Regulatory Affairs Manager

Posted on 07 July 26 by Ana Alborte

  • Saudi Arabia
  • AED - AED
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Job Description

A reputable and well-established Pharmaceutical company is actively recruiting a Regulatory Affairs Manager to be based 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:

  • Develop and execute regulatory strategies aligned with business objectives.
  • Drive product registrations and ensure timely regulatory approvals.
  • Maintain and strengthen relationships with the Saudi Food and Drug Authority (SFDA) and other GCC health authorities.
  • Ensure compliance with local regulatory requirements throughout the product lifecycle.
  • Collaborate closely with cross-functional regional and global teams.

To be successful, you will need to meet the following:

  • Minimum 5 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 managing variations, renewals, pricing submissions, and lifecycle management.
  • Solid knowledge of SFDA and GCC regulatory requirements and submission processes.
  • Excellent stakeholder management, communication, and leadership skills.

Must Read: The 7 uncomfortable reasons you were rejected from the role you just applied for

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

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Job Information

Rate / Salary

AED - AED

Sector

Life Sciences

Category

Not Specified

Skills / Experience

Not Specified

Benefits

Not Specified

Our Reference

JOB-14893

Job Location