• Standardize quality assurance process for all existing products, new products and new suppliers • Ensure documentation & regulatory compliance for: Designing of SOP for clustering of products based on Haz/Non Haz, Liquid/Solid; MSDS approval; ISO procedure • Identifying Labeling Requirement (Product Labels) - destination specific, road transport, rail, shipping line; IIP requirement • Supplier evaluation for new supplier in quality practices & periodic review of existing suppliers • Cross functional Interface with Marketing- Logistic- Finance- Risk-Operation • Building strong relationship, evaluation & development of service providers like inspection services at various locations • Deciding course of action when deviation are observed and based on criticality take relevant approvals before action

Arrange appointments with doctors, pharmacists and hospital medical teams, which may include pre-arranged appointmentsKeep up to date with the latest clinical data supplied by the companyAchieving assigned targets for every brand of the company

Arrange appointments with doctors, pharmacists and hospital medical teams, which may include pre-arranged appointmentsKeep up to date with the latest clinical data supplied by the companyAchieving assigned targets for every brand of the company

Arrange appointments with doctors, pharmacists and hospital medical teams, which may include pre-arranged appointmentsKeep up to date with the latest clinical data supplied by the companyAchieving assigned targets for every brand of the company

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.

ValidationPlanning and execution of validation and qualification activityTo review the Validation Master PlanPrepare the Re-validation schedule and execute the activity as per scheduleTo update validation master planTo review the Media Fill Protocol and reportExecution for Process validationTo review Hold Time Study protocols and reportsHandling Cleaning ValidationPlanning and Execution for HVAC system with Third partyTo review the list of calibration and validation of all equipments / instrumentsTo review certificate receipt from third party validationTo review preliminary SOP of QA, Process/Cleaning validation protocols and report and get it finalize after approval of QA HeadTo review Quality Management DocumentTo review the documents as current SOP and regulatory requirements.