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.
We are seeking an Analyst for our Bioanalysis group located in Senneville, QC.
The following are responsibilities related to the Analyst Bioanalysis:
- Analysis of test Items (concentration, purity or stability).
- Perform various extraction techniques (solid phase, liquid, liquid/liquid et protein precipitation).
- Analysis of different biological fluids (plasma, serum, urine, CSF) or tissues.
- Perform analysis by LC-MS/MS and/or HPLC and/or other analysis instruments.
- Collect and process data in accordance with the GLPs.
- Collaborating with the scientific staff.
The following are minimum qualifications related to the Analyst Bioanalysis position:
- Possesses a DEC or B.Sc. in Sciences (Chemistry, Biochemistry, Biotechnology or equivalent).
- Is flexible and able to rapidly adapt to changes.
- Is meticulous, autonomous, reliable and has good organizational skills.
- Bilingualism (French/English).
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 14,000 employees within 80 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 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.
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 2018.Apply Now