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  • To provide QA oversight for production to ensure procedures are being followed in accordance with GMP compliance. To ensure and coordinate that all Manufacturing Quality Assurance activities in manufacturing plants are performed as per BPR, SOPs

  • To provide QA oversight for production to ensure procedures are being followed in accordance with GMP compliance. To ensure and coordinate that all Manufacturing Quality Assurance activities in manufacturing plants are performed as per BPR, SOPs

  • To provide QA oversight for production to ensure procedures are being followed in accordance with GMP compliance. To ensure and coordinate that all Manufacturing Quality Assurance activities in manufacturing plants are performed as per BPR, SOPs

  • QA API

    Omgi Consultants

    Aurangabad, Maharashtra

    To provide QA oversight for production to ensure procedures are being followed in accordance with GMP compliance. To ensure and coordinate that all Manufacturing Quality Assurance activities in manufacturing plants are performed as per BPR, SOPs

  • for regulatory agency inspections. Provide support and training to other staff members to develop additional auditing resources. Overall responsibility for strict Quality Assurance Controls such as line clearance and In-Process quality controls and continuous improvement of manufacturing compliance. Carrying out

  • for regulatory agency inspections. Provide support and training to other staff members to develop additional auditing resources. Overall responsibility for strict Quality Assurance Controls such as line clearance and In-Process quality controls and continuous improvement of manufacturing compliance. Carrying out

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • Monitoring and control of the manufacturing environment. Process validation is done as per established system. Monitoring of storage conditions for materials and products. Retention of records. Compliance with the requirements of GMP

  • To evaluate & maintain Risk Assessment. To evaluate & maintain Vendor qualification & Market Complaint To review system as per requirements of cGMP / statutory / regulatory. Conducting Plant & Laboratory round and ensuring Compliance

  • To evaluate & maintain Risk Assessment. To evaluate & maintain Vendor qualification & Market Complaint To review system as per requirements of cGMP / statutory / regulatory. Conducting Plant & Laboratory round and ensuring Compliance

  • To evaluate & maintain Risk Assessment. To evaluate & maintain Vendor qualification & Market Complaint To review system as per requirements of cGMP / statutory / regulatory. Conducting Plant & Laboratory round and ensuring Compliance

  • To evaluate & maintain Risk Assessment. To evaluate & maintain Vendor qualification & Market Complaint To review system as per requirements of cGMP / statutory / regulatory. Conducting Plant & Laboratory round and ensuring Compliance

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