• Involvement in analytical method Validation, and method feasibility studies.• Analytical testing of solid dosage form finished products for batch release purposes, as well as stability studies. • Performing in-Vitro Comparative studies to meet drug product filling requirements for foreign regulatory bodies. • Day to day testing mainly includes Assay, CU, RC, and dissolution Testing using HPLC (Empower III). As well as Testing using UV, IR apparatuses. In addition to Water content analysis (KF, LOD) and PSA (Laser Diffraction using malvern 3000, Sieve analysis)

• Ensuring finished drug products' overall physical and chemical quality, and their adherence to regulatory requirements while maintaining cGMP.• Experienced with HPLC (Shimadzu, waters, Agilent) with Empower 3 software, UV and IRspectroscopy, as well as Karl Fischer (KF), Dissolution, physical testing apparatuses for several dosage forms (tablets, capsules, syrups, lotions, creams, ointments, and suppositories).• Preparing the required reagents for testing according to the tests' perspective SOPs.• Experienced in cGMP regulations and guidelines as 21 CFR part 210, 211, 11 and ICH.

• Invigilating International General Certificate of Secondary Education (IGCSE) exams.• Making sure the exam conditions are up to par with the British Council’s quality standards.

•Assisting pharmacists in dispensing prescription medications accurately and efficiently.•Learning and applying knowledge of OTC medications and addressing the costumer'smedication-related questions and concerns under the pharmacist in charge's supervision.•Assisting with inventory management, including receiving, stocking, and organizing medications and supplies.

• Leading a research team in a pharmaceutical research project on a new nanoparticle formulation.• Writing the paper for publication under the supervision of Dr Hany Mahmoud.• Our team won 2nd place in the 2022 MIU senior conference for best research project.

• Training in QA department with practical involvement in the day to day tasks performed in the factory.• Learning the workflow of a sterile Pharmaceutical factory starting with Raw material receiving till finished product release.

• Reviewing patient medical records and medication histories to identify drug-related problemsand make recommendations.• Attending daily Clinical pharmacotherapy training sessions.

• Taking part in an online program to enhance our skills as medical representatives through live sessions from multiple sales and marketing mentors.

• Took part in Hikma’s Virtual Internship program • The internship included live interactive sessions about Pharmacovigilance, Drug manufacturing, Quality Control and Assurance, Sales and Marketing

• Training as a Medical Representative In addition to going on practical sales visits

• Participated in the EVA Talent Internship (ETI)• The internship included training in Drug manufacturing, Quality Control and Assurance, Medical Biotechnology, Scientific Research, Sales and Marketing

• Assisting the pharmacist in charge and helping with customers