427 Qms Implementation Jobs - Page 3

preparing Quality manual and procedures in line with ISO 9001:2015 Responsible for implementing Quality Management system Periodic review of QMS by continuous auditing the processes. Sheet metal Industry Experience & control panel industry preferable

V.K.Group of Companies Job Description of Assistant Manager or Manager Quality Assistant Manager or Manger Quality Designation Department Quality ( Team size 7-8 Inspactor) Experience Department 8 - 10 years (Department Expereince) Qualification B.E.Mechanical / Diploma Mechanical Eng. Up to 10 lakh CTC Salary Expectation CTC Roll & Responsibilities 1) Maintain all reports related quality and customer requirements. 2) Co ordination with other departmens and therid party inspection agency. 3) Implementation of Quality systems and Qc related document prepiration. 4) Ensure all quality report (inward,Inprocess,Final etc...). 5) CAPA completion and Audit prepairation. 6) A company and take participation in new product development 7)Implementation of quality tools and certification. 8)Continues improvement in quality processes. 7) Customer complain resolve and take immediate action, if required personal visit 8) Ensure Calibration activity and Lab 9) Team management Skills 1) Instruments Mesureing / CMM 2) Knowledge of Machining components 3) Drawing reading 4) Process Product 5) Quality tools 8D,CAPA, other core tools 6) NDT test 7) PPAP,FMEA,APQP 8) QMS Implementation 9) Management skill (Team size/Training/Gravience handling/Retention) KPI 1)To achieve Rejection and Rework as per objective 2) 0 ' Customer complain and satisfaction level with quality. 3)QMS implementation with zero ( 0 ) N.C. 4) PPC achivement at quality level 5)No of Incedence of Loss of out put due to team un avialablity 6) Improvement / Team Recruitment,Training and Retention of Team Targeted Companies Desired Industries Crankshaft, Transmition Shafts and auto component manufactureing Comapny. Location Rajkot www.vkengitech.com

Job Title: QMS Engineer Department: Quality Assurance. Location: Bangalore Rural, Dabaspete. Job Purpose: The QMS Engineer is responsible for developing, implementing, monitoring, and continually improving the organizations Quality Management System in alignment with IATF 16949, ISO 9001, ISO 14001, and other relevant standards. The role ensures compliance with customer-specific requirements (CSR), internal processes, and statutory/regulatory requirements while supporting cross-functional teams to achieve quality excellence. Key Responsibilities: QMS Implementation & Maintenance Implement and maintain Quality Management Systems as per IATF 16949 & ISO 9001 standards. Support in defining and controlling documented information (procedures, work instructions, forms, manuals). Monitor QMS performance metrics and ensure compliance with corporate and customer requirements. Audits & Compliance Plan and conduct Internal Quality Audits as per IATF 16949 requirements. Coordinate with certification bodies, customer audits, and regulatory audits. Drive closure of audit findings and ensure preventive/corrective actions are implemented effectively. Process Improvement & Risk Management Conduct risk assessments (PFMEA, process audits, layered audits) to identify gaps and improvement opportunities. Facilitate continual improvement projects (Kaizen, Lean, Six Sigma) related to QMS. Ensure effective problem-solving methodology (8D, 5 Why, Root Cause Analysis) is applied. Customer & Supplier Interface Support in addressing customer complaints, audit findings, and quality concerns related to QMS. Work with suppliers to ensure their processes align with QMS standards and requirements. Training & Awareness Conduct QMS awareness and training programs for employees at all levels. Ensure teams understand customer-specific requirements and compliance obligations. Reporting & Documentation Prepare QMS performance reports for management review. Maintain updated QMS records and ensure availability during audits/inspections. Qualifications & Experience: Diploma or B.E./B.Tech in Mechanical / Automobile / Industrial Engineering or equivalent. 3 to 6 years of experience in Automotive / Manufacturing industry with focus on QMS. Hands-on knowledge of IATF 16949, ISO 9001, ISO 14001. Experience in conducting internal audits, handling certification audits, and customer audits. Proficient in Core Tools (APQP, PPAP, FMEA, MSA, SPC). Good knowledge of problem-solving tools (8D, 5Why, Ishikawa). Skills & Competencies: Strong analytical and problem-solving skills. Excellent communication, documentation, and presentation skills. Ability to work collaboratively with cross-functional teams. Detail-oriented with strong organizational skills. Proficiency in MS Office and quality management software. Interested candidates can send resume at manohara.is@trmn.biz

Responsibilities: * Conduct ISO audits and provide feedback. * Ensure compliance with QMS standards through documentation. * Collaborate with clients on implementation projects. * Develop and maintain ISO documents.

