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Quality Assurance Engineer II, HST Health FoundationWe are seeking an experienced Quality Assurance Engineer II to lead testing initiatives for complex healthcare systems and mentor junior team members. You will own end-to-end quality processes for critical healthcare applications, drive automation strategies, and collaborate with cross-functional teams to deliver world-class healthcare products that impact millions of customers globally. About Amazon Health Amazon Health is transforming healthcare delivery through innovative technology solutions that make healthcare more accessible, affordable, and convenient for customers worldwide. We leverage Amazon's proven expertise in technology, logistics, and customer service to revolutionize how people access and experience healthcare services. Key job responsibilities * Own comprehensive testing strategy and execution for multiple healthcare applications and services * Lead test planning, design, and execution for complex, multi-platform healthcare systems * Develop and maintain automated test suites using modern testing frameworks * Mentor junior QAE team members and provide technical guidance * Collaborate with product managers, architects, and development teams on quality requirements * Drive quality engineering best practices and process improvements across the team * Lead API testing initiatives including REST/GraphQL services and microservices architectures * Ensure compliance with healthcare regulations (HIPAA, FDA, GDPR) and security standards * Design and execute performance, load, and scalability testing strategies * Participate in architecture and design reviews with quality engineering perspective * Lead incident response and root cause analysis for quality-related issues * Drive continuous integration and deployment quality gates * Establish quality metrics and reporting dashboards About the team Join Amazon Health's centralized Quality Engineering team in Bangalore as a senior contributor responsible for driving quality excellence across our healthcare product portfolio. Our team ensures that healthcare applications and services meet the highest standards of quality, security, and compliance while delivering exceptional customer experiences at scale.<h4>Basic Qualifications</h4> - 4+ years of quality assurance engineering experience - Experience in automation testing - Experience in manual testing - Experience as QA lead on medium to large sized projects - Advanced knowledge of industry technologies and expert proficiency with STLC and testing methodologies - Ability to create, optimize, and execute comprehensive test strategies for complex scenarios involving multiple engineering teams - Expert proficiency in multiple programming languages (Java, Python, JavaScript, C#, or Go) - Designs and implements test solutions that are reusable, reliable, scalable, and efficient - Extensive experience with advanced test automation frameworks (Selenium Grid, Cypress, TestNG, JUnit, Pytest) - Deep expertise in API testing tools and methodologies (REST, SOAP, GraphQL, gRPC) - Advanced database testing skills with complex SQL queries and data validation strategies - Proven ability to lead test plan reviews, code reviews, design discussions, team planning, and metrics analysis - Strong experience with CI/CD pipelines, DevOps practices, and infrastructure as code - Expertise with performance testing tools and methodologies (JMeter, Gatling, LoadRunner) - Extensive experience with cloud platforms and distributed systems testing (AWS preferred) - Demonstrated ability to mentor and guide junior QAEs on products, testing approaches, and solution architecture - Strong technical leadership and team development capabilities - Excellent problem-solving, analytical, and system design skills - Outstanding communication and cross-functional collaboration abilities - Experience working effectively across global teams and multiple time zones <h4>Preferred Qualifications</h4>- Experience with at least one automated test framework like Selenium or Appium - Experience in gathering test requirements to create detailed test plans and defining quality metrics to measure product quality - Experience in healthcare, pharmaceutical, or highly regulated industry testing - Knowledge of healthcare standards and regulations (HIPAA, HL7, FHIR, FDA guidelines) - Experience with microservices and containerized application testing - Advanced automation skills with frameworks like Selenium Grid, Docker, Kubernetes - Experience with security testing and vulnerability assessment - Knowledge of mobile application testing (iOS/Android) including device farms and mobile automation frameworks (Appium, Espresso, XCUITest) - Mobile testing and automation experience across different devices, operating systems, and form factors - Experience with AWS services and cloud-native testing approaches - Familiarity with machine learning model testing and data quality validation - Experience with chaos engineering and resilience testing - Knowledge of accessibility testing standards (WCAG, Section 508) - Experience with test data management and synthetic data generation - Certification in quality assurance or testing (ISTQB, CSTE, or similar) Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit <a href="https://amazon.jobs/content/en/how-we-hire/accommodations">https://amazon.jobs/content/en/how-we-hire/accommodations</a> for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.<h4>Experience Level</h4>Senior Level

