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Quality Assurance LeadProject Role : Quality Assurance Lead Project Role Description : Develop and maintain quality processes and conduct reviews working with global QA initiatives and processes. Must have skills : Microsoft Dynamics 365 Supply Chain Management Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary: 
As a Quality Assurance Lead, you will be responsible for developing and maintaining quality processes, conducting reviews, and collaborating with global QA initiatives and processes. You will play a crucial role in ensuring quality standards are met across the organization.
 
Roles &amp; Responsibilities: 
- Expected to be an SME.
- Collaborate and manage the team to perform.
- Responsible for team decisions.
- Engage with multiple teams and contribute on key decisions.
- Provide solutions to problems for their immediate team and across multiple teams.
- Lead and oversee quality assurance activities within the organization.
- Develop and implement quality assurance policies and procedures.
- Conduct regular quality audits and ensure compliance with regulatory standards.
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in Microsoft Dynamics 365 Supply Chain Management.
- Strong understanding of quality assurance principles and practices.
- Experience in developing and implementing quality assurance processes.
- Knowledge of regulatory standards and compliance requirements.
- Good To Have Skills: Experience with quality management tools and software.
 
Additional Information: 
- The candidate should have a minimum of 5 years of experience in Microsoft Dynamics 365 Supply Chain Management.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.

Accenture India Private Limited

Quality Assurance Associate

Professional, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleProfessional, Quality Assurance EngineeringProfessional, Test Engineer (Manual + Automation )What does a Test engineer do at Fiserv?As an experienced member of our Payment Exchange Testing Team, you will own Requirement Analysis, Test Case Design and Manual Testing, Automation script preparation of our Product. What You Will Do:<ul><li>Your Primary responsibility would be to independently Test or prepare automated test scripts for the assignments and maintain highest degree of quality for all deliverables. </li><li>Provide estimations for analysis, design, manual testing, and automation script preparation of application functionality for the assignment.</li><li>Requirement Understanding through different source of information/documents available with the team.</li><li>Perform QA activities for manual as well as automation testing - execute, maintain &amp; enhance the existing and new automation test suite.</li><li>Conduct peer reviews of test conditions/test cases/test data requirement by testers and follow up to close the review comments.</li><li>Applying innovative concepts in testing to enhance the test coverage, improve quality and reliability.</li><li>Refine the requirements with BA during the grooming calls.</li><li>Learning the best practices and the methodology used in the program and adhere to the standards.</li><li>Provide L3 support as and when necessary for production issues. Analyze production issues, reproduce them in lower environments and provide data points and patterns to the technical team and help provide short-term and long-term fix and help the client support team in the whole process.</li><li>Mentor/train existing and new team members.</li><li>Identify and collaborate with all necessary stakeholders to reach agreement in accordance with defined project goals with little to no assistance.</li><li>Track progress against assigned tasks, report status, and proactively identify issues and report to the Product Owners, Architects and Management team.</li><li>Work successfully in a team environment and demonstrate a willingness to help team members in achieving their project goals if required.</li><li>Ownership and accountability for delivering assigned tasks and deliverables within the established schedule.</li></ul>What You Will Need to Have:<ul><li>Minimum of 4+ years of experience as a QA with minimum 2+ years of experience in automated testing.</li><li>Good understanding of Software Test Lifecycle including Test Strategy, Test Planning, Test Case Design, Test Data Setup, Defect Management and Test Log, Test results, Test Traceability Matrix and Test Metrics Screening and validation of application through database and system logs.</li><li>Technical Skillset required –<ul><li>Strong Knowledge on Selenium, TestNG, SQL Server</li><li>Knowledge of .Net or Java would help</li><li>Strong knowledge of Agile processes &amp; tools associated with it, such as – JIRA, Git hub, Jenkins.</li><li>Very good understanding of security aspect for an application or project.</li><li>Need to have good debugging and problem-solving skills.</li><li>Should have good understanding of Framework and able to understand complex Architectural aspects.</li><li>Experience in integrating to third party applications.</li></ul></li><li>Require minimal supervision, is a fast learner and a team player</li><li>Hands on experience on black box testing</li><li>Understanding of application interfaces, xml, security etc,</li><li>Must have good written and verbal communication skills. </li><li>Must have an experience in retail banking domain.</li><li>Creative thinking and good problem-solving skills</li></ul>What Would Be Great to Have:<ul><li>Handson experience on CI\CD tools like Jenkins/Harness and GitHub.</li><li>Hands on experience in coding Automation framework using programming language like C# or Java.</li><li>Knowledge of Payments domain.</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>Mid Level

