401 Job openings found

Hiring for upcoming Battery Manufacturing Industry  Position:  Quality Engineer - 02 Experience: Min 3 Years Experiences in the Battery manufacturing Industry  Education: DME / BE Salary: Rs. 35,000/- to 45,000/- Work profile: Electrical parameter testing of the final finish battery product lot wise as per the control Plan. Preparing and maintaining Quality records, MIS for system audit ...

Maintain production quality standards by following the quality manual. Reviewing computer parts for quality before they enter the assembly area. Use manufacturing tools such as screwdrivers, wrenches, hammers, and other hand tools to assemble various parts. Test computer machinery before it is sent off for packaging. Follow safety regulations for the safe operation of machinery. Communicate ...

Responsibilitiesof the QA Engineer will include:-Participate in the full Information Technology project lifecycle withparticular emphasis on Quality Assurance activities in the properimplementation of the Information Technology projects.-Responsible for supporting the development of comprehensive test strategies,plans, reports and environments for manual or automated testing for multiple ITprojects in a release cycle.-Responsible ...

QMS – Engineer 01 Post Education: BE Mechanical / Diploma Mechanical Experience: Min 2 Years in Automobile, Auto Component Mfg. Industry Salary Budget: Rs. 15,000/- to 20,000/- PM Knowledge: All Type of Audit & Documentations Personal skills:  A competent professional in Quality assurance and Quality Management System, process planning and process improvements with hands-on experience in SAP QM processes. Experienced in managing ...

Quality control and standards:  Develop and implement quality control plans, test procedures, and quality standards for genset assembly and testing.    Inspections and testing:  Conduct incoming, in-process, and final inspections of gensets and materials. Ensure performance and noise level testing are performed to specifications.    Problem-solving:  Investigate and troubleshoot quality issues, conduct root cause analysis (RCA), and implement both intermediate ...

17-02-25   HPS/2025/83 Quality Engineer Male 1 0 to 1 ITI/ DME Testing: Test products and systems to ensure they meet specifications and standards Problem solving: Investigate and fix issues, and develop corrective actions Documentation: Document inspections, analyses, and improvements Reporting: Prepare reports on quality and performance Training: Provide training to quality assurance teams Process improvement: Review processes to identify and implement improvements Compliance: Ensure products comply with regulations and standards Risk ...

JOB DESCRIPTION Quality Engineer Male 1 2 to 7 DME/BEE Mechanical   Roles and Responsibilities ASNT level 2, NACE, TQM / 6 Sigma /  Core experience from steel Fabrication industry having exposure to standards and specifications related to Mtl , Mtl testing, Welding , WPS,PQR qualification , Paint and paint testing , Trouble shooting of paint defects etc   manufacturing an ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results i n compliance with the Quality Management Plan & authorize their release for medical devices  Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the c orrectness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like Medical Device ...

Responsible for: . Analyzing, collecting data, and providing accurate, documented information about the status of quality . Verifying the correctness of quality related development results in compliance with the Quality Management Plan & authorize their release for medical devices . Validation of compliance to basic requirements, e.g. ISO standards and regulations like ...