Job Description

- Producing medicine at a small scale according to the given formulation As well as reporting and providing useful Documenting the production steps and the results in the analysis sheet and preparing the FDA documentations. - Innovation to improve existing products in the company - Troubleshooting of solid dosage form and other pharmaceutical products. - Ability to implement safety procedures in the laboratory and familiar with the relevant standards - Development of analytical methods - Analysis of raw materials and finished products and interpreting data. - Documentation - Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms and as well as other dosage forms. - Evaluate patents and develop non-infringement strategies. - Scale-up and optimization of manufacturing process; execution of pre-exhibit and exhibit batches; - Scale-up and technology transfer from R&D to production to meet timelines. - Work proactively with other cross-functional groups to execute change controls associated with Manufacturing and Packaging master records, SOPs and protocols. - Create and review SOPs, as well as review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement. - Ability to develop new products - Ability to Work closely with marketing department for positioning of product & segmentation. - Fluent in specialized formulation courses