Biography

A detail-oriented Pharmacist with over 4 years of diverse experience spanning IP, Quality Assurance validation, R&D stability, and clinical pharmacy. Proven expertise in technical writing, regulatory compliance, data analysis, and evaluating complex technical frameworks. Highly motivated to leverage a strong pharmaceutical background and analytical mentality to transition into intellectual property and patent management.

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Recent Experience

  • Actively manages patent filings and patent prosecution workflows.
  • Authors and prepares comprehensive technical proposals.
  • Analyze substantive examination reports and leverages a strong pharmaceutical and technical background to draft precise, strategic responses for clients.

Prior to joining Al Tamimi & Company, Reem worked as:

QA Validation Specialist

-Authored, reviewed, and managed highly technical validation documents, including Risk Assessments, User Requirements, Functional Specifications, and Validation Plans. Reem also Oversaw site qualification protocols (HVAC, thermal mapping, machine/instrument qualification) and administered the site validation master plan.

R&D Stability Pharmacist

-Designed stability protocols, established SOPs, and developed advanced stability-indicating assays for pharmaceutical products. Reem also Analyzed complex formulation trials and applied rigorous problem-solving skills to troubleshoot analytical testing methods.

Language(s)

  • English
  • German
  • Arabic

Education

  • 2020-Faculty of Pharmacy (Clinical Program) -Cairo University.
  • 2025-Pharmacovigilance Training Course & Workshops.
  • Analytical Procedures Verification & Validation Course-Egyptian Drug Authority.

Admission

  • Innovation, Patents & Industrial Property (3IP)
  • Technical Writing & Validation Documentation (SOPs, Protocols, Risk Assessments) .
  • R&D Stability Analysis & Method Development.
  • Regulatory Documentation (ICSRs, PSMFs, PBRERs, RMPs)