Description

 

Analyst, Quality Control (RH2023-019)

Location: Laval, Canada
Number of positions available: 1 

CIRION BioPharma Research is lookg for an Analyst, Quality Control. Under the supervision of the Director, R&D Unit,(or the person delegated by management) the Analyste, Quality Control performs quality control activities relevant to his field of expertise and linked to assigned projects.  

Responsibilities

  • Contribute in increasing the quality of data and performance of all operational units.
  • Ensure the review of the data generated by the analysts (tables, forms, calculations, etc.) according to the current procedures, such as the Good Laboratory Practices (GLPs) and Standard Operating Procedures (SOPs).
  • Ensure the review of the scientific protocols and reports.
  • Report any findings to analysts and project managers, and follow-up on the necessary adjustments to be made.
  • Proactively report findings to the immediate supervisor in order to identify opportunities for data and procedure improvements
  • Perform the maintenance of instruments, write necessary deviations and ensure that forms are signed in a timely manner.
  • Ensure the management of expired reagents;
  • Support analysts and project managers to respond to audits reports to the Quality Assurance Unit.
  • Ensure proper record-keeping for each assigned project for the transfer to the Quality Assurance Unit.
  • Prepare the documentation for transferred to archives at the end of a project;
  • Assist in laboratory instrument/equipment validation by performing functional analysis required;
  • Complete tasks in compliance with GLPs and current procedures;
  • Assist in implementing good quality control practices. 

  

Qualifications

  • B.Sc. in Biochemistry (or a related field).
  • At least 1 to 2 years of work experience in a laboratory or in a research environment in the biopharmaceutical industry.
  • Basic scientific knowledge in biochemistry and immunology.
  • Knowledge of the GLP (Good Laboratory Practices) and GCP (Good Clinical Practices) regulations.
  • Verbal and written ability in French and English.
  • Knowledge of Microsoft Office programs, specifically Word and Excel.

If you are passionate about the biopharmaceutical industry and are looking to join our team in Laval; a professional, dynamic team and meet exciting challenges within a growing company, please submit your resume with the reference RH2023-019 at: humanresources@cirion.com . Competitive compensation is offered to the candidate who meets the selection criteria.

CIRION's Benefits:

  • Mobile and sick days
  • Group Insurance
  • RRSP with employer participation
  • EAP and telemedicine
  • Parking
  • Easy access to highways 15 and 440
  • Social activites    

 Only selected candidates will be contacted for an interview. CIRION is an equal opportunity employer.

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