-Gained valuable insights into key industry sectors including Manufacturing, Quality assurance, Quality control and Regulatory affairs.-Assisted in the review of Standard Operating Procedures (SOPs) and other quality documentation to ensure they comply with GMP guidelines.-Acquired proficiency in established protocols, and the operation of industrial equipments and materials.-Assisted in reviewing product labels, advertising materials, and promotional content to ensure compliance with regulatory standards.-Developed the ability to communicate effectively with team members and stakeholders.

-Perform administrative tasks such as managing inventory and processing prescriptions.-Acquired insights into health products, over the couter drugs and medical devices.-Managing stocking shelves and checking expiration dates.-Counsel patients on medication usage, side effects, and interactions.-Learned about insurance claims processing and patient billing procedures.-Learned how to monitor and report adverse drug reactions and medication errors to regulatory authorities.