 Amazon India Limited 

Quality Assurance Engineer

Executive - QA<h4>The Opportunity:</h4>Job Location: Bhiwandi, ThaneThe QA Specialist in IND plays a crucial role in overseeing the quality assurance processes across the company’s three manufacturing sites (Mumbai, Panoli, and Dehradun). The core responsibility of this position is managing and resolving non- product quality issues, ensuring adherence to quality control procedures, and maintaining product excellence by collaborating with various teams, the specialist acts as the primary contact for resolving non-conformance issues and minimizing the recurrence of quality problems. QA Specialist is a vital role that ensures high standards of product quality, operational excellence, and regulatory compliance across the company’s manufacturing operations. What we’re looking for:<ul><li>Education: B.Sc/M.Sc (Chemistry, Biology, Microbiology)</li><li>Experience: Minimum 5-8 years of experience</li></ul>How you will thrive and create an impact: 1. Non-Product Quality Issue Management:<ul><li>Identify, document, and resolve non-product related quality issues across the Mumbai, Panoli, and Dehradun manufacturing sites.</li><li>Ensure compliance with established quality control procedures, work instructions, and GMP standards.</li><li>Monitor and address non-conformance issues to prevent recurrence, coordinating with relevant teams and departments.</li></ul>2. Site Coordination &amp; Communication:<ul><li>Serve as a liaison between the three manufacturing sites, ensuring smooth communication and effective resolution of non-product quality issues.</li><li>Collaborate with site managers, production teams, and quality specialists to ensure consistent quality control practices across all sites.</li></ul>3. Compliance with Regulatory Requirements:<ul><li>Ensure actions taken to address non-product quality issues comply with internal policies and external regulatory requirements (e.g., GMP, ISO).</li><li>Perform audits, review documentation (e.g., COA/COC), and ensure adherence to quality standards at all times.</li></ul>4. Root Cause Analysis and Corrective Actions:<ul><li>Utilize problem-solving tools like 5M+E and 5 Why’s to identify root causes of non-product quality issues.</li><li>Implement corrective actions across all three sites to ensure issues are effectively addressed and do not recur.</li></ul>5. Continuous Improvement:<ul><li>Drive continuous improvement initiatives to optimize processes and reduce non-conformance issues.</li><li>Collaborate with site-specific and regional teams to improve overall product quality and operational efficiency.</li></ul>6. Documentation and Reporting:<ul><li>Oversee the documentation of non-product quality issues and track trends to ensure timely resolution.</li><li>Prepare and maintain accurate and timely reports on quality control activities and issues identified across all sites.</li></ul>7. Customer Complaint Investigations:<ul><li>Lead and manage all investigations related to customer complaints, ensuring thorough root cause analysis and timely resolution to improve customer satisfaction.</li></ul>8. Audit Oversight:<ul><li>Oversee internal and external audits to ensure compliance with ISO 9001:2015, Medical Devices, GDP, and other relevant standards.</li><li>Serve as the appointed Lead Auditor for relevant certifications, ensuring audits align with regulatory requirements.</li></ul>9. Quality Management Systems (QMS):<ul><li>Develop, implement, and maintain the QMS to ensure compliance with ISO regulatory standards.</li><li>Drive the continuous improvement of the QMS by incorporating best practices, process enhancements, and risk mitigation strategies.</li></ul>10. Document Management:<ul><li>Oversee the document control system to ensure all documentation is up-to-date, compliant, and easily accessible for review during audits.</li></ul>11. ETQ System Development and Training:<ul><li>Lead the development and training of the ETQ system across the DC IND to ensure teams are proficient in system usage for quality management and compliance.</li></ul>12. Quality Culture and Continuous Improvement:<ul><li>Foster a culture of continuous improvement at the IND manufacturing site, guiding cross-functional teams to optimize quality performance.</li><li>Spearhead quality improvement initiatives, encouraging a culture of excellence across all operations.</li></ul>13. Third-Party Logistics &amp; Warehouse Audits:<ul><li>Oversee audits of third-party logistics providers and extended warehouses, ensuring compliance with quality standards and regulatory requirements.</li></ul>14. Certification Management:<ul><li>Lead and maintain certification audits to ensure compliance with ISO and industry-specific standards.</li><li>Ensure the organization consistently meets regulatory demands.</li></ul>15. Essential Skills and Qualifications:<ul><li>Extensive experience in quality assurance within regulated industries (ISO 9001:2015, Medical Devices, GDP).</li><li>Strong knowledge of QMS, audit processes, and document control.</li><li>Proven ability to lead and manage cross-functional teams in driving continuous improvement and compliance.</li><li>Strong analytical skills, with experience in customer complaint investigations.</li><li>Certification in ISO lead auditing or similar credentials.</li><li>Excellent communication, leadership, and training skills.</li></ul>16. Support Label Replacement Requests:<ul><li>Work closely with the supply chain led to support label replacement requests.</li><li>Coordinate actions related to containment and corrective actions if needed to address any quality issues.</li></ul>Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.Why Avantor?Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.   The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.   We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!EEO Statement:We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.If you need a reasonable accommodation for any part of the employment process, please contact us by email at <a href="mailto:recruiting@avantorsciences.com" rel="noopener noreferrer" target="_blank">recruiting@avantorsciences.com</a> and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.3rd party non-solicitation policy:By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation<h4>Experience Level</h4>Executive Level

Avantor Performance Materials India Ltd

Quality Assurance Executive

Specialist, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleSpecialist, Quality Assurance EngineeringWhat does a successful Tech Lead, Quality Assurance Engineer do? A successful Tech Lead, Quality Assurance Engineer with .Net programming language at Fiserv plays a pivotal role in our mission to deliver reliable, high-quality financial services technology. They ensure that our products meet high standards of functionality, reliability, and performance, helping our clients provide dependable services to their customers. Working alongside a team of dedicated professionals, they contribute to the continuous improvement of our testing processes and drive the innovation needed to stay ahead in the fintech industry.What you will do:<ul><li>Develop and execute test plans and test cases to ensure the quality and performance of Fiserv products.</li><li>Design and implement automated testing frameworks and scripts.</li><li>Collaborate with software developers and product managers to identify test requirements, design test strategies, and troubleshoot issues.</li><li>Conduct thorough regression testing when bugs are resolved.</li><li>Monitor testing processes and ensure that software releases are timely and of high quality.</li><li>Document and report defects, and work with developers to resolve them.</li><li>Stay up-to-date with the latest industry trends and technologies to improve testing practices.</li></ul>What you will need to have:<ul><li>BE, BTech or MCA and/or equivalent military experience.</li><li>8+ years of experience in software testing and quality assurance.</li><li>6+ years of experience in automated testing tools such as Selenium, JUnit, or similar.</li><li>8+ years of experience with various testing methodologies and types of testing (functional, non-functional, regression, etc.).</li><li>6+ years of experience in .Net programming language and scripting languages like Python,or JavaScript.</li></ul>What would be great to have:<ul><li>7+ years of experience in performance and load testing using tools like Selenium.</li><li>6+ years of experience with continuous integration and continuous deployment (CI/CD) tools such as Jenkins or Travis CI.</li><li>6+ years of experience with API testing tools, e.g., Postman, SoapUI.</li><li>6+ years of experience with version control systems like Git.</li><li>ISTQB Certification in the relevant domain.</li></ul>Perks at Work:<ul><li>We’re #FiservProud of our commitment to your overall well-being with a growing offering of physical, mental, emotional, and financial benefits from day one.</li><li>Maintain a healthy work-life balance with paid holidays, generous time off policies, including Recharge &amp; Refuel time for qualifying associates, and free counseling through our EAP.</li><li>Plan for your future with competitive salaries, the Fiserv 401(k) Savings Plan, and our Employee Stock Purchase Plan.</li><li>Recognize and be recognized by colleagues with our Living Proof program where you can exchange points for a variety of rewards.</li><li>Prioritize your health with a variety of medical, dental, vision, life and disability insurance options and a range of well-being resources through our Fuel Your Life program.</li><li>Advance your career with training, development, certification, and internal mobility opportunities.</li><li>Join Employee Resource Groups that promote our diverse and inclusive culture where associates can share perspectives, exchange ideas, and elevate careers.</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.<h4>Experience Level</h4>Senior Level

