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  • 1. CQA (Audits, Validation, QMS) - Male Candidates Prefered. Required: B.Pharma / M.Pharma / MSc with 4-8 years of same CQA experience in Validation, QMS, Regulatory Audits etc. 2. CQA (Market Complaints review & Investigation, Packaging Specifications, Audit Expertise, good exposure of SAP etc ...

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • needs of production of personnel and prepare annual training schedule for GMP training · To reconcile the raw material & packaging material and finished products · To ensure that validations protocols are prepared and reviewed · He shall use his discretion to find alternatives Supervision, Coaching, Managing Processes, Process Improvement, Tracking Budget Expenses, Production Planning, Controls and ...

  • variations for filing the post approval changes in the US and EU region. 6. Review the analytical document of raw material and finished products specifications & test procedures, packaging material specifications & test procedures, in-process specifications & test procedures, analytical method validation Qualification : M.Pharm from reputed institute with more than 70% marks Skills : Person should have ...

  • C date should be able to join within a month. Should be a male candidate. Should be a North Indian Should have worked in good pharma companies. KEY RESULT AREA o Review and submission of ANDA o Review and submission of responses to the queries o Review of all documents related AD, PD, QA, MA &

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • and finished products specifications & test procedures, packaging material specifications & test procedures, in-process specifications & test procedures, analytical method validation protocols and reports etc. 7. Review the development documents like master formula records, product development reports Qualification : M.Pharm from reputed institute with more than 70% marks Skills : Person should have worked ...

  • products specifications & test procedures, packaging material specifications & test procedures, in-process specifications & test procedures, analytical method validation protocols and reports etc. Review the development documents like master formula records, product development reports and stability Mandate Skills required: Person should have worked for eCTD filing for injectable and ophthalmic. C date ...

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • Location: Chennai Job Introduction Handle end-to-end recruitment effectively fro Pharma vertical. To be passionate about providing permanent/temp Hiring to customers as per the timeframes using social networking sites, job portals & references . Key activities & deliverables Coordinate with key

  • and accurate reports on to inventory, stock, shipment, forecast for the smooth function of Purchase-Logistics-Supply chain Coordinating with warehouse and update the status of materials receipt, dispatch, proper utilisation. Analyze & develop packaging material & structures after conducting product

  • and accurate reports on to inventory, stock, shipment, forecast for the smooth function of Purchase-Logistics-Supply chain Coordinating with warehouse and update the status of materials receipt, dispatch, proper utilisation. Analyze & develop packaging material & structures after conducting product

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • Life cycle management of the Drug Master Files (Amendments, Annual Reports, CEP updates and Bi-Annual updates). Preparation, review and submission of Applicant's Part DMF (Open Part DMF) and Technical data package to customers. Handling of DMF deficiencies received from regulatory agencies

  • and accurate reports on to inventory, stock, shipment, forecast for the smooth function of Purchase-Logistics-Supply chain Coordinating with warehouse and update the status of materials receipt, dispatch, proper utilisation. Analyze & develop packaging material & structures after conducting product

  • and accurate reports on to inventory, stock, shipment, forecast for the smooth function of Purchase-Logistics-Supply chain Coordinating with warehouse and update the status of materials receipt, dispatch, proper utilisation. Analyze & develop packaging material & structures after conducting product

  • and accurate reports on to inventory, stock, shipment, forecast for the smooth function of Purchase-Logistics-Supply chain Coordinating with warehouse and update the status of materials receipt, dispatch, proper utilisation. Analyze & develop packaging material & structures after conducting product

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