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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

Quality and Release leadJob title: Quality and Release leadAbout the jobWe are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?Main responsibilities:<ul><li>Lead and collaborate closely with the Release Manager, Product Owners, and Team Leads to ensure timely and successful product releases (Veeva configuration and Integration developments).</li><li>Ensure all required GxP documentations is completed in compliance with regulatory and SANOFI standards and within agreed timelines.</li><li>Proactively identify potential risks and schedule deviations and communicate them promptly to relevant stakeholders and management.</li><li>Conduct software quality assessments through manual testing, with a transition towards automated testing, to identify and report defects.</li><li>Liaise with business stakeholders to ensure adherence to the QualiPSO process and maintain alignment with release schedules.</li><li>Actively participate in team meetings and Agile ceremonies to support collaborative planning and execution.</li><li>Serve as the primary Release Lead for QualiPSO, providing guidance and coaching to other release leads to ensure effective coordination with QualiPSO project teams.</li><li>Maintain and continuously enhance documentation templates and the release toolkit to support project release leads in their delivery activities.</li><li>Drive continuous improvement in quality assurance processes by coordinating with the Digital Risk Advisory team.</li><li>Collaborate with the Release Manager and Scrum Master to drive continuous improvement initiatives, aiming to streamline and simplify ways of working.</li><li>Actively contribute to inspection, audit and quality reviews in partnership with the Technical System Owner and Digital Risk Advisory team, ensuring alignment with organizational standards and objectives. This includes to</li><li>Review of the Change Control on regular basis  </li><li>Secure compliance Team training</li><li>Secure SANOFI procedures are followed and adapt our own work instructions</li></ul>About you<ul><li>Experience: 7 to 10 years of experience on release or project management and testing</li></ul>Primary skills:<ul><li>Familiarity with release management processes.</li><li>Experience working in regulated GxP environments.</li><li>Proficient in tools like Jira, Confluence and Service Now</li><li>Working knowledge of Agile and Scrum methodologies.</li><li>Proven experience in Quality Assurance testing or a similar role.</li><li>Hands-on experience with automation tools, preferably TOSCA.</li><li>Strong skills in defining test strategies and reporting defects.</li><li>Ability to perform peer reviews of test scripts.</li></ul>Soft skills<ul><li>Excellent verbal and written communication skills.</li><li>Strong attention to detail and commitment to accuracy.</li><li>Demonstrated ability to collaborate effectively within global, cross-functional teams.</li><li>Being proactive</li><li>Education: Bachelor’s degree in computer science or related field (or equivalent experience)</li><li>Languages: English</li></ul>Why choose us? <ul><li>Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.</li><li>Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.</li><li>Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas. </li></ul>Pursue Progress. Discover Extraordinary.Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!<h4>Pursue progress, discover extraordinary</h4>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!<h4>Experience Level</h4>Senior Level

