Specialist/Project Manager, regulatory affairs
QuebecFull Time, Temporary
FOP Consultants
1+ YOECandidates need a bachelor's or master's degree in science or biomedical engineering and 1 to 10 years in medical device or pharmaceutical work. Knowledge of ISO 13485, device classes I to III, and Health Canada and FDA rules is required, plus English and French writing and speaking skills.
Regulatory affairs, Staff training, Medical device regulations, Pharmacology, Biomedical engineering, Pharmaceutical industry
Specialist/Project Manager, quality assurance
QuebecFull Time, Temporary
FOP Consultants
1+ YOECandidates need a bachelor's or master's degree in science or engineering and one to ten years of medical device or pharmaceutical quality experience. They must know ISO 13485, FDA and Health Canada rules, and medical device classes I to III, and write well in French and English.
MS Office