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Petroleum Engineer (QA Specialist)We are looking for the right people — people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and their careers. Experience the challenges, rewards and opportunity of working for one of the world’s largest providers of products and services to the global energy industry.<h4>Job Duties</h4>Under broad direction, mentors a team of Software Testers that can be comprised of Manual and Automated Test Engineers. Comprehensive understanding of all elements of a successful software development program. Including but not limited to Code Inspections, Manual Testing, Automated Testing, Functional Requirements, Design, Usability, Test plans and Results and Defect Management. Assists with secure architecture design reviews and supports preparing applications for security testing. Ensures security vulnerabilities have been mitigated. This role is an integral part of the planning of future releases including estimating efforts required in Testing and Documentation and advising on product improvements based on experience gained from previous releases and customer feedback. Usually works on projects of moderate to complex scope. Requires completion of an undergraduate degree in Computer Science, Geo-science, Petroleum Engineering or similar discipline, and 4+ years of related experience, including software testing and/or development experience. Completion of a masters degree is preferred.<h4>Qualifications &amp; Experience</h4>Key Responsibilities <ul><li>Lead quality assurance efforts across upstream Oil &amp; Gas applications, ensuring robust testing coverage and high software reliability.</li><li>Design, develop, and execute effective test cases for various testing types including functional, integration, performance, regression, and UAT.</li><li>Collaborate with cross-functional teams including developers and Product Owners to align testing strategies with business goals.</li><li>Manage defect tracking and resolution processes, ensuring timely and accurate reporting.</li><li>Contribute to test automation initiatives and framework enhancements to improve efficiency and scalability.</li></ul> Qualifications <ul><li>Bachelor’s degree in Petroleum Engineering or a related discipline is required</li><li>Minimum 4 years of relevant experience in upstream Ol &amp; Gas software environments, preferably in a quality assurance role</li><li>Solid understanding of drilling and completions workflows such as well construction, fluids management, and performance monitoring.</li><li>Experience with the EDT suit of application is a plus</li><li>ISTQB Foundation Level Certification is preferred but not mandatory.</li><li>Excellent communication, analytical and decision-making skills are required </li></ul> Technical Expertise <ul><li>Proficient in software testing methodologies: Smoke, Functional, Integration, Performance, Regression, and UAT.</li><li>Hands-on experience with Agile methodologies and ALM tools like Azure DevOps/TFS or JIRA.</li><li>Familiarity with engineering software such as WellCat, WellPlan, and Compass is a plus.</li><li>Working knowledge of automation tools and test framework design.</li><li>Strong communication and documentation skills with a collaborative mindset.</li></ul>Halliburton is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation. Location4th Floor, Gardenia 2D, Bengaluru, , 560103,  Job DetailsRequisition Number: 201580   Experience Level: Experienced Hire  Job Family: Engineering/Science/Technology  Product Service Line: Landmark Software &amp; Services    Full Time / Part Time: Full TimeAdditional Locations for this position:  Compensation Information Compensation is competitive and commensurate with experience.

Halliburton

Quality Assurance Engineer

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 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>Execute detailed quality assurance testing for software products.</li><li>Develop and implement comprehensive test plans and test cases.</li><li>Collaborate with cross-functional teams to identify and resolve software defects.</li><li>Apply best practices in quality assurance to ensure high-quality deliverables.</li><li>Contribute to the development and maintenance of automated testing scripts.</li><li>Participate in peer reviews and contribute to continuous improvement initiatives.</li><li>Responsibilities listed are not intended to be all-inclusive and may be modified as necessary.</li></ul>Experience you'll need to have:<ul><li>3-7 years of experience in automation testing, with a focus on Open Text UFT.</li><li>Have good experience in Web and Desktop Automation - UFT/Selenium/Playwright using C# or Java.</li><li>Strong understanding of Banking Domain Knowledge, systems, processes, and regulations.</li><li>Proficiency in programming languages (e.g., VBScript, C# or Core Java) and test automation tools.</li><li>Experience with banking applications and related technologies. Good working experience in any CI/CD Tools (Jenkins) for Continuous Integration and Source Code Tools(Gitlab/GitHub/BitBucket)</li><li>Proficient in writing SQL queries to perform Database Testing.</li><li>Excellent analytical, problem-solving, and communication skills.</li><li>Ability to work independently and as part of a team in a fast-paced environment.</li><li>Working experience of DNA core is preferrable </li><li>Should have good AI exposure.</li></ul>Experience that would be great to have:<ul><li>Familiarity with security testing practices</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.<h4>Experience Level</h4>Senior Level

