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  • Cadila Pharmaceuticals

Audit Manager Jobs in Dholka

1 - 14 of 14
1 - 14 of 14
Search Results - Audit Manager Jobs in Dholka
Cadila Pharmaceuticals Limited-Dholka
exposure  •  Hands-on PLC/SCADA experience  •  Audit & validation experience  •  Team leadership capability  •  Digital / automation project exposure Qualifications  •  Experience: 10–20+ years (Pharma mandatory)  •  Role Level: Manager / Sr. Manager  •  Department...
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Cadila Pharmaceuticals Ltd-Dholka
Major purpose of the Job: To conduct Audit for BE Clinical, Clinical Trial, Medical Writing, Clinical Data Management, IT, Archival Department to ensure that activities are conduct as per applicable SOP and Regulatory Requirements. Responsibilities...
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Cadila Pharmaceuticals Ltd-Dholka
operations Maintain Laboratory Information Management Systems (LIMS) Assist users with software-related issues and training Ensure compliance with GMP, GxP, 21 CFR Part 11 guidelines Maintain audit trails and data integrity standards Support validation...
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Cadila Pharmaceuticals Ltd-Dholka
  1.  IT Infrastructure Management Maintain and monitor servers, networks, and hardware systems Ensure uptime and performance of IT systems across departments Handle installation, configuration, and troubleshooting of systems 2. Software & Application...
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Cadila Pharmaceuticals Ltd-Dholka
To make a daily plan based on the monthly plan and share to the reporting managers. • To ensure the availability of lubricated blend, core tablets, coating materials and equipment before plan. • To distribute the operational activities among...
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Cadila Pharmaceuticals Ltd-Dholka
Handling of internal audit.  •  Routine lab monitoring in ADL, Synthesis lab & PERL.  •  Tracking of SOP effectiveness and review requirements.  •  Handling of SOP management system.  •  Review and approval of outside sample testing and analytical test report...
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Cadila Pharmaceuticals Ltd-Dholka
required  •  Primary selection of vendor for new development by team.  •  Discussion with new vendor for their capabilities, plants, terms etc.  •  Ensure approvals of QA, QC, Plants for submitted Sample  •  Vendor audit if required & negotiations  •  Arrange...
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Cadila Pharmaceuticals Ltd-Dholka
Management of all receipt/storage /issuance and reconciliation of PM & Misc. Store as per SOP. Maintain cGMP in warehouse and give regular training to all employees. • Ensure receipt and on-line documentation of the materials received as per SOP...
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Cadila Pharmaceuticals Ltd-Dholka
updation, follow  •  up for the CAPA and to ensure effective implementation of CAPA.  •  Preparation, Review, Issuance, Revision, Control and Retrieval of SOP pertaining to functioning of the department.  •  Participation in GMP Audits (Audit Checklist Compilation...
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Cadila Pharmaceuticals Ltd-Dholka
Management of all receipt/storage /issuance and reconciliation of PM & Misc. Store as per SOP. Maintain cGMP in warehouse and give regular training to all employees. • Ensure receipt and on-line documentation of the materials received as per SOP...
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Cadila Pharmaceuticals Ltd-Dholka
Training Compliance in Regulatory Audits.  •  GMP Training to be conducted for new joiner and existing employee.  •  Support smooth Operation & Management of Training Information Management system (TIMS) and its Updation  •  as per regulatory requirement...
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Cadila Pharmaceuticals Ltd-Dholka
Major purpose of the job : • To maintain best practices for Document Management System • To maintain QMS documents and timely, accurately compiled it with all evidence to justify. Principal task and responsibilities : 1. Document Management system...
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Cadila Pharmaceuticals Ltd-Dholka
for the noncompliance found during self  •  inspection.  •  To participate in all internal and external audits.  •  To prepare compliance report of different customer and regulatory audits.  •  To make sure that internal and external audit compliance report is prepared within...
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Cadila Pharmaceuticals Ltd-Dholka
timers and other utilities in the section/department. 24. Coordinating with RQA during the facility audits and study based inspections and complying with RQA audit observations. 25. Preparation of Form B and obtaining its IAEC approval. Allied...
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