294 Quality Systems Jobs

Pl join us my whatsup group no 9356395439 Post - Quality & MR CNC & VMC Production line Current Position Asst Manager or Sr Engineer Directly F2F interview availability Pune chakan Industry automotive Machine Shop Age Max 40 yrs Qualification – Any graduate or DME / BE /BTECH Experience – 8- 12 years in CNC & VMC Production line Sound knowledge and experience in ISO & IATF 16949 .• Communication skill in English must speak, writing . *Automotive experience* is must. Person must have *sound knowledge in 7 QC TOOLS . APQP, PPAP , 8D CAPA , CPK study Mass production and daily dispatch experience is preferred. Person should have ability to lead the team of 25+ workman*

Ensure the effective deployment of the EV Quality Vision, Mission, and Policy across the plants by providing necessary resources and structuring quality systems. Establish a structured process to capture the voice of customers through dealers and customer care for Product Quality & Reliability improvement. Ensure outgoing quality of the product meets or exceeds customer requirements. Work towards ensuring product quality consistency and meeting critical parameters through the development of Product & Process using appropriate tools. Collaborate effectively with various teams such as PVT and SQE to drive Product Quality, Supplier Quality Improvement, and benchmark enhancements. Deploy quality management systems through structured product, process & component audits. Take the lead in organizing management reviews to provide updates on quality initiatives/goals and ensure timely escalations. Provide functional guidance to the quality assurance team and lead as a people manager for the team in terms of recruitment, setting KRAs, performance appraisals, and team development. Guide the team in enhancing functional excellence in Quality Systems and Quality Engineering to resolve quality issues effectively and efficiently. Education Qualification: Graduate in Engineering (Electrical, Mechanical, or Automobiles). ASQE/QMS certifications will be an advantage. General Experience: 15+ years in Quality Assurance in the EV Passenger Cars Vehicle segment. Thorough understanding of business operations, manufacturing, and quality assurance processes. Familiarity with various quality systems. High level of business acumen and process orientation. Ability to make strong decisions, possess analytical skills, and demonstrate resilience to pressure. Critical Experience: Exposure in deploying Quality Management Systems through structured audits. Experience in Quality Assurance function and manufacturing processes. Previous role handling CQA Head responsibilities for large plants. Experience in successful new product launches in automotive/passenger/commercial vehicle segments or Powertrain products. Experience in leading medium to large-sized teams.

Reporting to the Engineering Manager, this position would be responsible to lead engineering activities supporting manufacturing, testing and vendor management needs of Surface Pumping Units within Weatherford. Required Skills: B.Tech/B.E in Mechanical Engineering from an accredited college/university. Minimum 6 to 9 years of proven experience working in complex engineering projects, project management, mechanical engineering design, instrumentation engineering. Experience working with customers like Exxon, Shell, NOC, KOC, ADNOC, Total, National Oil Companies etc Proficient in Industry standards such as ASME B31.3, API, ASME BPVC, IOGP, NACE etc Proficiently use MS Office Suite to develop presentations, correspondence, reports, and schedules (Projects - Gantt Chart, Word, Excel, Power Point, etc). Demonstrate clear written and verbal communication skills and ability to promptly give and follow directions when working with others. Preferred Skills: 3+ years of hands-on experience in handling projects from conceptual stage to project closure including but not limited to RFQ, design, manufacturing, testing, inspection, etc Experience working with equipment s/instruments/systems used in the Oil and Gas industry. Working knowledge of PTC Creo, DraftSight, AutoCAD, Windchill. Experience of working with cross functional teams spread across geographies. Travel Requirement: This role may require domestic and potentially international travel of up to: Understanding customer specifications, requirements and preparing project scope clearly highlighting deliverables. Liaise with engineering, product line, manufacturing, and supply chain in reviewing manufacturing documents, procedures, material test certificates and other documents per customer specifications and requirements. Perform tasks such as reviewing engineering drawings, documentation, prototype and production testing, vendor management, and quality management. Interact with clients and vendors independently as needed to provide product technical support. Identify any opportunities for improvement (OFI) regarding design, planning and manufacturing processes. Preparation of engineering design files, test reports and investigation reports. Work independently as we'll as part of a project team, managing multiple tasks and working on multiple projects simultaneously to meet challenging deadlines. Review Nonconformance Reports, field incidents and assist in providing disposition. Understand Weatherford Policies and comply with all requirements of the Quality Systems Manual, Safety rules, Operating and Technical Procedures and Workplace Instructions. Provide continued support for projects after completion and field commissioning in the form of troubleshooting either remotely, or in person onsite when required.

