284 Quality Systems Jobs - Page 2

Amazon Ads is looking for a Research Science Manager with machine learning and deep learning background to build industry-leading technology for preventing ad fraud at scale. Advertising at Amazon is a fast-growing multi-billion dollar business that spans across desktop, mobile and connected devices; encompasses ads on Amazon and a vast network of hundreds of thousands of third party publishers; and extends across US, EU and an increasing number of international geographies. One of the key focus areas is Traffic Quality where we endeavor to identify non-human and invalid traffic within programmatic ad sources, and weed them out to ensure a high quality advertising marketplace. We do this by building machine learning and optimization algorithms that operate at scale, and leverage nuanced features about user, context, and creative engagement to determine the validity of traffic. The challenge is to stay one step ahead by investing in deep analytics and developing new algorithms that address emergent attack vectors in a structured and scalable fashion. We are committed to building a long-term traffic quality solution that encompasses all Amazon advertising channels and provides state-of-the-art traffic filtering that preserves advertiser trust and saves them hundreds of millions of dollars of wasted spend. We are looking for a dynamic, innovative and accomplished research science manager to lead machine learning and data science for the Advertising Traffic Quality vertical. Are you excited by the prospect of analyzing terabytes of data and leveraging state-of-the-art data science and machine learning techniques to solve real world problems? Do you like to own end-to-end business problems/metrics and directly impact the profitability of the company? As an research science manager for Traffic Quality, you will lead a team of applied scientists, research scientists, data scientists and engineers to deliver to conceptualize and build algorithms that efficiently detect and filter invalid traffic. You will be the single-threaded owner of the algorithms that go into our traffic quality systems and will be responsible for both near-term improvements to existing algorithms as well as long-term direction for Traffic Quality algorithms. Your team will include experts in machine learning, statistics and analytics that are working on state-of-the-art modeling techniques, as well as generating insights that fuel critical investments. You will also lead an engineering team that works on handling terabyte scale data and implementing features and algorithms that process billions of events per day. You will interface with product managers and operations teams to bring key advertising initiatives to customers. Your strong management skills will be utilized to help deliver critical projects that cut across organization structures and meet key business goals. Major responsibilities Deliver key goals to enhance advertiser experience and deliver multi-million dollar savings by building algorithms to detect and mitigate invalid traffic Use machine learning and statistical techniques to create new, scalable solutions for invalid traffic filtering Drive core business analytics and data science explorations to inform key business decisions and algorithm roadmap Establish scalable, efficient, automated processes for large scale data analyses, model development, model validation and model implementation Hire and develop top talent in machine learning and data science and accelerate the pace of innovation in the group Build a culture of innovation and long-term thinking, and showcase this via peer-reviewed publications and whitepapers Work with your engineering team and product managers to evangelize new algorithms and drive the implementation of large-scale complex ML models in production Keep updated on the industry landscape in Traffic Quality and identify algorithm investments to achieve an industry leading traffic quality solution. Learn continuously about new developments in machine learning and AI, as well as recent innovations in creative intelligence and malware detection. Identify how these can be rolled into building an industry leading solution for Amazon advertising * A MS in CS focused on Machine Learning, Statistics, Operational research or in a highly quantitative field * 5+ years of hands-on experience in big data, machine learning and predictive modeling * 3+ year people management and cross department functional experience * Knowledge of a statistical analysis package such as R, Tableau, and high-level programming language (E.g. Python) used in the context of data analysis and statistical model building * Strongly motivated by entrepreneurial projects and experienced in collaboratively working with a diverse team of engineers, analysts, and business management in achieving superior bottom line results * Strong communication and data presentation skills * Strong ability in problem solving and driving for results * Technical leader with 10+ years of exceptional, hands-on experience in machine learning in e-commerce, fraud/risk assessment, or an enterprise software company building and providing analytics or risk management services and software. * Ph.D. degree in in Statistics, CS, Machine Learning, Operations Research or in a highly quantitative field. * Knowledge of distributed computing and experience with advanced machine learning libraries like Spark MLLib, Tensorflow, MxNet, etc. * Strong publication record in international conferences on machine learning and artificial intelligence

Number of Openings* 1 ECMS Request no in sourcing stage * 530254 Duration of contract* 12 Total Yrs. of Experience* 10 years Relevant Yrs. of experience* 10 years Detailed JD *(Roles and Responsibilities) SAP PPQM Must have a minimum of 10 years of experience. Provide L2/L3 support for SAP PP (Production Planning) and QM (Quality Management) modules. Resolve incidents, service requests, and change requests within SLA. Support key business processes: MRP, production orders, process orders, BOM, routing, work centers, inspection lots, quality notifications, usage decisions. Perform root cause analysis and implement permanent fixes. Work closely with business users for issue resolution and minor enhancements. Test and validate changes in development and quality systems Ensure system stability, performance, and compliance with change management processes. Mandatory skills* SAP PPQM Desired skills* Good communication and Good Knowledge on SAP PPQM Domain* Manufacture Approx. vendor billing rate excluding service tax* (Currency should be in relevance to the candidate work location) 10,000 INR Precise Work Location* (E.g. Bangalore Infosys SEZ or STP) Bangalore Pune BG Check ( Before OR After onboarding) After onboarding Any client prerequisite BGV Agency* NA Is there any working in shifts from standard Daylight (to avoid confusions post onboarding)* 1:30 PM to 11: 30PM IST

