The Compliance Associate also communicates with the fabricator on any corrections or changes to process equipment, methods, specifications that may affect the…
A degree from a recognized post-secondary institution with acceptable specialization in sciences. Maintain filing system for all applicable quality records,…
Initiate, coordinate and analyze (e.g. Root cause analysis, trending, control charting, gap analysis) data and reports using statistical techniques; Analyze and…
Assist in the development of technical documents, including incoming inspections. _*Education: *_ Undergraduate degree or diploma in Electrical, Mechanical…
O Conduct annual reviews (APQR, ADR) consistent with applicable statutory and regulatory requirements; produce / distribute summary reports and notify Ministry…
Quality control certificate, HACCP, GMP certificate or Food safety certificate or industry experience would be an asset. Handle deviation and change control.
Direct and develop QA strategies, discipline, and framework. Monitor all QA activities, test results, defects, root cause analysis, and identify areas of…
A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data…
Bachelor’s degree preferably in technical/science field or equivalent combination of education and experience. Review design inputs for regulatory compliance.
Bachelor’s degree or equivalent experience in a relevant field. Support engineering team during new designs and modifications in during such stages as risk…
Ensure regulatory compliance and oversee the regulatory strategies for growth opportunities and product development in alignment with business priorities.
Ensures a qualitative output that meets the Hospital, provincial and federal healthcare standards and guidelines. Successful completion of high school diploma.
Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical…
As a condition of employment, all external hires will be required to submit proof of COVID-19 vaccination or documentation unless a valid accommodation under…
All employees of HRH share a common responsibility to act in accordance with the commitment to safe and compassionate patient care and a safe and healthy work…
Reviews incoming order forms for proper coding, quantities requested, and authorized approvals; inspects and verifies supplies received against invoice and…
Hands-on Engineering System/Software development or Quality Assurance in complex System environment with certification constraints (Transportation, Aerospace,…
Manage all incoming calls to the company general phone line including screening and directing calls, taking messages while ensuring knowledge of staff movements…
Centre for Commercialization of Regenerative Medicine
— Toronto, ON
You will help develop CCRM’s quality assurance and quality control teams to deliver on client demands, including fee-for- service work, contract manufacturing,…
We develop and manufacture innovative new products on a contract basis for our customers that bring enhanced therapeutic value and impact the lives of the…
You will be submitting local and foreign medical device problem reports (MDPRs) to local regulatory authorities in accordance with the applicable regulations…
In addition, you will develop and maintain templates and resource to guide clinical research staff in the conduct of clinical research to facilitate regulatory…