Taking stringent quality measures including preparation / maintenance of necessary documents to ensure compliance with above standards customer requirements. Resolving all internal and external customer complaints; taking timely corrective preventive actions and preventing the recurrence. Restitution of the Audit vehicles from Attribution to the Closure of the Issues. Quality improvement - Reactive vs. Proactive. Quality Measurement to Customer Value Management. Establishing Priorities for Projects and implementing on time deliverables. Coordinate with all department including engineering, quality, manufacturing, supply chain to achieve new product development milestones. Support new product implementation and design changes . Ensure compliance to PPAP requirements during production trial run. Review of Design Change Request/Process Change Request Supplier Change Request. Co-ordinating and managing the tracking sheet with concerned department for DCR/PCR/SCR implementation. Update maintain all project management process engineering documents according to IATF-16949 standard. Assessing the process and product quality developed in compliance with pre-set technical specifications Detecting defects / faults and initiating corrective actions. Ensuring that the products produced and dispatched are in confirmation with the established quality standards and customer requirements. Practicing quality standards like 5S, TPM, MQS, POKA YOKE, KAIZEN, IATF, QMS systems standards responsible for quality up gradation productivity with key emphasis on Customer specific requirements. Lead role participation PCRN/APQP/SPC/PFMEA (Process Change Request Notification)/ MPPAP /for process improvements. Active participation in launching new projects w r t Quality systems FTR , Change management, PPAP, ECN Change with QMS management Champion in leading QCRT Meeting conducted for user plant concerns. Preferred Industries Automobile Education Qualification Bachelors of Technology in Mechanical; Bachelor of Engineering General Experience If BE 3 to 5 yrs Critical Experience System Generated Core Skills 7 QC Tools Analytical Thinking Microsoft Office People Management Presentation Skills Team Building System Generated Secondary Skills Communication Skills Consumer Focus Leadership Skills

Position: Senior Officer Job Title: Senior Officer Job Grade: Function: Corporate Quality Compliance Sub-function: Complaints Manager s Job Title: Senior Manager-1 Skip Level Manager s Title: Function Head Title: Head of Global Quality Systems Complaints Location: Vadodara No. of Direct Reports (if any) Nil Job Summary Logging of Product Quality Complaints (PQC) in the database (TrackWise). Acknowledge the complaints to the complainants. Providing the response letter to the complainant. Reconciliation of received market complaints. Review of Product Quality Complaint Investigation Reports (India Market). Coordinate with other stakeholders involved in the complaint handling process. Areas of Responsibility Product Quality Complaints Management Travel Estimate Approximately 5% Job Scope Internal Interactions (within the organization) Yes External Interactions (outside the organization) Nil Geographical Scope India Financial Accountability (cost/revenue with exclusive authority) Nil Job Requirements Educational Qualification M. Sc (Life Sciences) / B. Pharm Specific Certification Nil Skills Good Technical Communication Skills, minimum 1 year experience in complaints handling process, candidate should have worked in USFDA work environment. Experience 3-5 years Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title: Manager, Global Clinical Solutions Career Level: D Introduction to role: Are you ready to drive innovation in clinical solutions? As a Manager in Global Clinical Solutions (GCS) at AstraZeneca, youll be at the forefront of delivering services and technology that enhance process effectiveness and performance. Youll support teams in developing and maintaining processes, systems, and services that are crucial for Clinical Development programs. Your leadership will be pivotal in coordinating and delivering GCS services across projects, ensuring timely, cost-effective, and quality outcomes. Accountabilities: Providing input to eCOA and DPS systems based on CSP, previous practical experience from end users and consultancy with eCOA SME/ Solutions Implementation Lead/Study Management/Business Analyst and other relevant members to ensure clinical study needs are properly captured in eCOA and DPS user requirements specification. DPS stands for Digital Patient Solutions and means for the entire digital patient services in a clinical trial (can include but not limited to eCOA with integrated sensors, devices and/or wearables , spirometry, patient engagement, telemedicine, eConsent, HBS) The eCOA and DPS Manager is a member of GCS and acts as co-Project Manager of the study together with system suppliers teams and is responsible for the coordination/leading the activities ensuring delivery and lifecycle management for eCOA and DPS systems as defining, testing, training strategy for the system and maintaining system in validated state. The eCOA and DPS Manager work across drug projects with internal and external stakeholders to enable delivery of DPS clinical systems in agreed time, cost, and quality across all AZ portfolio. Essential Skills/Experience: Digital Patient Solutions systems, P roject Management experience & Stakeholders / Vendor Management & Risk/issues reporting University degree in related discipline, preferably in biological science or healthcare-related fields, such as medicine, nursing, or equivalent experience Ability to work collaboratively; proven organizational and analytical skills, and proven skills to deliver to time, cost and quality Good project management skills Excellent knowledge of spoken and written English Strong business communication, stakeholder management and presentation skills Well-developed organisational and interpersonal skills Ensures risks and issues management to ensure effective delivery. Expertly utilises escalation routes and governance to gain traction and deliver rapid solutions Shares lessons learned and best practice recommendations with relevant stakeholders to drive continuous improvement Builds relationships and achieve results without line management input Curious and self-motivated Desirable Skills/Experience: Expert in their relevant service Experience of utilizing standard process improvement methodologies (e.g. Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement Some experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment Experience in multiple fields of clinical development At least 2 year experience in Drug Development within a pharmaceutical or clinical background Understanding ICH GCP guidelines in relation to study delivery Experience of working in a global organisation with complex/geographical context At AstraZeneca, curiosity drives us to explore new scientific horizons. We are committed to making a difference by fusing data and technology with scientific innovations to tackle complex diseases. Our inclusive environment encourages collaboration across academia, biotechs, and industry, creating opportunities for lifelong learning and career development. With a focus on advancing scientific knowledge, we aim to shape the future of healthcare and impact patients lives globally. Ready to make an impact? Apply now to join our team! 27-Jun-2025 11-Jul-2025