Fiserv India Pvt Ltd

Senior Quality Assurance Engineer

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

Manager - Quality
In a world where customers consistently interact with your brand across multiple channels-including digital and social-we at Startek value our ability to effectively garner those interactions and CX insights, analysing, unlocking, and providing intelligence that drives digital transformation and further revenues for you, our client.Put simply: we break down the complexity of your customer lifecycle and help your customers build and sustain emotional connections with your brand.Our tech-enabled and Human assisted digital solutions build both on your CX requirements and our business transformation expertise and willingness to consistently pivot, innovate, and take advantage of new digital technologies.It’s a robust approach. We’ve partnered with global brands for over 3 decades now -working with them across their consumer value chain and providing new age customer experience solutions and insights that are helping them define and reach their target audiences with greater efficiency and better value for every dollar spent.Our partnerships have always been about more than building emotional connections with customers; they are about using artificial intelligence, omnichannel orchestration and providing CX insights &amp; technologies, that has the power for digital transformation We do this across 46 locations in 13 countries, with over 40,000 employees managing almost half a billion customer interactions every year for over 150 clients in different industries.*** DISCLAIMER***With the increase of remote positions since COVID, many companies have seen an increase in false representation recruiters and offering fraudulent positions/pay rates that do not exist.These messages are from anonymous sources and crafted to appear as they are being sent from Startek recruiters.  All communication from Startek will have an email address from  “startek.com”.  Additionally, a scam message can request funds or other personal information prior to the offer letter being released.  This is not a standard operating procedure for Startek to be employed with the organization.Startek is not responsible for any fraudulent representing the company.  <h4>Experience Level</h4>Mid Level

Startek

Quality Manager

Quality Engineer <ul><li>Role involves end-to-end testing in an Agile Scrum setup, collaborating with stakeholders, and ensuring quality delivery.</li><li>Skills: Playwright, TypeScript, Agile/Scrum, Testing Methodologies</li><li>Nice to have: DevOps / CI-CD exposure</li><li>Experience: 3–4 years</li><li>Work Hours: 12 PM – 10 PM</li></ul> Share your resume now.