Fiserv India Pvt Ltd

QA Engineer

Q.A OFFICER<h4>Job Purpose and Impact</h4>The Food Safety Quality Technician III will complete a variety of monitoring and verification tasks to ensure that the plant operates in compliance with food safety programs, policies and certifications. In this role, you will influence people who are not direct reports to achieve overall quality standards and meet governmental agency quality standards.<h4>Key Accountabilities</h4><ul type="disc"><li>Complete food safety, sanitation, operational, risk material and control room monitoring.</li><li>Review daily material processing procedures and verify all applicable monitoring documents, taking immediate corrective actions when deviations are identified.</li><li>Maintain quality records, imputing and assigning deviation reports as required.</li><li>Conduct daily inspections of the plant for each one of the critical control points and sanitation monitoring zones, ensuring all monitors are adhering to the written food safety programs.</li><li>Perform unbiased audits throughout the facility to ensure adherence to sanitation procedures for critical job tasks.</li><li>Communicate deviations to management and ensure they are documented, assigned correctly and completed in a timely manner and follow up on corrective actions and preventative measures to ensure they are effective.</li><li>Provide and administer food safety and quality certification training to plant employees including theoretical training related to quality programs.</li><li>Handle complex clerical, administrative, technical or customer support issues under minimal supervision, while escalating only the most complex issues to appropriate staff.</li><li>Other duties as assigned</li></ul><h4>Qualifications</h4><h4>Minimum Qualifications</h4><ul type="disc"><li>Degree in chemistry or bachelor’s in pharmacy level or equivalent</li><li>Experience with email, spreadsheet and word processing applications</li><li>Knowledge of food safety concepts, including hazard management and governmental agency requirements</li><li>Able to represent the company during third party audits and governmental agency verifications</li></ul><h4>Preferred Qualifications</h4><ul type="disc"><li>Bachelor's degree in a science related field</li><li>Minimum of two to three years of experience in a bulk drug manufacturing facility</li><li>Experience or knowledge of QMS, GMP, GDP, Data integrity and QRM Documentation. </li></ul><h4>Experience Level</h4>Senior Level

Cargill India

Quality Assurance Officer

Manager II, QualityJob Title:Manager II, QualityJob DescriptionConcentrix is a technology-enabled global business services company specializing in customer engagement and improving business performance. We partner with ambitious, progressive executives around the world to future-proof their business and stay ahead of the competition and customer expectations.Key Responsibilities<ul><li>Team Leadership &amp; Management: Lead, manage, and mentor a team of Quality Analysts and QA Leads, providing coaching and development to ensure consistent and strong quality performance.</li><li>Quality System Implementation: Develop, implement, and drive quality management systems (QMS) and processes to ensure compliance with client and industry standards.</li><li>Performance Analysis &amp; Improvement: Analyze quality and performance trends, aggregate audit findings, and provide actionable insights to identify and resolve quality issues and drive business KPIs.</li><li>Stakeholder Collaboration: Develop strong working relationships with business stakeholders, both internal and external, to collaborate on improvement action plans.</li><li>Metric Reporting: Track and maintain accurate metrics for direct reports and overall team performance, and present findings at MBRs and QBRs.