Position: Site QA Head Reports to: Site Quality Head Department: Quality Location: Halol POSITION SUMMARY Manage overall quality assurance oversight and site activities wrt to quality systems: documentation review and SOP update, in-process quality assurance, sampling and batch release, preventive maintenance / calibration / qualification / validation , internal audit, compliance, quality oversight of electronic systems, budget, and continuous improvement of quality systems, RA support, monitoring of pest control, retention sample management as per Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key responsibilities: Responsible for defining operational strategy and road map for quality assurance management at site. Define site quality assurance goals and strategy in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Effectively manage the site Quality Assurance activities and resources necessary to smoothly run the QA operation at site. Provide strong leadership and expertise to ensure achievement of all Quality Assurance accountabilities at site. Identify and implement solution for improving existing site quality assurance systems and processes. Coach and develop both direct and, as appropriate, indirect reports through ongoing, example-based performance feedback, annual performance reviews and the provision of training and development opportunities. Ensure that performance issues are managed in a consistent and timely manner. Develop site quality assurance revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams. Responsible for executing Quality Management Reviews at site, monitor individual Performance and set improvement areas. Responsible for ensuring market complaints, failures, deviations are investigated and corrective and preventive actions are implemented as per set timeline. Responsible for ensuring compliance to regulatory requirements on product, process and release procedures. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and leveraging synergies. Review & tracking of quality assurance metrics e.g. deviation, change control, OOS/OOT, CAPA effectiveness, market complaints with site manufacturing / QC Management and driving them down. Ensure processes for supply chain management / Global Material Sourcing for vendor selection is followed for vendor selection, qualification and monitor vendor quality performance Provide inputs to manufacturing, R&D and PDL work processes to ensure Quality by Design. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and QA systems at the site. Facilitate internal and regulatory agency audits, ensuring that findings from site audits are understood, assessed and addressed site wide in a comprehensive manner. Monitor industry trends/issues faced internally and identify scope for improving Site quality assurance management and processes. Responsible for fulfilling all training requirements of quality assurance employees. Ensure the quality policies, standards and procedures for computerized systems are implemented and adhered at site. Ensure all GxP computerized systems are validated in compliance with the quality policies, standards and procedures and are maintained in validated state throughout the lifecycle with adequate security and controls to ensure data security. Review and approve the documents as per quality procedures. Work in partnership with the site cross functions and corporate functions for implementation of new initiatives. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS B.Pharm / M.Pharm 17 to 18 Yrs ( with QA experience in - OSD)

Job Description Mission Identify non-quality factors continuously, conduct or have other departments conduct in-depth analyses and monitor quality improvement plans. Identify potential issues before they occur and implement preventive solutions. Solve quality manufacturing issues affecting customers quickly and effectively through containment, correction and prevention steps. Plan and take any necessary actions to provide adequate confidence/evidence that a product or service will satisfy given contractual/explicit customer requirements. Make audits and analyze results as specified by quality systems and methods Responsibilties Takes any necessary actions to make sure that a product or service will satisfy customer requirements and is the driving force in implementing continuous quality improvement, with a coordination role (hierarchical or functional) of quality manufacturing/logistics assurance engineers and sometimes quality control teams. Main Activiites In charge of the Quality of one or several production sectors Ensure that the Process Control Plan is applied Lead continuous improvement on its production lines Lead root cause analysis of quality issue and Problem solving Be a member of the Short Interval Management of the production lines Create and maintain quality control documentation Lead Process Audits and Process Failure Mode & Effect Analysis (FMEA) Provide inputs and challenge about quality for new product or product evolution (PMP and PEP) and regularly assess the Process execution of PEP, including the right usage of the tools (Symphony, Tempo, NextGen PDM, ) Manage derogations Be the local expert of the assembled products in his sector Management (hierarchical or functional) of the QCT/QCS, and QAT4 Manage his team according to SPS / SIM rules and cycle event of the plan Key competencies C009:Communicate Effectively FQ08:Continuous Improvement L05:Focus on Customer L06:Foster collaboration and networking C005:Issue Resolution FQ05:Quality Authority FQ12:Quality Manufacturing /Logistics C011:Business Acumen C014:Digital Acumen L03:Influence and Convince FQ02:Customer Experience Performance FQ03:Customer Quality Analytics Working knowledge of Microsoft Office Suite Quality improvement tools, techniques & models Statistical quality techniques and analysis Qualifications Profile Experience Graduate degree (Mechanical /Electronics Engineering) +8 Years of experience in similar role (Manufacturing quality) - Professional in Manufacturing quality assurance (trained in SPC,PPAP, MSA, FMEA, APQP, CSQ, Preferably Six Sigma Green Belt) - Good knowledge of the manufacturing processes - Machining, Molding, Plating, stamping, Electronics part - PCBA/Active/Passive components Quality Assurance, - Fully fluent in English communication Schedule: Full-time Req: 008Y5Z