Sanofi India Ltd

Quality Assurance Tester

Manager, Global Quality Complaint SurveillanceWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Key ResponsibilitiesResponsible for managing and reporting of accurate and on time Global Quality metrics for Product Quality Complaints (PQC) in a fast-paced environment that support Tier Councils, Product Quality Complaint compliance &amp; trending across the organization, internal &amp; regulatory audits. Expertise with data management and analysis using electronic software solutions, eg VEEVA, Tableau, SpotFire, and Microsoft Office, with focus on Excel, PowerPoint, and SharePoint.Responsible to maintain a high level of knowledge &amp; understanding of Pharmaceutical/Biologic Quality Assurance, Device Quality Assurance, cGood Manufacturing Practices as applicable in global GMP regulations (including FDA, EMA, MHRA, PMDA, ENVISA, TGA).Responsible to develop &amp; maintain tools and dashboards in support of PQC trending, data surveillance and PQC user support.Responsible to provide PQC data assessments, highlighting trends, signals and risks and business critical information related to Product Quality Complaint data to Quality leadership in a timely fashion. Data &amp; trend assessments will be communicated with stakeholders in a manner commensurate with risk, and enabling appropriate action taking to protect BMS and our patients. Responsible to complete required training and provide support for Product Complaints, Product Surety and Quality Serialization business process activities.You are accountable for other key activities that support the business such as:<ul><li>SharePoint design, data requests/analysis, and providing communication of trends, signals and risks in addition to business critical information to leadership</li><li>Maintain expertise on PQC data management at BMS, including data sources, data quality, data management, data users</li><li>Report at appropriate intervals (weekly, monthly, quarterly, year-on-year etc) metrics on key compliance indicators related to PQC performance and procedural compliance (for example on-time closure, increasing/decreasing trends by product/defect category/market etc).</li><li>Review signals and trends that may present a risk to the organization and/or to our patients. Engage with PQC management and appropriate stakeholders to identify corrective actions. Align with PQC management for escalations to Quality leadership.</li><li>Provide recommendations and communications based on output from analytical tools and visualizations.</li><li>Provide risk assessment support for PQC processes, data management and related activities</li><li>Continuously improve process for assessment and reporting PQC data to drive consistency and understanding of Quality compliance-focused metrics</li><li>Use Operational Excellence and similar approaches to support the design of metric tools that facilitate proactive discussion and provide visibility/transparency to drive continuous improvement, prioritization and product quality related decisions</li><li>Lead teams in the development of tools and reports to optimize and standardize metrics</li><li>Lead collection and review of PQC data in response to health authority requests</li><li>Lead collection and review of PQC data in support of audit requests (internal and external audits)</li><li>Lead metrics initiatives related to product quality complaint programs and processes</li><li>Facilitate and drive standards for communication, management and visibility of product quality support metrics</li><li>Implementation and timely update of information to ensure content is current and accurate</li><li>Establish appropriate procedural documents for product quality support metrics</li><li>Cross train in other areas of the Global Quality organization to assist the business in developing its employees</li><li>Develop and maintain high quality relationships with key stakeholders</li><li>Work on multiple projects at one time and manage priorities based on timelines</li><li>Work independently with a high degree of professional integrity, be highly organized, and be detail-oriented</li><li>Perform duties as aligned with PQC management</li></ul>Qualifications &amp; ExperienceDegree/Certification/LicensureBachelor of Science degree in data analytics/statistics/biostatistics, engineering, chemistry, biology, or other quantitative field.Advanced degree preferred.Required Competencies<ul><li>Fluent in English, with proven professional working proficiency in English for reading, writing and speaking</li><li>Excellent communication with management, peers, and other functional areas</li><li>Excellent ability to analyse data to extract useful information and trends, and to translate data to effective messaging to  stakeholders and leaders supporting effective decision-making</li><li>Ability to work well cross-functionally with stakeholders</li><li>Ability to influence positively in a matrix environment</li><li>Proven ability to understand complex processes/problems and propose alternate solutions</li><li>Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders</li><li>Demonstrated Enterprise mindset to be able to think and act across functions and divisions</li><li>Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives</li><li>Excellent teamwork, interpersonal, and communication skills, with the ability to communicate and collaborate with employees and management at all levels and through various formats</li><li>Demonstrated strategic thinking capability and ability to balance conflicting priorities</li><li>Ability to provide innovative ideas or alternatives that create value including seeking new information and external insights without compromising compliance</li><li>Ability to clearly articulate analytical needs to functional partners</li></ul>Experience – Responsibility and minimum number of years<ul><li>A minimum of 5 years of experience in a data analytical role, or in a Quality role where data analytics was a key component in the pharmaceutical/ biotech/ device industry</li><li>Strong working knowledge/experience with systems such as QMS, SAP/ERP, Veeva</li><li>Experience with understanding how to respond to trend signals within the context of quality surveillance</li><li>Strong problem solving skills are required</li><li>Strong program and project management</li><li>Ability to manage multiple, simultaneous projects</li><li>Thorough understanding of Quality Risk Management</li><li>Mastery of relevant Quality compliance processes and regulations</li><li>Understanding of technical areas related to pharmaceutical and/or biological manufacturing, chemical and/or biochemical analyses, microbiological</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

