Regulatory Affairs Specialist
Farabi Medical
- Riyadh
- Permanent
- Full-time
- Manage product registrations and maintain up-to-date records of regulatory submissions.
- Conduct thorough reviews of product labeling and promotional materials for compliance.
- Collaborate with cross-functional teams to ensure that product development aligns with regulatory requirements.
- Monitor changes in regulations and assess their impact on the company's products.
- Provide guidance and training to internal teams on regulatory requirements and best practices.
- Prepare for and participate in regulatory inspections and audits.
- Develop and maintain relationships with regulatory agencies.
- Assist in the preparation of responses to regulatory inquiries and issues.
- Support the development of regulatory strategies for new products and market expansions.
- Excellent communication and interpersonal abilities.
- Detail-oriented with a high level of accuracy.
- Ability to work independently and manage multiple projects simultaneously.
- Proficient in regulatory documentation and submission processes.
- Experience in the medical device or healthcare industry.
- Knowledge of quality management systems and standards.
- Ability to adapt to changing regulations and industry trends.
- Strong organizational skills and time management.
- Commitment to continuous professional development in regulatory affairs.
Bayt