Develop, implement, and maintain quality assurance policies, procedures, and standards. Monitor day-to-day operations and identify areas for improvement. Maintain documentation & prepare reports on quality metrics, audit results, process performance

Conduct quality assurance and quality control activities in compliance with company standards. Perform testing on products and processes to ensure adherence to quality standards Maintain accurate documentation of all QA QC activities and test results

Develop and implement quality management standards Production process improvement Supplier and MILL partnership Good at QMS Implementation Preferably from Home Textile background Exposure to Bed sheet / Terry towel division

Improve reliability of new product development processes Review products, processes, and systems to determine improvements Quality Inspection & Control Rejection analysis OEE Audit Function Incoming Quality Control System monitoring Manpower Handling Required Candidate profile Previous work experience as a Quality Manager or similar role Educational Qualification: CIPET/ B. Tech Experiences: Min. 3-5 years’ Exp. in Plastic industry will be preferred at the same level.

We are hiring for the role of Assistant Manager / Manager QMS (Quality Management System) based at Noida (NSEZ, PH 2). Quality Management System professional having more than 10 Years of experience in implementing & auditing various ISO standards specially ISO9001, ISO14001, ISO45001 & IATF16949 as well as VDA . TISAX audit exposure preferable. Key responsibility includes: Implementing & maintaining the quality management systems for ISO9001:2015, IATF16949:2016, ISO14001:2015, HSE into our processes to achieve the desired results by meeting all the applicable standard, customer, legal & other requirements. Handling end-to-end certification activities for ISO9001:2015, IATF16949:2016 & ISO14001:2015 independently. Taking care of the internal audits for ISO9001, IATF & ISO14001 and HSE Implementing & maintaining the end-to-end document management system throughout the company processes. Help the process owners in get to preparing the manuals, process approach, WI, Check sheets, Records etc. as per the process requirements. Maintaining the Master List of documents for changes, revisions & obsoletion. Help the process owners in get to preparing the risk assessments, control plans, etc. as per the process requirements. MRM: Prepare and conduct the Management Reviews half-yearly basis. Circulate the MOM for action closure. To have exposure in training & development process & performance management system to achieve the customer & organizational desired goals and objectives. Responsible for aligning quality system initiatives with organizational programs & business objectives, ensuring that quality system & technologies are adequately protected. Document Management System: Creating, updating, review, control & record maintenance for all the process documents. Document Preparation: Help of process owners into preparing their process approaches, WI, Check sheets, records, Does & Donts, OPL, Drawings etc. as per the defined standard templates. Implementing & maintaining: the end-to-end document management system throughout the company processes. Maintaining the Master List of documents for live, changes, revisions & obsoleted documents. Maintaining training records: TNIs, Training Plan Vs Actual, Training Execution, Maintaining Training Records. Training to his team: Training to his team on QMS & applicable standards ISO9001, ISO14001, IATF16949 & HSE. Educational Qualification: B. Tech/BE in any stream (preferably in EC) Key Competencies : Good communication and presentation skills Must be a Lead Auditor for ISO9001:2015, 14001, 45001 Must be Internal Auditor for IATF & VDA 6.3 & HSE TISAX Compliance

Role & responsibilities 1. Managing the quality documents and conducting internal Audit & data review etc. 2. Maintaining all records and documentation as per 17025:20053. 3. Maintaining regularly and tracked calibration and standard log books, 4. Directing all quality activities for the laboratory such as ILC, IQC, Training, etc. 5. Preparing compliance report for the audit or for the closure of various shortcomings or NCs. 6. Having sound knowledge of QMS and LIMS. 7. Knowledge of 21cfr, OOS, Market complaints, APQR.

