Regulatory Local - Medical Devices

Key Responsibilities:

• Demonstrated expertise in product management, development, or commercialization of medical devices.
• Strong understanding of regulatory requirements and quality assurance standards for medical devices.
• Excellent communication and interpersonal skills for effective stakeholder management.
• Proven ability to work collaboratively in a fast-paced, cross-functional environment.
• Analytical mindset with strong problem-solving abilities.
• Experience in preparing regulatory documentation and supporting audits.
• Ability to manage multiple projects and prioritize tasks effectively.
• Willingness to work onsite and travel as required.