- Dispensing of prescription medications and provide information to patients about
the drugs and their use. 
- Completes pharmacy operational requirements by organizing and directing
technicians’ workflow, verifying their preparation and labeling of pharmaceuticals,
and verifying order entries, charges, and inspections. 
- Meeting medical representatives, managing budgets, keeping statistical & financial
records, and inventory management of central drug store. 
- Arrange for distribution of the medical products and supplies to various
destinations by sorting, packing, and dispatching products. 
- Analyses inventory levels, inventory positioning, correct inventory system, verify
the accuracy and troubleshoots immediate inventory inaccuracies.

- Pharmaceutical product registration and renewals (local, export, and contract
manufacturing), pricing, export NOCs, CPP, and updating the comprehensive
product list for pharmaceuticals, healthcare, and consumer divisions.   
- Responsible for all regulatory affairs and international business development
documentation, standard operating procedures (SOPs), and the revision of leaflet
inserts and packaging artworks.   
- Managed F&R healthcare product enlistment (local, export, and contract
manufacturing) and F&R consumer division product registration with the Pakistan
Standard Quality Control Authority (PSQCA), as well as product enlistment
variations.   
- Responsible for registration and documentation with the Ministry of Narcotics
(ANF) and the Intellectual Property Organization of Pakistan (IPO) for trademark
registration.   
- Proficient in online web-based software, including DRIS, PRIMIS (renewals, eCTD),
IPO, import/export, GTIN GS1 product barcodes, and other online documentation.   
- Conducted presentations for official inspections, visits from delegates, and ISO
audits within the firm.

- Concerned with regulatory documents, including Technical Files, product
registration, renewals, price increases (CPI, SROs), updating product lists (local,
export, veterinary and toll manufacturing), deficiencies & other regulatory documentation.
- Communication (written, telephone, and direct) with regulatory agencies/DRAP.
- Form-5 dossiers (local and export) for human and veterinary sections.
- Common Technical Dossiers – CTD and ACTD.
- Work on the Drug Regulatory Information Management System (DRIM-S) site.
- Assisted in the development and maintenance of regulatory files, records, and 
reporting systems.
- Concerned with DTL (Drug Testing Labs) and Drug Inspector/FID letters. 
- Export NOC, CPP, COO, dossiers, agreements, and other documentation.