Senior Regulatory Affairs Consultant
2 weeks ago
Position Overview:
As a Senior Regulatory Affairs Consultant, you will play a crucial role in facilitating the development of innovative products for both local and global markets. Your expertise will be essential in shaping and refining regulatory strategies in response to evolving regulatory landscapes.
Key Responsibilities:
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
- Provide guidance on regulatory submissions and approvals for new products.
- Monitor and interpret regulatory changes to adapt strategies accordingly.
- Support the development of documentation and reports necessary for regulatory submissions.
Qualifications:
- Extensive experience in regulatory affairs within the medical device industry.
- Strong understanding of both domestic and international regulatory frameworks.
- Excellent communication and analytical skills.
Why Join Us:
At Stryker, we are committed to advancing healthcare through innovative solutions. Join our team and contribute to meaningful projects that impact lives globally.
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