Fiserv India Pvt Ltd

Quality Assurance Specialist

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

QA Engineer

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

Astrazeneca India Private Limited

Quality Manager

Quality Analyst II<h4>Who we are</h4>
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.<h4>How you’ll spend your day</h4><ul><li>In-depth knowledge of pharmaceutical quality and quality systems, with broad experience and exposure to best practices</li><li>Knowledge of cGxP requirements, Quality related IT applications, and computer system validation and deployment</li><li>Demonstrated experience with managing complex activities</li><li>Must have international experience and experience working with large cross-functional teams </li><li>Technical knowledge and expertise with Quality Management computer systems including Electronic Document Management Systems (EDMS)and Quality Management Systems (QMS) and processes (such as deviations, CAPA, laboratory investigations, complaints, trends, change control, document management, notification to health authorities, notification to Management, etc.).</li><li>Skilled with Excel, Word, PowerPoint, MS Project and SharePoint</li><li>Demonstrates resourcefulness and initiative and creates an appropriate level of urgency to meet objectives and deadlines</li><li>Fluent in English</li><li>Verbal and written communication excellence required</li><li>Veeva Quality system knowledge a plus</li></ul><h4>Your experience and qualifications</h4><ul><li>Bachelors in Science is required and advanced degree preferred in science/regulatory/computer science/management field </li><li>Minimum of 5-7 years in pharmaceutical or related industry is required</li></ul><h4>Already Working @TEVA?</h4>If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: <a href="https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P"> Internal Career Site </a>The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.<h4>Teva’s Equal Employment Opportunity Commitment</h4>
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.<h4>Experience Level</h4>Senior Level

Teva Pharmaceuticals

Quality Analyst

Advisor, 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 TitleAdvisor, Quality Assurance EngineeringAbout your role: As a Quality Assurance Engineering - Advisor I, you will play a critical role in ensuring the highest standards of quality and performance for our software products. Your in-depth expertise will help shape the quality assurance processes and frameworks, ensuring that our solutions are reliable and meet the needs of our clients. You will work closely with development and product teams, identifying issues and implementing best practices to drive continuous improvements in our QA operations. This role offers the opportunity to make a significant impact on the quality of our products and the overall user experience.What you'll do:<ul><li>Lead the execution of detailed quality assurance testing for complex software products.</li><li>Develop and implement comprehensive test strategies and plans.</li><li>Identify, report, and track software defects to resolution.</li><li>Collaborate with development and product teams to improve quality practices.</li><li>Mentor and guide junior QA team members to ensure adherence to best practices.</li><li>Participate in continuous improvement initiatives within the QA team.</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>6+ years of experience in software quality assurance</li><li>3+ years of experience in automation testing</li><li>3+ years of experience in performance testing</li><li>3+ years of experience in Agile methodologies</li><li>6+ years of an equivalent combination of educational background, related experience, and/or military experience</li></ul>Experience that would be great to have:<ul><li>Experience with automated testing tools</li><li>Knowledge of continuous integration and continuous deployment (CI/CD) tools</li><li>Familiarity with security testing practices</li><li>Understanding of software development lifecycles</li><li>Certification in software testing methodologies</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.<h4>Experience Level</h4>Senior Level

