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Support regulatory and compliance activities across assigned markets
Assist with product registrations, renewals, and lifecycle maintenance
Support quality system processes including SOPs, CAPA, and documentation updates
Review marketing and promotional materials for regulatory compliance
Assist with vigilance and post-market compliance activities
13 years experience in medical device registration, preferably with MDA; HSA exposure is a plus
Familiar with regulatory environments, including labeling requirements and controls
Able to work effectively with cross-functional teams and manufacturing sites
Strong project management and organizational skills
Flexible, detail-oriented, and able to prioritize tasks and meet deadlines in a fast-paced environment
Job ID: 136412779