Kairos Technologies

Quality Engineer

Assistant Manager - Quality Assurance AnalysyWho we are?  Johnson Controls is the global leader for smart, healthy and sustainable buildings. At Johnson Controls, we’ve been making buildings smarter since 1885, and our capabilities, depth of innovation experience, and global reach have been growing ever since. Today, we offer the world’s largest portfolio of building products, technologies, software, and services; we put that portfolio to work to transform the environments where people live, work, learn and play.This is where Johnson Controls comes in, helping drive the outcomes that matter most. Through a full range of systems and digital solutions, we make your buildings smarter. A smarter building is safer, more comfortable, more efficient, and, ultimately, more sustainable. Most important, smarter buildings let you focus more intensely on your unique mission. Better for your people. Better for your bottom line. Better for the planet. We’re helping to create a healthy planet with solutions that decrease energy use, reduce waste and make carbon neutrality a reality. Sustainability is a top priority for our company. We committed to invest 75 percent of new product development R&amp;D in climate-related innovation to develop sustainable products and services. We take sustainability seriously. Achieving net zero carbon emissions before 2040 is just one of our commitments to making the world a better place. Please visit and follow Johnson Controls LinkedIn for recent exciting activities.Why JCI: <a href="https://www.youtube.com/watch?v=nrbigjbpxkg" rel="noopener noreferrer" target="_blank">https://www.youtube.com/watch?v=nrbigjbpxkg</a>Asia-Pacific LinkedIn: <a href="https://www.linkedin.com/showcase/johnson-controls-asia-pacific/posts/?feedView=all" rel="noopener noreferrer" target="_blank">https://www.linkedin.com/showcase/johnson-controls-asia-pacific/posts/?feedView=all</a>Career: <a href="https://www.youtube.com/watch?v=EwhAYCz6x_4" rel="noopener noreferrer" target="_blank">The Power Behind Your Mission</a>OpenBlue: <a href="https://www.youtube.com/watch?v=bFbZIj0Sj6Y" rel="noopener noreferrer" target="_blank">This is How a Space Comes Alive</a>How will you do it?As a Quality Assurance Analyst II in the Collections department, you will be responsible for ensuring the quality and compliance of collections processes. You will work closely with collections teams to identify and resolve issues and contribute to the continuous improvement of our QA processes.What You Will Do:As a Quality Assurance Analyst II for the Collections department, your primary responsibilities will include:<ul><li>Ensuring Compliance: Conduct audits and reviews to ensure collections processes comply with regulatory requirements and company policies.</li><li>Identifying and Documenting Defects: Track and document any defects or inconsistencies found during auditing.</li><li>Collaborating with Teams: Work closely with collections leaders to understand requirements, calibrate, and provide feedback.</li><li>Data Analysis: Provide data analysis of audit findings.</li></ul>How You Will Do It:<ul><li>Defect Tracking: Document and track defects found during audits.</li><li>Compliance Audits: Regularly review collections processes to ensure they meet regulatory standards. This involves conducting internal audits and preparing compliance reports.</li><li>Calibration Meetings: Lead calibration meetings with collections leaders,  to discuss requirements, align quality standards, provide feedback, and ensure consistency in collections processes.</li><li>Continuous Improvement: Stay updated with industry best practices and emerging trends in collections and QA. Contribute to the development and improvement of QA methodologies and processes.</li></ul><ul><li>Experience: 2- 3 years of experience in quality assurance, preferably in collections or financial services.</li><li>Education: Bachelor’s degree in business, Finance, or a related field.</li><li>Skills:<ul><li>Strong analytical and problem-solving skills to identify and resolve issues effectively.</li><li>Excellent attention to detail to ensure thorough auditing and compliance.</li><li>Strong communication and teamwork abilities to collaborate effectively with various teams.</li><li>Intermediate to advanced skills in Microsoft Apps: Excel, Word and Outlook.</li></ul></li><li>Fluent in English for Business: Ability to communicate effectively in English for business purposes.</li><li>Certifications: Relevant certifications in quality assurance or collections are preferred.</li><li>Working experience within a shared services environment supporting India region is mandatory</li></ul>What we offer:We offer an exciting and challenging position. Joining us you will become part of a leading global multi-industrial corporation defined by its stimulating work environment and job satisfaction. In addition, we offer outstanding career development opportunities which will stretch your abilities and channel your talentsDiversity &amp; Inclusion Our dedication to diversity and inclusion starts with our values. We lead with integrity and purpose, focusing on the future and aligning with our customers’ vision for success. Our High-Performance Culture ensures that we have the best talent that is highly engaged and eager to innovate.  Our D&amp;I mission elevates each employee’s responsibility to contribute to our culture. It’s through these contributions that we’ll drive the mindsets and behaviors we need to power our customers’ missions. You have the power. You have the voice. You have the culture in your hands.<h4>Experience Level</h4>Mid Level