</li><li>Problem-Solving: Utilize methodologies such as <a href="https://www.google.com/search?q=Six+Sigma&amp;sca_esv=26624f0eb411dd2e&amp;source=hp&amp;ei=6GOjaPO6HenWseMP5KepoQI&amp;iflsig=AOw8s4IAAAAAaKNx-PH1ML81bgCHjcza7dKFM1aQQ89H&amp;ved=2ahUKEwjI-Iio8pSPAxWm8qACHaYXO0oQgK4QegQIARAN&amp;uact=5&amp;oq=job+description+Manager+Quality+II+concentrix&amp;gs_lp=Egdnd3Mtd2l6Ii1qb2IgZGVzY3JpcHRpb24gTWFuYWdlciBRdWFsaXR5IElJIGNvbmNlbnRyaXgyBBAhGApIkGBQqQ5YoV5wAngAkAEAmAGIA6ABgUKqAQkwLjEzLjE3Lja4AQPIAQD4AQGYAiagAptDqAIKwgIKEAAYAxjqAhiPAcICCxAAGIAEGLEDGIMBwgIFEAAYgATCAg4QLhiABBixAxjRAxjHAcICBRAuGIAEwgINEAAYgAQYsQMYigUYCsICDhAAGIAEGLEDGIMBGIoFwgIIEAAYgAQYsQPCAggQLhiABBixA8ICCxAuGIAEGLEDGIMBwgILEAAYgAQYsQMYyQPCAgsQABiABBiSAxiKBcICDhAAGIAEGLEDGIMBGMkDwgIHEAAYgAQYCsICDRAAGIAEGLEDGEYY-QHCAgYQABgWGB7CAgsQABiABBiGAxiKBcICCBAAGKIEGIkFwgIFEAAY7wXCAggQABiABBiiBMICBBAhGBXCAgYQIRgVGAqYAxbxBc0dwPafx4uUkgcJMi4xMy4xNy42oAe6-AGyBwkwLjEzLjE3Lja4B_1CwgcLNC4xOS4xMy4xLjHIB30&amp;sclient=gws-wiz&amp;mstk=AUtExfAmhDidYoAlxyiV4dhtxabUxjtmtZ6rs1lxh9_XPjBphppp9Qq4fNtrc5r3LT0pD8ZmIgDhYMjKjlbJ1YOfIq8zb4bGYMg0WtT6oUN-v3lKxx9rTJo_93M8MMfXDvPYay0&amp;csui=3" rel="noopener noreferrer" target="_blank">Six Sigma</a>, <a href="https://www.google.com/search?q=COPC&amp;sca_esv=26624f0eb411dd2e&amp;source=hp&amp;ei=6GOjaPO6HenWseMP5KepoQI&amp;iflsig=AOw8s4IAAAAAaKNx-PH1ML81bgCHjcza7dKFM1aQQ89H&amp;ved=2ahUKEwjI-Iio8pSPAxWm8qACHaYXO0oQgK4QegQIARAO&amp;uact=5&amp;oq=job+description+Manager+Quality+II+concentrix&amp;gs_lp=Egdnd3Mtd2l6Ii1qb2IgZGVzY3JpcHRpb24gTWFuYWdlciBRdWFsaXR5IElJIGNvbmNlbnRyaXgyBBAhGApIkGBQqQ5YoV5wAngAkAEAmAGIA6ABgUKqAQkwLjEzLjE3Lja4AQPIAQD4AQGYAiagAptDqAIKwgIKEAAYAxjqAhiPAcICCxAAGIAEGLEDGIMBwgIFEAAYgATCAg4QLhiABBixAxjRAxjHAcICBRAuGIAEwgINEAAYgAQYsQMYigUYCsICDhAAGIAEGLEDGIMBGIoFwgIIEAAYgAQYsQPCAggQLhiABBixA8ICCxAuGIAEGLEDGIMBwgILEAAYgAQYsQMYyQPCAgsQABiABBiSAxiKBcICDhAAGIAEGLEDGIMBGMkDwgIHEAAYgAQYCsICDRAAGIAEGLEDGEYY-QHCAgYQABgWGB7CAgsQABiABBiGAxiKBcICCBAAGKIEGIkFwgIFEAAY7wXCAggQABiABBiiBMICBBAhGBXCAgYQIRgVGAqYAxbxBc0dwPafx4uUkgcJMi4xMy4xNy42oAe6-AGyBwkwLjEzLjE3Lja4B_1CwgcLNC4xOS4xMy4xLjHIB30&amp;sclient=gws-wiz&amp;mstk=AUtExfAmhDidYoAlxyiV4dhtxabUxjtmtZ6rs1lxh9_XPjBphppp9Qq4fNtrc5r3LT0pD8ZmIgDhYMjKjlbJ1YOfIq8zb4bGYMg0WtT6oUN-v3lKxx9rTJo_93M8MMfXDvPYay0&amp;csui=3" rel="noopener noreferrer" target="_blank">COPC</a>, or <a href="https://www.google.com/search?q=PDCA&amp;sca_esv=26624f0eb411dd2e&amp;source=hp&amp;ei=6GOjaPO6HenWseMP5KepoQI&amp;iflsig=AOw8s4IAAAAAaKNx-PH1ML81bgCHjcza7dKFM1aQQ89H&amp;ved=2ahUKEwjI-Iio8pSPAxWm8qACHaYXO0oQgK4QegQIARAP&amp;uact=5&amp;oq=job+description+Manager+Quality+II+concentrix&amp;gs_lp=Egdnd3Mtd2l6Ii1qb2IgZGVzY3JpcHRpb24gTWFuYWdlciBRdWFsaXR5IElJIGNvbmNlbnRyaXgyBBAhGApIkGBQqQ5YoV5wAngAkAEAmAGIA6ABgUKqAQkwLjEzLjE3Lja4AQPIAQD4AQGYAiagAptDqAIKwgIKEAAYAxjqAhiPAcICCxAAGIAEGLEDGIMBwgIFEAAYgATCAg4QLhiABBixAxjRAxjHAcICBRAuGIAEwgINEAAYgAQYsQMYigUYCsICDhAAGIAEGLEDGIMBGIoFwgIIEAAYgAQYsQPCAggQLhiABBixA8ICCxAuGIAEGLEDGIMBwgILEAAYgAQYsQMYyQPCAgsQABiABBiSAxiKBcICDhAAGIAEGLEDGIMBGMkDwgIHEAAYgAQYCsICDRAAGIAEGLEDGEYY-QHCAgYQABgWGB7CAgsQABiABBiGAxiKBcICCBAAGKIEGIkFwgIFEAAY7wXCAggQABiABBiiBMICBBAhGBXCAgYQIRgVGAqYAxbxBc0dwPafx4uUkgcJMi4xMy4xNy42oAe6-AGyBwkwLjEzLjE3Lja4B_1CwgcLNC4xOS4xMy4xLjHIB30&amp;sclient=gws-wiz&amp;mstk=AUtExfAmhDidYoAlxyiV4dhtxabUxjtmtZ6rs1lxh9_XPjBphppp9Qq4fNtrc5r3LT0pD8ZmIgDhYMjKjlbJ1YOfIq8zb4bGYMg0WtT6oUN-v3lKxx9rTJo_93M8MMfXDvPYay0&amp;csui=3" rel="noopener noreferrer" target="_blank">PDCA</a> to identify root causes and implement solutions for process and agent-level improvements. </li></ul>Key Skills &amp; Knowledge<ul><li>Analytical &amp; Problem-Solving Skills: Strong ability to analyze data, interpret trends, and use various tools and methodologies to solve problems effectively.</li><li>Communication Skills: Excellent verbal and written communication skills to present findings, coach team members, and collaborate with stakeholders.</li><li>Technical Proficiency: Ability to work with Microsoft Office Suite (Word, Excel, PPT) and interpret data for decision-making.</li><li>Quality Certifications: Desirable to have certifications like Six Sigma Green Belt. </li></ul>Educational Qualification – Graduation  Disclaimer:-'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities Location:IND Gurugram - SP Infocity, Industrial Plot No. 243, 1st, 3rd, 4th, 5th &amp; 7th FloorsLanguage Requirements:Time Type:Full timeIf you are a California resident, by submitting your information, you acknowledge that you have read and have access to the <a href="https://www.concentrix.com/resource/job-applicant-privacy-notice-for-california-residents/" rel="noopener noreferrer" target="_blank">Job Applicant Privacy Notice for California Residents</a><h4>Experience Level</h4>Mid Level

