
Aniqa Asif, FPGEC
Officer New Product Development (Formulation) @ Pharmatec Pakistan (Private) Limited
About
🌟 Actively seeking entry-level opportunities in the U.S. as a Pharmacy Intern to apply my diverse pharmaceutical background and contribute to the healthcare system. 🎓 I am a Doctor of Pharmacy (Pharm-D) graduate from Pakistan with hands-on experience across research, regulatory affairs, and clinical pharmacy. I have worked as an R&D Officer in a pharmaceutical company, focusing on formulation development and product evaluation, and also trained in the regulatory department, gaining knowledge of compliance standards and drug registration processes. 🧪 I completed research internship at the International Center for Chemical and Biological Sciences (ICCBS), University of Karachi in the Stem Cell Department, where I developed research and laboratory skills including cell culture and experimental analysis. 🏥 My academic journey included clinical and hospital pharmacy rotations, providing me with essential skills in patient care, medication dispensing, and interdisciplinary collaboration. I’m passionate about advancing my career in a dynamic U.S. healthcare setting and eager to contribute through commitment, adaptability, and a global perspective.
United States
Bridgeport
Pharmaceuticals
Presentations, New Product Development, Regulatory Compliance, Ethics, Pharmacovigilance, Common Technical Document (CTD), Regulatory Submissions, Regulatory Requirements, Dossier Preparation, Research and Development (R&D), Healthcare Management, Computer Literacy, Good Laboratory Practice (GLP), Analytical Skills, Internal Audits, Hospital Pharmacy, Project Management, Medicine, Research, ISO Standards
Experience

Officer New Product Development (Formulation)
Proficient in doing Literature survey and preparing SOPs. Hands on experience in manufacturing of prototype, trial & stability batches according to GMP & ICH guidelines. Assist Manager in preparing protocols and reports of New Products. Coordinate with Supply chain , Production ,Quality Operations & Regulatory Affairs department for trial & scale up batches.

MTO Regulatory Affairs
Assisted in the preparation of CTD Dossiers, Export Dossiers & other related documents. Reviewed product labeling to ensure compliance with guidelines. Record keeping of product registration & inquiry letters from DRAP, PQCB DTL etc Coordinate with other departments for inquiry of references & testing methods related to dossier.

Industrial Pharmacy Workshop
MSQ foundation
Pakistan
Learned different areas of Pharmaceutical Industries and their way of working
Aniqa Asif, FPGEC's Contact Information
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