341 Customer Audits Jobs - Page 12

This role supports Quality Management System (QMS) activities including tracking and reviewing CRFs, CAPAs, deviations, and SOPs across multiple sites Responsibilities include documentation control, data analysis, digital transition support, and coordination with site teams to ensure compliance with cGMP standards The position also involves audit support, workflow optimization, and cross-functional collaboration to drive timely closure of quality events B. Pharm / M. Pharm / M.Sc. Chemistry / B.Sc. Chemistry or equivalent Track and follow up on pending TrackWise CRFs and CAPAs. Perform effectiveness checks for closed CAPAs and CRFs. Generate and maintain statistics on quality documents (e.g....

Key Responsibilities- is responsible for the acquisition of new business with the KA in the region (or country) develops a regional strategy for business with the KA negotiates price by.agreement with the GKAM together with Sales ensures transparency concerning the customers target prices and competitors prices is responsible for following up quotations given to the KA coordinates in-house exhibitions and presentations, top management events and meetings observes technological trends and requirements and the activities of the competition identifies and records the KA customer requirements carries out the sales planning with regard to the KA in the region executes and coordinates cost reducti...

Role & responsibilities Review Customer complaints trend & CAPA action of customer complaints. Monitor IHR PPM/ defect trend. Monitor IHR PPM trend & CAPA phenomenon reduction. Updation of Quality documents like PFA/ In process report/ Control Plan/ SOP/ PDI as and when required. Supporting in closure of audit NCS and monitoring the evidences. Tooling improvement suggestions/ Process improvement suggestion. Monitor in process rejection and give action plan Reduce in process rejection and monitoring before coating Area.

JOB RESPONSIBILITIES 1. Overall responsibility of continual improvement and implementation of the organization's Quality Management System 2. Overall responsibility for facing 3rd-party regulatory audits, including CE audits (as per EUMDR), ISO 13485 audits, USFDA inspections, customer audits, etc. 3. To work as PRRC (Person responsible for regulatory compliance as per EUMDR. 4. Leading proper conduct and closure of Internal Quality Audits 5. Management of customer complaints & CAPA. 6. Management of Product-related documentation including Risk Management files, Pre-clinical Test reports, Clinical Evaluation reports, Usability Engineering files 7. Conducting required validations, in particul...

customer quality, complaints, audits, customer satisfaction, manuals, 8D, CAPA, PDI, mis, IATF, Expertise in 7 QC tools, Statistical Process Control, Problem Solving & Root Cause Analysis, MiniTAB, fuel, engine, valve, powertrains, filters,

Responsibilities Roles and Responsibility of a Safety officer Under Rule - 61(A) of HP Factories act. Implementation of Safety trainings as per calendar schedule Safety management plan implementation Safety Incidents investigation with incident investigation team Conducting Safety observations & interactions & Contractor Safety Field Audit rounds as per the schedule Organize safety committee meetings and Implementation PPE stock management (Indenting PPE) Review and approval of Change request note, User requirement specifications &Major maintenance requests as per the safety compliance. Drive Safety promotional activities Monitor the safety performance of engineering department and ensure th...

Handling customer complaints Lead customer audits Lead engineering change management & NPI Lead team & quality risk controlling Customer Quality and Customer Complaint

1. Able to resolve the quality issues related to Ferrous Casting, Stamping and Spring products related processes independently. 2. Able to review independently Foundry and Press shop processes 3. Adequate Tool room machining exposure 4. Knowledge on Ferrous Casting and Press shop and Press tools 5. Responsible for Quality and process related topics for series purchased parts in Ferrous Casting, Springs and Stamping commodity. 6. Knowledge on Jigs and Fixtures 7. Single point of contact for technical communication for supplier 8. Lead the troubleshooting and root cause analysis of all technical issues using the principle of on-site, on-the-spot to ensure that products manufactured with pre-se...