We are a dedicated team of over 50 professionals within the Global ERP Solutions division, primarily based in India and Denmark. We always strive to leverage the existing SAP platform to bring in new ideas to the business to optimize and automate the business processes. We continuously rethink our ways of working to maximize the business value we deliver to our business. We have organized ourselves as small agile teams to plan, collaborate and focus on the priorities set by the product owners. We embrace the diversity and the cultures across geographies and bring in the synergy by working as one team. The position will offer you close collaboration with many stakeholders across the organization and the possibility to become a trusted advisor, challenging and championing both IT and business goals. In this role youll make an impact by : Key Responsibilities: Act as the SAP QM subject matter expert, understanding and documenting business requirements, and translating them into functional SAP solutions. Design, configure, and implement SAP QM modules including inspection types, quality notifications, results recording, and inspection planning. Analyze and document existing business processes, identifying gaps and recommending improvements. Provide technical support, end-user training, and troubleshooting for SAP QM-related issues. Collaborate with stakeholders to align SAP QM solutions with business objectives. Participate in and provide regular updates during project meetings. Plan and execute various testing phases including unit testing, UAT, and regression testing. Support and contribute to projects using Agile/Scrum methodologies. Stay current with the latest SAP technologies, tools, and industry best practices. Core SAP QM Functional Areas: Expertise in configuration of QM settings such as Plant parameters, Procurement control keys, Inspection lot creation and completion, Quality Certificate, DMR Creation of all QM master data like Sampling Procedure, Master Inspection Characteristics, Inspection Plan, Inspection method, etc., Quality Notifications were designed to use in product and customer complaints, vendor audit recording and OOS, Deviation and Change control Configure different type of Inspection such as In-process, Post-process, Recurring, Delivery, Stock transfer, Inventory, etc., Hands-on experience in LIMS integration, including middleware coordination, data exchange, and sample tracking Results Recording & Defects Recording Knowledge on Certificate Profiles and Certificate of Analysis (COA) both Inbound & Outbound and its printing process Good knowledge in Vendor Evaluation & Integration, Stability Studies & MQC process Sound understanding on Batch Management, Batch Derivation, and Serial Number Integration Integration processes with other modules SAP MM, SAP WM, SAP PP, SAP PM and SAP SD To succeed you must hold: At least 5-7 years of working experience as an SAP QM consultant with working knowledge in LIMS, preferably worked biotech, pharma, life science or other research and manufacturing business. Good to have 2-3 years of experience in Domain (Quality controls, assurance, laboratory, sample management, etc.,) Certification in ECC or S4 Hana added advantage Experience with agile methods and events/ceremonies. Experience with GxP compliance, added advantage.

Conduct quality assurance and quality control activities in compliance with company standards. Perform testing on products and processes to ensure adherence to quality standards Maintain accurate documentation of all QA QC activities and test results

Role & responsibilities Understanding customer expectations of and needs from a product. Developing quality control processes. Ensuring products are designed with adherence to standards. Supervising staff and monitoring standards. Monitoring and evaluating internal production processes and implementation of new procedures. Evaluating the final output of products to determine their quality. Rejecting products that fail quality standards. Engaging with customers and gathering product feedback. Producing statistical reports on quality standards. Reporting on management of quality standard issues. Evaluating product recalls. Improving production efficiency and managing waste. Plan projects or subtasks so they may be tracked and presented. Attend various meetings and action/communicate instructions. Monthly reports to managements through presentation. Perform root cause analysis and resolve problems to reduce the rejections with the Team. Independently determine approach and assigned tasks. Participate in the development and refinement of Design and Process FMEAs (Failure Mode and Effects Analysis). Manage the Supplier Key Performance Indicators (KPIs). Manage and coordinate customer PPM (Parts per Million), supplier PPM, supplier problem solving on time, cost recovery and supplier warranty indicators. Lead quality audits in the organization Take ownership of all the assets/information assigned and secure it in compliance with ISO 9001:2015 standard implemented in the company. Co-operate and co-ordinate for the internal audits conducted in the company (complying with ISO 9001 standard). Report to the Incident Response Manager, any incidents you come across in the office regarding Security threats like threats to physical asset & stored information or any risks detrimental to the Security Policies of the company, etc., Responsible for supervising in ensuring that all personnel reporting to you shall observe all Security requirements and be appropriately trained in Security. Preferred candidate profile Graduate Mechanical engineer/Diploma in mechanical with strong technical skill Require a deep understanding of quality standards with quality background with experience in mechanical components and related products. Knowledge of handling Aerospace components and Metal finishing (Surface treatment) is an added advantage. Excellent collaboration and work within team skills will help you to succeed in this position. Strong knowledge of Production Part Approval Process (PPAP), Failure Mode and Effect Analysis (FMEA). Understanding and interpretation of engineering drawings and manufacturing processes. Manufacturing process knowledge like Machining, Casting, Heat treatment & Surface treatment. Quality control certification is advantageous. Excellent attention to detail. Excellent verbal and written communication. Data analysis and statistical aptitude. Good interpersonal skills. Highly conscientious and diligent.

