Laboratory Analyst - Biomarkers

Laboratory Analyst - Biomarkers Req ID #:  87911 Location: 

Senneville, Quebec, CA, H9X 3R3 For 70 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. Job Summary  

We are looking for an Analyst for our Biomarkers department located In Senneville (West Montreal), Québec. Biomarkers department analyzes biological characteristics used for evaluating progression of a disease, normal biological processes and pharmacological reaction to the drug or a mechanism of action. Our scientific expertise is varied and covers key toxicological indications and a range of therapeutic areas, including oncology, inflammation, immunology, infectious disease, ocular disease, metabolism, and disease of the cardiovascular, renal, respiratory, and central nervous systems. Our team develop a large number of assays per year and is constantly increasing.

In this position you will performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.

Responsabilities:

Perform various immunoassays and enzymatic assays on several platforms including, among others, immunosorbent assay (ELISA), Luminex®, radioimmunoassay (RIA), ECL, SMCTM technology, Simoa® technology, Simple Protein ELLA. 

Carry out method development, validation and sample analysis assays.

Collect and process data in accordance with the GLPs (Good Laboratory Practice) in order to maintain high quality standards of the company. 

Collaborating with the scientific staff to optimize methods. Qualifications  

The requirements for this role:

Collegial diploma in science (biotechnology, biomedical or equivalent) or a B.Sc (Immunology, Biology, Biochemistry or equivalent).

Ability to work under time constraints, outstanding organizational skills and ability to adapt to changes. 

Work precisely, pay attention to details and strive to achieve quality work.

autonomous, have a collaborative sprit spirit and be positive.

Reading and writing English is required. Bilingualism is an asset.

What we can offer to you:

Advanced technology in a department who is expanding rapidly.

Good working atmosphere and team spirit.

New windowed laboratories and offices.

An excellent onboarding and training program for new employees. 

Ongoing training.

Opportunities for advancement in the department and within the company.

Flexible schedule.

Reimbursement of up to $1000 of moving expenses (some restrictions apply).

Competitive benefits: Health and Dental plans, REER/CELI with employer contribution.

Free access to the gym, cafeteria, paid Volunteer Time Off (7,5h paid per year).

Large free parking. Easy access to public transit with free shuttle service. 

A career in a company recognized as one of « Montreal’s Top Employers ». 

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.

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 17,000 employees within 90 facilities in 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. And in 2019, revenue increased to $2.62 billion.

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 supported the development of ~85% of the drugs approved by the FDA in 2019.

Equal Employment Opportunity 

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

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