Quality Assurance Associate

This job role involves the documentation activities conducted at the Par Formulation Indore Sterile Facility. As a personnel in this role, your main responsibilities include managing documentation and training, as well as handling various software such as Doc pro, Veeva, and Compliance wire (LMS). Your tasks will include: - Issuing Records of Analysis - Issuing controlled and uncontrolled copies of standard operating procedures - Issuing protocols, reports, layouts, and forms - Issuing logbooks and drawings - Following cGMP practices according to defined procedures - Performing distribution, retrieval, and destruction of documents as per procedures - Maintaining employee training files - Ensuring document controls on-site (Master Production Records/Packaging Records/Analytical Documents, etc.) - Managing master and controlled documents in the Documentation Cell - Assigning document numbers and equipment numbers as per defined procedures - Stamping controlled and uncontrolled copies and recording entries in respective formats - Initiating change control related to document cell activities - Generating Daily QMS data sheets as required and tracking pending documentation tasks. In this role, attention to detail, adherence to procedures, and proficiency in document management software are essential for successful completion of tasks.,