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