Performed raw material testing to verify compliance with pharmacopeial standards prior to production use
Conducted finished product testing including physical and chemical analysis to ensure quality specifications were met
Assisted in sampling procedures for raw materials, in-process samples, and finished products
Operated and calibrated laboratory instruments (e.g., HPLC, UV-Visible spectrophotometer, dissolution apparatus) under supervision
Documented test results accurately in compliance with GLP and GMP standards
Assisted in stability testing and shelf-life analysis of pharmaceutical products
Reported deviations and out-of-specification (OOS) results to senior QC staff for review

Assisted in batch manufacturing processes, ensuring adherence to Good Manufacturing Practices (GMP)
Reviewed and maintained Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for accuracy and completeness
Observed and supported tablet/capsule manufacturing operations including granulation, compression, and coating processes
Monitored in-process quality checks during production to ensure compliance with SOPs
Assisted in line clearance activities and documentation before batch changeovers
Gained exposure to production planning, equipment cleaning validation, and cGMP compliance protocols
Coordinated with QC and QA departments to ensure production standards met regulatory requirements

Assisted pharmacists in dispensing prescribed medications and verifying prescriptions for accuracy and completeness
Worked alongside oncology pharmacists, gaining exposure to chemotherapy protocols and specialized medication handling
Participated in rounds with clinical pharmacists, observing patient-specific therapy decisions and drug monitoring
Observed and supported inpatient and outpatient pharmacy operations, gaining exposure to hospital pharmacy workflow
Learned drug storage, labeling, and inventory management practices in compliance with hospital standards
Assisted in patient counseling on medication use under supervision of senior pharmacists
Supported documentation and record-keeping related to controlled substances and stock management

Assisted in preparing regulatory submission dossiers for DRAP (Drug Regulatory Authority of Pakistan)
Compiled and organized documentation required for drug registration and renewal applications
Reviewed product labeling, packaging inserts, and artwork for compliance with DRAP regulatory requirements
Assisted in maintaining regulatory records and tracking submission timelines
Supported preparation of variation applications for approved products (formulation, packaging, or labeling changes)
Coordinated with QA, QC, and Production departments to gather technical documentation for submissions
Gained familiarity with DRAP guidelines, drug registration process, and pharmaceutical compliance standards in Pakistan

Assisted pharmacists in dispensing emergency medications quickly and accurately under high-pressure conditions
Verified prescriptions for accuracy, dosage, and drug interactions in time-critical emergency cases
Supported medication preparation for trauma, resuscitation, and critical care patients
Assisted in maintaining emergency drug trolleys and crash carts, ensuring stock availability and expiry monitoring
Gained exposure to emergency pharmacotherapy including analgesics, antibiotics, and life-saving drugs
Coordinated with emergency physicians and nursing staff for timely medication administration
Assisted in documentation of controlled substances and emergency drug utilization

Dispensed prescribed medications accurately, ensuring compliance with hospital protocols and patient safety standards
Reviewed prescriptions for drug interactions, dosage accuracy, and contraindications
Counseled patients on proper medication use, dosage schedules, and potential side effects
Maintained accurate records of inventory, stock levels, and controlled substances
Coordinated with physicians and nursing staff to ensure timely and appropriate pharmaceutical care
Assisted in maintaining pharmacy compliance with hospital quality and safety regulations

Doctor of Pharmacy (Pharm-D) — completed coursework covering pharmacology, pharmaceutics, pharmaceutical chemistry, clinical pharmacy, and pharmacy practice, with practical training in hospital and industrial pharmacy settings. Gained strong foundation in drug development, quality standards, and regulatory frameworks relevant to the pharmaceutical industry.