About Us SEEPEX, part of Ingersoll Rand, a World Leader in progressive cavity pump (PCP) manufacturing (HQ based in Germany). SEEPEX core expertise lies in PCP solutions, the perfect choice for handling tough, viscous, abrasive, and high-consistency mediums. Equipped with state-of-the-art machinery and testing facilities, our integrated plant ensures precision manufacturing and rigorous quality control for every pump produced. Job Summary: This position will be responsible for product selection, quotes, tendering and order acquisition activities by closely working with mainly O&G customers, International Sales Team, operations and other stakeholders in fulfilling booking targets. Responsibilities: Study & technically Interpret enquiries received from existing and prospective new customers and establish an initial understanding of the customers requirements. Build further understanding of requirements by liaising with customers. In line with product decision, determine the key objectives and possible options to be covered in the proposal, coordinating the supply of necessary information, organizing the various estimates, and defining the scope of supply. Reviewing the P&ID and project specifications and arrive at the Bill of materials of every component in the dosing skids, going through Piping material specification, valve material specification, instrument specifications, inspection and quality requirements to arrive the complete technical requirements of the customer. Work in partnership with Engineering, Commercial, Project Managers and Parent Company Technical team, as appropriate, to need to evaluate technical risk and commercial terms. Prepare RFQ s for suppliers/subcontractors against specs and T&C s Compile comprehensive tender specifications defining prices, commercial conditions, comments and deviations and technical specifications for presentation to the customer. Support Sales Manager/Sector Managers /Sales Engineers during the bid-process. Act as a focal point for customer queries regarding Proposal submission and TQs, to reach agreement and build a positive on-going relationship. Monitor progress and status of Proposals, maintaining accurate records and keeping the Proposals Manager fully always informed. Support Project team during handover of Proposals that have resulted in orders. Maintain internal Quality systems as relevant to the processing of enquiries and proposals. Ensure that Health, Safety, Environmental and Quality management policies and procedures are adhered to in all work undertaken Basic Qualification: Bachelor s or master s degree in engineering or related technical field required Minimum 8-10 years experience in proposals and estimation, preferably from industrial pump products Being familiar with API Standards (API610, 676, ) Having been in contact with Middle East End-users or/and EPCs in the O&G Industry P&ID understanding. Instrument knowledge (Transmitters, Gauges, Switches, JB etc.) Completed at least 2 to 3 O&G Projects Cycles. Travel & Work Arrangements/Requirements: This position will be based on one of SEEPEX Sister Companies sites in India: Hydro Prokav in Coimbatore Key competencies: Excellent analytical and problem-solving skills Drives results and takes initiatives to achieve goals Negotiation skills - with Vendor & internal stake holders Good relationship builder with ability to merge different groups of people, processes and tools Excellent verbal and written communication skills. What we Offer: We are all owners of the company! Stock options (Employee Ownership Program) that align your interests with the companys success. Yearly performance-based bonus, rewarding your hard work and dedication. Leave Encashments Maternity/Paternity Leaves Employee Health covered under Medical, Group Term Life & Accident Insurance Employee Assistance Program Employee development with LinkedIn Learning Employee recognition via Awardco Collaborative, multicultural work environment with a team of dedicated professionals, fostering innovation and teamwork . Special Accommodation If you are a person with a disability and need assistance applying for a job, please submit a request . Lean on us to help you make life better We think and act like owners. We are committed to making our customers successful. We are bold in our aspirations while moving forward with humility and integrity. We foster inspired teams. Colorado Resident? Bicycle rights prism poutine austin. Drinking vinegar gluten-free iceland, typewriter farm-to-table selfies XOXO food truck four loko. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request and a member of our team will contact you.

