Lupin Recruitment -Send Resume TO HR mail

✅ Arrangement of documents and records in documents cell and timely tracking of documents for the effectiveness, submission, retrieval, discontinuation, obsoleting and destruction of the specific documents under the SOP guidance.
✅ Ensure retention of documents and records as per regulatory requirements.
✅ Ensure and monitor the document cell activity as per SOP and facility meets the GMP compliance level.
✅ Preparation and review of Specifications, Standard Test Procedure and Test data sheet such as Raw Material, Packaging Material, In- Process, Intermediate, API Finished and Finished products.
✅ Preparation and review of the SOP’s of Quality Assurance department.
✅ Initiation and review of change control, deviation and other quality system (QAMS system) documents. Tracking of QAMS events for closing and make sure the closure as per timeline.
✅ Issuance, Retrieval and Destruction of documents such as SOPs, Specification and Standard Test Procedure, Logbooks and all other documents.
✅ Documents updating in ‘Omni Docs’ as per SOP.
✅ Master BMR /BPR linking /delinking and printing from SAP.
✅ Preparation of master plan (Master Inspection Characteristic Report) in SAP.
✅ Preparation and review of E-TDS, SAP Annexure’s and related activities i.e. Merging, Uploading, Linking /delinking and Printing in SAP.
✅ E-TDS Merging, Uploading, Linking and Printing in SAP.
✅ Numbering of all type of QAMS document and logging into respective records/system.
✅ To perform the e-DMS Activity such as QA Authorizer.
  
 📝 Interested candidates can share their resume at 📧 parichayindore@lupin.com.