115 Manufacturing Quality Jobs - Page 4

Head QC & Customer Assurance for Precision Consumer Durable products Lead QC team PAN India at factories & People Mgmt Develop QC Strategy Conduct Audits to ensure sourcing & manufacturing QC Standards & Reliability strategy & implementation Required Candidate profile B.Tech / M.Tech LADY candidate 20+ Yrs exp in QC in FMCG / CD / Auto / Consumer Electronics / Pharma Currently leading QC in Manufacturing Exp in leading multi locational QC in mfg./assembly units Perks and benefits Best As Per Industry Standards

Responsibilities: * Lead quality initiatives across organization. * Conduct regular audits and inspections. * Ensure compliance with IATF standards. * Collaborate with cross-functional teams on improvement projects.

Title : Senior Analyst, Manufacturing Quality Applications Location: Bengaluru, KA We are seeking a skilled Manufacturing Quality Application analyst with 3 - 5 years of experience Digital Project and/or Support organization, along with a strong understanding of discrete manufacturing processes. Candidate should have experienced applications among those categories : Statistical Process Control application, Incoming Goods Inspections application, Tools Calibration Management application, Product Inspections Management application, Manufacturing or Engineering Change Notice application, Quality Surveillance Plan application, Quality modules of Manufacturing Execution Systems. Knowledge experience on Manufacturing Execution System (MES), Agile Project execution Outsystems lowcode platform is a plus. Responsibilities : Lead the continuous improvement, configuration, and maintenance of CSQ applications (Customer Satisfaction Quality) applied to Manufacturing domain to optimize manufacturing processes and data management. Collaborate with cross-functional teams to analyze, design, and improve Quality processes within applications and integrations to other systems Provide functional and technical guidance in Board of Change and provide functional specifications based on business requirements Analyze Level 2 tickets, trouble shoot the issues and coordinate with Level 3 Application Developers (internal or 3rd parties) and other Digital Teams to ensure minimal disruptions to production. Work with Application developers Digital / Business teams on building functional specifications coordinate agile project releases. Conduct training programs to educate end-users on system functionalities and best practices. Stay updated on industry trends and best practices in manufacturing systems to recommend and implement continuous improvements. Requirements : Bachelor s degree in engineering, Mechanical/Production, or related field. Proven experience (3 -5 years) in implementing and supporting quality applications. Knowledge of discrete manufacturing processes and industry standards. Proficiency in system integration, data analysis, and troubleshooting. Excellent communication skills and ability to collaborate with diverse teams. Exposure to Agile Project execution (optional) Exposure to Outsystems lowcode platform (optional) Bachelor s degree in engineering, Mechanical/Production, or related field. Proven experience (3 -5 years) in implementing and supporting manufacturing quality applications. Exposure to

Role & responsibilities : Candidate is responsible for 5 Star Audit IATF Audit Quality Core Tools New Project Development Business plan Preparation Customer Handling (QC, QA & SQA) APQP, PPAP, FMEA , Control Plan, SPC, MSA, IATF Documentation Product Development, Supplier Sourcing, VAVE / Cost Savings, Project Management QC Tools - Pareto & why why analysis Process Improvements, Problem solving, Internal Audit, Process Audit / Product Audit Supplier Evaluation, Performance Monitoring, CAPA Analysis Examine the Monthly Quality Results and developments, Reporting to Management Make ensuring that all the Customer Specific Requirements are met.

Role & responsibilities Position Overview: We are looking for a proactive and experienced CNC Quality Manager to lead and manage the quality assurance function in a CNC-based precision manufacturing environment. The ideal candidate must have a strong background in multiple CNC processes and machine types with proven leadership in quality systems, team management, and process improvement . Key Responsibilities: Lead the Quality Assurance team to ensure all CNC machined components meet or exceed customer and industry standards. Oversee the inspection of parts from various CNC processes (milling, turning, grinding, EDM, honing, lapping, polishing, etc.). Develop and implement quality control procedures , standard operating practices , and inspection protocols . Drive compliance with ISO 9001 / IATF 16949 / AS9100 or other applicable quality systems. Interpret and enforce engineering drawings , GD&T , and customer-specific requirements. Conduct regular audits, quality reviews, and team training sessions. Interface directly with customers on quality concerns , audits, and continuous improvement initiatives. Lead root cause analysis (RCA) and implement corrective and preventive actions (CAPA) . Analyze non-conformance data and drive efforts to reduce rework, scrap, and customer complaints. Ensure all measuring instruments and CMMs are properly calibrated and maintained. Required Skills & Experience: B.E. / B.Tech / Diploma in Mechanical or Production Engineering. 712 years of relevant experience in CNC quality management . Strong knowledge of CNC processes : milling, turning, grinding, EDM, honing, etc. Familiarity with machines from Fanuc, Mazak, DMG Mori, Haas, Makino , etc. Expertise in quality tools : 5 Why, Fishbone Diagram, FMEA, PPAP, SPC, MSA. Proficient in GD&T , surface finish measurement , and precision metrology . Excellent leadership, communication, and team development skills. Experience managing customer audits and working with cross-functional teams. Preferred Attributes: Exposure to Lean Manufacturing or Six Sigma methodologies. Hands-on experience with CMM software (Zeiss, Mitutoyo, Hexagon, etc.). Experience in high-precision industries like aerospace , medical , or automotive . Availability Requirement: Candidate must be available to join immediately or within 15 days .