01 Managing the entire QA activities in the plant & Overall implementation of Quality Systems in all units. 02 Design, Develop and approve all Quality systems in all units. Monitoring, Documentation, and implementation of process development. 03 Responsible to handle regulatory audits USFDA ISO 9001-14001, EU,WHO, and their compliance in all units without any Major Non Compliance. Making sure that there is stability data to support retest or expiry dates and storage conditions on APIs and/or intermediates where appropriate; and Performing product quality reviews 04 Handling of statutory audits like Quality, EHS, KSPCB, -CDSCO, weight & scale inspector, Director of Factories & Boilers, Social audits etc and their compliance (Evaluated by No show cause notice and no complaints) 05 Making sure that critical deviations are investigated and resolved; 06 Approving all specifications and master production instructions, Test methods, Qualifications 07 Approving all procedures impacting the quality of intermediates or APIs 08 Making sure that quality related complaints are investigated and resolved 09 Adhering to QA budget. 10 To qualify company for various certifications. 11 Assuring QMS in all Units. Experience 15 - 20 Years Salary Not Disclosed Industry Pharma / R&D / Biotech Qualification B.Pharma, M.Sc Key Skills Quality Assurance Supervisor USFDA Compliance and Audits Pharmaceutical Quality Assurance

4-8 years experience in food processing companies. 3-4 years in food quality Food Quality compliances, Audits, certifications, regulatory matters, Overall quality measures in the company

Hello Visionary! We empower our people to stay resilient and relevant in a constantly changing world. Were looking for people who are always searching for creative ways to grow and learn. People who want to make a real impact, now and in the future. Does that sound like youThen it seems like youd make an outstanding addition to our vibrant team. Siemens Mobility is an independent run company of Siemens AG. Its core business includes rail vehicles, rail automation and electrification solutions, turnkey systems, intelligent road traffic technology and related services. In Mobility, we help our customers meet the need for hard-working mobility solutions. Were making the lives of people who travel easier and more enjoyable while constantly developing new, intelligent mobility solutions! We are looking forSupplier Quality Engineer Youll make a difference by Your tasks include the independent assurance of the delivery quality of our purchased parts over the product life cycle. You are responsible for the identification and sustainable elimination of supplier caused quality problems (e.g., through root cause analyses) as well as for the implementation of pre-assessments and supplier audit according to VDA 6.3 and Siemens IRIS-based specifications. You are responsible for carrying out fault tree and value stream analyzes at the supplier, including deriving measures and monitoring implementation. You are responsible for supporting initial sample testing with the aim of releasing the product and the manufacturing and testing process. They are also responsible for the planning, preparation and implementation of the Product on Trial Run and a preventive inspection. You are responsible for the creation and implementation of a risk and supplier protection concept based on risk-based supplier selection. You work with the successful realization of the product and process development within the scope of the ramp-up safeguards at our suppliers and use experience. Such as APQP In your area of responsibility, you ensure the implementation of railway industry standards (DIN EN50155, DIN EN50657, ISO_IEC_27000, TSI2014-1300-EU. etc.) You accompany risk assessments of suppliers from a quality perspective. You calculate support expenses for suppliers to implement sourcing decision in the Cross. -functional sourcing team and work in strategy and project teams. Desired Skills: You should have experience in 5-8 years along with master's degree in engineering or. Alternatively. have undergone technical training with further training to become a state-certified technician specializing in mechanical engineering or electrical engineering and have many years of professional experience. You impress with many years of professional experience in a technology related function ((e.g., quality assurance / quality-related supplier management (supplier/product/process qualification (MQCP)). ideally in the environment of rail vehicles. You are familiar with procurement and technical planning processes. quality management project management. IT tools and methods (SAP, MS Office Suite, etc.). lessons learned methods, LEAN. 5S. Furthermore. You have experience with the requirements of quality systems (ISO 9001. IRIS and similar) and in the application of quality methods and analysis tools. such as APQP in the manufacturing or product development process.8D, FMEA. Root -Cause Analysis. You are a certified IRIS and/or VOA 6.3 Lead Auditor. You are fluent in spoken and written English. You have a confident appearance towards the supplier and the internal organization and work independently. analytically and in a structured manner. Frequent travel activities (approx. 50-70%) at home and abroad are not an obstacle for you. You are generally willing to do so. Join us and be yourself! Make your mark in our exciting world at Siemens. This role is based in Bangalore. You might be required to visit other locations within India and outside. In return, you'll get the chance to work with teams impacting - and the shape of things to come. Find out more about mobility athttps://new.siemens.com/global/en/products/mobility.html and about Siemens careers at

