Scientist - Development / Immunology - Jobs in Montréal, QC

Job Description

SummaryThe role of a Development Scientist at ImmuneCarta is to develop and implement novel approaches for cell-based assays including, but not limited to, flow cytometry and ELISpot. Equally important, the incumbent has the responsibility to serve as a technical and scientific resource for the assay development team. The Development Scientist in ImmuneCarta will work to establish Standard Operating Procedures (SOP) under Good Laboratory Practices (GLP). She/He is expected to remain current regarding the advances in the field regarding standardization, validation, reagents and in the field of immunology, overseeing experimental testing design.Main Responsibilities

• Develop new assays for clinical deployment;
• Perform work within specified timelines, proactively communicate any failure to meet timelines;
• When needed, design, execute and document troubleshooting activities;
• Present summaries of analysis results and interpretation in a professional, clear and concise manner;
• Perform in-depth data analysis and interpretation for each experiment performed;
• Present work internally as required;
• Design, execute method comparison studies for the implementation of novel methods or new technologies;
• Communicate effectively with Principal Scientist assigned to each specific project;
• Support the Principal Scientist assigned to each specific project.

Main Requirements

• M.Sc. with pharma/biotech/CRO experience or Ph.D. with demonstrated development skills;
• Immunology (human an asset) , immune monitoring methodologies;
• Experience with flow cytometry techniques and applications including assay design as well as handling complex data set of multi-color panels. Experienced in in the field of immune monitoring (an asset);
• Knowledge of non-flow cell-based assays to monitor adaptive and innate immune responses;
• Experience working with third party flow cytometry data analysis packages and Microsoft Office products;
• Knowledge and understanding of GLP regulations and other regulatory guidelines sufficient to carry out GLP studies;
• English and French proficiency (written and spoken) is required.

Skills

• Works methodically and systematically
• Critical and creative thinker
• Good team spirit
• Advanced level of understanding and analytical skills to interpret data and draw conclusions
• Communicates clearly and confidently and has excellent interpersonal and teaching skills
• Excellent time management and organizational skills to meet deadlines in a fast-paced, changing environment
• Excellent record keeping, attention to details and commitment to achieve good quality work
• Ability to prepare high-quality reports
• Excellent oral and written communications skills
• Ability to prepare project reports and make internal and client presentations
• Strong troubleshooting skills

Working Conditions

• Must be willing to perform duties or supervise activities in Bio Safety Level (BSL) 1 or 2 facilities where biological samples may be either naturally or experimentally infected with potentially hazardous viruses such as HIV, HCV, or CMV
• The role is predominantly conducted in a laboratory setting
• Employee is personally responsible for following Health and Safety guidelines/instruction

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