Reg Affairs

**Reg Affairs - P4**:

- Work mode: Hybrid- Onsite Location(s): Riyadh, SA**Additional Locations**: N/A

**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance**

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing - whatever your ambitions.

As an Regulatory Affairs Specialist, you will be responsible of supporting the regulatory submission and provide input on regulatory-related issues associated with compliance and achieving the business plan for assigned countries, in Middle East.
- Key Responsibilities:_
- Prioritize and plan on product registration for his/her respective product lines.
- Maintain an active knowledge of the status of pending approvals /submissions, and shepherd registrations through the approval process.
- Provide the management team with regular updates on product registration.
- Ensure product registrations files are reviewed and renewed as required.
- Supports tender operations by timely supply of accurate regulatory documents.
- Establish and maintain a good working relationship with regional RA peers to gain positive & timely support for document preparation.
- Ensures to meet additional Regulatory project requirements support if assigned and when needed.
- Required Skills and Qualifications:_
- BS in Scientific discipline/engineering preferred
- Has the at least 2 to 3 years’ experience in Regulatory environment
- Knowledge and experience of local regulations and standards.
- Must highly have organization skills / and can manage multitask in very competitive environment.

**Requisition ID**:573157

**Job Segment**:Compliance, Regulatory Affairs, Law, Engineer, Supply, Legal, Engineering, Operations