards.
On-site · Vaughan
The chemist is responsible for performing wet chemistry and HPLC analysis while ensuring adherence to quality assurance protocols and laboratory SOPs. They will also support the supervision and training of lab technicians while maintaining accurate data records and laboratory equipment.
On-site · Vaughan
The specialist is responsible for reviewing laboratory raw data, issuing Certificates of Analysis, and managing change controls for equipment and protocols. They also contribute to process improvements, review investigation documents, and ensure compliance with GMP and ISO 17025 standards.
On-site · Toronto
The Laboratory Technician will perform microbiology testing on incoming samples while ensuring compliance with ISO/IEC 17025 and internal SOPs. They are responsible for accurate data entry into the eLIMS system and maintaining a clean, safe, and organized laboratory environment.
On-site · Toronto
The Laboratory Technician is responsible for preparing and analyzing organic and inorganic samples using established analytical methods. They must also perform instrument maintenance, data entry into the LIMS system, and ensure compliance with quality and safety standards.
On-site · Vaughan
The Quality Assurance Manager will lead the QA/RA department, overseeing the Quality Management System, ISO 17025 accreditation, and regulatory compliance. They are responsible for managing team performance, conducting internal audits, and ensuring all laboratory operations meet GMP and regulatory standards.
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.