In this role you will perform documented inspections in the verification of conformance of parts to applicable drawings, procedures, specifications and all applicable statutory and regulatory requirements. The QC Inspector is responsible for the content of the Inspection Test Plan (ITP) and project quality plan according to customer s and Flowserve s specifications and international standards. Besides, the QC Inspector is responsible for defining, advising and controlling all project required QC documents. The QC Inspector reports directly to the QC Supervisor/Manager. Responsibilities Requirements: Documenting dimensional and visual inspections to the drawing or applicable procedures Documenting non-conforming material utilizing an NCR (nonconforming materials) process Reviewing and verify internal and external qualifications of suppliers, welders, NDE personnel with regard to Non-Destructive Examinations (NDE), welding procedures and/or other applicable requirements. Reviewing and approve supplier s manufacturing and testing documents/procedures and to take care for approval (when required) of these documents by the customer, his customer and the authorized inspection body Preparing and define test and inspection requirements for the required projects such as ITP and procurement specifications. HS Diploma / GED and / or 0-2 years relevant experience And any other duties assigned Preferred Experience / Skills: Knowledge of welding, NDE and quality systems Knowledge of the established quality standards, laws and regulations of national and international authorities Must have knowledge of inspection equipment generally found in machining, assembly and test operations Effective utilization of CMMs is a plus Flexible, eager to learn, accurate, analytical with positive, can-do attitude Flexibility and willingness to travel Good interpersonal, communication, negotiation, analytical and presentation skills Problem solving skills Operational Excellence High Level of Customer Service Standard

Job Purpose Performs administrative and technical duties in the Quality domain, such as complex report running, providing necessary support to Quality employees Follows internal procedures and Quality System (QS) and other governmental and customer requirements and specifications Collects and analyses data related to Quality, and identifies possible inconsistencies Participates in the calibration of equipment in laboratories Manages all documentation related to Quality Receives, classifies, reconciles, interprets, consolidates, and/or summarizes documents and information related to quality Maintains records and balance information for control purposes Compiles reports, drawing data from a variety of sources within the quality department Regularly contacts Quality employees outside the immediate work area to exchange information Assists with internal quality audits You are meant for this job if: Certificate or equivalent / technical background 3 to 5 years of experience Knowledge of Information Systems Skills

Project Name SAP PO/ CPI Application Development Service Experience Senior Service Type Development Mandatory Skills: Application Development activities in SAP PO/CPI. Optional Skills: Good Communication both written and oral in English Functional understating of the business applications Roles & Responsibilities A flexible team of highly experienced SAP PO/ CPI developers that will develop Integrations using SAP PO/CPI developers in accordance with the Novo Nordisk quality systems procedures and the Novo Nordisk SAP PO/ CPI implementation standards. The Integrations will be developed for different projects in different Business areas of Novo Nordisk. After the integrations has gone live the team must also be available to perform maintenance, enhancements, and changes for integrations/ i-flows developed. Key Deliverables SAP PO/ CPI Integrations with the Novo Nordisk quality systems defined documentation and according to Novo Nordisk SAP PO/ CPI standards and methods. During operation of the Application, it is required to be able to perform changes and maintenance of the application according to the Novo Nordisk Standards. Service Responsibility It is the vendors responsibility to provide skilled and experienced resources and ensure that Integrations are build according to the individual project requirements which is to be agreed in advance of commencing integrations together with the projects

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s mostinnovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as theyprovide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days arethe same. Key Responsibilities Be a part of core project team and support the quality engineering across the entire development cycle Participate in product risk management, usability, reliability and design validation efforts for new product development and design change projects. Contribute to the development and implementation of design verification and validation plans with project design lead. Participate and implement tools like Design of Experiments (DOE’s), FMEA sessions, Risk Management and ensure compliance. Manage electronic document control and version control on all project related documents. Having experience on adherence to the quality systems and design assurance SOPs of clients. Exposure with usability, reliability, testing, verification and validation testing – internal and local vendors. statistical skills and technical writing skills Provide quality and compliance guidance as needed to product development or design change project teams to assure country specific compliance . Ensure appropriate Project/Sustaining Quality Deliverables are created and properly executed (e.g. Project Design & Development Plan, Risk Management Plan, Hazard Analysis, Use and Design FMEA, Field Assessment Plan,). Co-Lead CAPA efforts, and apply sound, systematic problem-solving methodologies identifying, prioritizing, communicating and driving resolution of quality issues (e.g., 5 why’s analysis, Is-Is Not analysis, and preferably Six Sigma problem solving methodologies). Devise and support the implementation of effective quality assurance, process controls, , and metrics that assure products meet or exceed quality. Primary Skills Bachelors (or higher) degree in engineering with preference of engineering background. Professional training certification in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation is preferred. Sound understanding of medical device regulatory requirements for Class II and III medical devices. Preference for candidates with CQE certification or similar training and experience Proficient in project management tools like MS project. Experience in GD&T having experience on statistical tool like, MINITAB. Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end-to-end services and solutions leveraging strengths from strategy and design to engineering, all fuelled by its market leading capabilities in AI, cloud and data, combined with its deep industry expertise and partner ecosystem. The Group reported 2023 global revenues of "22.5 billion.