Johnson Controls Ltd

Quality Assurance Specialist

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

Lead Operational Excellence (Commercial Excellence)<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>We are looking for seasoned Marketing professionals looking to pivot their career into Operational Excellence while leveraging their rich marketing and branding experience. Job Summary We are seeking a dynamic and experienced Leader in Operational Excellence for overseeing the implementation of an operational framework, optimizing organizational processes through data analysis, and fostering continuous improvement. The role involves identifying and resolving operational issues, implementing knowledge management strategies, and enhancing employee proficiency in operational methodologies. The primary goal is to drive efficiency, resilience, and cost-effectiveness while ensuring adherence to performance metrics and targets. Roles &amp; Responsibilities <ul><li>You will be responsible to strategize and deploy the Process Excellence framework, Lean Management System, benchmarking and continuous improvement to enhance productivity across functions and teams in the business unit.</li><li>KAIKAKU (Radical change) across functions and team in the business unit.</li><li>You will be responsible to drive the process simplification and process improvement through leading a structured ideation process to drive innovation, eliminating non-value-adding activities, removing redundancies, digitizing tasks, outsourcing non-core activities and create more time for scientific endeavors.</li><li>You will be responsible to drive and implement a Cost Optimization program via Product and Cycle-time Excellence (PACE) methodology, identifying cost-saving ideas with functional leads, setting baselines and targets, and reviewing progress regularly.</li><li>You will be responsible for Business Process Redesign (BPR) and Metric Improvement through Strategic Initiatives. Also, evaluate and optimize business processes for scalability and future needs, conducting thorough analysis and workshops with stakeholders. Implement standardized work instructions and modifications to enhance efficiency and effectiveness.</li><li>You will be responsible to establish and manage knowledge sharing practices, overseeing implementation and application of knowledge, and maintaining a comprehensive repository for future reference.</li><li>You will be responsible to build leadership skills and motivate team members for improved Operational Excellence (OE) skills, enhancing their potential and resolving organizational challenges.</li></ul><h4>Qualifications</h4>Educational qualification: B.E/B.Tech preferably with an MBA Minimum work experience: 12 -15 years of experience in Pharma/ FMCG with core experience in Sales/ Marketing/ Commercial Excellence roles.  Skills &amp; attributes: Technical Skills<ul><li>Master Black Belt/ Black Belt Certifications in Lean Six Sigma, Certification in Project Management and other improvement methodology.</li><li>Prior experiences in internal/external process consulting, Process Excellence Framework</li><li>Good knowledge of Lean Six Sigma Methodology &amp; Tools</li><li>Understanding of Strategic Planning and business processes</li><li>Good in Data Analytics, visualization, deriving insights and providing recommendations</li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills</li><li>Business Acumen &amp; Decision Making</li><li>Strong analytical and problem-solving abilities</li><li>Ability to work collaboratively with own team and cross-functional teams</li></ul><h4>Additional Information</h4>About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com <h4>Experience Level</h4>Senior Level

Dr Reddys Laboratories

Team Leader - Operations

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 testing ideas, products, designs, planning and execution</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:09/10/2025<h4>Experience Level</h4>Mid Level