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Responsibilities may include the following and other duties may be assigned: Analyze returned products to identify failure modes and root causes. Conduct detailed assessments of device performance, including physical inspection and functional testing. Document investigation findings in the complaint handling system, ensuring accuracy and completeness. Review complaint data for trends and recurring issues. Identify opportunities for streamlining failure analysis workflows to improve efficiency and accuracy. Contribute to the development and implementation of standardized investigation procedures and tools. Support automation initiatives to reduce manual effort in complaint handling Ensure all complaint investigations comply with regulatory requirements (e.g., MDR, FDA). Maintain detailed and accurate records for audits and inspections. Support internal and external audits by providing investigation data and process documentation. Serve as a subject matter expert (SME) for failure analysis techniques and tools. Stay updated on industry standards and best practices for complaint handling and failure analysis. Train and mentor junior team members in complaint investigation and analysis methods. Monitor and report on key performance indicators (KPIs) related to complaint handling (e.g., FTQ, OCT). Drive improvements to meet or exceed quality and timeliness targets. Required knowledge, experience & skills : Bachelors degree in Engineering, Science, or Technical Discipline required and Minimum of 4 to 8 years of quality systems experience. Strong communication skills, both oral and written. Ability to understand the functionality / intended use of complex medical devices Computer literate with skills in Word, Excel, Access, PowerPoint and database trending analysis Comfortable working with international and multi-cultural department and groups in different time zones Accurate and delivers quality work, with a sense of urgency. Ability to work well under pressure and maintain positive, enthusiastic attitude. Ability to work in a fast-paced environment .Eagerness to learn and expand responsibilities & accountability . Skills - Nice to have : Knowledge of medical devices, their development and quality control. Knowledge of FDA, MEDDEV, Canadian Regulations. Technical Writing experience. Good interpersonal skills. Ability to work effectively in a team environment and build strong working relationships. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission to alleviate pain, restore health, and extend life unites a global team of 95,000+ passionate people. We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here

Role & responsibilities include providing Solutions & Services for ISO standard for Quality & Business Excellence to Corporate clients, in Manufacturing & Services sector. Preferred candidate are those with extensive experince in providing ISO QMS Consulting , implementaitons, training of Quality Stadards , Continuous Improvement methodologies to enterprise customers. Excellent opportunity to build a long terms carrer in Quality Mansgement consulting & enablement.

Competencies Overall Feedback Responsibilities & Key Deliverables Improve Receipt Quality through improving RIR time, escalation of repetitive issues, suppliers etc. Liaise with Supplier Quality Improvement group by communicating the supplier non conformances and ensure the action plan from SQI. Monitor the effectiveness of the actions taken. Improve DOL performance. Ensure adherence of process and product audits. Monitoring and Improving line rejection and customer line rejection RPH to achieve the Quality targets. Coordinate daily ORC meetings and ensure faster resolution of issues. coordination with manufacturing, supplier Quality, Design for resolution of the issues. Ensure adherence to Quality systems and maintaining the MIS, Ensuring proper data and document control. coordination with other manufacturing plants for horizontal deployment of actions and improvements. Ensuring faster resolution of field issues and External Customer Handling. Act as Customer representative in CFTs like APPAP, PFMEAs, New product, etc. Can identify and apply latest techniques in measurement, statistical analysis and quality assured processes. Can conduct Statistical analysis to aid decision making relating to process improvements. Meet M and M Quality expectations by solving problems / making improvements with the help of advanced statistical tools and drive continual Improvements Preferred Industries Automobile Tractor Manufacturing Education Qualification Bachelor of Engineering; Diploma in Engineering in Mechanical; Diploma in Engineering in Automobile; Bachelor of Engineering in Mechanical; Bachelor of Engineering in Automobile; Diploma in Engineering General Experience 10 to 12 years in Automobile Manufacturing in Quality Assurance or manufacturing Critical Experience System Generated Core Skills 7 QC Tools Analytical Thinking Communication Skills Cost Optimization Creative Thinking Customer Sensitivity Hydraulics Interpersonal Skills ISO 9000 - Quality Management ISO TS 16949 - Quality Management ISO/IEC 17025 Testing & Calibration Measurement System Analysis (MSA) Dimensional Metrology Process Control Plan (PCP) Product Knowledge & Application Statistical Analysis Statistical Process Control (SPC) Product Knowledge - Transmission Service Orientation Quality Control Service Management System Generated Secondary Skills

