Medical Technologist - Clinical Laboratories

• Req ID #: 235171
• Montreal, QC, CA
• Full time

For 75 years, Charles River employees have worked together to help discover, develop, and safely manufacture new pharmacotherapies. When you join our family, you will have a significant impact on the health and well-being of people around the world. Regardless of your background in the life sciences, finance, IT, sales, or another field, your skills will play an important role in the work we do. In return, we will help you build a career you can be passionate about.

Job Overview

Medical Technologist – Clinical Laboratories

As a Medical Technologist (Technician III) for our Clinical Laboratories team located at the Senneville site, you will perform technical tasks and follow the directives of study/phase plans and SOPs.

The main responsibilities for this position include:

• Perform sample preparations and analyses.
• Perform quality control and maintenance on various instruments.
• Complete activities on time by following established schedules.
• Perform venipunctures.
• Ensure study integrity and meet regulatory agency requirements by executing activities and collecting data in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), and health and safety regulations.
• The minimum qualifications sought for this position are as follows:
• Diploma in Biomedical Analysis;
• Valid OPTMQ practice permit is required;
• Relevant experience is an asset;
• An equivalent combination of education and experience may be considered as an acceptable substitute for the specific education and experience listed above;
• Ability to work under time constraints and adapt to changes;
• Ability to read and write in English is required. Bilingualism is preferred;
• Demonstrate flexibility and be capable of working autonomously.

Specific Job Information

• Location: 22022 Transcanada Highway, Senneville, QC, H9X 1C1
• Transportation: We offer shuttle service from Sainte-Anne-de-Bellevue train station, John Abbott College, and the Anse à l’Orme REM station to the Senneville site. Free parking. Electric vehicle charging station.
• Salary: $26.00/hr, possibility to start at a higher level with a higher salary with specific research experience;
• Annual performance-based bonus;
• Schedule: Monday to Friday, 8:00 AM to 4:15 PM;
• Permanent position upon hire, full-time at 37.5 hours per week.

Why Charles River?

• We offer competitive benefits and perks upon hire to support your well-being;
• Free on-site gym;
• Employee and family assistance program;
• Excellent onboarding program for new employees and opportunities for internal growth and professional development;
• Access to a doctor and various healthcare professionals at all times (telemedicine);
• 3 weeks of vacation and 5 days of personal leave;
• Numerous social activities organized!

If you wish to contribute to the well-being of our communities, not only across the country but around the world, join the team. It's Your Moment.

About Toxicology Evaluation

Charles River is a company committed to helping its partners accelerate the preclinical development of their drugs with exceptional toxicity evaluation services, state-of-the-art facilities, and expert regulatory advice. From specialized toxicology and studies enabling Investigational New Drug (IND) applications to customized formulas and full support for laboratories, our experienced team can design and execute programs that anticipate challenges and avoid bottlenecks for a smooth and efficient path to market. Approximately 300 IND studies are conducted annually at our toxicity evaluation centers.

About Charles River

Charles River is an international contract research organization (CRO) in early-phase research. We have leveraged our strong foundations in laboratory medicine and veterinary science to create a diverse portfolio of discovery and safety assessment services, compliant with Good Laboratory Practices and others, to provide our clients with comprehensive support from target identification to preclinical development. Charles River also offers a range of products and services to support our clients' laboratory clinical trial needs and manufacturing activities. This extensive portfolio of products and services allows our clients to create a more flexible drug development model, reducing costs, increasing productivity, and improving efficiency for a faster time to market.

With over 20,000 employees at 110 sites in 20 countries, we are strategically positioned to coordinate global resources and apply multidisciplinary perspectives to address our clients' unique challenges. Our client base includes international biotechnology and pharmaceutical companies, public agencies, and hospitals, teaching, and research institutions worldwide.

Charles River takes very seriously its contribution to the efforts made to improve the quality of life for as many people as possible. The sense of our mission, our scientific excellence, and our determination motivate us every day. We approach each day knowing that our work contributes to improving the health and well-being of countless men, women, and children around the world. We are proud to have contributed to the development of 86% of the FDA-approved drugs in 2021.

For more information, visit www.criver.com.