Hello, Good Day! & we are one of the most aggressively & rapidly growing company named A. M. Designs Private Limited (AMD) (http://www.amdindia.in/) is an AS9100D Certified company specifically focused on providing precision Engineering Solutions to Space, Aviation & Defense Industries worldwide. Position: QC Engineer. Qualification: Diploma/BE/B. Tech (Mechanical/Production Engineering/CAD-CAM) Reporting To: QA-QC Lead Engineer/Operation Manager. We are looking for QC Engineer with following capabilities. Having expertise in handling measuring instruments like Vernier caliper, Height gauge (TRIMOS), Micrometer, Radius Gauge, Go-No Go Gauge, Thread Gauge, Slip Gauges, Profile projector, Hardness Tester- etc. Knowledge of GD&T. Define measurement strategy. Stage inspection of Machined part as per drawing and give first piece approval. Ensure Product & Process characteristics for In-process management at Shop floor. Maintain Quality documents. Rejection analysis of ongoing process & control. Prepare Rejection Report & Quality Performance Report on daily basis Responsible for Rework and Rejection (Yellow/Red bin) analysis at shop floor & initiate CAPA. In-process manufacturing of the products and their online inspection. 100 % Visual Inspection. Root Cause analysis using problem solving tools like 7QC Tools, 8D, Why-Why Analysis and coordinate with production team. Follow-up of Corrective and Preventive Action Implementation. Coordinate with production team and generate Quality alert at shop floor over customer complain. Knowledge of CMM Machine. Knowledge of operating of CNC/VMC Machines. Ability to give training to Operator. If you are interested, Please send your updated Resume to Email: career@amdindia.in Place Of Work: A. M. Designs Pvt. Ltd. Kathwada GIDC, Plot No 24, Road No 5/A, Odhav Road,Ahmedabad-382430 (INDIA) Regards Contact Details : Mrs. Juhi Suthar Ms. Saloni Pandit Mo: 63577723 / 9712950735 Email ID : hradmin@amdindia.in / career@amdindia.in Call between 11:00 to 6:00

. Implementing Quality management systems . Review & approval of Process validation, cleaning validation, Water Validation, HAVC Validation, Analytical Method Validation. . Annual product reviews and reviews of stability reports Required Candidate profile 20+ years of experience in Pharmaceuticals Industry with Quality Management Systems, Quality Assurance, Validation, Greenfield Projects in dosage form -. Solid orals ,liquid injectable,

Roles and Responsibility 1. Implementation of Final Quality testing as per manufacturing Quality Plan 2. Final Quality Audit as per Defined Frequency and manufacturing Quality Plan 3. NC management and Identification and Traceability of Non-conforming Materials 4. Perform Data Analysis for Post- Lamination Defects(Visual / EL / IV/ HV) and preparation of Root cause analysis and Action plan for Reduction of Post-Lamination Defects 5. Ensure quality audits; record and analyze feedback and initiate follow-up audits where necessary and review of the Corrective action implemented. 6. Devise test methods and inspection processes to ensure adherence to specifications based on international standards and best practices in the industry. 7. Monthly reporting and analysis of rejection levels with root cause and identify action areas to ensure early detection and reduction in rejections to enable productivity. 8. Perform Root cause /FMEA / SPC / 7 QC tools analysis of process/Production/Quality Issues associated with Module Production line 9. Implement and Execution of On-Job training to shop floor Operators for corrective actions of issue. 10. Daily and Monthly MIS

