naukri
Regulatory Affairs Executive
CorDx Drug Stores LLC
Dubai, UAE
Mid
2 weeks ago
Regulatory AffairsProduct RegistrationMOHAPIVD ProductsMedical Device ClassificationLabeling Compliance
Free
Job Fit Check
Base Career helps you apply smarter for this job.
?%
Ready to ScanKey skills for this role
Regulatory AffairsProduct RegistrationMOHAP
About the Role
Key Responsibilities: Prepare, compile, and submit product registration dossiers for IVD products to MOHAP and other relevant authorities. Ensure timely renewal and maintenance.
Key Skills for This Role
Regulatory AffairsProduct RegistrationMOHAPIVD ProductsMedical Device ClassificationLabeling Compliance
Responsibilities
- Prepare, compile, and submit product registration dossiers for IVD products to MOHAP and other relevant authorities
- Ensure timely renewal and maintenance of product licenses and regulatory approvals
- Classify medical devices and IVD products according to UAE and international regulatory requirements
- Review product labeling, packaging, and promotional materials for regulatory compliance
- Liaise and communicate with MOHAP officers and other health authorities for registration follow ups and clarifications
- Maintain regulatory databases, documentation, and product registration records
- Monitor and interpret changes in regulatory requirements and ensure company compliance
- Collaborate with internal departments (Quality, Operations, Sales) to ensure all regulatory documentation supports business needs
- Support importation and post market surveillance activities as required
Requirements
- Prepare, compile, and submit product registration dossiers for IVD products to MOHAP and other relevant authorities
- Ensure timely renewal and maintenance of product licenses and regulatory approvals
- Classify medical devices and IVD products according to UAE and international regulatory requirements
- Review product labeling, packaging, and promotional materials for regulatory compliance
- Liaise and communicate with MOHAP officers and other health authorities for registration follow ups and clarifications
- Maintain regulatory databases, documentation, and product registration records
- Monitor and interpret changes in regulatory requirements and ensure company compliance
- Collaborate with internal departments (Quality, Operations, Sales) to ensure all regulatory documentation supports business needs
- Support importation and post market surveillance activities as required
Full Job Posting
Key Responsibilities
- Prepare, compile, and submit product registration dossiers for IVD products to MOHAP and other relevant authorities.
- Ensure timely renewal and maintenance of product licenses and regulatory approvals.
- Classify medical devices and IVD products according to UAE and international regulatory requirements.
- Review product labeling, packaging, and promotional materials for regulatory compliance.
- Liaise and communicate with MOHAP officers and other health authorities for registration follow ups and clarifications.
- Maintain regulatory databases, documentation, and product registration records.
- Monitor and interpret changes in regulatory requirements and ensure company compliance.
- Collaborate with internal departments (Quality, Operations, Sales) to ensure all regulatory documentation supports business needs.
- Support importation and post market surveillance activities as required.
Apply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career