Job Order Detail

Description

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, supervising QA/QC Specialists, 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.

Qualifications
        BSc in a related field is required; MSc or higher is preferred. Advanced degrees in quality, analytical monitoring, or assay development are advantageous.
        Strong familiarity with applicable regulatory regulations and guidelines for veterinary and human biologics manufacturing.

Experience
        Experience in regulated biologics, assay development, technical transfer, and quality management systems is required.

Knowledge and Skill Requirements
        Strong analytical and problem-solving skills.
        Excellent communication and presentation skills.
        Ability to manage multiple projects and priorities.
        Proficiency in quality management software and tools.
        Strong organizational skills and attention to detail.
Work Environment, Physical Demands, and Safety Considerations
        Must be willing to be vaccinated/blood tested for antibody titer for products manufactured within the facility, if required
        Work in environments with large mechanical equipment, piping and pumps serviced by high-pressure steam, water and air, and strobe lights
        Work with hazardous materials and chemicals