Technician, Clinical Laboratories(Optmq Member)

5 days ago

Senneville, Canada Charles River Laboratories Full time

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

**Job Summary**:
We are seeking a Technician in Clinical Laboratories to join our team located in Senneville, Qc.

The Clinical Laboratory technician does the reception of blood, urine and other body fluids samples, must centrifuge decant and proceed to the analysis as required by the protocol.

**Work schedule**:

- Daytime schedule: Tuesday to Saturday, 08:00 to 16:15.
- Full time 37.5 hours with occasional overtime.
- Permanent position (benefits/savings plan).

**Competencies**:
The following are minimum qualifications related to the Technician in Clinical Laboratories position:

- Must be member of the OPTMQ
- Experience analysing hematology, biochemistry and urine with the appropriate instruments
- Have attention to detail
- Have knowledge of computer software
- Experience in centrifugation and analysis of blood, urine and other fluids.
- Ability to multi-task
- Have a good team spirit

**Competencies**:
**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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

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