Quality Assurance Officer

Quality Assurance Engineer, Aladdin Engineering, AnalystAbout this roleAre you interested in building innovative technology that crafts the financial markets? Do you like working at the speed of a startup, and solving some of the world’s most exciting challenges? Do you want to work with, and learn from, hands-on leaders in technology and finance? At BlackRock, we are looking for Software Engineers who like to innovate and solve sophisticated problems. We recognize that strength comes from diversity, and will embrace your outstanding skills, curiosity, and passion while giving you the opportunity to grow technically and as an individual. We invest and protect over $9 trillion (USD) of assets and have an extraordinary responsibility to our clients all over the world. Our technology empowers millions of investors to save for retirement, pay for college, buy a home, and improve their financial well-being. Being a technologist at BlackRock means you get the best of both worlds: working for one of the most sophisticated financial companies and being part of a software development team responsible for next generation technology and solutions.  What are Aladdin and Aladdin Engineering? You will be working on BlackRock's investment operating system called Aladdin. Aladdin is used both internally within BlackRock and externally by many financial institutions. Aladdin combines sophisticated risk analytics with comprehensive portfolio management, trading, and operations tools on a single platform to power informed decision-making and create a connective tissue for thousands of users investing worldwide. Our Quality Assurance teams reside inside the Aladdin Engineering group. We collaboratively build the next generation of technology that changes the way information, people, and technology intersect for global investment firms. We build and package tools that manage trillions in assets and supports millions of financial instruments. We perform risk calculations and process millions of transactions for thousands of users every day worldwide!  Being a member of Aladdin Engineering, you will be: <ul><li>Tenacious: Work in a fast paced and highly complex environment </li></ul><ul><li>Resourceful problem solver: Analyze multiple solutions and deploy technologies in a flexible way. </li></ul><ul><li>Great teammate: Think and work collaboratively and communicate effectively. </li></ul><ul><li>Fast learner: Pick up new concepts and apply them quickly. </li></ul>Job Purpose / Background: Aladdin Private Markets Quality Engineering is a globally distributed team supporting Quality Engineering initiatives for Apps on Aladdin. The team employs use of industry-leading tools (Selenium, Cypress, Cucumber, Jenkins, Azure dev ops) to support the testing activities. As a QA Engineer you will work as part of the Global testing team supporting Quality Engineering activities for applications on the Aladdin platform.  Responsibilities include: <ul><li>Guide and mentor junior team members from both technical and functional standpoint. Foster a culture of continuous improvement and accountability within the team. </li></ul><ul><li>Being hands-on and owning functional deliveries. </li></ul><ul><li>Apply expertise in Java Script, Performance Testing tool (JMeter), or other test frameworks to design, develop and maintain performance test suites. </li></ul><ul><li>Responsible for managing comprehensive testing phases from planning to execution for functional and non-functional requirements including design, development, and delivery. </li></ul><ul><li>Work closely with collaborators, customers, partners, and team members to capture client needs, provide design insights, and deliver outstanding work. </li></ul><ul><li>Analyze and report on QA metrics, trends, and opportunities for improvement, presenting findings to senior management and recommending corrective actions. </li></ul><ul><li>Champion a culture of quality within the organization, driving awareness and consistency with Quality standards. </li></ul><ul><li>Prioritize and develop enhancements to continuously improve application stability and scalability. </li></ul><ul><li>Conduct reviews of applications and workflow processes to target automation effectiveness. </li></ul><ul><li>Drive a strong culture by bringing principles of inclusion and diversity to the team and setting the tone through specific recruiting, management actions and employee engagement. </li></ul>Qualifications: <ul><li>B.E. / B.Tech. MCA