Responsibilities & Key Deliverables Improve Receipt Quality through improving RIR time, escalation of repetitive issues, suppliers etc. Liaise with Supplier Quality Improvement group by communicating the supplier non conformances and ensure the action plan from SQI. Monitor the effectiveness of the actions taken. Improve DOL performance. Ensure adherence of process and product audits. Monitoring and Improving line rejection and customer line rejection RPH to achieve the Quality targets. Coordinate daily ORC meetings and ensure faster resolution of issues. coordination with manufacturing, supplier Quality, Design for resolution of the issues. Ensure adherence to Quality systems and maintaining the MIS, Ensuring proper data and document control. coordination with other manufacturing plants for horizontal deployment of actions and improvements. Ensuring faster resolution of field issues and External Customer Handling. Act as Customer representative in CFTs like APPAP, PFMEAs, New product, etc. Can identify and apply latest techniques in measurement, statistical analysis and quality assured processes. Can conduct Statistical analysis to aid decision making relating to process improvements. Meet M and M Quality expectations by solving problems / making improvements with the help of advanced statistical tools and drive continual Improvements Preferred Industries Automobile Tractor Manufacturing Education Qualification Bachelor of Engineering; Diploma in Engineering in Mechanical; Diploma in Engineering in Automobile; Bachelor of Engineering in Mechanical; Bachelor of Engineering in Automobile; Diploma in Engineering General Experience 10 to 12 years in Automobile Manufacturing in Quality Assurance or manufacturing Critical Experience System Generated Core Skills 7 QC Tools Analytical Thinking Communication Skills Cost Optimization Creative Thinking Customer Sensitivity Hydraulics Interpersonal Skills ISO 9000 - Quality Management ISO TS 16949 - Quality Management ISO/IEC 17025 Testing & Calibration Measurement System Analysis (MSA) Dimensional Metrology Process Control Plan (PCP) Product Knowledge & Application Statistical Analysis Statistical Process Control (SPC) Product Knowledge - Transmission Service Orientation Quality Control Service Management System Generated Secondary Skills