Quality Specialist

Quality AnalystJoin us as a Quality Analyst<ul><li>If you have a keen eye for detail, then this could be the role for you as you make sure that only well designed and built work packages get through quality testing</li><li>You’ll be the quality conscience of the team, assisting them to write and maintain automated tests as a standard way of working</li><li>Joining us in this fast paced role, you'll have excellent opportunities for progression and developing your analyst capabilities</li><li>We're offering this role at associate level</li></ul><h4>What you'll do</h4>As a Quality Analyst, you’ll be assisting the feature team to define testable work that is technically robust, high performing, stable and secure and ensures excellent customer experiences and outcomes. Promoting continuous improvement, you’ll identify opportunities to maximise the customer experience and reduce the test cycle time by improving techniques, tooling, eliminating waste and creating a collaborative, proactive approach to quality in the feature team.As well as this, you’ll be:<ul><li>Supporting the Quality Manager and the team in executing against the test strategy and quality by determining and advising which tests should be automated at which layer</li><li>Making sure that test plans are adequately covered by test scenarios</li><li>Creating different test and automation suites, such as smoke tests, full regression and progression tests, and end-to-end system regression tests</li><li>Analysing the results of automated tests</li><li>Providing data to the business and the team that focuses on quality and quality improvement</li></ul><h4>The skills you'll need</h4>We’re looking for someone with an extensive understanding of all stages of the product or service life cycle. This will include in-depth and hands on experience in areas such as product testing, static testing, systems testing, systems integration testing, user acceptance testing, compliance testing and operational readiness testing.Along with this, you’ll have experience of applying a wide range of testing automation tooling, as well as testing methodologies, including a range of Agile testing methods such as test driven development and behaviour driven development.We’ll also expect:<ul><li>Experience of manual, ETL and database testing with hands on experience in writing SQL queries</li><li>Experience in functional and non-functional testing such as system, system integration, user, load, volume, stress, security, accessibility, compatibility, penetration and back-out</li><li>Demonstrable knowledge of Agile methodologies with experience of working in an Agile team</li><li>A very capable communicator with the ability to communicate complex technical concepts clearly to your peers and management level colleagues</li><li>Good collaboration and stakeholder management skills</li></ul>Hours45Job Posting Closing Date:06/11/2025<h4>Experience Level</h4>Mid Level

NatWest Group

Quality Analyst

Process Improvement Specialist - Lean Six Sigma CertifiedProcess Excellence (PEx) Black Belt Leader is responsible for being a change agent, leading improvement teams and working projects focused - Early Development as part of the PEx team.  During this full-time assignment, PEx consultants are expected to complete the following:  Lead and complete black belt projects within Early Development both locally and globally, coach and mentor business departments leaders, including green belt candidates and provide training to broaden the culture of process excellence within the business unit.Duties and Responsibilities:<ul><li>Leads process improvement teams and directs timely completion of projects that support critical goals and customer satisfaction requirements and serves as the departmental point of contact for specific project initiatives and best practices.</li><li>Assists process owners, project champions, and business unit leaders to facilitate setting priorities, developing agendas and designing objectives related to Labcorp Drug Development Process Excellence.</li><li>Train, mentor, coach and challenge others in the use of statistical tools and Process Excellence approaches and techniques to establish a process acumen mindset at the department or process level.</li><li>Demonstrates Project Management techniques on existing projects by managing multiple priorities effectively and meeting commitments in an accurate and timely manner.</li><li>Identify and present opportunities to business leaders and champions to improve customer satisfaction, increase net income, enhance productivity and further employee performance across business units within the Early Development business.</li><li>Identifies and shares leveraging opportunities or best practices across business units within the Early Development business.</li><li>Support ED project management and process excellence efforts with other duties as assigned.</li></ul>Education / Qualifications:<ul><li>Six Sigma Black Belt certification preferred, Six Sigma Green Belt will be considered.</li><li>BSc/BA is required; relevant experience may be substituted for education.</li><li>Engineering degree or other technical background preferred.</li></ul>Experience:<ul><li>7+ years in Process Excellence/Improvement roles</li><li>Direct experience working in a global matrix organization.</li><li>Project Management skills, including an ability to plan and execute projects and meet commitments in an accurate and timely manner.</li><li>Strong facilitations skills as demonstrated with various levels in an organization.</li><li>Strong technical skills as applied to obtaining and analyzing business metrics</li><li>Strong leadership and communication skills to senior leadership at the executive level and above.</li><li>Pharmaceuticals or Drug Development regulatory (GLP) experience highly preferred but not essential</li></ul>Labcorp is proud to be an Equal Opportunity Employer:Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to applyIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a href="https://careers.labcorp.com/global/en/accessibility" rel="noopener noreferrer" target="_blank">accessibility site</a> or contact us at <a href="mailto:Disability_apply@LabCorp.com" rel="noopener noreferrer" target="_blank">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a href="https://www.labcorp.com/about/web-privacy-policy" rel="noopener noreferrer" target="_blank">Privacy Statement</a>.<h4>Experience Level</h4>Senior Level

