Global Medical Device Specialist
4 days ago
About the Role
We are seeking an experienced APAC Regulatory Expert to join our team. In this role, you will be responsible for ensuring that our medical devices comply with regulatory requirements in Australia, New Zealand, and other APAC countries.
Key Responsibilities:
- Develop and implement regulatory strategies for medical devices in the APAC region
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements
- Review and approve product labeling, advertising materials, and other documentation
- Assess the impact of new regulations and provide recommendations for implementation
Requirements:
- Minimum 2-5 years of experience in medical device regulation or a related field
- Strong knowledge of Australian, New Zealand, and international medical device regulations
- Excellent communication and problem-solving skills, with the ability to work independently and collaborately
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