Pricing analyst Jobs in Saint-Eustache, QC

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.

Job Summary

As an Analyst for our Laboratory Science team located at the Senneville site, you will be involved in the analysis of samples using various techniques to evaluate the safety of a compound.

In this role, the main responsibilities of an analytical chemistry analyst will include:

• Performing various analytical techniques on the substances to be tested, enabling the identification and quantification, as well as the verification of different parameters.
• Working collaboratively with scientific staff.
• Performing these analyses using high-performance liquid chromatography (HPLC) and spectrometry.

In this role, the main responsibilities of a bioanalytical Analyst will include:

• Conduct technical assays using various extraction techniques (protein precipitate extraction, solid phase extraction) and LC-MS/MS to quantify molecules of interest, , in compliance with the Good Laboratory Practice (GLP) and FDA regulations
• Handle and analyze biological samples
• Validate the analysis of samples, in a multidisciplinary laboratory using a variety of extraction techniques, manual assays, automated equipment and analytical instruments
• Work closely with the Scientific team.

In this role, the main responsibilities of a biomarkers will include:

• Perform sample analysis based on a variety of immunoassays and enzyme assays such as ELISA, Luminex, radioimmunonalysis, ECL, MSC technology, Simoa technology, and Simple Protein ELLA
• Oversee method development and perform validation and data analysis to determine if results are as expected, in compliance with Good Laboratory Practice (GLP).

In this role, the main responsibilities of a genetic toxicology analyst will include:

• Perform the following techniques:
  
  • Bacterial Mutation Test (BMT)
  • Chromosome Aberration Test (CAT)
  • InVitro Micronucleus (IVM)
  • Mammalian Cell Mutation Test (MCM)
  • Micronucleus Test (MNT), Comet Assay
  • Cytotoxicity Test and Mode of Action Assay (MOA)
• Analysis of bacterial or cell cultures; manipulation of animal organs
• GLP-compliant collection and processing of analytical data
• Documentation of activities and data processing
• Work in collaboration with scientific staff
  

Key Elements

If you have the following qualifications, we will train you for the rest:

• Holder of an AEC, a DEC or a BAC in Laboratory Sciences;
• Ability to work under time constraints;
• Ability to adapt to changes;
• Detail oriented.

Role Specific Information

• Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
• Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
• Salary: 23,50$/hrs;
• Annual bonus based on performance;
• Schedule: Monday to Friday, 8am to 4:15pm. Depending on business needs, you may have to do overtime;
• Permanent full-time position as of the hiring, 37.5hrs per week

Why Charles River?

• Competitive benefits upon hire. We pay up to 85% of premiums (medical & dental coverage)
• Paid development training
• Employee and family assistance program
• 24/7 access to a doctor and various health care professionals (telemedicine)
• 3 weeks’ Vacation & 5 Personal day policy
• Numerous organized social activities

If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team.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 supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity

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.

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 crrecruitment_US@crl.com. 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.