Division- Production Department- Assembly Job Location- Kharkhoda, Haryana Job Title- Quality Supervisor - Assembly - (3~5 yrs) Job Role : 1. Should have experience of working in manufacturing quality. 2. Knowledge of vehicle manufacturing processes like Weld, Paint & assembly are desired. Reporting To :Shift Incharge Level in the organization JE/SE Educational Qualification Diploma in Mechanical/Automobile Engineering. Graduation (With Specialization): Work Experience (Years) in treasury activities. 3 5 years Job Responsibilities : 1.Lead quality operation in defined shift. 2.Resolution of Defects using Problem solving tools 3.Drive containment actions along with other stakeholders. 4.Validate and monitor the countermeasure and provide correct feedback to stakeholders. 5.Handling voice of customer and resolution of problem at earliest. 6. Organising daily quality review meeting. 7. Preparation of weekly & monthly reports for management reporting. Competencies / Skills 1. Hand on Experience of MS Excel and power point. 2. Experience of quality abnormality Handling 3. Experience of Vehicle Inspection & Manufacturing Process of 4 Wheeler Industry 4. ISO 9001-2015 System & procedure Knowledge 5. Planning and Problem solving Skills 6. Co-ordination and communication with other stake holders 7. Can read engineering drawings.

Develop 2D/3D CAD models and engineering drawings using tools such as SolidWorks, AutoCAD. Perform design calculations, tolerance stack-ups, and feasibility analyses. Work on new product development and modifications of existing designs. Collaborate with manufacturing, quality, and RD teams to ensure design feasibility and manufacturability. Participate in prototype development and support testing and validation. Review and revise technical documentation in accordance with company standards. Ensure compliance with applicable industry standards and safety regulations.

Responsibilities: * Conduct field surveys on manufacturing quality * Provide IT support at service desk * Conduct market research for industry associations * Report findings to stakeholders * Collect data through market survey. 50+ Vacancies All MH Flexi working Work from home Over time allowance

Handle QMS (ISO 9001: 2015), QC & Customer Assurance for Consumer Durable products Handle EMS (14001:2015) Be the Certified internal auditor for the both systems People & Process Mgmt. Quality Management OHSAS Six Sigma Lean manufacturing Required Candidate profile LADY B.Tech 3-5 Years exp in QMS & EMS in manufacturing, engineering comp. QMS (ISO 9001 : 2015) CERTIFIED INTERNAL AUDITOR EMS (14001 : 2015) CERTIFIED INTERNAL AUDITOR Six Sigma, TQM, OHSAS etc. Perks and benefits Best As Per Industry Standards

Dear Candidate, Greetings from Grupo Antolin India Pvt. Ltd. We are one of the largest players in the car interiors market internationally and number 1 worldwide supplier of headliner substrates. We offer products with high added value to outfit automobile interiors: Overhead Systems, Doors, Cockpits, Lighting, Electronic Systems & Integrated Products. We dominate the complete component cycle from component conception and design, through development and validation to parts industrialization and sequenced delivery. We have an opening with us for the position of Quality Manager in for our Grupo Antolin India Pvt. Ltd. (Chakan Plant) Responsibilities: To boost the Quality Culture and continuous improvement focusing the company operations in the Customer Satisfaction. Define the quality assurance and improvement plan of the company managing all activities described in the process P10. Principal Duties and Responsibilities Should define the Objective parameters against each of the KPI indicator to monitor the Performance of the Reporting team against the defined targets linked to the Management objectives QMS systems. Should have the Customer Requirements and the Quality targets defined by the customer and ensure that there is an action plan for higher/ equal or lesser than customer quality targets.. Mechanism for sharing these defects and Objectives throughout the Plant. Should be conversant with IATF requirements ,GA QMS process. IATF CSR requirements VW- Formal Q Audits , GMI -BIQS , FCA -PCPA Renault -Supplier Health Check and M&M- MSES Audit Co ordination and NC closure along with Yearly Audits- TLD ( VW in case of Concerns ) , PCPA ( Incase of TML, FCA and GMI and adhere to the Quality Routine Plan Product & Process Changes-Responsible to Track the Changes in the Process and Product as per the GA Application guide Procedure GA P 06 Knowledge of NC monitoring system for NC with Open/ Close status and action plan for delayed / Pending NC. -Customer Audits Knowledge of Quality Routines and Evaluation of P10 Process and Staff meetings , GAPS Audits. Customer claims -Should have strong Knowledge and skill on Problem solving tools and Management tools for giving guidance to the team in Problem section and mentor the weak areas --QMS -Customer Specific Action Plan review and Closure in the Portal Progress Monitor for Effectiveness and Phenomena Recurrence. Should Ensure that Customer Satisfaction with Customer Visit and Satisfaction survey sign off . Should be a Part of Phase 3 and Phase 4 Customer Documentation closure - PPCR-IPA-CPA-IPH-CPH along with the Customer PPAPA document submission in coordination with the Quality Engineering. NQC for Customer Rejections and GAPS Audit Compliance Capture Lessons Learnt and the Process Know How and its Horizontal deployment for the NQC Issues. To implemented the CSR requirements related to the EMS & OHSMS. To implemented the TQM & TPM system with the great approach. To implemented the CSR requirements related to the EMS & OHSMS. Responsible for the developing child part and the P10.3 Responsible for the DVP & NDP activity To implement lab at NABL level. Qualifications: Experience in Automotive sector at least 15 years Experience Communication skills, analytical thinking, attention to detail, problem-solving capabilities, leadership qualities, ability to influence others, a strategic approach, and a focus on continuous improvement. What can we offer you: You will be part of a highly engaged multinational with international career opportunities. We offer you a learning journey adapted to your professional experience. You will work on international projects for world- renowned companies in Automotive sector. You can find an open Environment to learn new technologies. We can offer you a competitive salary & benefits. If you are interested for the said position, kindly revert back with your updated profile on below email Id - reshma.renukar@antolin.com

