McGill University
Healthcare
CourseLecturer-BMDE654BiomedicalRegulatoryAffairs-MedicalDevices
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Course Lecturer -BMDE 654 Biomedical Regulatory Affairs - Medical Devices at McGill University. Skills: Biomedical regulatory affairs, Medical devices, Quality management systems. Prepare course lectures. Prepare teaching materials”
Industry & Context.
What They're Looking For.
Must Have
Understand FDA requirements, Understand Health Canada requirements, Understand ISO 13485:2003, Understand ISO 14971:2007, Understand IEC 62304:2006, Understand 21 CFR 820, Bachelor of Science, Bachelor of Engineering, Bachelor of Arts, More than 5 years experience
Nice to Have
Fluency in French
What You'll Do.
Prepare course lectures
Prepare teaching materials
Prepare grading rubrics
Facilitate classroom discussions
Assess student performance
Evaluate student performance
Prepare students for leadership
Participate in curricular discussions
Hold regular office hours
Full Job Description
**Please refer to the[How to Apply for a Job (for External Candidates)](https://www.mcgill.ca/hr/files/hr/apply_at_mcgill_university_-_guide_for_external_candidates_en.pdf) job aid for instructions on how to apply.** **If you are an active McGill employee (ie: currently in an active contract or position at McGill University), do not apply through this Career Site. Login to your McGill Workday account and apply to this posting using the Find Jobs report (type Find Jobs in the search bar).** **COURSE DESCRIPTION** The Department of Biomedical Engineering of the Faculty of Medicine, McGill University, is seeking applications for a Course Lecturer for the 2026-2027 academic year to teach BMDE 654 Biomedical Regulatory Affairs - Medical Devices (3 credits) Course overview: Biomedical Engineering : Regulatory strategies and quality management systems are critical for medical device development. This course provides an overview of regulatory requirements, and familiarize students with the important ISO and IEC standards pertaining to medical device development. This course will provide biomedical engineers with an understanding of the regulatory and quality requirements to translate a medical device idea into a commercial product, and will draw upon the expertise of invited speakers currently working in the medical devices industry. **RESPONSIBILITIES** Preparing the students with the required knowledge, facilitating classroom discussions, assessing and evaluating student performance and preparing students to be successful leaders in their profession. **OTHER MAIN RESPONSIBILITIES** **INCLUDE:** • Preparation of course lectures and teaching materials • Preparation of assignments, tests and grading rubrics • Participation in curricular discussions • Hold regular office hours **T****EA****C****H****I****N****G Q UALIFICATION REQUIREMENTS** * Understand the FDA’s and Health Canada’s requirements for medical devices. * Understand best practices required for timely regulatory c
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