Select with space bar to view the full contents of the job information. Executive - Quality Systems Job Details | AdvanzPharma We use cookies to offer you the best possible website experience. Your cookie preferences will be stored in your browser s local storage. This includes cookies necessary for the websites operation. Additionally, you can freely decide and change any time whether you accept cookies or choose to opt out of cookies to improve the websites performance, as well as cookies used to display content tailored to your interests. Your experience of the site and the services we are able to offer may be impacted if you do not accept all cookies. Modify Cookie Preferences Reject All Cookies Accept All Cookies Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Andheri (East), IN, Mumbai 400 ADVANZ PHARMA is a global pharmaceutical company with the purpose to improve patients lives by providing and enhancing the specialty, hospital, and rare disease medicines they depend on. Our ambition is to be a partner of choice for the commercialisation of specialty, hospital, and rare disease medicines in Europe, Canada, and Australia. In line with our ambition, we are partnering with innovative biopharma and pharmaceutical development companies to bring medicines to patients. Headquartered in London, UK, we have c700 employees based across more than 20 countries, including key countries in Europe, the US, Canada, and Australia. Our Centre of Excellence in Mumbai, India, as well as an established global distribution and commercialisation partner network complement our global operations. ADVANZ PHARMA s product portfolio and pipeline comprises innovative medicines, specialty generics & biosimilars, and originator brands. Our products and pipeline cover a broad range of therapeutic areas, including hepatology, gastroenterology, anti-infectives, critical care, endocrinology, CNS, and, more broadly, rare diseases. We can only achieve our ambition with the passion of our dedicated and highly qualified people, acting in line with our company values of entrepreneurship, speed, and integrity. About the Role As ADVANZ PHARMA continues to strengthen its position as the partner of choice for specialty, hospital, and rare disease medicines, we have an exciting opportunity for an Executive- Quality Systems. Execute Complaints investigations in accordance with the defined procedures ensuring that: Complaints are raised in the system. Complaints are investigated to the required standard and that root cause is identified (leading to appropriate CAPA). Complaint s resolution is appropriately documented with supporting evidence. Liaising with CMOs and relevant stakeholders to ensure that complaints are investigated, resolved and closed in a timely manner. Interact with complaints reporter in the course of investigations and communicate the outcome of investigations accordingly. Follow up with CAPA owners to ensure that actions are implemented in a timely manner. To assist in executing Recalls as required. To assist in investigation of deviations when required. Creation of Quality related documentation (SOPs, Risk Assessments etc.) Carry out internal audits as required. Report Quality Systems metrics. Other activities as may be required, at the discretion of management. Thrive in an entrepreneurial environment and take accountability for results. Embrace challenge and change, applying a growth mindset approach. Have a bias for action and fast decision making. Consistent demonstration and embodiment of company core values: Entrepreneurship, Speed, and Integrity. Drive the spirit of One Team by working collaboratively across all business functions with an open, honest, and respectful cooperation. Contribute to making ADVANZ PHARMA a desired place to work. We are looking for highly motivated individuals who are passionate about making a meaningful difference to patients lives. For this role, you will also have the following: Qualifications: Minimum Honors Degree in Chemistry, Pharmacy or Microbiology. Knowledge, Skills & Experience: Decent experience of working in a similar role within a pharmaceutical company. Ability to use eQMS (eg. TrackWise, Veeva Vault etc.) for Quality Systems management. Knowledge of ICH Q9, ICH Q10 and Eudralex- Volume 4 Good manufacturing practice (GMP) guidelines. Capable of working to deadlines & remain calm under pressure. Good working knowledge of MS Office. Well organised with logical & methodical approach to work. Excellent communication skills, both oral and written, to include senior management where escalation is required. A positive and can-do approach , biased towards finding solutions and embracing change. Inspired by our values of entrepreneurship, speed and integrity. Learning agility and scalability , with a desire to continuously improve and develop as ADVANZ grows. Work collaboratively across all business functions with an open, honest, and respectful cooperation. Ability to have fun and thrive in a growing, unique, and inclusive work environment. The success of any company is driven by its people, and we are no different. At ADVANZ PHARMA, we believe in empowering our people to be entrepreneurs and embrace challenges to enable personal and company growth in an agile and fast-paced environment. We strive to do that inclusively and responsibly, treating all employees with integrity whilst rewarding outcomes and impact. Our teams are made up of people from all walks of life and backgrounds. We thrive in an environment where uniqueness is celebrated, but we are all united by the same passion to help improve patients lives by providing and enhancing the specialty and hospital medicines they depend on. But there s more to you and us than just work, which is why our culture, vision and values are so high on our agenda. We believe in gender equality and actively encourage women into senior roles we have an active ADVANZ PHARMA Women s Network; almost 40% of our managers are women. We work hard to recognise and reward talent, and we actively promote from within - last year, approximately 25% of our people across the company achieved promotions. In addition, we recognise talent with our annual Impact Awards, in which our top performers are rewarded for their hard work and dedication. We offer flexible, agile working options, and you will also enjoy a highly competitive salary and benefits package. *Please include a CV and Cover letter. When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. Because we respect your right to privacy, you can choose not to allow some types of cookies. However, blocking some types of cookies may impact your experience of the site and the services we are able to offer. These cookies are required to use this website and cant be turned off. 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About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar and specialty products. For more information visit: www.apotex.com . Job Summary Planning and executing various analytical method development, validation for new products, comprehensive testing of API and finished dosages with all established regulatory and compliance and safety requirements. Review of laboratory data, instrument logbook and reports wherever applicable. Initiation of departmental CCRs and tracking the progress to execute the proposed changes through QMS system. Preparation of TAP (Transfer of Analytical Procedures) protocol and Report for various sites. Procuring respective samples and Impurities accordingly. Planning and executing the assigned TAP projects to various sites. Preparation, maintenance and archival of regulatory submission documentation like SOP, protocols, reports for method development and validation. Job Responsibilities Prepares working plan for assigned projects and provides timeline to Deputy Manager. Develops stability indicative analytical methods for drug substance and finished product Responsible for all activities in Analytical Development, including cGLP, documentation and implementation of departmental quality systems. Responsible for protocol preparation, planning, execution, review and report preparation of various analytical method validation parameters. Ensures analytical methods validation is conducted according to approved validation protocol in a timely manner with accuracy and precision in compliance of laboratory SOP and guidelines. Responsible for method verifications and publishing of analytical methods Maintenance and archival of analytical method validation documents. Performs all analytical tests for drug substance, including assay, related compounds, identifications and wet chemistry for API evaluation. Performs all analytical tests for PE/PO samples, including assay, degradation products and dissolution. Performs all analytical tests for API releasing, including assay, degradation products, dissolution and physical testing. Conducts other tests required for dosage submissions. Conducts lab investigations for OOS and OOT results. Raising Change control for various analytical activities (Method SOP and department SOPs)by QMS trackwise To prepare General, Operation and Calibration Standard Operating Procedures. Responsible for initiation, execution and completion of technology transfer and collaborative validation activities of analytical methods to and / or from other departments of Apotex wherever applicable. Responsible for technology transfer and Transfer of analytical procedures activity to support the supervisor. Communicating the requirements for the Leaders and within the team members for effective cGLP procedures and departmental quality systems to achieve all outcomes. With guidance of scientists, performs troubleshooting on complex issues with respect to the stability of drug substances and drug products. To participate in the mandatory trainings to execute the day to day job responsibilities. Develops and maintain strong relationships within Analytical R&D to ensure that the projects are delivered on time. Practice and up-gradation of knowledge with respect to cGMP. Performs all work in accordance with all established regulatory and compliance and safety requirements. Participates in departmental housekeeping and other pertinent duties as assigned in accordance with safety and GMP requirements. Ensures all instruments assigned with responsibility within group/department are well maintained. Work as a member of a team to achieve all outcomes. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education A graduate/post graduate in analytical chemistry, organic chemistry, pharmaceutical sciences, or related field. Knowledge, Skills and Abilities knowledge of the instrumentation such as HPLC, GC, spectrophotometer and dissolution apparatus, wet chemistry and analytical bench techniques. Knowledge in HPLC method development and method validation. Knowledge on preparation and review of various documents like SOPs, Formats, Protocols, Reports, analytical data, investigation and deviation reports. Should have well versed knowledge on regulatory guidelines and thorough knowledge on cGMP activities Should possess troubleshooting knowledge on Instruments and analysis. Knowledge of wet chemistry, analytical bench techniques, Window-based software, and automated data acquisition systems. Working knowledge of LIMS is an asset. Good written and verbal English communication skills. Experience BSc with 5 years or MSc with 3-4 years experience in a pharmaceutical lab in an R&D environment. Chromatographic method development and validation. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Ensure implementation and maintenance of ISO 9001 & IATF 16949 standards. Lead internal & external audits – customer, third-party & surveillance. Maintain and update all quality manuals, SOPs, work instructions, and control plans.

QMS Experience of IATF EMS Certification Audits, Internal Auditors in IATF and EMS Certification. Sound knowledge of PPAP, 8D, MSA, SPC,7 QC Tools, DOJO training module SAP QA module AutoCAD Drawing awareness, change systems, 5S, safety.

