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scientific research department manager
Title posted on Jobillico - Senior Scientist ? Bioanalysis (LC-MS MS
Posted on December 11, 2024 by Employer details ITR Laboratories Canada Inc.
Job details
<p>At ITR Laboratories Canada INC</p><p>Our Mission is to bring new medicines to the world which relieve patients suffering from serious diseases.</p><p>ITR Laboratories Canada has been servicing the pharmaceutical and biotechnology industries for over 30 years and has established itself as a trusted partner worldwide in Drug Safety Testing. We are actively seeking a <strong>Senior Scientist- Analytical Department ? Bioanalysis (LC-MS/MS) </strong>to join our team as we continue to expand our reach and services.</p><p><strong> </strong></p><p><strong>Responsibilities:</strong></p><p>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.</p><p><strong> </strong></p><p><strong>Tasks Performed:</strong></p><p></p><ul><li>Strong understanding of LC-MS/MS theory and applications.</li><li>Experienced in serum/plasma and tissue sample extraction techniques.</li><li>Research and development for LC-MS/MS assays including troubleshooting ongoing assays.</li><li>Conduct analytical pre-clinical and clinical studies in compliance with the Study Plan/Amendments, GLPs, SOPs, and current industry best practices.</li><li>Provide research project planning and deliver on time solutions.</li><li>Interpretation, analysis, documentation, and reporting of results on Analytical projects (validation and sample analysis).</li><li>Co-ordinate results with various Clients, Consultants and Toxicology Study Directors.</li><li>Generate reports, or reporting of results, within study timelines, and ensure any deviations/exception events are acceptable, including their impact on study data.</li><li>Keep up to date with respect to pertinent regulatory developments in the industry.</li><li>Write, review and apply all relevant SOPs.</li></ul> <br> <p><strong>Experience</strong></p><p> </p><ul><li>A minimum of 8 years Scientific experience of project management.</li><li>Excellent understanding of bioanalytical analysis and the associated regulations.</li><li>Experience and hand son knowledge of analytical instrumentation (LC-MS/MS).</li><li>A strong team player with excellent oral and written communication skills.</li><li>Skilled in data interpretation and report writing. </li><li>Bilingual English and French</li></ul><p> </p><p> </p><p><strong>This position offers:</strong></p><ul><li> Permanent full-time position, </li><li> Group insurance plan and group RRSP.</li><li> A stimulating and friendly work environment.</li></ul><p><br> </p><p>Start Date: ASAP </p>- LocationBaie-d'Urfé, QC
- Workplace information On site
- SalaryNot available
- Terms of employment Permanent employmentFull time
- Starts as soon as possible
- vacancies 1 vacancy
- Source Jobillico #12020801
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