Pharmacist Regulatory Affairs - DRAP

Description

Latif Brothers (Instruments) is seeking a diligent and detail-oriented Pharmacist Regulatory Affairs professional specializing in DRAP compliance to join our team. This role focuses on managing the regulatory submissions and compliance for electromedical equipment and medical devices in accordance with Drug Regulatory Authority of Pakistan (DRAP) guidelines. The ideal candidate has at least one year of relevant experience and is skilled in preparing, compiling, and reviewing applications for product registration and licensing through the DRAP online portal. The Pharmacist will work closely with internal teams and external stakeholders, ensuring all documentation is complete, accurate, and compliant with current regulatory requirements. Though this position does not involve managing a team, it demands excellent organizational and communication skills to coordinate activities with different departments and international manufacturers effectively. In this role, the pharmacist ensures that all regulatory submissions are properly tracked and completed in a timely manner, addressing any queries or documentation deficiencies promptly. The pharmacist is responsible for maintaining comprehensive records related to applications, including acknowledgments, correspondence, deadlines, and current status updates. Staying informed about updates to DRAP policies, forms, and portal procedures is essential to identify and address compliance gaps early. This position offers an opportunity to contribute significantly to ensuring the safety, efficacy, and regulatory integrity of medical and electromedical products distributed by Latif Brothers (Instruments).

Responsibilities

• Prepare, compile, and review DRAP applications related to electromedical equipment and medical devices for submission via the DRAP online portal.
• Gather and verify technical, regulatory, company, manufacturer, and product information from internal teams, principals, and manufacturers.
• Identify required documentation and data for each regulatory application, ensuring completeness, accuracy, and proper organization of files.
• Accurately enter application data and upload supporting documents to the DRAP portal, maintaining high attention to detail.
• Manage the entire application process by tracking status, monitoring queries or deficiencies, coordinating responses, and ensuring timely follow-up until resolution or approval.
• Review forms and supporting documents for consistency, completeness, validity, and proper formatting before submission.
• Coordinate with internal departments and overseas manufacturers or principals to obtain missing documents, clarifications, and updated information.
• Maintain well-organized records of applications, including acknowledgments, reference numbers, correspondence, deadlines, and current status.
• Stay current with relevant DRAP requirements, portal procedures, forms, and regulatory updates that impact medical devices and electromedical products.
• Identify early compliance gaps or missing information, communicate issues effectively, and coordinate prompt resolution.
• Manage multiple regulatory submissions simultaneously, prioritizing tasks to meet all submission and follow-up deadlines.

Experience

1 Year

Apply By

Dec 10, 2026

Required Skills

• DRAP Regulatory Compliance
• Drug Registration And Licensing
• Regulatory Submission Management
• Medical Equipment DRAP Management
• Regulatory Documentation
• Attention to detail
• Compliance Monitoring

Nice to Have Skills

• Application tracking
• Records Management
• Coordination
• Time management