Scientist, Immunoassay
Caprion
Montreal, Quebec, CA
18h ago

Caprion Biosciences Inc. is a leading clinical research organization (CRO) laboratory in immune monitoring, protein characterization and tissue pathology solutions for immunotherapy and drug development.

Located in Montreal, California, Chicago, Belgium, UK, Australia and soon in China. Employees at Caprion are true scientific partners working together to enhance people'™s health and quality of life.

SUMMARY

Caprion is seeking a highly motivated and enthusiastic Scientist with strong background and hands-on experience n immunoassays (MSD and ELISA).

This individual will play a key role in analyzing samples on a variety of biological fluids and tissue study samples following Standard Operating Procedures (SOP) and Good Laboratory Practices (GLP).

He will also be required to perform method optimization / qualification and validation.

MAIN RESPONSIBILITIES

  • Process biological samples for analysis by Immunoassay (ELISA and MSD)
  • Develop, and validate Immunoassay (ELISA and MSD)
  • Autonomously design and perform experiments for troubleshooting
  • Apply technical expertise to modify and improve sample preparation workflow
  • Execute work as per established procedures
  • Maintain study-related documentation according to GLP and regulatory guidance
  • Monitor the performance of equipment and recording activities in logbooks
  • Perform general laboratory duties
  • Prepare and review documentation for experiments
  • Perform work in a GLP environment and occasionally in a containment level 2 (CL2) environment
  • EDUCATION

  • B.Sc. or M.Sc. in life sciences, chemistry or biochemistry (or equivalent)
  • EXPERIENCE AND SKILLS REQUIRED

  • A minimum of 2 years of relevant experience;
  • Knowledge and experience with ELISA and MSD assays is a must
  • Knowledge of sample processing for proteomics analysis, such as immuno-depletion and digestion techniques is an asset
  • Hands on method Qualification / Validation experience in compliance with regulatory requirements is highly desired.
  • Knowledge and understanding of GLP regulations;
  • Excellent time management and organizational skills to meet deadlines in a fast-paced, changing environment;
  • Ability to work independently, autonomously and as part of a team;
  • Skill to accurately test large numbers of samples with reliable repeatability;
  • Good record keeping, attention to details and commitment to achieve good quality work;
  • Critical thinking, troubleshooting is highly desired
  • Experience working in industry.
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