Concentrix

Quality Manager

Senior Manager- Commercial Quality- India & SAARC     <h4>JOB DESCRIPTION:</h4>PURPOSE This position will provide Commercial Quality Leadership to India and SAARC markets in Abbott ID Rapid Diagnostics business. RESPONSIBILITIES: • Accountable for being Management representative with Responsibility &amp; Authority forthe Quality and Regulatory requirements; ensuring compliance to Abbott Global Quality/Regulatory Framework, Divisional Policies/ Procedures. • Responsible for proactively creating Quality Culture w.r.t People, Process, Products &amp; Services to meet customer needs. • Maintain QMS in the market and continually evaluate and monitor the quality system for suitability and adequacy for the commercial business. • Must interface and represent commercial leader in areas of quality decisions, such as escalations, field actions and/or other significant quality issues. • Engage as required for the Quality Complaints for Abbott products, ensuring timely investigation, resolution, closure &amp; customer follow-ups through the Legal Manufacturers and Tech Support Team. Proactively reviewing product complaints and address the trends in a timely manner.Collaborate with other global entities in fulfilling Field Corrective actions (FCA) resulted from Regulatory Field Safety Notifications. • Provide relevant quality support for post market surveillance (PMS) activities, ensure timely executions to minimize, any product supply interruption. • Facilitating Audits (Corporate Quality Audits, Regulatory Audits, ISO-Notified Bodies) • Ensuring implementation of effective CAPA program across operational site. • Driving Supplier Qualification Program (Identification, Evaluation through Audits, Monitoring, Maintenance &amp; Re-Qualification). • Review/Approve Changes, Deviations, Investigations, Market Complaints &amp; CAPA. • Responsible for Budgetary Planning for Quality Operations. • Evaluate the existing Quality Management System implemented in the country with the Abbott QMS and Business Unit Quality Standards and Procedures and conduct gap analysis , develop a remediation plan and drive it to achieve highest level of compliance. • Responsible for the Quality Control program for imported products that are distributed in the market o Has final decision making responsibility for product release. o Has final decision making and reporting responsibilities for field corrective actions. o Collect information on product quality and when concerning information is obtained, provide timely written report to appropriate management so that necessary and appropriate measures be taken. • Responsible for administration of and compliance with all major quality system activities including but not limited to document control, record control, training, CAPA, quality incidents, risk management and internal audit. • Continuously drive for compliance with Abbott quality standards and regulatory requirements. • Responsible for management and satisfactory resolution of product issues in a timely manner. Coordinate cross-functionally to ensure implementation of containment, mitigation, remediation and corrective activities as necessary. • Coordinate with entity management and facilitate Quality Management Review activities, including quarterly quality objective reporting, escalation of issues with QMS impact and closure of open actions from previous meetings. • Responsible for coordination and management of site Quality metric tracking, trending and reporting activities. Assure metrics appropriately characterize the key performance indicators of the quality system. • This position will be the Commercial Quality representative for internal compliance and 3rd party audits / inspections. Coordinate and manage all commercial audits in conjunction with the Commercial office lead. • Implement new or modify existing processes to maintain compliance with local entity, business unit, division, corporate, voluntary standards and regulatory requirements. • Develop Commercial Quality team in the Cluster and the talent pool and ensure capabilities are in place to become self- sufficient in the necessary aspects of Quality. • Implement Talent Strategies to grow quality capabilities, provide development opportunities for key talent, and drive a global mindset within the cluster. • Other duties as assigned.BASIC QUALIFICATIONS | EDUCATION: • Bachelor Degree in Pharmacy/Science/Engineering. • Must have been employed in the Medical Device/Pharmaceutical /In-Vitro Diagnostics/Healthcare industry for a minimum of 7 years. • Minimum of 10 years of experience in Quality Assurance and /or Compliance in a regulated industry. • Minimum of 3 years supervisory / managerial experience • Ability to effectively communicate in English.COMPETENCIES: • Strong leadership influence. • Strong analytical, communication, decision-making and leadership skills for interaction with external and internal customers and partners. • Strong ability to negotiate with stakeholders. • Able to manage multiple priorities and pull information together from multiple business units to ensure concise consolidated business picture is communicated to the commercial businesses. • Superior attention to accuracy and details. • Strong leadership skills, including the ability to set goals and provide constructive feedback respectfully in order to build positive relationships and improve business results. • Capable of understanding and overcoming different cultural and language barriers to provide solutions that satisfy corporate, regional, and local objectives. • Strong English verbal and written communication skills with the ability to convey appropriate information with clarity and effectiveness. • Strong knowledge of relevant medical device industry regulations for quality systems and compliance. • Ability to work in a highly matrixed and geographically diverse business environment. • Ability to work effectively within a team in a fast-paced changing environment. Multitasks, prioritizes and meets deadlines in timely manner. • Experience in conducting and handling audits and inspections. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities.     The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.     <h4>JOB FAMILY:</h4>Operations Quality     <h4>DIVISION:</h4>ID Infectious Disease        <h4>LOCATION:</h4>India &gt; Mumbai : BKC Building     <h4>ADDITIONAL LOCATIONS:</h4>     <h4>WORK SHIFT:</h4>Standard     <h4>TRAVEL:</h4>Not specified     <h4>MEDICAL SURVEILLANCE:</h4>Not Applicable     <h4>SIGNIFICANT WORK ACTIVITIES:</h4>Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)               <h4>Experience Level</h4>Senior Level

Abbott India Ltd

Quality Head

Executive - Quality / FEDDate Posted:2025-09-29Country: IndiaLocation: MK Towers, #27, Longford Road, Shanti Nagar,Bangalore - 560 027, IndiaJob Title: Executive - Quality / FED Location: BangaloreQualification: Diploma / BE in Electrical and ElectronicsExp: 3 to 5 years in elevator Industry Job description:<ul><li>Be fully conversant and complaint with Otis EH&amp;S policies</li><li>Follow safety procedures as per OSS (Otis safety standards) based on training and certification processes</li><li>Ensure adherence to ethics guidelines</li><li>Portraying right skills to understand layout drawings, FIM and other product wiring diagrams and procedures about installation quality.</li><li>As a quality inspector he must do full checking entire installation quality of elevators and escalators, as per FIM within allocated timeline.</li><li>Minimum 150 to 200 units he must complete on yearly basis.</li><li>This includes high speed gearless units and escalators / travellators, managing other quality teams on multi-unit sites to ensure safe and efficient quality checks.</li><li>Undertaking client liaison during the testing of large multi-unit sites and attending site meetings if required.</li><li>Undertaking quality readings on completion of a project, providing a seamless handover from New Equipment to Service and supporting service on technical issues on site during the Quality Operating Period and on an ad-hoc basis.</li><li>Trouble shooting and RRCA of electrical / mechanical fault in elevators.</li><li>Prepares the new installation inspection report, field test data report, safety check report and Otis safety audit.</li><li>Need to report on-site field turn backs at product level.</li><li>Ensure 100% on-time delivery to customer as agreed.</li><li>Ensure all internal customer complaints are addressed and acknowledged.</li><li>Carry-out pre-NIS checks and share the list.</li></ul>If you live in a city, chances are we will give you a lift or play a role in keeping you moving every day. Otis is the world’s leading elevator and escalator manufacturing, installation, and service company. We move 2 billion people every day and maintain approximately 2.2 million customer units worldwide, the industry's largest Service portfolio.  You may recognize our products in some of the world’s most famous landmarks including the Eiffel Tower, Empire State Building, Burj Khalifa and the Petronas Twin Towers! We are 69,000 people strong, including engineers, digital technology experts, sales, and functional specialists, as well as factory and field technicians, all committed to meeting the diverse needs of our customers and passengers in more than 200 countries and territories worldwide. We are proud to be a diverse, global team with a proven legacy of innovation that continues to be the bedrock of a fast-moving, high-performance company.  When you join Otis, you become part of an innovative global industry leader with a resilient business model. You’ll belong to a diverse, trusted, and caring community where your contributions, and the skills and capabilities you’ll gain working alongside the best and brightest, keep us connected and on the cutting edge.  We provide opportunities, training, and resources, that build leadership and capabilities in Sales, Field, Engineering and Major Projects and our Employee Scholar Program is a notable point of pride, through which Otis sponsors colleagues to pursue degrees or certification programs.   Today, our focus more than ever is on people. As a global, people-powered company, we put people – passengers, customers, and colleagues – at the center of everything we do.  We are guided by our values that we call our Three Absolutes – prioritizing Safety, Ethics, Quality in all that we do. If you would like to learn more about environmental, social and governance (ESG) at Otis click <a href="https://www.otis.com/en/us/our-company/esg" rel="noopener noreferrer" target="_blank">here</a>.  Become a part of the Otis team and help us #Buildwhatsnext! Otis is An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other protected class according to applicable law. To request an accommodation in completing an employment application due to a special need or a disability, please contact us at careers@otis.com.Privacy Policy and Terms:Click on this <a href="https://www.otis.com/corporate/privacy-policy/Job-Applicant/" rel="noopener noreferrer" target="_blank">link</a> to read the Policy and Terms<h4>Experience Level</h4>Executive Level