Quality Assurance / Manufacturing Quality / Customer Quality / Root cause Analysis / PPAP / APQP / 8D / Plant Quality / Six Sigma / Quality Audit

Quality Assurance Leadership, Compliance Oversight: Ensure all processes comply with cGMP, ICH, and other relevant regulatory requirements, Process Improvement: Identify and implement continuous improvement initiatives to enhance product quality .

Division- PLT-KB Department- PQC-KB Job Location- PQC Line Job Title- Supervisor Job Role- Quality Supervisor Reporting To- DPM Level in the organization- JE-ER Educational Qualification- Diploma in Mechanical/Automobile Engineering. Any Other: - 1. Should have experience of working in manufacturing quality. 2. Knowledge of vehicle manufacturing processes like Weld, Paint assembly are desired. Work Experience (Years)- 3- 6 years Job Responsibilities 1.Lead quality operation in defined shift. 2.Resolution of Defects using Problem solving tools 3.Drive containment actions along with other stakeholders. 4.Validate and monitor the countermeasure and provide correct feedback to stakeholders. 5.Handling voice of customer and resolution of problem at earliest. 6. Organising daily quality review meeting. 7. Preparation of weekly monthly reports for management reporting. Competencies / Skills 1. Hand on Experience of MS Excel and power point. 2. Experience of quality abnormality Handling 3. Experience of Vehicle Inspection Manufacturing Process of 4 Wheeler Industry 4. ISO 9001-2015 System procedure Knowledge 5. Planning and Problem solving Skills 6. Co-ordination and communication with other stake holders 7. Can read engineering drawings. 8. Body CMM scanning report reading

Theres never been a more exciting time to be at McCormick India. Were a respected global flavour leader with more than 12,000 employees across 27 countries. From favourite drinks to iconic burgers and in every aisle in the grocery store, McCormick is flavouring many of the biggest brands you know. What makes us a great place to work? Simple. We put people first. We champion growth, respect everyones contributions and do whats right for our business, our people and our planet. The best part: we get to bring our passion for flavour to work every day. Join us on our quest to make every meal and moment better. Position Overview To ensure customer and McCormick quality standards are met and to provide disposition for out of specification products. Key Responsibilities Conduct and participate in customer, regulatory, AIB and vendor audits, and visits. Work closely with the Production Teams to conduct investigations and studies to determine cause, effect and corrective actions required to resolve deviations from quality and customer standards. Management of documents status at Intelex , Food safety Culture Survey Interact with customers at any and all levels required to establish and maintain effective business relationships. Lead the management and disposition of Out of Specification and defective Finished Products. Participate or lead the development of new or revised QA procedures as assigned by the Global Quality and Regulatory. Identify opportunities for improved efficiency of the operation (capital, expenses, people, equipment, etc.) Maintain and distribute updated specifications for products as needed. Administer return goods process. Participate in or Lead mock recalls, Traceability and material trace ability exercises. Assist the Quality Team in determining the annual Quality Program training needs. Secondary Responsibilities Management of Operational Quality operations Validation and verification of processes, CCPs and OPRPs Change management system Required Qualifications & Experience Bachelors Degree in Food Science or related field with 3-5 years of experience in manufacturing Quality Control experience required with food manufacturing and supervisory experience preferred. Have the ability and experience writing technical procedures. Have the knowledge and experience working with HACCP Programs and other Food Safety pre-requisite programs. Other Skills and HPO Competencies Have the ability to read and interpret technical documents, such as specifications, procedure manuals and technical data sheets. Our ambitions are bold. If you are a change-maker with a passion for flavour and an appetite for a good challenge, come have a seat at our table. Your application will be treated in strict confidence. WHY WORK AT MCCORMICK? United by flavor. Driven by results. As a McCormick employee you ll be empowered to focus on more than your individual responsibilities. You ll have the opportunity to be part of something bigger than yourself to have a say in where the company is going and how it s growing. Between our passion for flavor, our 130-year history of leadership and integrity, the competitive and comprehensive benefits we offer, and our culture, which is built on respect and opportunities for growth, there are many reasons to join us at McCormick.