degree in Computer Science, Engineering, or a related subject area or its equivalent </li></ul><ul><li>1-3 years of proven experience </li></ul>Skills and Experience: <ul><li>Experience in senior QA role within the financial services industry, ideally in asset management. Deep understanding of investment management processes, risk management methodologies, regulatory compliance requirements or Investment Accounting skills. </li></ul><ul><li>Hands on Performance Testing experience (3+ years) using tools like JMeter </li></ul><ul><li>Good understanding of performance test frameworks, tools, and scripting languages along with strong analytical and problem-solving skills to address complex issues. </li></ul><ul><li>Consistent record of successfully leading and implementing QA programs that drive continuous improvement. </li></ul><ul><li>Comprehensive understanding of software quality assurance and engineering processes, methodologies, and proven methods. Good understanding of Agile software development methodologies. </li></ul><ul><li>Excellent communication, interpersonal and leadership skills, with the ability to influence and collaborate effectively across diverse teams. </li></ul><ul><li>Strong foundation in RDBMS, SQL and application infrastructure technologies, performance testing tools &amp; methodologies (JMeter or other), API testing for handling complex distributed systems. </li></ul><ul><li>Self-motivator, that looks for challenges and rolls up their sleeves to identify and understand the core issues and works closely with all levels and across teams to implement solutions. </li></ul>Nice to have and opportunities to learn: <ul><li>Experience of working in Agile Development Team </li></ul><ul><li>AZURE Dev Ops, CI/CD integration and associated tools and processes (Jenkins, Maven, SonarQube). </li></ul><ul><li>AI and Machine Learning (ChatGPT or GitHub CoPilot) </li></ul><ul><li>Specflow/Cucumber and BDD </li></ul><ul><li>Cloud based testing. </li></ul><ul><li>API testing (Postman, Soap UI) </li></ul>Our benefits To help you stay energized, engaged and inspired, we offer a wide range of benefits including a strong retirement plan, tuition reimbursement, comprehensive healthcare, support for working parents and Flexible Time Off (FTO) so you can relax, recharge and be there for the people you care about.Our hybrid work modelBlackRock’s hybrid work model is designed to enable a culture of collaboration and apprenticeship that enriches the experience of our employees, while supporting flexibility for all. Employees are currently required to work at least 4 days in the office per week, with the flexibility to work from home 1 day a week. Some business groups may require more time in the office due to their roles and responsibilities. We remain focused on increasing the impactful moments that arise when we work together in person – aligned with our commitment to performance and innovation. As a new joiner, you can count on this hybrid model to accelerate your learning and onboarding experience here at BlackRock.About BlackRockAt BlackRock, we are all connected by one mission: to help more and more people experience financial well-being.  Our clients, and the people they serve, are saving for retirement, paying for their children’s educations, buying homes and starting businesses. Their investments also help to strengthen the global economy: support businesses small and large; finance infrastructure projects that connect and power cities; and facilitate innovations that drive progress.This mission would not be possible without our smartest investment – the one we make in our employees. It’s why we’re dedicated to creating an environment where our colleagues feel welcomed, valued and supported with networks, benefits and development opportunities to help them thrive.For additional information on BlackRock, please visit <a href="http://careers.blackrock.com/" rel="noopener noreferrer" target="_blank">@blackrock</a> | Twitter: <a href="https://twitter.com/blackrock" rel="noopener noreferrer" target="_blank">@blackrock</a> | LinkedIn: <a href="http://www.linkedin.com/company/blackrock" rel="noopener noreferrer" target="_blank">www.linkedin.com/company/blackrock</a>BlackRock is proud to be an Equal Opportunity Employer.  We evaluate qualified applicants without regard to age, disability, family status, gender identity, race, religion, sex, sexual orientation and other protected attributes at law.<h4>Experience Level</h4>Mid Level