Otis Elevator Company India Ltd

Quality Executive

Senior Process and Compliance ManagerJob Description SummaryResponsible for ensuring operational excellence related to clinical trial activities within Translational Clinical Oncology (TCO). Track progress to key quality indicators (KQIs), Quality Plan and overall compliance to applicable processes and regulations. Lead and assist in the development and implementation of process improvement initiatives within the function; ensure changes are adequately communicated and managed. Work collaboratively with clinical QA (CQA) and appropriate line functions to ensure that TCO upholds high quality standards. Job Description Major accountabilities: <ul><li>Accurate and timely execution of process improvement and quality initiatives as measured by meeting key milestones effectively.</li><li>Successful implementation of process improvements as measured by sustainable changes and improved efficiency.</li><li>Increased compliance with relevant processes.</li><li>Establish business partnerships with all relevant TCO functional groups, CQA, training and other LFs as required.</li><li>Training programs implemented in a timely fashion, and tracked to ensure compliance and maintenance</li></ul><h4> Impact on the Organization: </h4><ul><li>Improved quality of outputs</li><li>Increased compliance with SOP, GCP and training</li><li>Decreased audit/inspection findings</li><li>Efficient use of resources through operational effectiveness</li></ul><h4>Additional Details</h4><ul><li>KQIs - Responsible to track, report and reinforce adherence to applicable performance measures. Support in recommending corrective actions based upon report outputs and root cause analysis; and support implementing training/communication as applicable to ensure remediation (preventative actions). Support Clinical Trial Quality Risk Management (CTQRM) review by evaluating studies to ensure adherence to CTQRM SOP and follow-up with respective study leads.</li><li>SOPs - provide input into new SOPs/WPs on behalf of TCO as applicable, may serve as subject matter expert. Contribute to identifying training opportunities and ensuring compliance with new SOPs and Working Practices. Track quality issues and ensure their documentation within the quality event management system and implementation of corrective actions. Support the implementation and tracking of compliance to the clinical trial processes.</li><li>Quality Plan - Ensure that actions required of TCO are appropriately tracked.  Support the conduct of self-assessments for TCO in conjunction with CQA. Proactively ensure procedural deficiencies within TCO are corrected and prevented. Liaise with BR TM and CS&amp;I and appropriate Development LFs to ensure quality outcomes.</li><li>Process Expertise – identify or support the identification of procedural gaps and their correction with process improvements where applicable. Represent TCO/BR in cross-functional initiatives aiming for continual process improvement and ensuring a compliance focused environment either by direct involvement or by ensuring appropriate TCO/BR representation. May serve as Managed Access Program Champion.</li><li>Training -Support training/communications to assure understanding of new processes or findings.  Assure remediation. Identify gaps and assign action where needed to promptly gain compliance. Assist with change management activities related to new processes or organizational changes. Support/organize timely Lessons Learned sessions.</li><li>Compliance – As applicable based on assignment, ensure Corrective Actions Preventative Actions (CAPA) commitments are adequate, submitted and completed in a timely manner. Initiate and document root cause investigations of critical issues. Support inspection preparation and inspection readiness.  Ensure the timely submission and completion of adequate Corrective Actions Preventative Actions (CAPA). Ensure audit and inspection outcomes requiring corrective action are managed.</li><li>Act as TCO Protocol Review Committee Manager, as assigned: run PRC Office independently (meetings and agenda planning, uploading of documents in review system), maintain the PRC SharePoint site, system owner of the TCO PRC submission tracker, providing training and access and working with IT on system updates; maintain revisions to the PRC charter.</li><li>Act as BR-DOC Manager, as assigned – manage end-to-end document QC function with BR Translational Medicine – BR Doc function. Provide vendor management, track submissions and provide guidance to TCO teams.</li><li>As assigned, participate as a reviewer on the TCO Protocol Review Committee or assist with quality checks of documents (protocols, ICFs, etc) as appropriate per TCO process.</li><li>Escalate issues to TCO management and CQA in a timely manner.</li></ul> Minimum Requirements: Work Experience: <ul><li>A minimum of 5 years of relevant pharmaceutical clinical development experience</li><li>Extensive knowledge of clinical development process, GCP and clinical quality management; including strong understanding of regulation and guidance for clinical studies</li><li>Proficiency/Fluency in English</li><li>Experience working in matrix environment and in global teams.</li><li>Excellent interpersonal, problem-solving, negotiation and conflict resolution skills</li><li>Excellent organizational skills, as well as predisposition to quality management and process improvement</li><li>Excellent communicator and presenter (oral and written).</li></ul> Education: <ul><li>Bachelor of Science (BS) or advanced degree in scientific discipline or equivalent education in life science/healthcare required</li></ul> Languages :<ul><li>English.</li></ul> Skills DesiredAnalysis, Databases, Decision Making Skills, Operations, Problem Solving Skills, Reporting, Team Management, Waterfall Model<h4>Experience Level</h4>Senior Level

Novartis India

Process Manager

Quality AnalystJob Title:Quality AnalystJob DescriptionThe Sr Quality Evaluator is responsible for monitoring and evaluating inbound and/or outbound calls and other customer contact methods (e.g. email, chat) for accuracy and adherence to established quality standards. This position assists in the output of assessing quality standards, provide insight to customers to contribute to program performance improvements.Concentrix is a technology-enabled global business services company specializing in customer engagement and improving business performance. We partner with ambitious, progressive executives around the world to future-proof their business and stay ahead of the competition and customer expectations. Role and Key Responsibilities<ul><li>Define, standardize and monitor quality parameters including both non-critical &amp; critical parameters (End-User, Business critical, &amp; Compliance) and thereafter make recommendations for ongoing improvements in the process.</li><li>Ensure the team meets the assigned audit targets and compliances set as per SLA and performance scorecard for each process through continuous improvement methodologies.</li><li>Design and document standard practices to be carried out-  business processes.</li><li>Work closely with all functions for consistent delivery of service standard.</li><li>Interact actively with the clients at an operational level. Responsible for consistent delivery of service standards as per SLAs.</li><li>Drive a Metrics Driven Culture amongst the Team and establish reliable systems for measurement.</li><li>Monitor systems and process to provide ongoing feedback for continuous improvement to the service delivery standards</li><li>Attention to detail in supporting management reporting with clear and concise data handling and presentation</li><li>Evaluate and identify the capabilities of all processes within the system, introduce metrics to monitor the same and report to management on improvements necessary to meet customer and industry standards.</li><li>Leverage quality tools and techniques to effectively disseminate knowledge on the floor</li><li>Incorporate &amp; establish TQ standards across all LOBs in the span.</li><li>To identify root causes of variances in metrics (if any)</li><li>Responsible for leading, motivating and supervising the team of Quality analysts</li></ul>Key Skills and knowledge:<ul><li>Good Quality domain knowledge &amp; Tool management</li><li>Analytical, logical, reasoning &amp; numerical ability</li><li>Ability to interact with internal and external stake holders</li><li>Excellent oral &amp; written communication skills.</li><li>Expert in Excel &amp; PowerPoint</li><li>Knowledge of basic life insurance terminology</li><li>Graduate in any discipline</li><li>Good People Management skills.</li></ul>Education: Graduation Disclaimer:-'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities.Location:IND Kolkata - 10th Floor on Block A, DLF IT Park I, New TownLanguage Requirements:Time Type:If you are a California resident, by submitting your information, you acknowledge that you have read and have access to the <a href="https://www.concentrix.com/resource/job-applicant-privacy-notice-for-california-residents/" rel="noopener noreferrer" target="_blank">Job Applicant Privacy Notice for California Residents</a><h4>Experience Level</h4>Senior Level

