Kinetic has partnered with a leading Pharmaceutical company who are actively recruiting a Regulatory Affairs Specialist for their team in Riyadh.
Please note that you must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.
The main responsibilities will include but not limited to:
- Prepare, compile, review, and submit regulatory dossiers for new product registrations, renewals, variations, and post-approval changes.
- Works closely with cross-functional teams to facilitate product registrations, lifecycle management activities, and timely approvals.
- Ensure all submissions comply with applicable regulations, guidelines, and company standards.
- Track submission timelines and ensure regulatory commitments are met.
To be successful, you will need to meet the following:
- Minimum 3 years of experience in a Regulatory Affairs role within the pharmaceutical industry.
- Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field.
- Experience in preparing CTD/eCTD submissions.
- Strong knowledge and understanding of pharmaceutical regulatory requirements and guidelines.
- Well experience of interacting with SFDA.
- Must be based in Riyadh currently.
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