Quality Head of garment export unit, you will be responsible for ensuring products meet and exceed the expectations of clients. implement strategies to maintain and improve the quality of our garments throughout the production process. Required Candidate profile Quality Assurance, Quality Control, Supplier Management, Process Improvement, Compliance, Team Leadership, Customer Satisfaction, Documentation, Risk Management, Customer Complaints, export-oriented

Manage cost effective GxP Compliance and/or Audit activities, operations and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements, and through internal audits, KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators) -Performs preparation and management of external and corporate audits and Health Authority inspections. About the Role: The eCompliance Manager is responsible for providing Quality Assurance oversight and guidance with regard to computerized systems validation (CSV), operating within the framework of regulations (GxP, 21CFR11, etc. ) and requirements defined in the Novartis Quality Manual and global procedures. eCompliance Manager provides the needed operational support such as approving the GxP impacted changes, Periodic Review Reports, deviations etc. , Provides the guidance to the project and operations team on the CSV related topics and related information. Reviews and/or approves the global Computerized Systems key validation deliverables as a part of the eCompliance support to the GxP projects. Key Responsibilities: Quality oversight of operational activities of GxP systems (e. g. , Changes, Periodic Reviews, Deviations etc. , ) Provide needed support to meet the applicable Novartis and regulatory requirements for GxP regulated computerized systems projects. Point of Contact for all CSV related matters for GxP Computerized Systems and act as an interface between IT and Business for eCompliance topics in relation to GxP classified Computer Systems promoting a Quality Culture. Review and approve project related documents for GxP relevant systems including determination of GxP applicability for all GxP and non-GxP relevant systems. Establish trusted partnership with assigned IT Function with understanding of business drivers, and provide the needed day to day operational support. Review and approve the GxP Changes and the associated deliverables. Review and approve the GxP impacted deviations, ensure appropriate CAPA are implemented. Contribute for the preparation of VMP and execute the plan for the systems associated with the respective functions. Review and approve the Periodic Review Reports for the GxP computerized systems and the associated gaps within CAPA Management System. Manage GxP supplier qualification activities Provide Audit support as assigned and in case of CAPAs, provide the required Quality support. Essential Requirements: 10-15 years of overall IT experience, and a minimum 7 years of relevant experience in the Pharmaceutical Industry and in particular within regulated functions such as IT Quality and Compliance Solid understanding of global regulations and Health Authorities expectations governing computerized systems (CSV, Part 11, etc. ) Solid experience in the development, implementation and lifecycle management of computerized systems in regulated environments Experience in quality management of Cloud, SaaS platform, mobile and digital application used in regulated environments Highly experienced in the operational management of GxP solutions including its related technologies to support the operation Good understanding in system application management, its Quality support approach and industry best practices (ITIL, ITSM, etc. ) Experience in the development, implementation and lifecycle management of key computerized systems in the Pharmaceutical Development, Manufacturing, Quality, Commercial and Infrastructure space (e. g. ERP/SAP, MES, LIMS, CRM, IAM, etc. ) Desirable Requirements: Degree in Information Technology, Life Sciences, Pharmacy, Engineering or equivalent.

