akuabemahntiedu

1. Analyzed bulk and finished product samples of drugs quantitatively and qualitatively to ensure the product’s assay was within British pharmacopeia (BP) or USP specifications. 2. Competent in using and calibrating lab instruments, including liquid particulate counters, PH meters, analytical ba lances, conductivity balances, UV spectroscopy, HPLC, and digital polarimeters. 3. Conducted stability analysis of products for both accelerated and long-term periods. 4. Strict adherence to all Good Laboratory Practices and safety procedures while handling corrosive and dangerous chemicals. 5. Maintained up-to-date records of all laboratory activities, including analysis, device usage, calibration log books, and other records.

1. Assisted in organizing workshops in training all workers including the security men on Good Manufacturing Practices guidelines and applications 2. In solving the problem of the possibility of missing documents, I assisted in organizing all documentation (BMRs, SmPcs) for each of the products in chronological order. 3. Helped to ensure that, in terms of GMP rules, comprehensive in-house inspections were performed more than twice a day. 4. I was able to improve product quality by ensuring that all in-process tests were done and ready on time before the production of a batch began. 5. I assisted in the review of all SOPs for each of the operations carried out in the industry and made sure they were ready before the review date expired. 6. Ensuring that interns comprehend the activities of a pharmaceutical company, I assisted in tutoring interns by organizing quizzes and presentations. 7. I assisted in ensuring that all samples stored in the retained room were subject to the right temperature and humidity