Regulatory Affairs Specialist

Regulatory Affairs Specialist - Smith+Nephew, Saudi Arabia

We are seeking a dynamic and detail-oriented Regulatory Affairs Specialist to join our team at Smith+Nephew in Saudi Arabia. In this role, you will play a pivotal part in ensuring our medical devices comply with regulatory requirements and maintain our high standards of quality and safety.

Your key responsibilities will include:

• Preparing and submitting regulatory documents to the Saudi Food and Drug Authority (SFDA) and other relevant authorities.
• Monitoring regulatory changes and their impact on our products.
• Collaborating with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.
• Maintaining regulatory documentation and ensuring its accuracy.

To excel in this role, you should have a Bachelor's degree in a relevant field, such as Biology, Chemistry, or a related discipline. Previous experience in regulatory affairs, preferably within the medical device industry, is highly desirable. Strong communication skills, both written and verbal, are essential, as is proficiency in Arabic and English.

If you are a proactive, organized individual with a keen eye for detail, we would love to hear from you. Join us and be part of a global leader in medical technology, where you can make a real difference to patients' lives.