Regulatory Affairs Specialist

Kinetic is working with a reputable Pharmaceutical company actively recruiting a Regulatory Affairs Specialist for their team in Riyadh.

***Please take the time to read the job description, you must meet all the criteria set out below for your application to be considered. We do check all applications and 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.***

Key aspects of the role include:

• 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.

Hiring If you need help filling a similar position in your company, please contact us on +971(0)4 433 4579 or click here.

***We check all applications and 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.***