- Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices according to regulatory requirements.
- Identifies, analyzes and implements country specific requirements necessary for product related submissions.
- Recommend strategies for earliest possible approvals for marketing applications.
- Performs regulatory projects or acts as a member of the project steering group.
- Submits required documentation/information to local authorities or Varian internal.
- Initiates and escalates necessary activities if deviations are identified.
- Ensures creation of adequate documentation for audits/inspections.
- Performs training within the organization in country specific regulatory requirements, if applicable.
- Write and maintain submissions procedures, work instructions and templates relevant for maintaining regulatory compliance.
- Performs review of promotional material for regulatory compliance according to country specific requirements.
- 5-8 years' experience.
- Product Registration Experience:
- Experience with FDA 510(k) applications, Health Canada license applications and EU MDR technical files.
- Knowledge of regulatory guidance documents and requirements for product classification determination, FDA 510(k) submissions, Health Canada license Applications and EU MDR technical files.
- Knowledge of regulatory guidance documents (FDA, Health Canada, and EU MDR) for determining if a product change requires a regulatory submission (software and hardware devices).
- Working knowledge of ISO 13485, IEC 62304, IEC 62366, ISO 14971, and ISO as evidenced by coursework or submissions that required use of each standard.
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Sr. Regulatory Affairs Specialist - Palo Alto, United States - Hired by Matrix
Description
Job Description
Job DescriptionHybrid Role - Onsite 2D/Week
What You'll Do:
What You Bring: