Regulatory Affairs Intern- Tamheer , Riyadh
الوصف الوظيفي
About Boston Scientific
At Boston Scientific, we empower professionals to reach their full potential by fostering an environment of diversity, innovation, and high performance. Recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, we are committed to advancing healthcare through cutting-edge medical technologies. Our global teams tackle critical industry challenges, supported by state-of-the-art tools, comprehensive training, and a culture that values collaboration and excellence. Whether your ambition is to grow your expertise or contribute to life-changing innovations, Boston Scientific provides the platform to achieve your career goals.
The Role
As a Regulatory Affairs Intern in Riyadh, you will play a pivotal role in supporting the entry, maintenance, and accuracy of Unique Device Identification (UDI) data within the Saudi Food and Drug Authority (SFDA) Saudi-DI system. This internship offers a unique opportunity to gain hands-on experience in implementing SFDA MDS-REQ-007 guidance while developing a deep understanding of regulatory processes in Saudi Arabia. You will collaborate closely with cross-functional teams to ensure data integrity and compliance with stringent regulatory requirements, contributing to the advancement of healthcare solutions that improve patient outcomes.
Key Responsibilities
- Data Management: Enter and update UDI data in the Saudi-DI system in strict alignment with SFDA requirements, ensuring accuracy and completeness at all times.
- Documentation & Tracking: Maintain meticulous UDI trackers and ensure precise documentation of all submissions to support regulatory compliance.
- Cross-Functional Collaboration: Support the regulatory affairs team with UDI-related submissions and updates, fostering seamless communication with internal stakeholders.
- Issue Resolution: Coordinate with teams to address missing, incomplete, or inconsistent data, ensuring timely and accurate resolutions.
- Process Improvement: Assist in enhancing data accuracy and process efficiency by identifying opportunities for optimization and implementing best practices.
- Compliance Adherence: Follow established procedures and maintain strict compliance with quality and regulatory standards to uphold Boston Scientific’s commitment to excellence.
Qualifications
- Education: Currently pursuing a bachelor’s degree in regulatory affairs, life sciences, biomedical engineering, or a closely related field.
- Skills & Competencies:
- Exceptional attention to detail and strong organizational abilities to manage complex data and deadlines.
- Proven ability to follow instructions and adhere to established procedures with precision.
- Proficiency in Microsoft Office tools, particularly Excel, to support data analysis and reporting.
- Excellent communication and collaboration skills to engage effectively with diverse teams.
- Preferred Qualifications:
- Familiarity with regulatory requirements or medical device industry standards, demonstrating a foundational understanding of the field.
- Genuine interest in regulatory affairs and compliance within the healthcare industry, with a passion for driving impactful change.
Why Join Boston Scientific?
As a global leader in medical technology for over 45 years, Boston Scientific is dedicated to transforming lives through innovative solutions that address unmet patient needs and reduce healthcare costs. Our portfolio includes high-performance devices and therapies that empower physicians to diagnose and treat complex conditions across cardiovascular, respiratory, digestive, oncological, neurological, and urological specialties. By joining our team, you will contribute to groundbreaking advancements that make a tangible difference in patient care while growing your expertise in a dynamic and supportive environment. Explore our mission and values further at www.bostonscientific.com and connect with us on LinkedIn.
يمكن أن يرتكب الذكاء الاصطناعي أخطاءً.