LabCorp

Process Analyst

Quality Engineer<h4>Position:</h4>Quality Engineer<h4>Job Description:</h4>* Detailed Description of the Job Profile (Role and Responsibility)<ul><li>Performing quality audits as per CMMI / ISO 13485 / ISO 62304 / IEC 14971</li><li>Understanding of software lifecycle</li><li>Medical QMS with regulatory requirements knowledge</li><li>Guiding and facilitating projects for effective process &amp; metrics implementation</li><li>Work product reviews for quality and process</li><li>Writing, updating and implementation of quality management system</li><li>Conducting trainings</li><li>Prepare &amp; Present Management Reviews</li><li>Defining processes and conduct Quality Management System related activities</li><li>Review documents (such as proposals / SoWs /</li></ul>Project plans) to ensure the quality<ul><li>Take other global initiatives such as external audits, Customer surveys, knowledge management, training</li></ul>* Technical Skill [Required]<ul><li>CMMI</li><li>ISO 13485 / ISO 62304 / IEC 14971</li><li>AS 9100</li><li>ISO 9001</li><li>Experience in Process Definition/ Improvement/ Implementation</li><li>Software Quality Assurance</li><li>Proficiency in Project Management</li><li>Sound knowledge of Product Lifecycle Management</li><li>Understanding of audit cycles and processes</li><li>Good in MS Excel, Project, Word and Presentation</li><li>Six Sigma</li><li>VBA Programming</li></ul>* Soft Skills [Required]<ul><li>Positive attitude &amp; Good team player</li><li>Excellent communication (written and oral), presentation &amp; interpersonal skill</li></ul><ul><li>Ability to work independently and collaboratively</li></ul><ul><li>Ability to prioritize and manage work to critical project timelines in a fast-paced environment</li></ul><h4>Location:</h4>IN-GJ-Ahmedabad, India-Ognaj (eInfochips)<h4>Time Type:</h4>Full time<h4>Job Category:</h4>Supply Chain Services<h4>Experience Level</h4>Senior Level

Arrow Electronics India Pvt Ltd

Quality Engineer

Assistant Manager, Quality Control
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4><h4>Responsible and accountable for Analytical Method Transfer /Verification related to Site Technology Transfer, SDC/Compendia and Cleaning methods; Training &amp; Documentation, Change Control management, Sample management and SOP updates.</h4><h4>Monitoring and ensuring the readiness of QC laboratory for audits at all time for the respective sections.</h4><h4>Job Responsibilities</h4><ul><li>Assessment/Review of scheduled projects with respect to Analytical method transfer/ verification, SDC and Compendia activities</li><li>Execution of method transfer/ verification activities related to STT, SDC and Compendia with proactive discussions and planning</li><li>To ensure initiation and completion of Analytical Method Transfer/verification studies within the stipulated time lines</li><li>Review and approval of Analytical Method Transfer/verification protocols, reports or any related documents</li><li>Monitoring of Lab investigations and providing guidance in the execution and closure of the same</li><li>To ensure alignment and engagement of manpower and equipment in a sustainable manner</li><li>To develop Analytical competency in the team through Qualification and Training for the required techniques</li><li>To ensure availability of all materials/requirements for the execution with pre-planning</li><li>Coordination/meetings with the cross functional teams within ARPL and GTA as and when required.</li><li>Awareness/ training on safety procedures to the team to ensure no major safety issue occurrence</li><li>Handling of LIR/Deviations if any related to method transfer/ verification activities</li><li>Ensuring the compliance to the adhered procedures in the functional area.</li><li>Any other additional responsibilities assigned by Department head, as and when required.</li><li>Participate and lead performance conversations with employees, including monthly one on ones, to connect on performance; check in on employee’s progress toward achieving Objectives, offer support and remove barriers; and, communicate and revisit performance expectations to reinforce and encourage high performance culture and a safe working environment for all employees.</li><li>Utilize open, honest, two-way communication to build trust-based relationships with employees, business partners and direct leader while continuously improving leadership capabilities by personally seeking feedback and development.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>Utilize your networks to attract and hire talent in a comprehensive, differentiated and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.</li><li>Ensure adherence of team members (direct reports) with all compliance programs and company policies and procedures.</li><li>All other duties as assigned.</li></ul><h4>Job Requirements</h4><ul><li>Education:
<ul><li>MinimumMSc/B. Pharm or any equivalent degree</li></ul></li><li>Skills and Abilities
<ul><li>Proficient in Analytical Method development, validations and transfer activities</li><li>Knowledge on regulatory guidelines and compendial procedures</li><li>Ability to resolve the issues related to day to day analytical activities</li><li>Ability to manage the work to meet the commitments despite challenges</li></ul></li><li>Experience
<ul><li>Minimum 7 to 14years of experience in GMP regulated Pharmaceutical Industry</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Mid Level

