Technician, Clinical Laboratories

BioTalent Canada; Senneville; On-site; CAD 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a dedicated Technician to join their Clinical Laboratory team in Senneville. In this full-time role, you will be responsible for sample preparation, quality control, and ensuring compliance with regulatory standards. This position offers a unique opportunity to contribute to groundbreaking research that impacts global health. With a supportive environment that values your contributions, you will receive comprehensive training and competitive benefits, including health coverage and vacation time. If you are passionate about science and eager to make a difference, this is your moment to shine.

Benefits

Free Parking

Free Shuttle Service

Health & Dental Coverage

Employee Assistance Program

3 Weeks Vacation

5 Sick/Personal Days

Qualifications

• College diploma in Medical Technology required.
• Understanding of written English is mandatory; bilingualism preferred.

Responsibilities

• Perform preparation and analysis of samples.
• Ensure integrity of studies and adhere to GLP and SOP.
• Conduct quality control procedures on various instruments.

Skills

Sample Preparation

Quality Control Procedures

Data Collection

GLP Compliance

Bilingualism (French and English)

Education

College Diploma in Medical Technology

Tools

Laboratory Instruments

Computer Systems

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

As a Technician for our Clinical Laboratory department located in Senneville, you will perform technical activities and follow directives from the study/phase plan and the procedures. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

• Perform the preparation and the analysis of samples
• Perform the quality control procedure and maintenances on different instruments.
• Perform the activities in a timely fashion by adhering to preset schedules.
• Use a computer system for accurate and detailed data collection.
• Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules.
• Perform all other related duties as assigned.

If you possess the following qualifications, we will train you in the rest:

• College diploma, Medical Technologist.
• Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
• Understanding of written English is mandatory. Bilingualism French and English is preferable.

Role Specific Information:

• Location: Senneville / Free parking / Free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site.
• Annual bonus based on performance plan.
• Schedule: Tuesday to Saturday, 8:15am – 16:30pm.
• Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage) .
• Employee and family assistance program.
• Access to a doctor and various health professionals (telemedicine).
• 3 weeks’ vacation & 5 sick/personal days per year.
• Many social activities.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

About Safety Assessment Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [e-mail]. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.