Meeting management QA Targets Skilled in QC tools Responsible for Customer complaint/query QA Improve plan as per last yr defects Controlling internal/external PPM RedBin/RCA/WHY-WHY Analysis Enhance QA Strategy CFT Wiring Harness knowledge is a must

Perform final inspection of finished products to verify conformity with specifications, drawings, & customer requirements. Document inspection findings & maintain quality control reports, checklists. Proficiency in using measuring & inspection tools. Required Candidate profile 2–5 years of experience in final quality inspection. Experience in rubber products like hoses, seals, gaskets, molded or extruded parts. Hands on experience in final inspection.

Brief The Quality Engineer will provide FMEAs (Failure Mode and Effects Analysis) and Control Plans, drives Continuous Improvement, performs audits, ensures performance to workmanship standards. Investigates and leads Corrective Actions. Plans, implements, and coordinates applicable corrective, preventive and technical controls of processes and products as required. Develops and implements an effective quality system related to manufacturing elements; including, but not limited to quality planning, receiving inspection, and Quality Management System audits. Responsibilities: - Leads the identification of problem root cause and the development and implementation of effective corrections and preventive methods Participates in product and process development teams as applicable Analyzes various failure reports and recommends corrective action Collects, analyzes and reports on various measurement statistics and metrics Maintain an interactive plant quality relationship focused on effective transition of product releases to a manufacturing quality support role. Facilitate creation of control plans, process flows and Process Failure Mode Effect Analysis (PFMEA) specific to new product development. Interface closely with Engineering, Service, Manufacturing and Product Management to understand and improve product and service quality. Investigate and resolve QA projects, as assigned. Ensure communication and interaction with Supplier Quality. Participate as Auditor of the Vertiv Quality Management System. Other duties and responsibilities as assigned. Qualifications: - Minimum Job Qualifications: BA or BS or equivalent experience Bachelor of Science in Mechanical Engineering, Industrial Engineering, Industrial and Systems Engineering, or other relevant degree preferred No experience required with a bachelor s degree Minimum of 5 years relevant experience in lieu of degree Preferred Qualifications: Excellent communication skills, both written and verbal Proficient in MS office Ability to design special tooling, develop and manufacturing processes, and assess new manufacturing technologies Highly adaptable with the ability to learn and apply new skills quickly Possesses a strong work ethic and sets high standards for quality and quantity of work Education And Certifications: Bachelor of Science in Mechanical Engineering, Industrial Engineering, Industrial and Systems Engineering, or other relevant degree preferred Physical Requirements: - Heavy Lifting (over 50 Ibs. ) Frequent Standing Frequent kneeling / crawling / stooping Frequent bending / twisting Frequent climbing (stairs, ladders) Environmental Demands: - Protective Equipment Required (earplugs, gloves, eyewear, safety toed shoes/boots) Travel Time Required: - 10% domestic/international

Handle QMS (ISO 9001: 2015), QC & Customer Assurance for Consumer Durable products Handle EMS (14001:2015) Be the Certified internal auditor for the both systems People & Process Mgmt. Quality Management OHSAS Six Sigma Lean manufacturing Required Candidate profile B.Tech 3-5 Years exp in QMS & EMS in manufacturing, engineering comp. QMS (ISO 9001 : 2015) CERTIFIED INTERNAL AUDITOR EMS (14001 : 2015) CERTIFIED INTERNAL AUDITOR Exp. in Six Sigma, TQM, OHSAS etc. Perks and benefits Best As Per Industry Standards

Greetings From Xelentra!!! One of Our Top Manufacturing Client Based at Coimbatore is On The Look Out For: Quality Inspector Machine Shop Qualification: BE / DME Age: 25 35 Years Location: Coimbatore – Thennampalayam Years of Experience: 4 – 8 Years CTC: 3.50 Lacs – 4.00 lacs Number of Vacancies : 3 Job Description: 1. Machine shop in process/final inspection 2. New part Development 3. Feasibility review 4. Supplier management quality side 5. Instrument maintenance, calibration and other quality activities 6. Experience in special process 7. Problem solving techniques like 8D, Pareto, why why analysis, cause and effect diagram 8. Quality system documentation 8. Well Experience in machine shop process and foundry process Interested and Relevant Talents Send Your Updated CV to My Mail Id hr@xelentra.in and Contact Akilabalan @ 98940 40086 Regards Akilabalan | Xelentra

Quality engineer required for a steel company(press shop) Qualification- Any diploma or iti mechanical Exp- min 6 month in quality Saalry- 15k to 20k Location- kundli, sonipat Wtsapp me resume at 8295842337 - Mr. Bansal Required Candidate profile Skills- Vernier caliper, micrometer, gauges meter