We are looking for a Management Representative (MR) with experience in ISO 9001:2015 standards. Candidates with backgrounds as Metallurgists , Production Supervisors , Operations , or Quality Control professionals are preferred. Health insurance Annual bonus Free meal Maternity benefits in mediclaim policy Accessible workspace Provident fund

The Quality Management System Engineer is responsible for the development, implementation, maintenance, and continual improvement of the organization's Quality Management System in compliance with applicable standards (e.g., ISO 9001, ISO 9001, ISO 14001, ISO 45001).This role ensures that quality processes and documentation meet regulatory, customer, and internal requirements. Primary Responsibilities: Develop and maintain QMS documentation, including quality manuals, procedures, work instructions, and forms. Ensure compliance with relevant quality standards (e.g., ISO 9001, ISO 14001, ISO 45001) Manage document control systems and ensure version control and proper distribution of QMS documents. Assist in risk management activities, including risk assessment and mitigation planning. Knowledge and experience of various certifications like ISO 9001:2015, ISO14001,ISO 45001). Ability to demonstrate the Core Values of Jakson - Integrity, Customer Centricity, Innovation, Team work and Care, in all aspects of work.

Knowledge of Rotary machines inspection details Experience in EIL preferred approved Cos 1. Implementing and Controlling of Quality parameters. 2. Daily/Weekly and monthly Report Record Preparation and attending quality review meetings. 3. Preparation of daily Inspection Reports like Stage Wise Inspection of All fabrication activities, Visual Examination, Nozzle Marking, Machining, Fit Up Examination, Examination After Head Forming, Dimensional Inspection, Final Inspection & Testing 4. New Product Trail, Inspection of New Model, Indoor & outdoor Testing. 5. QMS ISO 9001 6. RCA, CAPA, PDCA CYCLE, TPM & ISO Audit 7. Timely Escalation and closer of issue & analysis (why issue occur & past record) 8. Overall responsibility for testing or inspection of item according to approved drawing, procedures, applicable codes & specifications. 9. To prepare & maintain all documents & procedures in guidance for ASME/ISO audit. 10. Welder Qualification (Verification of WPS, PQR & WPQ). 11. Knowledge of NDT like DPT, MPI, UT, RT etc. 12. Knowledge of ASME SEC- IX, V, II, III & VII, EN & IS Standard. 13. Responsible for maintaining quality according to QAP. 14. Responsible for all stage inspections. 15. Responsible for verification of Hydro/pneumatic test and maintain reports & records. 16. Responsible to inspect brought out or inward material. 17. To visit the supplier when needed or while inspection is needed at vendor end across India. 18. To perform Red bin analysis daily 19. Review and validate nonconforming material reports throughout the process (incoming, in-process and final). 20. To plan schedule and arrange conducting of internal & external audits. 21. Management & Calibration of Instruments etc. 22. Final inspection or review of final inspection documents. Keywords: Knowledge of Rotary machines inspection details Experience in EIL approved Cos preferable Personality Traits: Strong documentation, Qty Audit communication skills Skills & knowledge: In-depth knowledge of quality systems

Responsible 4 smooth functioning in processing of various products & systems as per the laid down procedure.Customer Complaint Handling.Corrective & Preventive Action for External & internal Product Quality Issues.Suppliers audit & Internal Audit Required Candidate profile Problem solving tools,knowledge of workshop kaizen, knowledge of system standards.Identifying & solving problems,Setting goals & targets,Commitment,Time management & Prioritizing,Training & Delegating

Job Description: Position : Quality Control (QC) Engineer Manufacturing Plant Experience : Min 5 years of experience in QC or QA within a manufacturing environment Salary : 5-7 LPA Location : Lkapadvanj, Gujarat Qualification: Bachelors degree in Engineering (Mechanical, Electrical, Industrial, etc.). JOB SUMMARY: The QC Engineer is responsible for maintaining the quality of products and production processes in a manufacturing unit. The individual will perform a range of quality control functions such as inspecting raw materials, monitoring production processes, testing finished products, and ensuring compliance with quality standards. The role also includes collaborating with cross-functional teams to implement continuous quality improvements. Job Duties : Inspect raw materials, in-process items, and finished products. Conduct dimensional, visual, and functional tests to ensure compliance with quality standards. Document test results, analyze findings, and initiate timely corrective actions when necessary. Continuously monitor production processes to ensure adherence to established quality standards. Identify potential quality risks in real-time and take corrective measures as required. Ensure that quality checkpoints are integrated into the production flow and are consistently maintained. Investigate defects, non-conformities, and deviations from product specifications. Analyze production data to identify trends, patterns, or recurring issues that impact quality. Prepare detailed reports on quality findings and provide recommendations for corrective actions. Ensure full compliance with industry standards, including ISO, GMP, and other regulatory requirements. Participate in and support internal and external quality audits, providing necessary documentation. Maintain and update QC documentation, such as inspection checklists, reports, and records. Develop and implement corrective actions to address identified quality issues. Collaborate with cross-functional teams to prevent recurrent quality problems through preventive measures. Monitor and assess the effectiveness of implemented CAPA actions to ensure continuous improvement. Ensure that all testing tools, measuring equipment, and QC instruments are properly calibrated and maintained. Oversee the scheduling and execution of regular maintenance for QC equipment to guarantee accuracy and reliability. Lead and manage quality improvement projects to enhance the efficiency and effectiveness of production processes. Implement continuous improvement strategies focused on reducing defects and improving product quality. Stay updated on industry trends, new technologies, and best practices in quality control. Provide ongoing training to staff on quality control procedures, testing methods, and inspection techniques. Promote a culture of quality awareness across the manufacturing plant, ensuring all staff adhere to best practices. Required Qualification & Experience: Bachelors degree in Engineering (Mechanical, Electrical, Industrial, etc.). Min 5 years of experience in QC or QA within a manufacturing environment. Experience with quality systems (ISO 9001, Six Sigma, etc.). Proficient in QC tools (calipers, micrometers, CMM). Familiarity with SPC, root cause analysis, and quality software. Knowledge of Microsoft Office (Word, Excel, PowerPoint). KRA Ensure the quality of raw materials, in-process items, and finished products through rigorous inspection and testing, documenting results and initiating corrective actions as needed. Monitor production processes to identify risks and implement preventive measures, ensuring compliance with industry standards and internal quality protocols. for more jobs- https: / / glansolutions.com / jobs.php Google search: Glan Management Consultancy Key Skill: QC, QA, Quality control engineer, Quality assurance engineer

