Regulatory Affairs Specialist

We’re Hiring: Regulatory Affairs Specialist

On behalf of a leading multinational pharmaceutical company

A renowned multinational pharmaceutical company is seeking a talented and motivated Regulatory Affairs Specialist to join its dynamic regional team.

If you have solid experience with GCC regulatory submissions and a passion for ensuring compliance in a fast-paced, innovative environment — we want to hear from you!

Key Responsibilities:

Prepare and submit registration dossiers in line with GCC health authority requirements (SFDA, DHA, NHRA, etc.).

Maintain up-to-date knowledge of regulatory guidelines and legislation across GCC countries.

Collaborate with cross-functional teams to ensure timely and accurate submissions.

Support product lifecycle activities including renewals, variations, and labeling compliance.

Communicate effectively with regional regulatory bodies and internal departments.

Qualifications:

Bachelor’s degree in Pharmacy, Life Sciences, or a related field.

Strong understanding of regional regulatory frameworks.

Excellent organizational and communication skills.

• 3-5 years GGC experience ,
• eCTD knowledge (compiling and lifecycle management using any eCTD tools )
• Excellent communication and documentation skills
• Attention to detail and analytical thinking
• Proficiency in English and Arabic

Job Types: Full-time, Part-time