Apotex Pharmachem India Pvt Ltd

Quality Control Manager

Snr. Engineer Quality AssuranceJob title:  Senior Engineer   Job function and sub function: Quality Assurance –NPD &amp; Customer complaint. Reports to (role):Quality Manager<ol><li>Involve in new product launch with CFT </li><li>Preparation of PPAP documents </li><li>Handling pre launch stage customer </li><li>Handling customer complaint by 8D methodology</li></ol>  Team size (Direct and total): 2 Nos Works closely with: CFT team -MET ,Launch ,Program ,RnggLocation: ChakanKey responsibilities: Experience: Diploma/ B.E. with 7-10 years from experience in sheet metal &amp; welding<ol><li>Participate in the program meetings</li></ol><ol start="2"><li>Follow APQP time line</li></ol><ol start="3"><li>Do feasibility study of drawing with CFT</li></ol><ol start="4"><li>Preparation of PPAP documents</li></ol><ol start="5"><li>Participate in fixture design approval process with CFT</li></ol><ol start="6"><li>Participate in inspection gauge design approval process with CFT</li></ol><ol start="7"><li>Do CMM  of inspection gauge</li></ol><ol start="8"><li>Do internal PTR</li></ol><ol start="9"><li>Follow up of closing of observations of internal PTR</li></ol><ol start="10"><li>Do meeting with customer </li></ol><ol start="11"><li>Do PPAP with customer</li></ol><ol start="12"><li>Follow up of closing of observations of customer PPAP</li></ol><ol start="13"><li>Handling of complaint after 1 months from PPAP date</li></ol><ol start="14"><li>Make 8D of customer complaints</li></ol><ol start="15"><li>Customer audits handling and closure.</li><li>Customer complaints analysis and CAPA submission to customers.</li><li>Involve in APQP Documents preparation with CFT. Participate in design &amp; gauge/fixture reviews to identify potential quality risks early in NPD process.</li><li>Maintained the quality documentation throughout the NPD cycle. &amp;follow-up to PPAP approval.</li><li>Process documents like-SPC/MSA/PFMEA/CONTROL plan all PPAP documents good knowledge.</li><li>TATA,M&amp;M,VW,EICHER, customer handling experience.</li></ol><h4>Experience Level</h4>Senior Level