Job Description Role & responsibilities Ensure the development and implementation of quality management systems, analyze data to identify areas for improvement, and promote a culture of continuous improvement. Develop and Implement Quality Management Systems. Manage all Internal & External QC & QA Standards Ensure compliance with relevant industry standards and regulations. Analyze performance data to identify trends, inefficiencies, and improvement opportunities. Set and track key performance indicators (KPIs) related to quality. Participate in ISO/IATF certifications and ensure compliance. Lead APQP and QMS initiatives, focusing on customer satisfaction. Face internal and external audits. Act as a liaison between customers and the organization to address quality-related concerns. Manage Documentation, Records & Reports for all Quality Systems. Take initiative and share critical insight for Process Improvement & Optimization Ensure customer feedback is integrated into quality improvement plans. Candidate Profile (Qualification, Experience, Skills & Abilities): M.E/M.Tech./ B.E. / B. Tech in Mechanical Engineering with 10-12 years of experience. OR Diploma in Mechanical Engineering with more than 15 years. Must have held a managerial role for 6-8 years in the QC Department of HVAC/Engineering/Automotive Component, Tubing, or Heat Exchanger manufacturing unit. Proficiency in 5S/KAIZEN, quality audit systems, statutory and factory compliances, and safety norms. Exposure to Quality Management Systems such as Lean,and Six Sigma will be preferred, though not mandatory. Excellent written and verbal communication skills in English & Hindi. Basic computer literacy, including email and MS Office. Exposure to ERP systems will be an advantage. Enthusiastic and proactive in taking new initiatives. Knowledge of industry-specific regulations and standards. Leadership and team management capabilities. Must be willing to travel to Customer Sites and other production units. Willing to work in shifts. (Occasional)

QMS Experience of IATF EMS Certification Audits, Internal Auditors in IATF and EMS Certification. Sound knowledge of PPAP, 8D, MSA, SPC,7 QC Tools, DOJO training module SAP QA module AutoCAD Drawing awareness, change systems, 5S, safety.

Inspect CNC machined/turned/VMC precision components visually & using instruments: Detect defects Meet specs,Standrds & Quality; Ensure complince ISO 9001 Reporting & documention Perform PPAP, Root cause analysis, Audits, Interpret Engg drawings Required Candidate profile 3-5 Yrs exp in QC/QA in machining Co. Knowledge of QC process in CNC machines like Turning, Turnmill, Sliding Head Stock Automats, VMCs.. & GD&T, Tolerances, Calibration documents & Inspection

•PPAP APPROVAL FOR NEW PARTS DEVELOPMENT • NEW PARTS DEVELOPMENT TECHNICAL ACTIVITY FOR POWERTRAIN PARTS • Knowledge of quality systems such as QC tools, GD&T, SPC, MSA, PFD, FMEA, Control plan etc., • DRIVABILITY ISSUES ANALYSIS & EVALUATION SKILLS RELATED TO POWERTRAIN • ECU & TCU S/W FLASHING (PT CODIING) BY USING INCA TOOL • CAN DATA MONITORING THROUGH INCA & CANOE • INCA DATA ANALYSIS & CALIBRATION DATA VERIFICATION through MDA • RIDE & DRIVE (Real road test) ACTIVITY RELATED TO POWERTRAIN • POWERTRAIN DURABILITY ISSUSE DIAGONISIS & ANALYSIS • KNOWLEDGE ABOUT COST SAVING & VALUE ENGINEERING PROPOSALS • KIN VEHICLE CCL LIST VALIDATON FOR POWERTRAIN PARTS • SYSTEM VALIDATION FOR POWERTRAIN BASIC EMISSION RELATED UNDERSTANDING

