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Quality Manager

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Job Order #: 6163199

NOC: 20011
Employer Name:
Vaccine and Infectious Disease Organization
Posted Date:
23-Sep-2024
Location:
SASKATOON
 
# of Positions:
1
Employment Terms:
Full Time
Education:
University Bachelor's Degree
Experience:
3-5 Years
Apply By:
06-Oct-2024
How to Apply?:
Interested candidates are asked to submit their application including a cover letter, CV, and the names of three references online via the following link: https://vido.applytojobs.ca/vaccine development centre/33183

Application Information

Employer Name:
Vaccine and Infectious Disease Organization
Employer Address:
 
120 Veterinary Road
SASKATOON,SK
CANADA
S7N5E3
Contact Name:
Human Resources
Contact Email:
hr@vido.org
Employer Website:
https://vido.applytojobs.ca/vaccine development centre/33183


Description

The Vaccine and Infectious Disease Organization (VIDO), Canadas Centre for Pandemic Research, is a world leader in infectious disease research and vaccine development for humans and animals. Located at the University of Saskatchewan in Saskatoon, Canada, VIDO is home to one of the largest and most advanced containment level 3 facilities in the world. To strengthen the preparedness for emerging infectious diseases we are currently expanding our infrastructure to include containment level 4 capacity, a GMP vaccine manufacturing facility, and a new animal housing facility. Our vision includes having the capacity to study any emerging disease in any animal model embracing a One Health approach to prevent emerging and re-emerging infectious diseases in humans and animals.

We are seeking a Quality Manager to join our team. Reporting to the Manager, Regulated Vaccine Manufacturing, the Quality Manager will oversee all Quality Assurance (QA) and Quality Control (QC) activities within the VIDO Vaccine Development Centre, ensuring compliance with regulatory requirements and maintaining the highest quality standards for all products. This role involves managing the quality system, reviewing and approving SOPs, overseeing the calibration program, and ensuring timely release of all batches of the final product. The Quality Manager will also contribute to regulatory submissions, staff training programs, and continuous improvement initiatives to achieve full GMP compliance.

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