Senior Research Scientist

• Execution of NCE projects, generic projects and line extension projects using QbD principle.
• Preparation and/or review of literature summary and development report to the assigned product.
• Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches to the assigned product.
• Preparation and/or review of technical documents like MFC, BMR, BPR and Stability protocol etc. following the GDP.
• Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same.
• Team management and motivation.
• Execution and/or supervision of scale up and pilot batches in pilot under GMP condition.
• Preparation and/or review of technical documents like product development report, batch manufacturing record, technology transfer documents and transfer of technology to manufacturing site, if required.
• Communicating with cross-functional team within within Piramal and client via mails and meetings.
• Preparing/ reviewing department relevant SOPs.
• Performing and/or supervision calibration and maintenance of R&D instruments and equipment
• Procuring/ indenting materials and machines change parts related to concern projects
• Maintain safe and hygienic condition in respective department
• Ensuring the use of personal protective equipment whenever required during batch execution
• Attending training related to FD, EHS and QA (if applicable)
• To complete any task or projects given by management or organization for product development and organization improvement.
• All generated waste to be sent to concerned person and must be comply with EHS requirements
• Communicating and interacting with international and national clients

Master in Pharmacy with minimum 10 years of experience in formulation development