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  • Experience: Minimum 6 years experience into Internal Audits. Qualification: Qualified Chartered Accountant. Designation: Manager/ Senior Manager. Location: Pune. Outstation Candidates can also apply. CTC: Upto 22 L/A Job Profile: Accountable for the identification and reporting on all Desired Profile: Candidate should have atleast 6 years of experience into Internal Audits. Candidate should have Corporate Work ...

  • 4 years of experience in the quality team out of which min 2 years handling the below responsibilities Experience Required: Experience is conducting ISO/ISMS audits. Experience in conducting data analysis using MS excel/ Minitab to identify the improvement areas Implement process / analyst

  • Responsible for conducting calibration and performance review call in terms of quality with client as well as the internal team. Conduct refresher training based on the errors identified. Maintaining update log and communicate process updates by conducting a session. Perform weekly analysis aiming

  • Engineering, or related discipline. Must Have Skills Good knowledge of Software Development Life Cycle and Quality Assurance concepts, metrics, SDLC methodologies and documentation standards (Agile Environment) Hand-on experience of at least one object oriented programming language (Java, C# or python ...

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager-Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager-Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager-Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • -Set up Quality Mgmnt System as per ISO13485 / D&C Act/New Medical device Rule at Distributors place under Manager -Lead Distributor Audit, follow up for CAPA Response plan, tracking the action plan till the closure

  • Job Description: Handling Quality Assurance. Heading entire QA Team. Responsible for setting all processes related to quality, standard operating procedures (SOPs) that are to be followed in the plant. Exposure to UK, US, European buyers. To carry out other tasks as assigned by management from

  • Overall Responsibility from Stitch to Pack Handling man power of complete production floor Handling Training dept. with better technical solutions Maintaining records and status for the order Maintaining discipline and memorandum of floor Must have Technical background in Quality in buying house Residing near by location Must have exp in to Garments Strong into Co-ordination Problem solving skills

  • Hands on experience in plastic injection molding and painting. Adhere to APQP requirements and ensure linkages of Process flow, PFMEA, Control Plan. Ensure PPAP review in compliance to automotive standards. BE + CIPET specialization with 6+ years of relevant experience (or) Diploma + CIPET specialization with 8+ Years of experience Six sigma and Problem solving tools Good Planning Skills Having Good Experience ...

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