Quality Analyst

Team Leader - Testing<h4>About SLK</h4>SLK is a global technology services provider focused on bringing AI, intelligent automation, and analytics together to create leading-edge technology solutions for our customers through a culture of partnership, led by an evolutionary mindset. For over 20 years, we've helped organizations across diverse industries - insurance providers, financial service organizations, investment management companies, and manufacturers - reimagine their business and solve their present and future needs. At SLK, we champion diversity and inclusion, valuing the unique perspectives and talents each individual brings. We empower specially abled talent by fostering a supportive environment that welcomes every member's abilities. Our goal is to create an innovative workspace enriched by diversity, providing reasonable accommodations to ensure everyone can contribute to our success. We invite candidates from diverse backgrounds to help us build a more inclusive future.<h4>BASIC INFORMATION ON THE POSITION</h4> Position Name: Team Leader - Testing <h4>Mandatory/Required Skills &amp; Location</h4>Location:Mandatory/Required Skills : <h4>PURPOSE OF THE ROLE</h4> The Senior Test Lead handles large or multiple end to end testing projects/programs and is responsible for all phases of the STLC cycle including test strategy/planning, estimation, test design, testing and release/ support of high complexity projects/programs.  The Sr. Test Lead is responsible for leading, tracking progress, mentoring the testing team and ensuring that the team adheres to testing process standards, procedures and goals. The Sr. Test Lead is also responsible for driving key automation (test automation coverage) &amp; process optimization initiatives in the project/program<h4>KEY RESPONSIBILITIES AND ACCOUNTABILITIES</h4> <ul><li>Understand &amp; analyse project/program requirements and business expectations</li><li>Conduct status update calls and manage customer escalations/query resolution, chair the DRB and Defect Management meetings. Coordinate with various stakeholders for smooth operations</li><li>Get required approvals and sign offs against project deliverables</li><li>Create Test Strategy/Plan, Test Estimations &amp; Resource Planning, Work Allocations, Track the testing progress &amp; report Status</li><li>Review the key test deliverables produced by the team and ensures they meet quality standards</li><li>Ensure complaince of self and team to organizational policies and processes</li><li>Develop ideas for improvements (Testing, Organization processes etc.) or create accelerator/tools/utilities to improve productivity.</li><li>Ensure project cost savings by efficient utilisation of resources in the team</li><li>Identify training needs of the team and ensure completion of mandatory trainings of the team</li><li>Is responsible for Work allocation and tracking the performance of reportees</li><li>Mentor and coach the team to ensure succesful completion of the project</li></ul><h4>EDUCATION QUALIFICATION</h4> <ol><li>Degree: B.E\B.Tech\M.Tech\MCA\M.Sc</li><li>Certifications (if any): ISTQB</li></ol><h4>MINIMUM EXPERIENCE REQUIRED</h4> <ol><li>Overall (in years): 8+ years</li><li>Relevant (in years): 2+ years</li></ol><h4>DOMAIN/ FUNCTIONAL SKILLS</h4> <ul><li>Test Strategy/Planning, Test Management, Test Concepts, Tools, Automation</li><li>BFSI/M&amp;SC Domain</li><li>Analytical skills, Logical Reasoning</li></ul><h4>Experience Level</h4>Senior Level

SLK Software Private Limited

Test Supervisor

Manager - Process Design<h4>Description</h4>Manager - Process Design<h4>Skills Required</h4>Design thinking, problem solving, Fraud risk management<h4>Education/Qualification</h4>Graduation<h4>Desirable Skills</h4>Process Excellence

Flipkart

Professional, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleProfessional, Quality Assurance EngineeringAbout your role: As a Quality Assurance Engineering - Sr Professional I, you will be a key contributor to ensuring the quality and performance of our software products. Your expertise will be critical in upholding our high standards and delivering reliable solutions to our clients. You will collaborate closely with development and product teams to identify issues, implement best practices, and drive continuous improvement in our QA processes. This role offers an opportunity to leverage your skills to make a significant impact on our product offerings and the overall user experience.What you'll do:<ul><li>Develop and implement comprehensive test plans and test cases.</li><li>Prepare/Create mock data needed for executing user stories for positive and negative test cases</li><li>Setup data for integrated testing.</li><li>Contribute to the development and maintenance of automated testing scripts.</li><li>Write test automation scripts using SOAP utilities or Rest Assured</li><li>Execute test automation scripts manually or automatically using Jenkin. Setup CICD process to automate the execution of test cases.</li><li>Collaborate with cross-functional teams to identify and resolve software defects. Work with development team to get the issues resolved and retest</li><li>Provide the demo to stakeholders and get approval for release.</li><li>Certify software adhering to standards and business requirements.</li><li>Ensure that JIRA and time entries are in place for QA work</li><li>Under limited direction, research, define, document, and prototype additions and changes to ESF product.</li><li>Apply best practices in quality assurance to ensure high-quality deliverables. Adhere to technical and functional standards</li><li>Participate in peer reviews and contribute to continuous improvement initiatives.</li></ul>Basic Qualifications for Consideration:<ul><li>Education: A Bachelor’s Degree in Computer Science, an associate degree in Computer Programming, or equivalent education in a related discipline is required.  Related work experience can be substituted for educational requirement</li><li>6+ years experience testing  technical solutions</li><li>2+ years of experience in automation testing</li><li>2+ years of experience in performance testing</li></ul>Preferred Skills &amp; Experience<ul><li>Candidates should be creative, self-motivated, problem solver with the ability to analyze a broad range of technologies. They should also possess good communication and writing skills, be able to effectively multi-task, and have a strong analytical skill</li><li>Experience with manual and automation testing of Java applications and RestAPIs.</li><li>Experience with Postman, SOAP API</li><li>Experience in RestAssured is must</li><li>Experience in Groovy or Python is a plus</li><li>Familiarity with security testing practices</li><li>Understanding of software development lifecycles</li><li>Certification in software testing methodologies</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.

