Formulation & Development: Conduct pre-formulation and formulation trials for MOH products, while optimizing existing commercial formulas when required.Scale-Up & Pilot Batches: Oversee the scaling-up process to production and lead the manufacturing of pilot batches (internally and externally).Technology Transfer: Monitor the Technology Transfer process with QA and Production, and execute consecutive validation/site transfer batches.Documentation & Reporting: Prepare Product Development Reports, Master Formula/Packaging Cards, and document all trial results and manufacturing data.Compliance & SOPs: Ensure full adherence to GMP guidelines and quality policies, and author standard operating procedures (SOPs) for the R&D department.Analysis & Troubleshooting: Prepare samples for stability and bioequivalence testing, analyze test result variances, and provide troubleshooting solutions for production.Equipment & MSDS Management: Operate and qualify R&D instruments, while maintaining up-to-date Material Safety Data Sheet (MSDS) files.EHS & Team Support: Participate in job risk analysis, report workplace hazards/incidents, and train new employees on safe working instructions. Bachelor’s degree in pharmacy or a related field 2–5 years of experience in Research & Development within the pharmaceutical or related industries Good knowledge of GMP standards