Job Description

Role & responsibilities 1) Responsible to monitor overall compliance in Research and development. 2) Review documents pertaining to analytical development and formulation development activity for completeness and accuracy as per regulatory requirement. 3) Monitor day to day activity in analytical development laboratory and formulation development for all time readiness. 4) Responsible to monitor project folders and department folders on the common server. 5) Responsible to review method validation/ verification protocol and report, analytical development report, formulation development report and technology transfer documents etc. 6) Preparation of standard operating procedure pertaining to Research and development. 7) Review and verification of raw data and electronic data generated at analytical development laboratory. 8) Responsible to verify the outside laboratory analysis and ensuring it is within specification. 9) Evaluation of change control and discrepancy with appropriate remedial action. 10) Identified the training needs to the team member and conduct of the GLP Studies. 11) Responsible to maintain the documents with systematic manner pertaining to the Research and development. 12) Responsible for issuance, distribution and control of documents pertaining to research and development Responsible to perform other duties allotted by reporting Manager as required or necessary. Preferred candidate profile M.Pharma Perks and benefits As Per Company Standard