Venus Aesthetic Intelligence
Vice President of Regulatory Affairs in Canada
Job Description
Join the senior leadership team at Venus as Vice President of Regulatory Affairs, focusing on Quality Assurance and Quality Control. This strategic role demands extensive experience in regulatory environments, ideally within medical devices, either in Toronto or East Coast, USA.
As a strategic driver of regulatory and quality excellence, you will oversee regulatory affairs and quality assurance, leading compliance and safety initiatives. With at least 10 years in the medical device industry, including 3 years at the Vice President level, you will define global regulatory strategies, manage quality systems, and foster talent development across the organization.
Key Responsibilities:
• Provide executive leadership and oversight of regulatory affairs and quality assurance
• Lead global regulatory strategy for product development and compliance
• Interface with FDA and international regulatory authorities
• Ensure continuous improvement of global Quality System policies
As a strategic driver of regulatory and quality excellence, you will oversee regulatory affairs and quality assurance, leading compliance and safety initiatives. With at least 10 years in the medical device industry, including 3 years at the Vice President level, you will define global regulatory strategies, manage quality systems, and foster talent development across the organization.
Key Responsibilities:
• Provide executive leadership and oversight of regulatory affairs and quality assurance
• Lead global regulatory strategy for product development and compliance
• Interface with FDA and international regulatory authorities
• Ensure continuous improvement of global Quality System policies