Analyst Bioanalytical
at Charles River Laboratories
Laval, QC, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 12 Jun, 2024 | Not Specified | 13 Mar, 2024 | N/A | Reading Comprehension,French,English,Biochemistry,Chemistry | No | No |
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Description:
Req ID #: 221722
Location:Laval, Quebec, CA, H7V 4B3
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.
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
JOB SUMMARY
As an Analyst for our Bioanalysis department located at the Laval site, you will be involved in the analysis of samples using various techniques to evaluate the safety of a compound.
In this role, responsibilities may 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.
Responsibilities:
ROLE SPECIFIC INFORMATION
Location: Laval / Shuttle service between Montmorency metro station and the Laval site, Free parking
Schedule: Weekday schedule, Monday to Friday
Permanent position as of the hiring, full time 37.5hrs per week
In this role, responsibilities may 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
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
Laval, QC, Canada