Roles & Responsibilities

1. Batch Manufacturing Record
2. Enter the data in Equipment usage log, Batch Manufacturing Record, Cleaning log and other required document.
3. Timely submit the samples and result collection from Quality Control department.
4. Follow cGMP & Safety rules during working in the plant.
5. Perform labeling as per SOP.
6. Write the status on equipment status board.
7. Perform cleaning of equipment as per SOP.
   
   
   * Pharma /API Background Must
   * Working Volume: Reactor Capacity: 50L - 5KL
   * Experience in Chemical Area (Only Hazardous)
   * Experience in Documentation

Company manufacturing facility at Masar, Gujarat, is at par with international standards. It complies with cGMP norms complying to the standards of WHO and is in the process of getting CEP for the active pharmaceutical ingredient Epirubicin , Lovastatin
This adequately reflects Company commitment towards quality. Efforts to attain such standards have also opened the key to gain foothold in the regulated and semi regulated markets throughout US and Europe

Company strives to become leaders in API pharmaceutical area by developing state of the art facility for research and development, contract manufacturing of active pharmaceutical ingredients. Company build quality in every aspect of manufacturing with particular laid down emphasis based on current Good Manufacturing Practices.
Company is committed to scaling new heights and creating new dimensions in Fermentation based API and Synthetic API.  This way Company shall support aspiration to "Live better and live longer".