BlackRock Services India Pvt Ltd

Quality Assurance Engineer

ISO Quality & Performance AnalystNTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now.We are currently hiring for Quality &amp; Performance Analyst to join our team in Bangalore or Noida locations. This role demands expertise in ISO and CMMI standards, Internal Audits, Metrics Analysis, Statistical Analysis, Reporting, Quality Consultation and Effective Communication, Key Responsibilities<ul><li>Planning: Process definition and implementation of QMS across projects.</li><li>Audit: Conduct internal process audits to assess the functioning and process compliance, support for external audit.</li><li>Support: Assists in coordinating with relevant groups for continuous refining and improving of processes.</li><li>Performance Metrics: Collating, monitoring and analysing performance by gathering relevant data and contribute to organizational metrics.</li><li>Project Lifecycle: actively involve in projects meetings and analyse feedback obtained from Customer.</li><li>Quality Improvement: Identify areas for improvement and implement best practices to enhance product and service quality.</li><li>Reporting: Prepare and present detailed reports on quality metrics, project progress, and outcomes to senior management.</li><li>Innovation: Stay updated with the latest trends and technologies in quality management and integrate innovative solutions into the company's processes.</li><li>Good to have: knowledge on CMMI model, Six Sigma, ISO 9001, ISO 27001, ISO 20K standard implementation.</li></ul><h4>Experience Level</h4>Mid Level

NTT DATA Global Delivery Services Ltd

Quality Engineer (Tester)Project Role : Quality Engineer (Tester) Project Role Description : Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process. Must have skills : TOSCA Testsuite Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary: 
As a Quality Engineer, you will enable full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Your typical day will involve engaging with various teams to ensure that testing processes are efficient and effective, while also focusing on continuous improvement and automation strategies. You will be responsible for creating automated scripts and supporting data and environment configuration, ensuring that the quality of applications meets the highest standards throughout their lifecycle.
 
Roles &amp; Responsibilities: 
- Expected to perform independently and become an SME.
- Required active participation/contribution in team discussions.
- Contribute in providing solutions to work related problems.
- Assist in the development and implementation of testing strategies to enhance the quality assurance process.
- Collaborate with cross-functional teams to identify and resolve defects in a timely manner.
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in TOSCA Testsuite.
- Experience with test automation frameworks and tools.
- Strong understanding of software testing methodologies and best practices.
- Ability to analyze requirements and create comprehensive test plans.
- Familiarity with continuous integration and continuous deployment processes.
 
Additional Information: 
- The candidate should have minimum 3 years of experience in TOSCA Testsuite.
- This position is based at our Pune office.
- A 15 years full time education is required.

