About the Job
Key Responsibilities:
- Lead the regulatory affairs department ensuring compliance with DRAP and international guidelines.
- Oversee product registrations, renewals, and variations.
- Liaise with health authorities, auditors, and global regulatory bodies.
- Provide regulatory strategy for new product development and market entry.
- Lead the regulatory affairs department ensuring compliance with DRAP and international guidelines.
- Oversee product registrations, renewals, and variations.
- Liaise with health authorities, auditors, and global regulatory bodies.
- Provide regulatory strategy for new product development and market entry.
Requirements:
- Pharm-D / Master’s in a relevant field.
- 8+ years of experience in Regulatory Affairs within the Pharma sector.
- Strong knowledge of DRAP regulations and global regulatory standards.
- Pharm-D / Master’s in a relevant field.
- 8+ years of experience in Regulatory Affairs within the Pharma sector.
- Strong knowledge of DRAP regulations and global regulatory standards.