venus
Vice President, Regulatory Affairs, Quality Assurance and Quality Control
New York, New York, United States · Exec
Sponsorship not specifiedDetected 7 hours ago
ComplianceStakeholder ManagementNegotiationPerformance ManagementFDA RegulatoryMedical DevicesLeadershipCommunicationMentoringMicrosoft OfficeRegulatory Affairs
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odds of building a lasting career here
37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
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About the role
- This role will provide proactive global leadership across regulatory, quality, ensuring safety, compliance, product excellence, and operational rigor across the organization.
- The successful candidate will be a seasoned executive who has operated at a Vice President level for a minimum of 3 years, with demonstrated experience leading global, regulated medical device organizations.
- Serve as the executive interface with the FDA and international regulatory authorities, including direct participation in inspections, audits, and regulatory meetings.
Responsibilities
- Lead and execute global regulatory strategy for new product development and sustaining product maintenance, including FDA submissions and international product approvals and renewals.
- Establish, maintain, and continuously improve global Quality System policies and procedures to ensure compliance with applicable international regulations, directives, and standards related to Venus Concept products and services.
- Perform and oversee comprehensive risk assessments, ensuring risk management activities and documentation are incorporated into regulatory and quality systems.
- Demonstrated success identifying, developing, and mentoring talent.
Requirements
- Mandatory: 3+ years of experience performing this role at the Vice President level, leading enterprise‑wide regulatory and quality organizations.
- Proven experience implementing, scaling, and optimizing Quality Management Systems. must be proficient in Arena and Salesforce.
- Proficiency with Microsoft Office and enterprise business tools.
Benefits
- Partner with executive leadership to establish and execute the long‑term strategic vision for regulatory compliance and quality excellence.
- Bachelor's or Master's degree in a scientific, engineering, or healthcare‑related discipline.
- Minimum 10+ years of progressive experience in Regulatory Affairs, Quality Assurance, and/or Quality Control within the medical device industry.
- Medical device experience is a must - medical aesthetic experience is preferrable.
Company info
- What you will be part of - our Venus Culture Venus believes in pushing boundaries while embracing creativity and innovation.
- Our employees are a critical part of our company's performance and are at the core of its success.
- At Venus, we promise to give you Endless Opportunities, allow you to Foster Innovation and be part of Delivering a Best-In-Class Offering.
- What you will be part of - our Venus Culture
This listing is sourced directly from venus's careers page and normalized into a canonical job model.