Quality Engineer

Quality SpecialistWe help the world run better At SAP, we enable you to bring out your best. Our company culture is focused on collaboration and a shared passion to help the world run better. How? We focus every day on building the foundation for tomorrow and creating a workplace that embraces differences, values flexibility, and is aligned to our purpose-driven and future-focused work. We offer a highly collaborative, caring team environment with a strong focus on learning and development, recognition for your individual contributions, and a variety of benefit options for you to choose from.WHAT YOU'LL DOAs a Quality Assurance Specialist, you will play a key role in ensuring the successful delivery of high-quality software products by supporting test planning, execution, and defect analysis. You will work closely with development and product teams in an agile environment to maintain testing standards and contribute to continuous improvement initiatives.You will in addition contribute to a compliant delivery of the artefacts built in the programs following established delivery processes.· Experience working in agile/scrum mode and adapt test plans to evolving project needs.· Assist in defining and executing manual and automated test plans.· Use test management tools (e.g., JIRA with xRay or GTP) and bug tracking systems to manage test cycles and report issues.· Monitor and evaluate test results, identifying risks and areas requiring corrective action.· Collaborate with developers and analysts to perform root cause analysis of defects.· Support integration testing and CI/CD pipeline executions.· Maintain compliance with SAP’s product framework and applicable ISO standards.· Contribute to quality documentation and test reporting to support release decisions.· Contribute to the compliant delivery of developed artefacts to customers following established delivery processes. This includes monitoring of the delivery backlogs and the completeness of functional and non-functional requirements.· Support project members and management regarding the delivery status and the release decision meetings. WHAT YOU BRING· 3–5 years of experience in software testing or quality assurance.· Working knowledge of test management and bug tracking tools (JIRA, xRay, GTP).· Experience working in agile development environments.· Understanding of ISO and corporate compliance standards (preferred).· Strong analytical and problem-solving skills.· Good communication and documentation abilities.MEET YOUR TEAMOur team is delivering a single platform to simplify our customers’ data management, analytics, planning and AI needs. We establish data engineering workloads on top of critical SAP business applications through semantically unified data access across the SAP portfolio and Databricks. Finally, we enable our customers to unlock the value of all this data with unique Apps directly integrated to the data stack. ​Bring out your bestSAP innovations help more than four hundred thousand customers worldwide work together more efficiently and use business insight more effectively. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-end business application software and related services for database, analytics, intelligent technologies, and experience management. As a cloud company with two hundred million users and more than one hundred thousand employees worldwide, we are purpose-driven and future-focused, with a highly collaborative team ethic and commitment to personal development. Whether connecting global industries, people, or platforms, we help ensure every challenge gets the solution it deserves. At SAP, you can bring out your best.We win with inclusionSAP’s culture of inclusion, focus on health and well-being, and flexible working models help ensure that everyone – regardless of background – feels included and can run at their best. At SAP, we believe we are made stronger by the unique capabilities and qualities that each person brings to our company, and we invest in our employees to inspire confidence and help everyone realize their full potential. We ultimately believe in unleashing all talent and creating a better and more equitable world. SAP is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to the values of Equal Employment Opportunity and provide accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with SAP and are in need of accommodation or special assistance to navigate our website or to complete your application, please send an e-mail with your request to Recruiting Operations Team: Careers@sap.com For SAP employees: Only permanent roles are eligible for the SAP Employee Referral Program, according to the eligibility rules set in the <a href="https://one.int.sap/me@sap/jobs_at_sap#17498858-1050-415e-8d82-21f91655666b_96fc">SAP Referral Policy</a>. Specific conditions may apply for roles in Vocational Training.EOE AA M/F/Vet/Disability:Qualified applicants will receive consideration for employment without regard to their age, race, religion, national origin, ethnicity, age, gender (including pregnancy, childbirth, et al), sexual orientation, gender identity or expression, protected veteran status, or disability. Successful candidates might be required to undergo a background verification with an external vendor.Requisition ID: 427047  | Work Area: Software-Quality Assurance  | Expected Travel: 0 - 10%  | Career Status: Professional  | Employment Type: Regular Full Time   | Additional Locations: #LI-Hybrid.<h4>Experience Level</h4>Mid Level