Multidimensions is looking for Assistant Manager - QMS to join our dynamic team and embark on a rewarding career journey Ensuring company policies are followed. Optimizing profits by controlling costs. Hiring, training and developing new employees. Resolving customer issues to their overall satisfaction. Maintaining an overall management style that follows company best practices. Providing leadership and direction to all employees. Ensuring product quality and availability. Preparing and presenting employee reviews. Working closely with the store manager to lead staff. Overseeing retail inventory. Assisting customers whenever necessary. Organizing employee schedule. Ensuring that health, safety, and security rules are followed. Ensuring a consistent standard of customer service. Motivating employees and ensuring a focus on the mission. Maintaining merchandise and a visual plan. Maintaining stores to standards, including stocking and cleaning. Completing tasks assigned by the general manager accurately and efficiently. Supporting store manager as needed.

Tasks Lead the Quality Assurance (QA) and Quality Control (QC) operations across all manufacturing units at HLL-KFB, ensuring compliance with cGMP, ISO 13485, WHO-GMP and other regulatory standards. Oversee batch release, deviation management, CAPA, change control, validation, and documentation systems. Ensure timely testing and release of raw materials, packing materials, in-process, and finished products through QC lab operations. Coordinate internal audits, external inspections (by CDSCO, State FDA, WHO, ISO), and ensure audit preparedness at all times. Guide the implementation of Quality Management Systems (QMS) and drive continual quality improvement initiatives. Lead the development and training of QA/QC personnel to build a technically competent and regulatory-ready workforce. Supervise qualification and validation activities (process cleaning, equipment, facility, analytical methods). Coordinate with production, regulatory, R&D, and supply chain departments for smooth product flow and compliance. Maintain quality records, trend analysis, product quality reviews (PQR), and ensure compliance to data integrity principles. Serve as the key spokesperson during audits and regulatory inspections; represent quality interests in management reviews. Requirements Maximum Age : 45 years as on 01.09.2025 Scale of Pay (For Regular appointment): Rs. 70000 200000/- Annual CTC : Rs.19.93 Lakhs (Non-Metro) (approx.) at the minimum of the scale. Qualification: Essential: Master in Pharmacy Desirable: Additional certifications in GMP, QMS or Regulatory Affairs preferred Post Qualification Experience : Essential: Minimum 10 years of experience in pharmaceutical QA/QC functions. At least 5 years of experience in a managerial/leadership role in a WHO-GMP compliant pharmaceutical or medical device manufacturing facility. Skills and Competencies required: In-depth knowledge of cGMP, WHO, ISO, USFDA, and other applicable regulatory guidelines. Strong leadership in QMS implementation, audit management, and team building. Experience in handling regulatory audits (CDSCO, WHO, USFDA, etc.) Proficiency in analytical techniques, instrument calibration, documentation, and validation procedures. Excellent communication and cross-functional coordination skills. Candidates from CPSUs should be holding posts in the scale of Rs. 60000 - 180000 (Revised 2017 scale) / Rs. 24900 - 50500 (Pre-revised 2007 scale) for a period of two years as on 01.09.2025 No. of Positions : 1 Posting Location : Kanagala, Belguam, Karnataka Contract Type : Executive – Permanent

The Quality Manager is responsible for ensuring that products and services meet all necessary requirements before they reach the customer. This role involves developing quality control processes, supervising inspection teams.