Job Title: QMS Specialist # Salary: As per Industry Standards (Depend on Experience/Knowledge) # Job Summary: We are seeking a highly skilled and experienced QMS Specialist to join our team in the plastic molding industry. The successful candidate will be responsible for implementing, maintaining, and continuously improving our QMS, ensuring compliance with international standards and regulations. # Key Responsibilities: 1. Develop, implement, and maintain QMS in accordance with international standards (e.g., ISO 9001, IATF 16949). 2. Ensure compliance with regulatory requirements, industry standards, and customer-specific requirements. 3. Conduct internal audits to ensure the effectiveness of the QMS and identify areas for improvement. 4. Lead corrective action and continuous improvement initiatives to address quality issues and improve processes. 5. Develop and maintain quality-related documentation, including procedures, work instructions, and records. 6. Provide training and support to employees on QMS policies, procedures, and requirements. 7. Manage and analyse quality data, including customer complaints, internal rejects, and supplier performance. 8. Collaborate with cross-functional teams, including production, engineering, and procurement, to ensure quality requirements are met. 9. Maintain relationships with external parties, including customers, suppliers, and certification bodies. 10. Stay up-to-date with changes in regulations, standards, and industry best practices. # Requirements: 1. Bachelor's degree in a relevant field (e.g., QMS/BE/MBA). 2. Minimum 8 -10 years of experience in a QMS role, preferably in the plastic molding industry. 3. Certification in a recognized quality management standard (e.g., ISO 9001, IATF 16949). 4. Strong knowledge of quality management principles, including lean manufacturing, Six Sigma, and continuous improvement. 5. Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams. 6. Strong analytical and problem-solving skills, with the ability to interpret data and make informed decisions. 7. Proficient in Microsoft Office and quality management software. # Nice to Have: 1. Experience with industry-specific regulations and standards (e.g., FDA, EU MDR). 2. Certification in a related field (e.g., quality engineering, supply chain management). 3. Job Title: QMS Specialist # Salary: As per Industry Standards (Depend on Experience/Knowledge) # Job Summary: We are seeking a highly skilled and experienced QMS Specialist to join our team in the plastic molding industry. The successful candidate will be responsible for implementing, maintaining, and continuously improving our QMS, ensuring compliance with international standards and regulations. # Key Responsibilities: 1. Develop, implement, and maintain QMS in accordance with international standards (e.g., ISO 9001, IATF 16949). 2. Ensure compliance with regulatory requirements, industry standards, and customer-specific requirements. 3. Conduct internal audits to ensure the effectiveness of the QMS and identify areas for improvement. 4. Lead corrective action and continuous improvement initiatives to address quality issues and improve processes. 5. Develop and maintain quality-related documentation, including procedures, work instructions, and records. 6. Provide training and support to employees on QMS policies, procedures, and requirements. 7. Manage and analyse quality data, including customer complaints, internal rejects, and supplier performance. 8. Collaborate with cross-functional teams, including production, engineering, and procurement, to ensure quality requirements are met. 9. Maintain relationships with external parties, including customers, suppliers, and certification bodies. 10. Stay up-to-date with changes in regulations, standards, and industry best practices. # Requirements: 1. Bachelor's degree in a relevant field (e.g., QMS/BE/MBA). 2. Minimum 8 -10 years of experience in a QMS role, preferably in the plastic molding industry. 3. Certification in a recognized quality management standard (e.g., ISO 9001, IATF 16949). 4. Strong knowledge of quality management principles, including lean manufacturing, Six Sigma, and continuous improvement. 5. Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams. 6. Strong analytical and problem-solving skills, with the ability to interpret data and make informed decisions. 7. Proficient in Microsoft Office and quality management software. # Nice to Have: 1. E xperience with industry-specific regulations and standards (e.g., FDA, EU MDR). 2. Certification in a related field (e.g., quality engineering, supply chain management). 3. Experience with quality management software (e.g., QMS, EQMS)

Role & responsibilities : Maintain , upgrade and implement the Quality Management System (QMS) / MR and Quality Assurance throughout organisation. Ensure zero customer complaints by introducting quality gate cocept. Ensure inprocess rejection and rework is within target set by the management, Assure the reliability and consistency of production by ensuring inprocess control by having internal process and product audits. Communicate and interaction with customer for QAP (Quality Assurance Plan) & Customer Complaints. To develop and implement the Quality Assurance & Quality Management Strategy in conjunction with Senior management to satisfy quality requirements defined by customers, applicable standards and internal requirements for the products, processes and services. Preferred candidate profile

QA/QC Lead Role Purpose Leads the QA/QC function, ensuring raw materials, processes, and products meet technical and client standards. Enforces quality systems and ensures regulatory compliance. Key Responsibilities Develop and maintain the Quality Management System (QMS). Implement QA/QC procedures for material and product testing. Supervise inspections across production and final stages. Manage in-house lab operations for material testing. Coordinate third-party inspections and audits. Train staff on quality norms and corrective actions. Perform RCA on NCRs. Maintain quality documentation and traceability. Qualifications & Experience B.E./B.Tech in Civil Engineering. 12-20 years in QA/QC in precast/infrastructure manufacturing. Core Competencies & Skills Knowledge of precast QA processes. Documentation and analytical skills. Training and communication ability. Familiar with ERP and lab testing tools. Quality and compliance focus.