Planit are world leaders in application testing and quality engineering. We provide solutions that support organizations to deliver high quality systems, applications, and IT architecture. Planit is now a proud NRI company and part of a global movement to deliver a sustainable and secure future through better Information Technology exchanges. Our team offer expert consultancy, bespoke services, tailored training and unique solutions to complex projects. Specializing in digital quality, Planit have a geographic footprint across many continents, with 1700+ permanent employees and have been recognized in Gartners Magic Quadrant for Application Testing Services. Our values and ethos are focused on an intrinsic connection to our people, the awareness of our environment and our pursuit to be better than yesterday. We continue to lead the industry with unrivalled ideas, ability, and a quest to discern paradigms. About the Role: As an Engineer, you will consult to our top tier client base, covering all areas of the testing lifecycle in multiple domains. Knowledge and expertise on all software delivery methodologies and test processes, you will use your testing capability to deliver large scale projects on schedule and to the highest quality. Responsibilities: Willingness to share relevant technical, process and/or industry knowledge and expertise to other resources Resourceful and proactive in gathering information and sharing ideas Experience of working in an Agile environment is a plus Strong written and verbal communication skills are a must. Prior presentation and Client interaction skills is a must. Skills & Experience: Require an automation tester with a minimum of 4-7 years of hands-on experience. The ideal candidate should have automation skills like Tosca, TCD. Excellent verbal and written communication skills to coordinate efficiently with clients, products, offshore & onshore teams and bridge the communication gaps. Culture and Benefits: For the right person we will provide:- A competitive remuneration package with career pathways within the team as we continue to expand globally An open, flexible hybrid working environment where you can immediately see the impact of your work and delivery towards the business success All of the tools, software and support you need (weve just undergone a migration of our ATS platform with bleeding edge tool /process to enable success) Benefits including health insurance, Free LinkedIn Learning licences,Training platforms & internet reimbursement among others

Ensure appropriate testing documents and artefacts are documented and maintained Have excellent communication skills (written and oral), attention to detail and gravitas to communicate with senior stakeholders Impact assess and keep track of requirements (original/new/changes) on projects ensuring there is appropriately prioritized test coverage A professional and confident style, with drive & enthusiasm and with a strong ability to multi-task. Applies strong knowledge of QA principles, methodologies, and techniques to test and ensure the quality of the software. Detects problems where standard practice and / or software has failed to meet customer requirements. Addresses escalated technical defects identified by less experienced team members. Provides support in areas such as feasibility studies and design review.

Ensure appropriate testing documents and artefacts are documented and maintained Have excellent communication skills (written and oral), attention to detail and gravitas to communicate with senior stakeholders Impact assess and keep track of requirements (original/new/changes) on projects ensuring there is appropriately prioritized test coverage A professional and confident style, with drive & enthusiasm and with a strong ability to multi-task. Applies strong knowledge of QA principles, methodologies, and techniques to test and ensure the quality of the software. Detects problems where standard practice and / or software has failed to meet customer requirements. Addresses escalated technical defects identified by less experienced team members. Provides support in areas such as feasibility studies and design review.

Responsibilities: As Senior Automation Test Engineer, you will consult to our top tier client base, covering all areas of the testing lifecycle in multiple industries. Using your expertise in all levels of test methodologies and processes, you will work in a team responsible for the analysis and planning of large-scale projects and providing estimates for test resources. Skills & Experience: Required skills include Selenium with Java Overall experience: 4 - 8 Years Require a proactive, committed quick-thinking automation engineer having hands-on experience in Selenium. Strong technical experience in the programming language Java or C# or JavaScript Experienced in developing automation frameworks such as BDD, Data-Driven, Hybrid frameworks Excellent analytical and debugging skills Experience of working in an Agile environment is a plus Strong written and verbal communication skills, good presentation skills are a must. Experience in CI/CD tools: Jenkins/Azure Devops is a plus. Culture and Benefits: For the right person we will provide: - A competitive remuneration package with career pathways within the team as we continue to expand globally An open, flexible hybrid working environment where you can immediately see the impact of your work and delivery towards the business success All of the tools, software and support you need (weve just undergone a migration of our ATS platform with bleeding edge tool /process to enable success) Benefits including health insurance, Free LinkedIn Learning licenses, Training platforms & internet reimbursement among others

Responsibilities: As Senior Automation Test Engineer, you will consult to our top tier client base, covering all areas of the testing lifecycle in multiple industries. Using your expertise in all levels of test methodologies and processes, you will work in a team responsible for the analysis and planning of large-scale projects and providing estimates for test resources. Skills & Experience: Required skills include Selenium with Java Overall experience: 4 - 8 Years Require a proactive, committed quick-thinking automation engineer having hands-on experience in Selenium. Strong technical experience in the programming language Java or C# or JavaScript Experienced in developing automation frameworks such as BDD, Data-Driven, Hybrid frameworks Excellent analytical and debugging skills Experience of working in an Agile environment is a plus Strong written and verbal communication skills, good presentation skills are a must. Experience in CI/CD tools: Jenkins/Azure Devops is a plus. Culture and Benefits: For the right person we will provide: - A competitive remuneration package with career pathways within the team as we continue to expand globally An open, flexible hybrid working environment where you can immediately see the impact of your work and delivery towards the business success All of the tools, software and support you need (weve just undergone a migration of our ATS platform with bleeding edge tool /process to enable success) Benefits including health insurance, Free LinkedIn Learning licenses, Training platforms & internet reimbursement among others

