Development Scientist

Overview

CellCarta, a Contract Research Organization, is hiring a Development Scientist to join our dynamic team. As a Development Scientist, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being.

Summary

The Development Scientist is responsible for developing and implementing novel approaches for cell-based assays, immunoassays, and biochemical assays, including but not limited to flow cytometry (conventional and spectral), cell sorting, CyTOF, ELISpot, ELISA, MSD, or single-cell genomics. The incumbent also has the responsibility to lead and perform development studies and serve as a technical and scientific resource for the assay development and operation teams. In addition, method development, interpretation, and reporting of scientific results, along with working in close collaboration with cross-functional teams, are important aspects of the position. The Development Scientist is expected to stay current with advances in the field, including standardization, validation, reagents, and immunology, while overseeing experimental test design.

Responsibilities

• Lead R&D and development studies.
• Evaluate, design, test, and implement novel methods and new technologies.
• Design, execute, and document troubleshooting activities.
• Perform in-depth data analysis, interpretation, and reporting of scientific results.
• Present summaries of analysis results and interpretations in a professional, clear, and concise manner to clients and other relevant stakeholders.
• Perform work within specified timelines and proactively communicate any delays in meeting those timelines.
• Work in close collaboration with cross-functional teams.
• Work as a member of a team, leading own projects and supporting other projects and team members when needed.
• Train other laboratory members on complex methods.
• Write and review methods.
• Record associated documentation relevant to the tasks at hand, as per appropriate SOPs, GLP regulations, and GCLP guidelines.

Education

• M.Sc. with pharma/biotech/CRO assay development experience, or Ph.D. in life sciences, preferably in immunology, virology, or molecular biology, with demonstrated development skills.

Main Requirements

• Knowledge of modern immunology and keeping abreast of current literature, IM methodologies.
• Clear and concise written and verbal communication in English (French is a plus).
• Experience with flow cytometry techniques, instruments, and applications, including assay design, as well as handling complex datasets of multi-color panels.
• Experience working with third-party flow cytometry data analysis packages and Microsoft Office products.
• Experience with spectral flow cytometry, cell sorting, and mass cytometry (CyTOF) is preferred, but not essential.
• Experience with immunoassays (ELISA, MSD) including assay development and validation.
• Knowledge of non-flow cytometry-based and biochemical assays to monitor adaptive and innate immune responses is a plus.
• Experience in the field of immune monitoring and clinical trial design and regulations is an asset.
• Knowledge and understanding of GLP regulations and other regulatory guidelines sufficient to conduct GLP studies is considered a benefit.
• Approaches work methodically and systematically.
• Demonstrates and applies an advanced level of understanding and analytical skills to interpret data and draw conclusions within the project goals.
• Critical and creative thinker.
• Communicates clearly and confidently, with excellent interpersonal skills.
• Strong team spirit.
• Excellent time management and organizational skills to meet deadlines in a fast-paced, changing environment.
• Excellent record-keeping, attention to detail, and commitment to delivering high-quality work.

Working Conditions

• 100% onsite.
• The role is predominantly conducted in a laboratory setting.
• 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 employee is personally responsible for following Health and Safety guidelines and instructions.

Benefits

• Competitive Wages.
• Vacation and Personal Days.
• Comprehensive Group Insurance Plans.
• RRSP Contribution with Employer Matching.
• Employee Annual Incentive Plan (EAIP).
• Dialogue Telemedicine Service and Employee Assistance Program (EAP).
• OPUS & Cie Contribution.
• Parking Reimbursement.
• Referral Program.
• Career Advancement Opportunities.

About CellCarta

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China. Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world.

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