NatWest Group

Quality Analyst

Quality Assurance Principal AssociateAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Position Brand Description:Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The PIP (person in plant) API EM Quality Assurance Principal Associate will provide support to all quality activities within a dynamic external manufacturing environment. The PIP position is based in Hyderabad, India with travel as required to Visag. The candidate must be within commute distance.The QA Associate’s position is essential for ensuring that all batches meet specifications, are manufactured in accordance with the validated process and are compliant to cGMPs and regulatory commitments. The QA Associate will need to interact daily with a wide variety of people, primarily external partners team members and site management.Key Objectives/Deliverables:<ul><li>Serve as a liaison between CMs and Lilly.</li><li>Provide quality oversight of CMs including being the initial point of contact for all quality-related issues.</li><li>Escalate quality issues at CMs to Lilly QA management.</li><li>Assist in the establishment and revisions of Quality Agreements with affiliates and customers.</li><li>Provide quality oversight of Lilly/APIEM Quality Plans</li><li>Coordinate and perform QA responsibilities of API shipments.</li><li>Participate in regulatory inspection preparations with CMs.</li><li>Provide on-site support during manufacturing events and inspections.</li><li>Participate on the Technical Review Board</li><li>Evaluate and disposition API batches, if required.</li><li>Ensure that documented checks have been completed for the Certificates of Testing and Certificates of Environmental Monitoring (where applicable), and deviations, changes and batch documentation that demonstrates requirements have been met prior to batch release.</li><li>Provide quality support of API manufacturing with the focus on holistic review of key activities associated with or impacting the manufacturing processes including deviations, change controls and countermeasures.</li><li>Assess the impact of deviation investigations and changes and ensure that all appropriate records are documented and retrievable.</li><li>Ensure all processes are in an appropriate state of control.</li><li>Maintain awareness of external regulatory agency findings which individually or collectively reference the quality of the product.</li><li>Review and approve documents including, but not limited to, procedures, master production records, change control proposals, deviations, equipment qualifications, and computerized system validations.</li><li>Participate in APR activities.</li><li>Participate in projects to improve productivity.</li><li>Participate in Joint Process (JPT) and Post Launch Optimization (PLOT) Teams.</li></ul>Basic Requirements:<ul><li>BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences.</li><li>Previous GMP manufacturing experience in API manufacturing in a Quality Assurance role (minimum 5 years of GMP QA on the floor support)</li><li>Minimum 10 years of experience in a Quality Assurance role in “big pharma” as the Market Authorization Holder for non-generic products.</li><li>Demonstrated foundational knowledge of ICH and EMA regulations.</li><li>Experience participating in internal, customer, and regulatory inspections</li><li>Process Validation and Technical Transfer experience</li><li>Fluent in English</li></ul><ul><li>Additional Preferences:</li><li>Demonstrated coaching and mentoring skills.</li><li>Experience in root cause analysis.</li><li>Demonstrated application of statistical skills.</li><li>Demonstrated strong written and verbal communications skills.</li><li>Strong attention to detail.</li><li>Proficiency with computer system applications.</li><li>Excellent interpersonal skills and networking skills.</li><li>Ability to organize and prioritize multiple tasks.</li><li>Ability to influence diverse groups and manage relationships.</li></ul>Education Requirements:<ul><li>BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences.</li><li>Master of Science preferred</li></ul>Other Information: <ul><li>Must complete required training for API EM Quality Assurance.</li><li>No certifications required.</li><li>Required onsite 2-3 days a week and must be able to support 24 hour/day operations.</li><li>Some travel (&lt;25%) is required primarily to Vizag</li></ul>Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Senior Level

Eli Lilly and Company India Pvt Ltd

Quality Assurance Associate

Quality Lead : Green Proposal<ul type="disc"><li>Develop and implement comprehensive testing strategies, including functional, regression, and performance testing. </li><li>Oversee the execution of test plans, analyze results, and identify defects. </li><li>Work closely with package Managers, Engineering and other stakeholders to ensure quality standards are met. </li><li>Manage and track defects using bug tracking tools, working with developers to resolve issues. </li><li>Monitor and report on project quality metrics, providing insights and recommendations. </li><li>Continuously improve testing processes and methodologies to enhance efficiency and effectiveness. </li><li>Ensure adherence to quality standards throughout the project lifecycle. </li><li>Identify and assess project risks related to quality and develop mitigation strategies. </li><li>Create and maintain test documentation, including test plans, test cases, and test scripts. </li><li>Motivate, coach, and mentor QA engineers, ensuring efficient and effective testing processes. </li><li>Keep abreast of industry best practices and emerging technologies in quality assurance. </li><li>Communicate effectively with all stakeholders, providing regular updates on project status and quality metrics. </li></ul>

