We are looking for a motivated, honest, and dedicated professional with a strong command of written and spoken English and a solid understanding of the pharmaceutical industry. The successful candidate will play a key role in briefing doctors and patients, managing pharmaceutical documentation, and ensuring strict compliance with regulatory requirements. This position demands hands-on experience with dossier submission to DRAP for product registration, as well as active involvement in inventory control and stock management. Candidates should be committed to a long-term role and not planning to relocate abroad within the next six months.
Key Responsibilities:
- Prepare and submit dossiers to DRAP for pharmaceutical product registration, ensuring accuracy and completeness.
- Manage store stock issuance and receiving processes, verifying releases against invoice details, batch numbers, and expiry dates.
- Conduct monthly stock level assessments and review expiry reports, communicating updates to manufacturers as needed.
- Cross-check daily purchase and sales records to maintain precise inventory records.
- Coordinate with the CDC office to promptly resolve any licensing issues.
- Update and maintain company Standard Operating Procedures (SOPs) and ensure documentation compliance in line with manufacturer requirements.
- Provide clear and effective briefings to doctors and patients about pharmaceutical products, supporting their understanding and safe use.
Required Qualifications:
- Proven experience in pharmaceutical dossier submission and regulatory compliance, particularly with DRAP.
- Strong knowledge of pharmaceutical stock management, including batch control and expiry monitoring.
- Excellent command of written and spoken English to communicate effectively with stakeholders.
- Ability to manage documentation and ensure compliance with manufacturer standards.
- Experience liaising with regulatory bodies such as CDC for licensing matters.
- Commitment to a full-time, in-person role with no plans to relocate abroad within six months.
Preferred Qualifications and Benefits:
- Prior experience in updating and managing company SOPs is highly desirable.
- Ability to work collaboratively within a team environment.
- Competitive monthly salary ranging from Rs45,000 to Rs55,000.
This full-time, in-person position offers a valuable opportunity to contribute significantly to pharmaceutical operations and regulatory compliance within a dedicated and professional team.