1. Develop and maintain 70% Standard Operating Procedures (SOPs) in compliance with the National Pharmaceutical Regulatory Agency (NPRA) audit requirements and the Department of Occupational Safety and Health (DOSH) guidelines.2. Effective record-keeping ensures adherence to regulatory standards and guidelines, providing a clear audit trail of CAPA activities for regulatory authorities to review.3. Conduct validation studies for media, including Growth Promotion Test (GPT), and method suitability on pharmaceutical products, ensuring the accuracy and reliability of both counting and test methods.4. Conduct microbiology tests on water, food, cosmetics, traditional products, and supplements, following the workflow outlined in the British Pharmacopoeia.5. Perform hygiene monitoring of the environment and stability testing of products toensure the cleanliness of the production line and product safety.

1. Assist in conducting experiments, analyzing raw materials, and evaluating product stability and efficacy.2. Perform analytical testing, such as pH measurements, viscosity tests, and ingredient compatibility studies.3. Prepare detailed reports and documentation of experiments, results, and observations.4. Conduct quality control checks on finished products to ensure they met specifications and made recommendations for adjustments if needed.