Specialist/Project Manager, quality assurance
QuebecFOP Consultants
1+ YOECandidates need a bachelor's or master's degree in science, cosmetology or a related field, plus 1 to 10 years of industry experience, ideally in cosmetics or biopharma. Knowledge of ISO 22716 and Health Canada, FDA and EMA regulations is required, along with strong French and English writing skills.
MS Office Suite
Specialist/Project Manager, regulatory affairs
QuebecFOP Consultants
1+ YOECandidates need a science-related degree, one to ten years of industry experience (preferably in biopharmaceuticals), and knowledge of Health Canada, FDA and EMA regulations. Fluent French and English writing skills and MS Office are required.
MS Office
Specialist/Project Manager, regulatory affairs
QuebecFOP Consultants
1+ YOECandidates need a science-related bachelor's or master's degree and 1 to 10 years of industry experience, ideally in agri-food. Knowledge of CFIA, Health Canada and FDA rules, SQF and HACCP, and strong French and English writing are required.
MS Office Suite
Specialist/Project Manager, quality assurance
QuebecFOP Consultants
1+ YOECandidates need a science degree (food technology, chemistry, biology or related), 1 to 10 years of industry experience, ideally in agri-food quality assurance. Knowledge of CFIA, Health Canada, FDA, SQF and HACCP, plus French and English writing skills, is required.
MS Office Suite
Specialist/Project Manager, regulatory affairs
QuebecFOP 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
QuebecFOP 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
Specialist/Project Manager, pharmacovigilance
QuebecFOP Consultants
1+ YOECandidates need a bachelor's or master's degree in a science or related field and one to ten years of industry experience, ideally in pharmaceuticals. They need demonstrated pharmacovigilance experience, knowledge of Health Canada, FDA and EMA regulations, and good French and English communication skills.
MS Office
Specialist/Project Manager, regulatory affairs
QuebecFOP Consultants
1+ YOECandidates need a bachelor's or master's degree in science or a related field and 1 to 10 years of industry experience, preferably in (bio)pharmaceuticals. Regulatory affairs experience with Health Canada, FDA or EMA rules and good French and English writing skills are required.
MS Office Suite
Specialist/Project Manager, quality assurance
QuebecFOP Consultants
1+ YOECandidates need a science degree (bachelor's or master's) and 1 to 10 years of industry experience, preferably in pharmaceuticals. Knowledge of Health Canada and FDA regulations, quality assurance experience, and French and English writing skills are required.
MS Office, MS Excel