Larsen & Toubro Ltd

Associate Manager Quality AssuranceROLE SUMMARY<ul><li>Responsible for reviewing documents related to product development, analytical data (including electronic data, chromatographic data, and audit trails), as well as instrument and equipment qualification</li><li>Accountable for ensuring data integrity compliance and adherence to SOPs during the review of both hard copy and electronic records</li><li>Conduct periodic system audit trail reviews and ensure compliance with 21 CFR Part 11 requirements</li><li>Liaise effectively with global BL and OQ colleagues to achieve organizational objectives</li><li>Maintain a thorough understanding of ICH quality guidelines and relevant regulatory guidance on microbiology method development pertaining to sterility, BET, CCIT, and associated development requirements</li><li>Possess in-depth knowledge regarding sterility requirements and filter validation activities in accordance with PDA technical reports</li><li>Demonstrate familiarity with requirements for sterile ANDA product development and combination products</li><li>Exhibit strong proficiency in MS Office applications, including Excel, Word, and PowerPoint presentation preparation</li></ul>ROLE RESPONSIBILITIES &amp; SKILL SETS<ul><li>Awareness of DI and ALOCA principles</li><li>Basic understanding of cGMP requirements, including 21 CFR part 210 and 211, ICH guidelines, and sterile product requirements</li><li>Maintain compliance in laboratories and during document review</li><li>Ability to perform statistical evaluation and analysis of analytical data during method development and validation review</li><li>Effective communication skills.</li><li>Adherence to discipline and self-motivation.</li><li>Participate in the implementation of new initiatives and goals within the QA function and with business line partners to support consistency, efficiency, and compliance.</li><li>Manage time to meet agreed targets and plan work activities for projects within assigned teams.</li><li>Suggest improvements and participate in continuous improvement activities.</li><li>Contribute to the development and compliance of quality and business line partner procedures</li><li>Provide support for inspection readiness efforts, internal audits, and regulatory inspections as required</li></ul>QUALIFICATIONS Education:<ul><li>Master of science in chemistry</li><li>Master of pharmacy</li></ul>Relevant experience:<ul><li> Relevant work experience in an analytical data review and Technology transfer and cGMP pharmaceutical   sterile manufacturing area</li></ul>Location: On premise   Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and Control<h4>Experience Level</h4>Mid Level

Pfizer Ltd

Technical Auditor Eligibility:<ul><li><a rel="noopener noreferrer" href="\&quot;http://b.tech/B.E\&quot;" target="_blank">B.Tech/B.E</a>. (Food Tech, Dairy Tech, Biotech, Chemical, Textile &amp; Fibre, Agri, Petrochemical) OR <a rel="noopener noreferrer" href="\&quot;http://m.sc/\&quot;" target="_blank">M.Sc</a>. (Chemistry, Biochemistry, Microbiology)</li><li>Minimum 60% marks / 6.0 CGPA / First Division</li><li>2–5 years of relevant experience (Graduated before Feb 2023)</li></ul> Role Highlights:<ul><li>Conduct on-site factory inspections under BIS standards</li><li>Assess processes, raw materials &amp; lab facilities</li><li>Ensure compliance across Food, Chemical &amp; Textile sectors</li></ul> Share your resume now.

