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Quality & Regulatory Director
Not specifiedFull-timeRegulatory Affairs ManagementMedical DevicesBusiness Consulting
Join a senior leadership team supporting medical device clients with quality assurance, regulatory affairs, certification, and clinical trial programs.
Responsibilities
- Lead complex quality assurance and regulatory affairs projects for medical device clients.
- Define and execute regulatory strategies to achieve timely global market clearances.
- Drive project strategy, technical precision, and commercial efficiency.
- Provide leadership within the senior management team.
Requirements
- B.Sc. in Engineering.
- At least 10 years of experience in a medical device manufacturing company.
- Proven management and team leadership experience.
- ISO 13485 Lead Auditor certification.
- Full professional proficiency in written and spoken English.
- Strong stakeholder management, interpersonal, and service-oriented skills.