DRAP Regulatory Affairs Officer

We are seeking a detail-oriented and experienced DRAP Regulatory Affairs Officer to join our expanding team. The successful candidate will play a crucial role in ensuring full compliance with regulatory requirements for medical and laboratory equipment within Pakistan. This position involves managing product registrations, maintaining up-to-date knowledge of DRAP regulations, and collaborating closely with regulatory authorities to support the company’s compliance and marketing efforts.

Key Responsibilities:
- Manage product registrations with DRAP for Class A, B, C, and D medical devices.
- Ensure strict adherence to DRAP rules, guidelines, and documentation standards.
- Prepare and submit comprehensive regulatory dossiers and technical files.
- Liaise effectively with DRAP officials and other regulatory bodies to facilitate approvals.
- Monitor regulatory updates and implement necessary changes within the organization.
- Support the marketing team by ensuring product claims and advertisements comply with regulatory requirements.

Required Qualifications:
- Bachelor’s or Master’s degree in Pharmacy or a relevant field.
- 1 to 3 years of mandatory experience in DRAP regulatory affairs.
- Strong knowledge of DRAP regulations and medical device classification systems.
- Proven experience in product registration and licensing processes.
- Excellent documentation skills coupled with effective communication abilities.

Preferred Qualifications and Benefits:
- Competitive salary package along with additional company benefits.
- Opportunities for career growth within a rapidly expanding organization.
- A professional work environment focused on compliance and regulatory excellence.
- Work location is on-site, fostering direct collaboration with the team and regulatory bodies.

Only shortlisted candidates will be contacted for further steps in the recruitment process.