Sap India Private Limited

Quality Specialist II<h4>Who we are</h4>
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.<h4>The opportunity</h4>This incumbent<ul><li>Ensures that the review of CMC documentation is completed in timely &amp; compliant manner as per Teva CORP standards and related Guidance’s.</li><li>Review of Method Development/Validation Protocols &amp; Reports, Stability Protocols &amp; Reports received from various Teva contracting sites, R&amp;D units, Method Development &amp; Stability Testing Centres.</li><li>Review of Instrument/Equipment Qualification records.</li><li>Review of BMR.</li><li>Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva’s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance.</li><li>Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system</li><li>Liaising with third party contract manufacturers and QA/QC/Technical support personnel located globally for data collection and arranging responses.</li><li>Recommend actions and professionally communicate to sites/ Quality units for continuous improvement in quality of products Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, other Managers in Quality Strategy &amp; Shared Services, EMSO Quality affiliates, Commercial Quality EU &amp; IM, TGO sites</li></ul><h4>How you’ll spend your day</h4><ol><li>Review of CMC Documentation</li></ol><ul><li>Review of Method Development / Validation protocols &amp; reports.</li><li>Review of Stability Study protocol, reports &amp; grids.</li><li>Review of Instrument / Equipment Qualification records.</li><li>Review of Batch Manufacturing Records.</li><li>Liaising with contracting Teva units and QA/QC personnels located globally for arranging required documents and query responses.</li><li>Escalation of issues to Supervisor, Group Leader, Manager Global Quality GBS.</li><li>Contemporaneous updation of SharePoint data base</li></ul><ol start="2"><li>Data requesting and Compilation of PQR’s</li></ol><ul><li>Compilation of high-quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and systems</li><li>Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs.</li><li>Follow up with the CMO‘s for the receipt of data within time.</li><li>Check quotation received from CMO and initiate PR/PO for QP’s approval.</li><li>Once the data is received responsible for filling the PQR receipt checklist and scheduling the PQR in SharePoint.</li><li>Escalation of PQR issues to Supervisor, Group Leader, Manager PQR Centre.</li><li>Contemporaneous updation of SharePoint data base</li></ul><ol start="3"><li>Quality Management Systems</li></ol><ul><li>Initiate the process of change controls and deviations</li><li>Preparation of local SOP’s and its related documents.</li><li>Participate in self-inspection process</li></ul><ol start="4"><li>Performance Management</li></ol><ul><li>Participate in continuous process improvement projects to improve efficiency of the unit</li></ul><ol start="5"><li>Training</li></ol><ul><li>Prepare the Training Materials for GMP training and on the job training.</li><li>Imparts training on procedures as needed.</li></ul><ol start="6"><li>Miscellaneous Support</li></ol><ul><li>Any other tasks assigned by the management for smooth functioning of the team</li></ul><h4>Your experience and qualifications</h4><ul><li>2 to 8 years of experience in QA / QC function in the pharmaceutical industry</li><li>Master’s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences</li><li>Basic knowledge on worldwide cGxP regulations</li><li>Good English language skills, other language skills could be helpful</li><li>Good communication skills</li><li>Basic knowledge of Computerised Systems. Knowledge of Systems in TEVA´s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya etc.) would be of advantage</li><li>Basic understanding of manufacturing, QC and Contract manufacturing processes</li><li>Engagement to drive improvements and ability to manage complexity</li><li>Hands-on experience on Analytical Method development, Method Validation for API and FP of different analytical methods (e.g. Assay, impurities, dissolution etc.) &amp; Stability Studies.</li><li>Hands-on experience on Review of Instrument/Equipment qualification records.</li><li>Basic knowledge / hands on experience of review of BMR.</li><li>Basic knowledge / hands on experience on Product Quality Reviews.</li></ul><h4>Teva’s Equal Employment Opportunity Commitment</h4>
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Quality Specialist

Junior Manager-PSV Quality
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>Preparation, review and reporting of process and cleaning validation studies, APQRs &amp; trending. Review of equipment/ support system qualifactions, calibrations and production support activities.<h4>Job Responsibilities</h4> <ul><li>Validation studies.</li><li>Preparation of Annual quality product review &amp; Cleaning verification periodic review ..</li><li>Review of the excuted BPCR's /GCR's and Manufactiring related documentation support.</li><li>Supporting and co-ordinating for dispatch activities.</li><li>To perform the SAP related activities.</li><li>To perform viable sampling for environmental monitoring activities.</li><li>Preparation of trending reports for key starting materilas, intermediates and finished products.</li><li>Performing daily production activities like plant rounds, equipment visual cleaning clearance &amp; RMDC release.</li><li>Preparation and revision of the Departmental SOP's, Form's and exhibits.</li><li>Monitoring of the cGMP compliance through Plant rounds.</li><li>Documentation &amp; issuance activities.</li><li>To perform unannounced audits.</li><li>To review and take retained sample area temperature printouts.</li><li>Review of alarm summary and audit trail report in data logging system (PiSCADA).</li><li>Handling eResidue pro application.</li><li>Preparatoin of quality risk assessment reports and other related activities.</li><li>Preparation of validation master plan and exhibits.</li><li>Handling of QMS activities in trackwise (change control).</li><li>Review of equipment/ support system qualification documents.</li><li>Review of calibration certificate and monitoring of preventive maintanace activities.</li><li>Preparation of Quality trending documents for OM water, environmental monitoring and nitrogen trending etc.</li><li>To co-ordinate with the manufacturing team to address any Quality issues arises during manufacturing.</li><li>To adhere the EHS policy &amp; procedure in routine activities.</li><li>To involve in EHS related activities on need basis.</li><li>Works in a safe manner collaborating as a team member to achieve all outcomes.</li><li>Demonstrate behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance and Passion.</li><li>Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.</li><li>All other relevant duties as assigned.</li></ul><h4>Job Requirements</h4><ul><li>Education
<ul><li>Minimum Masters Degree in Science /Pharmacy </li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Knowledge of Relevant procedure and applicable regulatory guidelins.</li><li>Knowledge of cGMP activities.</li><li>Knowledge on API Manufacturing activity.</li><li>Knowledge on relavent applications. </li></ul></li><li>Experience:<ul><li>9.0 years of experience in Quality Assurance &amp; Compliance functions.</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>Entry Level

