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Summary
I am a highly motivated and detail oriented professional, boasting over four years of
successful experience in the dynamic fields of Pharmacy. My career goal is to
leverage this expertise to foster growth within a competitive and adaptable learning
organization. I am eager to embrace constant challenges that will not only enhance
my skill set but also drive significant change within the industry.
Experience
Pharmacist (MOH - UAE)
- 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.
Senior Officer Regulatory Affairs
- 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.
Regulatory Affairs Co-ordinator
- 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.