Tenneco

Quality Assurance Engineer

Quality Assurance / EngineeringOur PurposeMastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we’re helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential.Title and SummaryQuality Assurance / EngineeringJob Summary: We are seeking a detail-oriented and analytical Quality Test Engineer to join our team. The ideal candidate will be responsible for designing, implementing, and executing tests to ensure the quality and functionality of products before they reach customers. This role involves close collaboration with development, product, and operations teams to identify issues and drive continuous improvement. Key Responsibilities: Develop and execute test plans, test cases, and test scripts based on product requirements and specifications. Assist in writing and maintaining automated test scripts using Java and Selenium. Perform manual and automated testing of software/hardware systems. Identify, document, and track bugs and issues using tools like JIRA, Bugzilla, or similar. Collaborate with developers and product managers to understand features and technical implementation. Conduct regression, performance, and stress testing. Familiarity with Selenium WebDriver or other automation tools (preferred). Analyze test results and provide feedback for product improvements. Ensure compliance with industry standards and best practices. Participate in design and code reviews to provide a quality perspective. Maintain and improve test automation frameworks and CI/CD pipelines.Corporate Security Responsibility All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must:<ul><li>Abide by Mastercard’s security policies and practices;</li><li>Ensure the confidentiality and integrity of the information being accessed;</li><li>Report any suspected information security violation or breach, and</li><li>Complete all periodic mandatory security trainings in accordance with Mastercard’s guidelines.</li></ul>

Mastercard India Services Pvt Ltd

QA Test Engineer

Quality Assurance SubleadThe Quality Assurance Sublead will be responsible for ensuring the quality of products and services, implementing quality control processes, and leading a team of quality assurance professionals. The role involves developing and executing test plans, identifying defects, and providing recommendations for improvement.

Sterlite Technologies Ltd

Senior QA AnalystBachelor's degree in engineering / science. 3+ years of experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Experience with the implementation of Quality Management systems (Track wise/ Master control / ETQ/ CEBOS) Should be able to Develop validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Should be able to create project Deliverables which will encompass validation plans, specifications, test protocols and standard operation procedures Good communication and technical writing skills are a must. Should be able to work Independently. Should be Flexible to handle multiple projects parallelly. Should have experience in Managing clients and Stakeholder. Strong Manufacturing or Business process knowledge will be added advantage. Any Automation skill set /ability is added advantageIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" rel="noopener noreferrer" target="_blank">https://jobs.iqvia.com</a><h4>Experience Level</h4>Senior Level

IQVIA

QA / QC Analyst

Process Excellence Lead - Quality<ul><li>Identify, design, and execute process improvement initiatives using methodologies such as Lean, Six Sigma, and Kaizen.</li><li>Excellent leadership and communication skills with the ability to collaborate effectively across multidisciplinary teams.</li><li>Provide Lean Six Sigma training and mentorship, governance and reporting of in progress and implemented projects and measure their success</li><li>Create a culture focused on Continuous Improvement, challenging status-quo, thinking outside-the-box, and coach, mentor Green-Belts and Yellow-Belts</li><li>Ensuring operational efficiency by analysing operational data to identify trends, root cause of issues and opportunities of improvement </li><li>Create, review, edit, and format documents, including standard operating procedures (SOPs), work instructions, manuals, workflows, templates, and reports, ensuring accuracy, clarity, and compliance with established guidelines and standards.</li><li>Establish and maintain document control processes, including version control, document tracking, distribution, change control process and archival, to ensure that documents are current, accessible, and properly managed throughout their lifecycle.</li><li>Conduct quality reviews and audits of documents to identify errors, inconsistencies, and non-compliance issues, and recommend corrective actions and improvements to enhance document quality and integrity.</li></ul> Qualifications:<ul><li>Bachelor’s degree </li><li>2-3 years of experience in six sigma project/PEX team leading and mentoring projects within Finance, Procurement, HR and IT </li><li>Proficiency in six sigma tools and techniques, strong Excel skills, including advanced functions and data analysis.</li><li>Experience working with tools like VSM, Kaizen, DMAIC/DMADV, 5S, Kaizen, 8D</li><li>Excellent communication, presentation, change management, and project management skills</li><li>Ability to work independently and as part of a team.</li></ul>Preferred Qualifications:<ul><li>Knowledge of other automation tools and technologies.</li><li>Knowledge of Visio and other tools to create workflow, manuals, Document management etc</li><li>ISO 2001:2015 Lead Auditor </li></ul><h4>Experience Level</h4>Senior Level

