Spécialiste, Affaires Réglementaires/ Regulatory Affairs Specialist (contrat 12 mois)
McKesson(4 days ago)
About this role
A Regulatory Affairs Specialist at McKesson is responsible for ensuring compliance with regulatory requirements related to drug and medical device licensing. The role involves preparing submissions, reviewing labels, managing product registrations, and supporting regulatory processes within the pharmaceutical industry.
Required Skills
- Regulatory Submissions
- Health Canada
- eCTD
- GMP
- Labeling
- Product Monographs
- Regulatory Compliance
- Documentation Management
- Project Management
- Bilingualism
About McKesson
mckesson.comThe leading healthcare company for wholesale medical supplies & equipment, pharmaceutical distribution, and healthcare technology solutions.
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