Project Quality ManagerBe part of the solution at Technip Energies and embark on a one-of-a-kind journey. You will be helping to develop cutting-edge solutions to solve real-world energy problems.We are currently seeking a Project Quality manager reporting directly to Head of Quality – IOC to join our Quality team based in  Chennai &amp; Delhi Operating CentersAbout us:Technip Energies is a global technology and engineering powerhouse. With leadership positions in LNG, hydrogen, ethylene, sustainable chemistry, and CO2 management, we are contributing to the development of critical markets such as energy, energy derivatives, decarbonization, and circularity. Our complementary business segments, Technology, Products and Services (TPS) and Project Delivery, turn innovation into scalable and industrial reality.Through collaboration and excellence in execution, our 17,000+ employees across 34 countries are fully committed to bridging prosperity with sustainability for a world designed to last. About the mission we offer you:<ul><li>To manage and coordinate Project quality assurance and quality control activities providing leadership, expertise and direction.</li><li>To apply high level of competencies and capabilities (tools, procedures, organization and resources) in discharging quality assurance functions in the assigned projects (Engineering / EPC).</li><li>To define the quality assurance and quality control execution methodology for the project assigned </li><li>Represent project on quality matters with Client and  stakeholders </li></ul>Relationship Responsibilities:Reports to: Head Quality - IOCDirectly supervises (operationally): Nil Key Interactions:Internally: Project Managers, Other Department Managers/Project Leads (Engineering, Construction, QHSE, Procurement, P&amp;C, Proposals, Subcontract, Planning, IT, Administration Externally: Clients Quality Representatives, PMC, Subcontractors Quality team, Third Party Inspection Agencies , Certification agencies.Major Responsibility Areas:<ul><li>Define and implement Project Quality Plan.</li><li>Ensure implementation of Disciple Quality Plans where applicable. </li><li>Establishment of an approved Project Internal IMS audit plan and schedule. </li><li>Define and implement Project quality objectives / KPIs in liaison with Project management.</li><li>Plan, schedule, conduct / participate in project internal IMS audit as per project internal audit plan and schedule.</li><li>Follow up to ensure timely closure of audit findings ( internal / external).</li><li>Develop and conduct Project quality inductions, where mandated.</li><li>Facilitate Client / PMC audits in Projects and Home Offices. </li><li>Liaise and coordinate with other Operating Centers on quality matters where the scope of work is shared. </li><li>Conduct lesson learned workshops and quality awareness sessions.</li><li>Participate in non-conformity investigations, root cause analysis and validate corrective action proposals.</li><li>Review of Client / Contract quality assurance requirements and ensure collation, communication and maintenance of the same.</li><li>Review of Project Quality Plan and procedures in liaison with Project Manager. </li><li>Close coordination with Vendor performance Management and Site Quality Control on Quality performance</li><li>Document and facilitate investigation into quality incidents and non-conformities customer complaints. </li><li>Participate in Project quality reviews/ meetings. </li><li>Participate in CNQ review and root cause analysis as needed.</li></ul>Starting Date: Sept -Oct 2025About you:We love to hear from you and how you match this position. To be successful in this mission you should consider the following requirements:<ul><li> Bachelor’s degree in engineering</li><li>Minimum 7 years of experience including experience of handling FEED, Detailed Design and EPC projects of large and complex nature.</li><li>Familiarity with Project Life Cycle principles and significant project milestones </li><li>Conversant with Quality Management System standard ISO 9001:2018 and related guidelines with familiarity on ISO 45001:2018 and ISO 14001 :2015 standards.</li><li>Lead Auditor or Internal Auditor qualifications on ISO9001/ ISO45001/ ISO14001 desirable</li><li>Proficiency in writing plans, procedures, process flow mapping, etc.</li><li>Familiar with project / discipline objectives, targets, goals, KPIs and QHSE metrics </li><li>Possess an investigative and analytical mindset </li><li>Proficient in the use of root cause analysis methods (e.g. Fishbone, FMEA, FTA, ETA, 5 Whys…)</li><li>Project management knowledge in a multi discipline engineering project is desirable</li><li>Very good report writing skills  </li><li>Excellent management and leadership skills</li><li>Excellent interpersonal and influential skills</li><li>Knowledge on ASME/ API/ ASNT/ EN/ IS codes desirable </li><li>Fluency in professional English</li></ul> Your career with us:Working at Technip Energies is an inspiring journey, filled with groundbreaking projects and dynamic collaborations. Surrounded by diverse and talented individuals, you will feel welcomed, respected, and engaged. Enjoy a safe, caring environment where you can spark new ideas, reimagine the future, and lead change. As your career grows, you will benefit from learning opportunities at T.EN University, such as The Future Ready Program, and from the support of your manager through check-in moments like the Mid-Year Development Review, fostering continuous growth and development What’s next?Once receiving your application, our Talent Acquisition professionals will screen and match your profile against the role requirements. We ask for your patience as the team completes the volume of applications with a reasonable timeframe. Check your application progress periodically via personal account from created candidate profile during your application. We invite you to get to know more about our company by visiting  and follow us on LinkedIn, Instagram, Facebook, X and YouTube for company updates.#LI-MS2<h4>Experience Level</h4>Senior Level

Technip Energies

Sky-Team Manager-Service Quality-Sky Channel-Service Quality
Quality AnalystThe Internal Quality Auditor ensures that department processes – and the goods and services that result – comply with the requirements of standards, as well as customer, regulatory, and the organization’s own requirements. Role / Responsibilities: <ul><li>Evaluate production processes for compliance with quality requirements</li><li>Periodically inspect and calibrate auditing tools </li><li>Complete audit targets designed for the day / week / month for various processes</li><li>Assist in development of audit plans, audit schedules</li><li>Identify processes, situations, etc., where department is meeting requirements, as well as identify opportunities for improvement</li><li>Assist audit team in developing audit reports; prepare audit reports and  present audit reports to seniors, as needed</li><li>Assist with follow-up audits, as required</li><li>May be required to develop internal auditing/testing parameters</li></ul>Reporting Structure: Reports to the Quality Manager – Senior Manager Requirements:·         A bachelor’s degree is required·         Two or more years of internal auditing experience is desirable. Broking background will be given more preference ·         Must have an eye for detail and above-average analytical ability ·         Strong analytical and problem solving abilities are a must·         Must have solid experience with auditing tools·         Need exceptional listening, communication, and presentation skills.·         Must be able to work well with people at all levels of the organization ·         Must be able to work independently and as part of a diverse team of auditors <h4>Experience Level</h4>Mid Level

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Quality Assurance Officer

Quality Manager

Quality Head

Quality Executive

Process Manager

Quality Analyst

Test Supervisor

Process Manager

Quality Assurance Engineer

Quality Head

Quality Auditor

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