Our client is a leading innovator in the medical device industry, developing cutting-edge products that address complex health challenges. As a Senior Regulatory Specialist, you will play a critical role in ensuring compliance with regulatory requirements and facilitating the approval process for new products.
**Job Description:**
This exciting opportunity requires an individual with extensive knowledge of regulatory affairs and experience in managing projects to deadlines. You will work closely with cross-functional teams to develop and execute regulatory strategies, manage submissions, and maintain compliance with evolving regulations.
* Develop and implement comprehensive regulatory plans for product registration and approval.
* Manage day-to-day regulatory activities, including submission preparation, review, and maintenance of documents.
* Collaborate with QA, R&D, Operations, Clinical Affairs departments to integrate regulatory requirements into QMS processes.
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