Responsibilities
The Scientist will be experienced in research and development for Bioanalytical LC-MS / MS assays. They will need to develop innovative solutions to mass spectrometry challenges.
They will troubleshoot, optimize and develop assays to current GLP regulatory requirements.
Tasks Performed :
- Strong understanding of LC-MS / MS theory and applications.
- Experienced in serum / plasma and tissue sample extraction techniques.
- Research and development for LC-MS / MS assays including troubleshooting ongoing assays.
- Conduct analytical pre-clinical and clinical studies in compliance with the Study Plan / Amendments, GLPs, SOPs, and current industry best practices.
- Provide research project planning and deliver on time solutions.
- Interpretation, analysis, documentation, and reporting of results on Analytical projects (validation and sample analysis).
- Co-ordinate results with various Clients, Consultants and Toxicology Study Directors.
- Generate reports, or reporting of results, within study timelines, and ensure any deviations / exception events are acceptable, including their impact on study data.
- Keep up to date with respect to pertinent regulatory developments in the industry.
- Write, review and apply all relevant SOPs.
Qualifications :
- Masters of Science (Chemistry, Biochemistry, Biotechnology, Pharmacology or related field).
- Scientific industry experience of project management.
- Excellent understanding of bioanalytical analysis and the associated regulations.
- Experience and good hands on knowledge of analytical instrumentation (LC-MS / MS).
- A strong team player with excellent oral and written communication skills.
- Skilled in data interpretation and report writing.
- Bilingual English / French;
This position offers :
- Permanent full-time position,
- Group insurance plan and group RRSP.
- A stimulating and friendly work environment.
Start Date : ASAP
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