Quality Austria Central Asia

External Auditor

Quality Assurance Engineer SpecialistIt’s not just about your career or job title… It’s about who you are and the impact you will make on the world. Because whether it’s for each other or our customers, we put People First. When our people come together, we Expand the Possible and continuously look for ways to improve what we create and how we do it. If you are constantly striving to grow, you’re in good company. We are revolutionizing the way the world moves for future generations, and we want someone who is ready to move with us.It’s not just about your career or job title… It’s about who you are and the impact you will make on the world. Because whether it’s for each other or our customers, we put People First. When our people come together, we Expand the Possible and continuously look for ways to improve what we create and how we do it. If you are constantly striving to grow, you’re in good company. We are revolutionizing the way the world moves for future generations, and we want someone who is ready to move with us.Who are we? Wabtec Corporation is a leading global provider of equipment, systems, digital solutions, and value-added services for freight and transit rail as well as the mining, marine, and industrial markets. Drawing on nearly four centuries of collective experience across Wabtec, GE Transportation, and Faiveley Transport, the company has grown to become One Wabtec, with unmatched digital expertise, technological innovation, and world-class manufacturing and services, enabling the digital-rail-and-transit ecosystems. Wabtec is focused on performance that drives progress and unlocks our customers’ potential by delivering innovative and lasting transportation solutions that move and improve the world. We are lifelong learners obsessed with making things better to drive exceptional results. Wabtec has approximately 27K employees in facilities throughout the world. Visit <a href="http://www.wabteccorp.com/" rel="noopener noreferrer" target="_blank">our website</a> to learn more!Job Description:  We are seeking a skilled Automation Test Engineer to join our dynamic team. The successful candidate will be responsible for conducting automated testing on our software applications to ensure efficiency and effectiveness. RESPONSIBILITIES Develop and update scripts to automate testing processes, ensuring they are both efficient and effective.  Identify, analyze, and meticulously document test results.   Work closely with cross-functional teams to develop effective strategies.   Verify that software applications meet both functional and non-functional requirements.   Perform thorough post-release and post-implementation testing.   Participate in troubleshooting and triaging issues with various teams to identify root causes and drive resolutions.   Confirm and validate identified defects.   Continuously maintain and improve the automated scripts  and framework.   Regularly assess and implement new tools and technologies  to enhance testing efficiency. QUALIFICATIONS REQUIRED:  Hands-on experience of less than 1.5 years as an Automation Test Engineer.   Basic Python programming knowledge and hands-on experience.   Familiarity with testing concepts and process management.   Excellent communication and presentation skills.   BE in Computer Science, Engineering, or a related field.  DESIRED:   Domain knowledge in Positive Train Control or Locomotive domain.   Good understanding of IBM test management tools.   Exposure to Eclipse/PyCharm.Our Commitment to Embrace Diversity: Wabtec is a global company that invests not just in our products, but also our people by embracing diversity and inclusion. We care about our relationships with our employees and take pride in celebrating the variety of experiences, expertise, and backgrounds that bring us together. At Wabtec, we aspire to create a place where we all belong and where diversity is welcomed and appreciated.   To fulfill that commitment, we rely on a culture of leadership, diversity, and inclusion. We aim to employ the world’s brightest minds to help us create a limitless source of ideas and opportunities. We have created a space where everyone is given the opportunity to contribute based on their individual experiences and perspectives and recognize that these differences and diverse perspectives make us better.We believe in hiring talented people of varied backgrounds, experiences, and styles… People like you! Wabtec Corporation is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or expression, or protected Veteran status. If you have a disability or special need that requires accommodation, please let us know.Who are we? Wabtec Corporation is a leading global provider of equipment, systems, digital solutions, and value-added services for freight and transit rail as well as the mining, marine, and industrial markets. Drawing on nearly four centuries of collective experience across Wabtec, GE Transportation, and Faiveley Transport, the company has grown to become One Wabtec, with unmatched digital expertise, technological innovation, and world-class manufacturing and services, enabling the digital-rail-and-transit ecosystems.Wabtec is focused on performance that drives progress and unlocks our customers’ potential by delivering innovative and lasting transportation solutions that move and improve the world. We are lifelong learners obsessed with making things better to drive exceptional results. Wabtec has approximately 27K employees in facilities throughout the world. Visit our website to learn more! <a href="http://www.WabtecCorp.com" rel="noopener noreferrer" target="_blank">http://www.WabtecCorp.com</a>Our Commitment to Embrace Diversity:Wabtec is a global company that invests not just in our products, but also our people by embracing diversity and inclusion. We care about our relationships with our employees and take pride in celebrating the variety of experiences, expertise, and backgrounds that bring us together. At Wabtec, we aspire to create a place where we all belong and where diversity is welcomed and appreciated.  To fulfill that commitment, we rely on a culture of leadership, diversity, and inclusion. We aim to employ the world’s brightest minds to help us create a limitless source of ideas and opportunities. We have created a space where everyone is given the opportunity to contribute based on their individual experiences and perspectives and recognize that these differences and diverse perspectives make us better.We believe in hiring talented people of varied backgrounds, experiences, and styles… People like you! Wabtec Corporation is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or expression, or protected Veteran status. If you have a disability or special need that requires accommodation, please let us know.<h4>Experience Level</h4>Senior Level

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