Quality Engineer Graduate Jobs in Navi Mumbai

Monitor and ensure quality of construction work as per approved drawings and specificationsConduct site inspections, tests, and audits to ensure compliance with standardsPrepare and maintain quality documentation, reports, and checklistsCoordinate with site engineers, contractors, and consultants for quality-related mattersEnsure materials used at site meet required quality standardsIdentify defects and suggest corrective and preventive actionsEnsure compliance with BMC and other regulatory guidelinesMaintain records of tests (concrete, soil, materials, etc.)Participate in client/authority inspections

Key Responsibility.Incoming material inspection.in-process Quality inspection.pre- Dispatch inspection.(PDI)Documentation.

We are hiring for Quality Engineer- Chemical A) Qualification : To become a QA person in the pharmaceutical industry, one should have a degree in a science-related field, such as chemistry or pharmacy, to better understand pharmaceutical products.B) Experience : 0 to 2 years in R&D Pharmaceutical Industry from QA Department.C) Responsibility :1. Review of Manufacturing Processes.2. Knowledge of All regulated Guideline & Pharmacopoeia.3. Preparation & implementation of SOPs related to the concerned department & Justification of Specification.4. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.5. QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.6. The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.7. A QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements8. The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.9. The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA).10. A QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.11. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.12. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.Qualification- Graduate in Chemical Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Production Manager position. Looking after daily production of medical devices and following SOP and maintaining QMS as per required. Looking after waste management, production management, raw material management and quality assurance in production. Looking after production time frame for dispatch

Designation : QA ManagerLocation : MumbaiQualifications : Degree in a science-related field, chemistry or pharmacyExperience : 3+ years in R&D Pharmaceutical Industry from QA DepartmentResponsibility :* Review of Manufacturing Processes.* Knowledge of All regulated Guideline & Pharmacopoeia.* Preparation & implementation of SOPs related to the concerned department & Justification of Specification.* Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.* QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.* The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.* QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements* The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.* The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA)* QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.* Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.* Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.* Implementation & verification, in-process checks, online entries in BPR of product at Pilot plant manufacturing site.* Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site.Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Need a candidate who has good amount of production management knowledge with minimum 5 to 6 years of experience in the same field. He should have qualities like Production control, quality control, stock management waste management, error control, costing control, QMS, SOP, 5 P of production. production staff management. We looking for candidate for long term for at least 5 years.