Division TM-MPT Department TMHT Job Location Manesar-Gurgaon Job Title Production Supervisor, level - Engineer Job Role Production Shift Supervisor Reporting to Department head Level in the organization L-08 (Engineer) Educational Qualification Diploma /BE/B-Tech Graduation (With Specialization): Mechanical/Automobile Post Graduation (With Specialization): - Any Other (Certification / Diploma etc.): Mechanical/Automobile Work Experience (Years) in treasury activities. Minimum: 4 Yrs. Maximum: 5Yrs. > For Production Shift Supervisor Techanical: a )Experience in gear and shaft machining manufacturing . b) Hands on working on grinding machines, CNC lathes, gear checker machines, Distortion correction machines. c) Part programming on CNC machine, work setup, grinding process improvement and troubleshooting. d) Knowledge of cycle time study, efficiency and loss time analysis e) Experience of abnormality handling tools, rejection reduction by process improvement. f) Knowledge of quality systems (ISO-9001), safety and Environment standards (ISO-14001). g) Production planning and inventory control, setup change and tool change management. h) Knowledge of SAP usage Behavioral: Target oriented, Good Analytical Skills, Interpersonal, communication & presentation skills, Team player with Networking skills etc.

Tenneco is one of the worlds leading designer, manufacturers and marketers of automotive products for original equipment and aftermarket customers, with approximately 78.000 team members working at more than 300 sites worldwide. Through our four business groups, DRiV, Ride Performance, Clean Air and Powertrain, Tenneco is driving advancements in global mobility by delivering technology solutions for diversified global markets, including light vehicle, commercial truck, off-highway, industrial, motorsport and the aftermarket.. Position: Assistant Manager Manufacturing Engineer. Experience?5-8 years. Qualification: Graduate or above, Mechanical & Mechatronics.. Location: Bhiwadi. Roles and Resonsibilities. Complete engineering releases for new or revised Ignition Products to include process specifications, tooling and tool charts.. Review and process Manufacturing / Engineering Documentation Request (MEDR).. Directly support the APQP / product launch management process.. Develop and revise Process FMEA’s.. Maintain current process standards and develop new standards for emerging process technology.. Design, Develop and Implement projects to enhance existing process technology to improve efficiency, quality and reduce manufacturing cost.. Each employee has the authority to initiate action to prevent the occurrence of non-conformities relating to the product, process and quality system and has the authority to stop further work on non-conforming suspect product until the deficiency or conditions have been corrected.. Work with global team to meet customer requirements.. Experience Required. Master the design and manufacture of fixture and tooling.. Master industrial automation device, PLC control Assembly equipment.. Have good judgment ability and operation ability.. Have English communication ability.. Have 3D mechanics drawing and reading drawing ability,. Have strong sense of responsibility, team-cooperation and hard working spirit,24 hours quick response.. Job Specific Training. Ignition Group ECN Process. Ignition Group EDB System. Problem Solving Methods and Tools. Project Management. Statistical Process Control. Failure Modes and Effects Analysis. Problem Solving Methods. Design of Experiments. Show more Show less

Key Responsibilities: Supplier Quality Management: Monitor and evaluate supplier performance through audits, scorecards, and metrics. Lead supplier root cause analysis and corrective/preventive actions (CAPA). Ensure compliance with industry and company-specific quality standards (e.g., ISO 9001, IATF 16949, AS9100). Supplier Development: Partner with strategic suppliers to implement quality improvement plans. Drive supplier process improvements using Lean, Six Sigma, or other CI methodologies. Conduct supplier capability assessments and risk evaluations. New Product Introduction (NPI): Collaborate with Engineering, Sourcing, and Operations to support supplier readiness for new products. Oversee PPAP, APQP, or similar quality assurance processes during product launch phases. Problem Solving & Quality Tools: Facilitate 8D, 5 Whys, FMEA, SPC, and other problem-solving tools. Utilize data analytics to drive decisions on supplier quality performance and improvement areas. Leadership & Supervision: Supervise a team of Supplier Quality Engineers or Auditors. Provide mentoring, coaching, and performance management for direct reports. Develop training materials and lead supplier quality training sessions, internally and externally. Qualifications: Bachelor s degree in Engineering, Quality, or related field (Master s preferred). 12+ years in supplier quality or supplier development roles, with at least 5+ years in a supervisory capacity. Strong knowledge of manufacturing processes and quality systems. Experience in industries such as automotive, aerospace, electronics, or heavy equipment preferred. Proficiency in quality tools: PPAP, APQP, FMEA, SPC, MSA. Certifications such as CQE, CSSBB, or ASQ are a plus. Skills and Competencies: Excellent analytical and problem-solving skills. Strong communication and interpersonal abilities for cross-functional collaboration. Proficiency in MS excell Ability to lead and influence suppliers and internal stakeholders. Willingness to travel (domestic/international) up to 30-50%. Qualifications: Bachelor s degree in Engineering, Quality, or related field (Master s preferred). 12+ years in supplier quality or supplier development roles, with at least 5+ years in a supervisory capacity. Strong knowledge of manufacturing processes and quality systems. Experience in industries such as automotive, aerospace, electronics, or heavy equipment preferred. Proficiency in quality tools: PPAP, APQP, FMEA, SPC, MSA. Certifications such as CQE, CSSBB, or ASQ are a plus. Skills and Competencies: Excellent analytical and problem-solving skills. Strong communication and interpersonal abilities for cross-functional collaboration. Proficiency in MS excell Ability to lead and influence suppliers and internal stakeholders. Willingness to travel (domestic/international) up to 30-50%.