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ITR Laboratories Canada Inc.

Scientist- Bioanalysis (LC-MS/MS)

ITR Laboratories Canada Inc.

Scientist- Bioanalysis (LC-MS/MS)

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ITR Laboratories Canada Inc.

Scientist- Bioanalysis (LC-MS/MS)

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ITR Laboratories Canada Inc.

Scientist- Bioanalysis (LC-MS/MS)

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    ITR Laboratories Canada Inc.

    Scientist- Bioanalysis (LC-MS/MS)

    ITR Laboratories Canada Inc. Baie-D'Urfé, Quebec

    Engineering and science
    Posted 27 day(s) ago | Still Open
    Permanent 37.5 h - Full time As soon as possible Work shift: Day

    Description

    At ITR Laboratories Canada INC

    Our Mission is to bring new medicines to the world which relieve patients suffering from serious diseases.

    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 Scientist- Analytical Department – Bioanalysis (LC-MS/MS) to join our team as we continue to expand our reach and services.



    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.


    Education/Qualifications :



    Masters of Science (Chemistry, Biochemistry, Biotechnology, Pharmacology or related field).


    Experience:



    A minimum of 5 years of Scientific industry experience of project management.
    Excellent understanding of bioanalytical analysis and the associated regulations.
    Experience and hand son 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
    Salary benefits : Oui
    Relocation/Travel requirements : Non
    ITR Laboratories Canada Inc.

    ITR Laboratories Canada Inc.

    At ITR Laboratories Canada Inc, our mission is to bring new medicines in the world and help improve health and well-being of individuals across the globe. ITR Laboratories Canada has been servicing the pharmaceutical and biotechnology industries...

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