Research Assistant II

CIRION BioPharma Research is looking for a Research Assistant II. Under the supervision of the Director, Research and Development Unit, the Research Assistant II, R&D will participate in experiments and technical activities related to clinical and preclinical projects for which he or she is assigned to.

Responsibilities

As a qualified member of the Research and Development team, the principal responsibilities are:

• Assist the Project Managers and project team members in the planning and follow-up of R&D activities relevant to the domain of expertise and relating to preclinical and clinical studies.
• Apply the technical methods required for the development and validation of assays
• Verify, compile and analyze the research information and results/data in order to assure their quality and in accordance with concerned protocols.
• Write and maintain laboratory notes on assays and protocols.
• Observe secure laboratory working practices.
• Perform quality control functions with the documentation of the associated projects.
• Perform general laboratory tasks and aid in project preparation.
• Maintain the functionality of the laboratory which will include: maintenance and inventory of work devices and instruments, etc.
• Perform all tasks in compliance to GLP (Good Laboratory Practices) regulations.

Qualifications

• MSc. degree in Cellular Biology, Virology, Immunology or Biochemistry or a related area combined with 1 to 2 years of relevant experience conducting research in laboratory in the Biopharmaceutical Industry.

OR

BSc. degree in Cellular Biology, Virology, Immunology or Biochemistry or a related area combined with a minimum of 4 years of relevant experience conducting research in laboratory in the Biopharmaceutical Industry.

• Proven experience in the use of the following basic techniques such as ELISA, PCR, flow cytometry and cell culture
• Ability to maintain instrumentation, production, compilation and analysis of results
• Knowledge of the GLP (Good Laboratory Practices) and GCP (Good Clinical Practices) regulations is considered an asset
• Oral and written ability in French and English
• Excellent knowledge of Microsoft Office Word and Excel

Interested candidates should submit their resume immediately to the following address: **************@******.*** with the reference RH2021-010. A competitive compensation will be offered to the candidate who meets the selection criteria. Only selected candidates will be contacted for an interview. The use of the masculine is only intended to lighten the text. We are an equal opportunity employer.

COMPANY DESCRIPTION

Since 1996, CIRION BioPharma Research has been offering contract research laboratory services to the international pharmaceutical industry. In our state-of-the-art facilities in Laval, we value the knowâ€'how, the expertise, the innovation and the quality, proof of success for our company. For more information, we invite you to visit our website at www.cirion.com.