1.Knowledge of machining,welding,plating & painting process. 2.Customer Quality issues handling & Reporting. 3.Customer defective parts analysis & 8D preparation,Warranty claim settlement,PPM monitoring. 4.new product development act. -PPAP ,APQP. Required Candidate profile 5.Train and guide quality teams for identifying & developing problem solving methodologies to resolve quality issues. 6.Customer visit during any quality issueCustomer visit during any quality issue

KRA's: Quality check of all raw materials, in-process and finished goods on a FIFO basis QMS Implementation Audit Documentation Internal/ external as well as 3rd party/ regulatory audit compliances Required Candidate profile 5+ years of experience in Quality [quality inspection, auditing, testing, reporting] in a medical device/ pharmaceutical manufacturing co. Should be ready to travel or relocate to Taloja Navi Mumbai

POSITION : Quality analyst II Customer Quality LOCATION : India BU : Global Automotive SEGMENT : Transportation Solutions (India) COMPANY TE Connectivity Ltd. is a $14.9 billion global technology and manufacturing leader creating a safer, sustainable, productive, and connected future. For more than 75 years, our connectivity and sensor solutions, proven in the harshest environments, have enabled advancements in transportation, industrial applications, medical technology, energy, data communications, and the home. With 80,000 employees, including more than 7,500 engineers, working alongside customers in approximately 150 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at www.te...

KRA's: Ensure SOPs are followed & quality standards are met Quality check of raw materials, in-process & finished goods on a FIFO basis QMS Implementation Audit Documentation Audit facilitation - Internal/ external & 3rd party/ regulatory audits Required Candidate profile 5+ years of experience in Quality [quality inspection, auditing, testing, reporting] in a pharma/ medical device mfg. co Ready to relocate to Medchal, Hyderabad Accommodation & food will be provided Perks and benefits Accommodation and Food provided

Manager – Quality B.E/B.Tech (Metallurgy/Mechanical) 5–10 yrs experience Strong in ISO 9001, IATF 16949, APQP, PPAP, 8D, CAPA, MSA, SPC Knowledge of ASTM, EN, IS standards CTC: 10-15 LPA Required Candidate profile Send your resume via WhatsApp: 8013014471 Ideaspot Consultant / Kolkata

Division- Production Department- Assembly Job Location- Kharkhoda, Haryana Job Title Quality Analysis Incharge - Assembly - (3~5 yrs) Job Role: 1. Should have experience of working in automobile manufacturing quality. 2. Knowledge of vehicle manufacturing processes like Weld, Paint assembly are desired. Reporting To Shift Incharge Level in the organization AM/DM Educational Qualification B.E./B. Tech. in Mechanical/Automobile Engineering. Graduation (With Specialization): B.E./B. Tech. in Mechanical/Production/ Automobile Engineering Post Graduation (With Specialization): Not Required Any Other (Certification / Diploma etc.): Not Required Work Experience (Years) in treasury activities. 3- 5 ...

QMS develop implement & maintain QMS that meets industry standards (e.d ISO 9001 IATF 16949) Quality Process, Product Quality Process Control Quality Planning, Supplier management, inspection testing, training development, technical knowledge strong Required Candidate profile Should have good experience electronics plant ( PCBA (SMT ). Individual handling of overall SMT PCBA.

The ISO Quality control / Assurance is responsible for supporting the Quality Assurance Department with all ISO 9001 related quality assurance requirements for the ISO 9001 Quality Management System (QMS) Internal audit; External/Customer audit.... Required Candidate profile The ISO Quality will ensure the ISO 9001 QMS demonstrates its ability to consistently provide products &services that meet customer & statutory & regulatory Lead investigations of customer complaints

Handle in-process & final inspection, IMS documentation, root cause analysis, process, product &system audits, continuous quality & process improvement projects. Coordinate with production R&D & purchase to ensure quality compliance Required Candidate profile know IMS 7 QC tool CAPA FMEA &inspection instrument Strong documentation communication &team handling Mfg or eng industry background pref with hands-on qlty assurance exp Handle customer complaints

Independently lead and manage all production/operations related activities of the plant, on time dispatch with desired Safety, Quality & Productivity Output Can run plant with ensuring proper safety and housekeeping in the plant. Closely monitoring and controlling of better utilization of equipment to get maximum Lead plant improvements and modification projects in Pilot & existing plant Experience of handling Mechanical, Electrical and instrumentation will be an advantage. Can handle multiple products and multiple purpose plant Accountable & responsible for all Plant/Factory operation activities & making manufacturing processes more profitable, lean and efficient by TQM practices such as 5 ...

