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  • of Medical checkup SOP. 11. To monitor compliance and effectiveness of Personnel Hygiene SOP. 12. To monitor compliance and effectiveness of Pest control SOP. Key Skills: Preference to candidate working in medical devices Industry. Sound knowledge of ISO 9001 & 13485, Certified Lead Auditor from any ISO

  • of Medical checkup SOP. 11. To monitor compliance and effectiveness of Personnel Hygiene SOP. 12. To monitor compliance and effectiveness of Pest control SOP. Key Skills: Preference to candidate working in medical devices Industry. Sound knowledge of ISO 9001 & 13485, Certified Lead Auditor from any ISO

  • of Medical checkup SOP. 11. To monitor compliance and effectiveness of Personnel Hygiene SOP. 12. To monitor compliance and effectiveness of Pest control SOP. Key Skills: Preference to candidate working in medical devices Industry. Sound knowledge of ISO 9001 & 13485, Certified Lead Auditor from any ISO

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Responsible for overall quality of product and compliance of GMP at the site To review and approval of site master files Release the batches for distribution Investigate market complaint and prepare response and forward it further review

  • Experience in quality assurance a with at least 5-7 years hands on QA Lead experience preferably In EMS company . Manage multiple QA/ Testing project leads guiding the team Responsible for defining, reviewing and tracking engineering metrics like On-Time Delivery, Quality etc. Executes the project

  • Experience in quality assurance a with at least 5-7 years hands on QA Lead experience preferably In EMS company . Manage multiple QA/ Testing project leads guiding the team Responsible for defining, reviewing and tracking engineering metrics like On-Time Delivery, Quality etc. Executes the project

  • To ensure SOP compliance for entire facility. To supervise the IPQC activities of manufacturing plant. Is responsible for testing of all products i.e. In-process, Raw material, Packing material and Finished product by chemically. Is responsible to prepare and perform all the standardization activity of volumetric standard solution and maintain its record as per GMP. Must have experience of API ...

  • Monitoring and controlling product quality at each stage of manufacturing, Devising procedures to inspect and report quality issues, Complaint management and CAPA, QMS management and MR function, Managing regulatory compliance, Quality training, Handling customer audits and New Product Development ...

  • Monitoring and controlling product quality at each stage of manufacturing, Devising procedures to inspect and report quality issues, Complaint management and CAPA, QMS management and MR function, Managing regulatory compliance, Quality training, Handling customer audits and New Product Development ...

  • Designation: AGM QA- API - Dahej Reports to: VP â€" Corporate QA & RA Reportees: Manager / Assistant Managers / Executives in the QA & QC team Educational Qualification: M.Sc(Chemistry) / B.E (Chemical Engg) / B.Sc(Tech) in Pharmaceuticals preferable Masters in Regulatory. • Manage

  • Designation: AGM QA- API - Dahej Reports to: VP â€" Corporate QA & RA Reportees: Manager / Assistant Managers / Executives in the QA & QC team Educational Qualification: M.Sc(Chemistry) / B.E (Chemical Engg) / B.Sc(Tech) in Pharmaceuticals preferable Masters in Regulatory. • Manage

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