Job Responsibilities Planning and management of 45-50 workmen and 5-6 supervisors in weld body shop Process Improvement by analyzing the issues and countermeasures to enhance Safety/Quality/Productivity Administrative control of team, Manpower Management, Manpower Training, Skill Upgradation Production Quality Target Achievement Loss Recovery Hands on Experience on Line, Part loading Sequence, Line Data management Efficiency analysis and continuous Improvement(KAIZEN) Training of new supervisors and workmen Defect analysis and countermeasures Safety Production Quality cost(KPI) Target Achievement Efficiency analysis and continuous Improvement(KAIZEN) Emergency and loss recovery planning capability Direct and indirect consumables consumption optimization Functional/Technical In-depth knowledge of welding jigs/Safety Checks/Quality checks In-depth Knowledge of spot welding process/parameter control In-depth Knowledge of Robot teaching/programming of Fanuc and Kawasaki robots, Hands on Experience on Spot Reteaching, Sealer application teaching Detailed Knowledge of prevailing and latest quality systems to maintain weld body quality Knowledge of body accuracy analysis and body fit and finish Detailed Door line and white body line Knowledge - Hemming Sealer application and hemming process in doors Safety Production Quality cost(KPI) Target Achievement Hands on Experience on Line, Part loading Sequence, Line Data management Efficiency analysis and continuous Improvement(KAIZEN) Team building know and customer orientated attitude Emergency and loss recovery planning capability Behavioral Target orientation Customer orientation Good analytical skills Excellent Communication presentation skills Flexibility Team player Networking skills

Responsibilities: As Senior Automation Test Engineer, you will consult to our top tier client base, covering all areas of the testing lifecycle in multiple industries. Using your expertise in all levels of test methodologies and processes, you will work in a team responsible for the analysis and planning of large-scale projects and providing estimates for test resources. Skills & Experience: Required skills include Selenium with Java Overall experience: 4 - 8 Years Require a proactive, committed quick-thinking automation engineer having hands-on experience in Selenium. Strong technical experience in the programming language Java or C# or JavaScript Experienced in developing automation frameworks such as BDD, Data-Driven, Hybrid frameworks Excellent analytical and debugging skills Experience of working in an Agile environment is a plus Strong written and verbal communication skills, good presentation skills are a must. Experience in CI/CD tools: Jenkins/Azure Devops is a plus. Culture and Benefits: For the right person we will provide: - A competitive remuneration package with career pathways within the team as we continue to expand globally An open, flexible hybrid working environment where you can immediately see the impact of your work and delivery towards the business success All of the tools, software and support you need (weve just undergone a migration of our ATS platform with bleeding edge tool /process to enable success) Benefits including health insurance, Free LinkedIn Learning licenses, Training platforms & internet reimbursement among others

The role demands here that the candidate should have working experience into Excel, MS Office, Big Data and preferably from Health Insurance Domain. Along with this, stakeholder management, client interaction, and leadership qualities are an added advantage. Responsibilities : They need to have minimum 1 year experience in general insurance domain in either Motor or Health or Commercial Line of business Tester should have good understanding of Insurance business and should be able to define market scenarios using your library they will be responsible for end-to-end testing (including API s) They will be responsible of Test Scenario/Case creation, getting sign off from Stake holders on the same and UAT sign off from users, They need to publish daily status of Testing of all the projects and escalate wherever they anticipate slippage. Skills& Experience: 1 - 3 years of experience in Manual Testing and in General Insurance Domain (Health/Motor/Commercial line of Business). Culture and Benefits: For the right person we will provide:- A competitive remuneration package with career pathways within our talent team as we continue to expand globally An open, flexible hybrid working environment where you can immediately see the impact of your work and delivery towards the business success All of the tools, software and support you need (we ve just undergone a migration of our ATS platform with bleeding edge tool /process to enable success) Benefits including health insurance, Free LinkedIn Learning licences, Training platforms & internet reimbursement among others.

B.E. /B TECH (Mechanical Engg / Automobile / Production / Industrial) 4-5 yrs Experience in automobile Parts Procurement / Development / Logistics / Project Management Sourcing and Development of automobile parts Techno commercial assessment of supplier proposals Ordering & Scheduling of parts/RM/Consumables Management of Packaging and logistics for Raw material & Parts. Budget Planning and payment to suppliers Ensuring quality management of procured part etc. Competencies : Sound understanding of automobile part sourcing and development Basic knowledge of various manufacturing processes of Automobile industry Sound understanding of import and export logistics Supplier handling & negotiation skills Good communication skill, interaction with internal customer and suppliers Project management, execution, and monitoring skill Quality management system (ISO/TS) knowledge Budget Planning Inventory Management