Adani Enterprises Ltd

Business Process Lead

ExecutiveCandidate shall have detailed knowledge on equipment qualification, computer system validationReview of the Equipment Qualification Protocols and Final reports and Monitoring of the Equipment Qualification like IQ, OQ and PQ. Review of Qualification documents for IQ, OQ and PQ done by the Vendor/Third party related to Instrument integrated with equipment.Experience in handling of QMS related activities: Change control, Deviation, CAPA.<h4>Experience Level</h4>Executive Level

lupin ltd

Quality Technician

Senior Manager - Quality Management<ul><li>Job Title: Senior Manager - Quality ManagementCareer Level - EIntroduction to roleProtecting AstraZeneca's license to operate through the delivery and maintenance of compliant innovation, projects, and services. This function comprises Quality Management professionals who understand AstraZeneca's business processes and are experts at integrating business-appropriate risk management techniques. This function will also consult and educate the business and the broader workforce on effectively integrating Compliance Requirements into all IT Lifecycle activities. The function is truly global in scale with resources in Asia, EU, North America, and South America.<h4>Accountabilities</h4><ul><li>Accountable for the application of Quality Management processes and services to assure that projects, systems, solutions, and services delivered by IT and their 3rd party suppliers meet AstraZeneca internal and external regulatory requirements.</li><li>Act upon risks and issues to raise compliance and quality levels within IT and the business.</li><li>Support the development and roll-out of training, education, and awareness campaigns for quality and compliance.</li><li>Contribute to the continuous improvement of IT Policies, standards, and procedures.</li><li>Collaborate with system/business process owners to complete or update the Risk Impact Determination (RID) as per the procedure to ensure an understanding of the Regulatory applicability (GxP, SOx, Data Privacy etc.), business, technical, software category, and regulatory risks.</li><li>Review System lifecycle deliverables including RID, specifications, protocols, reports, and the Test Closure Memo with a focus on cGMP impact, validation lifecycle requirements, and quality, and compliance requirements.</li><li>Participate in the review and approval of Exceptions, CAPA, Deviations, Changes, Incidents, and Problems ensuring timely completion and update of System Lifecycle deliverables.</li><li>Collaborate with the IT Project Manager to define the Quality Plan, processes, validation planning, and reporting processes.</li><li>Lead/Participate in the Supplier Assessment to ensure that IT Suppliers meet AstraZeneca Regulatory requirements.</li><li>Act as a QC point of contact for any potential internal and/or regulatory inspection.</li><li>Drive accountability for the completeness, accuracy, and currency of Quality-related data through effective monitoring, tracking, and reporting.</li><li>Process authoring, ownership, lead, quality review, and/or approval as appropriate.</li></ul><h4>Essential Skills/Experience</h4><ul><li>BA, BSc in Computer or Life Sciences or equivalent, with 3-5 years of experience in the pharmaceutical industry regulatory requirements</li><li>Experience of providing regulatory support including validation of laboratory and business applications</li><li>Knowledge of industry good practice and standards such as ISO 9000, ISO 27002, CMMI, GAMP, GxP, ITIL, S404 Sarbanes-Oxley</li><li>Experience of contributing to implementation of a Quality and/or Compliance strategy with the ability to prioritise and understand the impact of the decisions made</li><li>Experience of operating across business functions and geographies in large, complex and sometimes uncertain IT environments</li><li>Strong communication, influencing and relationship building skills, capable of discussing technical IT terms with a non-technical business audience</li><li>Strong change leadership and team working skills</li><li>Ability to make pragmatic decisions by analysing complex situations and assessing risks</li><li>Concern for impact, analytically minded and able to prioritise and plan using initiative</li><li>High levels of drive, energy, resilience and a desire for professional excellence</li><li>Ability to hold self and others accountable for actions</li></ul><h4>Desirable Skills/Experience</h4><ul><li>Broad IT management experience including project or service management</li><li>Familiarity with technical concepts in infrastructure or applications</li><li>External qualifications such as ISPE PCC CPIP and ISACA CISM</li><li>Understanding of Lean principles, tools and techniques</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca, our work has a direct impact on patients by transforming our ability to develop life-changing medicines. We empower the business to perform at its peak by combining cutting-edge science with leading digital technology platforms. Join us at this crucial stage of our journey in becoming a digital and data-led enterprise.Ready to make a difference? Apply today!</li><li>A</li></ul>Date Posted09-Sept-2025Closing DateAstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Senior Level

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