Establishes, enforces, and oversees compliance for an effective Quality Management System within the scope of activities, ensuring streamlined and efficient QMS structures and documentation across all levels. Manages the deployment of the QMS. Required Candidate profile IATF-16949& ISO 9001, ISO 13485, AS 9100, ISO 14001 &ISO 45001 quality standards. knowledge in SPC, Gage R & R, MSA, FMEA, APQP, PPAP. IATF, ISO 9001, ISO 13485, AS 9100, ISO14001 and ISO 45001

Responsibilities: * Develop QMS strategies and plans * Conduct regular audits and assessments * Ensure compliance with ISO standards * Implement quality systems and documentation

Lead and manage the Quality Management System (QMS) as per IATF 16949, ISO 9001, and customer-specific requirements. Ensure compliance with Maruti Suzuki (MSIL) quality standards , audits, and reporting protocols. Prepare, coordinate, and successfully close VSA (Vendor System Audit) and MACE audits . Drive corrective and preventive actions (CAPA) to address audit findings and improve processes. Implement and sustain best practices for process control, documentation, and traceability . Collaborate with cross-functional teams to ensure adherence to OEM requirements and statutory compliance . Monitor and improve supplier quality performance through audits, assessments, and capability building. Conduct internal audits and provide training to enhance quality awareness across teams.

Investigate customer complaints and nonconformance; CAPA Maintain accurate quality documentation, reports, and data logs.Monitor and inspect welding and assembly processes to ensure compliance with quality standards.quality control operations

Key Responsibilties Develop, implement and maintain quality process across Prepress, Printing and Post press operations. Conducts inspections of Raw material, in process production and finished goods to ensure compliance with quality standards. Establish and maintain SOPs for all quality check points. Monitor and control printing parameters (Color consistency, registration, lamination etc) Identify defects, analyze root cause and implement corrective and preventive measures. Ensure customer complaints are investigated and resolve effectively within timelines. Ensure compliance with industry standards, certification and customer specific requirements. Prepare daily/ weekly quality reports and present findings to management. Manage quality audits both internal and external. Training and Development. Skill and Competencies Experience of Flexo Printing Processes (IML, Shrink Sleeves, adhesives etc) will be additional benefit. Indepth understanding of Raw Material such as Bopp films, Ink, Adhesives etc. Familiar with ISO, BRC, Sedex or other relevant quality standards. Ability to handle client quality audits and queries Good communication and documentation skills Relevant candidate can directly call on 9892-471-559. Co Website - www.tmppl.net

IATF Requirements as per Company's Standard, BIS Audit, Customer complaints & Handling , Glass Process Inspection Analysis & Knowledge, Related Lab Responsibility & Testing For further information, please call 8050070079 / 8050011328

We Have Urgent Vacancy of MR , Having Experience in Sheet Metal Industry , ensure the proper implementation of the quality management system.

Managing and implementing QMS with deep expertise in ISO 9001, ISO 14001, ISO 45001, and IATF 16949. Experience in Automotive manufacturing is a must. Drive continuous improvement initiatives, focusing on reducing waste & improving efficiency. Required Candidate profile Implement (CAPA) based on audits, customer feedback, and internal analysis. Exp of Export related compliances like Sedex, BSCI etc, with excellent communication skills. Must have dealt with customers

Key Responsibilities: Lead the implementation, maintenance, and enhancement of the Quality Management System as per ISO 13485:2016 and relevant international standards. Manage and oversee the Corrective and Preventive Action (CAPA) system, ensuring timely investigation, root cause analysis, and closure. Plan, schedule, and conduct internal audits across departments; coordinate and support external audits by customers, certification bodies, or regulatory authorities. Evaluate and resolve non-conformances (NCs), manage deviation records, and ensure corrective measures are implemented effectively. Collaborate with cross-functional teams to drive quality improvements and process compliance across the organization. Review and update quality documentation, SOPs, audit trails, and training records. Conduct training and awareness programs on QMS, CAPA, deviation handling, and audit readiness. Ensure regulatory preparedness and support documentation for submissions and inspections Manage the validation plan through out the organization. Qualifications & Experience: Bachelors / Master’s degree in Pharmacy, Biotechnology Minimum 5–8 years of relevant experience in QA/QMS roles within medical device, pharmaceutical. Strong understanding and hands-on experience with ISO 13485:2016, QMS, CAPA, audits, and regulatory documentation. Prior experience in handling customer audits and regulatory inspections is a must. Excellent written and verbal communication skills. Proficient in MS Office and electronic QMS tools (preferred).