The Position Organization : - Jubilant Ingrevia Limited Designation / Position: - Dy Manager QA Band / Grade / Level: - L2 Location : - Bharuch Job Summary (Optional): - Reporting Manager: - Sr. Manager -QA Direct Reports (Optional): - Nil Team Size (Optional): - 10 Matrix Relationship (Optional): - Key Responsibilities Quality professional with 15.0+ years of progressive experience with strong knowledge of Speciality Ingredient, Bulk Chemicals, Food additive/ Food supplement & API Manufacturing, QMS, Qualification, Validation and other Manufacturing functions. Personnel shall have experience to handle certification, customer & regulatory inspection i.e.: IMS, WHO-GMP, FSSC, FAMI-QS, EnMS, H...

To follow the safety rules in the premises according to the company norms. To ensure timely completion of SOPs training and on the job trainings related to production department. To review and maintain the training related log books in the department. To Coordinate new joiners for internal and cross functional trainings in coordination with cross functional departments. To coordinate with QA documentation cell for issuance of required documents and submission of completed documents. To prepare the SOP index, Equipment index and format index as per the frequency of QA001, QA007and QA002. To update the schedule manager for SOP related activities (to update SOP effective dates). To upload the S...

Role & responsibilities To Monitoring Customer Complaints & minimizing complaints through action taken. To Monitor all area PPM (Final Inspection & escalation to respective areas for improvement & provide support to achieved defined targets. Responsible for adherence of Quality management system & align with TS 16949/Customer requirements on monthly basis. Effectiveness Monitoring of Corrective & preventive action plan. Improve Customer Rating. Preferred candidate profile Btech Mechanical with 19+ years of work experience in Automotive Industry. Leadership quality, Analytical skills, knowledge of quality tools, Communication skills, Presentation skills 5 S & Safety audits

Role & responsibilities QA JD: GQCS Issue Monitoring and Control New Car Defect Monitoring [3MIS] and Control 12 MIS defect Monitoring and Control OEM Inline failure monitoring and Control Tier#1 Inline failure Monitoring and Control 8D report preperation & ontime issue closures Effectiveness Monitoring of Customer Complaint Actions DQRM presentation at Customer end for OEM inline failures Failure analysis and Process verification Customer Complaint Tracker QIS System GMES System IMDS Portal SAP Management PPAP Document Preparation, submission & Approval EO Change Document submission & Approval 4M Change Customer submission & Approval Deviation Approval submission & Approval MIP PPAP Audit a...

DesignationLab Chemist Full Time Opportunity LocationMultiple : - To collect samples of raw materials from Plant as per written down procedures, analyze and submit report. - Testing of all raw materials and finished goods as per the ASTM /ISO standard methods. - To prepare report of all lab testing. - To make record of all lab instruments and its calibration. - To attend customer audit and ISO audit. - To prepare documents related to internal & external audits. - Collection & testing of effluent sample in a shift is also an important activity. - Active participation in site projects as team member. - Participation in new product development work. - Provide training to labs workers, if requir...

Liaise with other managers to formulate objectives and understand requirements Estimate costs and prepare budgets Organize workflow to meet specifications and deadlines Monitor production to resolve issues Supervise and evaluate performance of production personnel (quality inspectors, workers etc.) Determine amount of necessary resources (workforce, raw materials etc.) Approve maintenance work, purchasing of equipment etc. Ensure output meets quality standards Enforce health and safety precautions Report to upper management

Key responsibilities: Plan and execute the Verification and Validation (V&V), reliability, and Quality strategies for new and existing products Preparing Quality Assurance Plan (QAP) for customer iFAT (Factory Acceptance Test). Coordinate with customers for factory acceptance tests (FAT), pre-commissioning tests and resolution of customer complaints RCA and Analyzing the failure by coordinating with Designs / Production / Quality Departments. Organizing routine, type & special tests as per the set standards and giving suggestions to take corrective actions. Updating of MIS reports to management like daily test report, weekly & monthly failure reports/analysis, Corrective & Preventive actions...