Apotex Pharmachem India Pvt Ltd

Quality Head

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 TPM QA     <h4>JOB DESCRIPTION:</h4>MAIN PURPOSE OF ROLEJob Responsibilities:<ul><li>Third Party Manufacturing (TPM) Site Compliance:<ul><li>Perform regular and ad-hoc visits to TPM facilities across the West Zone to evaluate compliance with current Good Manufacturing Practices (cGMP) primarily Revised Schedule M, Abbott’s internal quality standards, and applicable regulatory guidelines.</li><li>Identify non-conformities, process inefficiencies, and documentation gaps during site inspections.</li><li>Collaborate with TPM quality teams to develop robust corrective and preventive action (CAPA) plans.</li><li>Monitor CAPA implementation timelines and effectiveness through follow-up visits and reviews.</li></ul></li><li>Audit CAPA Oversight:<ul><li>Review audit findings from TPM sites and ensure timely development and implementation of CAPAs.</li><li>Track CAPA progress and verify effectiveness through follow-up assessments.</li><li>Maintain accurate CAPA documentation in line with Abbott’s quality systems and regulatory standards.</li><li>Coordinate with TPMs and internal teams to resolve recurring issues and drive systemic improvements.</li><li>Support audit readiness by reviewing CAPA histories and preparing TPMs for inspections.</li><li>Use digital tools (e.g., SolTraqs) to create Auditee records, manage CAPA workflows and ensure timely updates whenever necessary.</li></ul></li><li>Market Complaint Investigation:<ul><li>Receive and document product complaints from the market in compliance systems.</li><li>Lead or support investigations to identify root causes using structured problem-solving tools.</li><li>Coordinate with TPMs and internal teams to define and implement CAPAs.</li><li>Ensure timely resolution and closure of complaints with proper documentation.</li><li>Analyze complaint trends to identify recurring issues and recommend preventive actions.</li><li>Support Abbott audits by maintaining accurate complaint records and summaries.</li><li>Assess product impact and recommend actions such as holds or recalls if necessary.</li></ul></li><li>QMS: <ul><li>Quality Risk Assessment:<ul><li>Conduct risk assessments for identified issues, deviations, or changes in manufacturing processes.</li><li>Recommend mitigation strategies and escalate critical risks to senior management when necessary.</li></ul></li><li>Change Control, Deviation, OOS Management:<ul><li>Evaluate change control proposals and deviation / OOS reports from TPMs.</li><li>Ensure changes are scientifically justified, risk-assessed, and compliant with regulatory and internal standards.</li></ul></li><li>Trackwise Task Management:<ul><li>Initiate Exception Reports, Planned deviations</li><li>Manage CAPA tasks associated with ER, PD, Market Complaints and on time closure.</li><li>Tracking and closure of ageing documents impacting metrics.</li><li>Approve and manage artwork-related tasks within the Trackwise system</li></ul></li></ul></li><li>Stability Data &amp; Control Sample Review:<ul><li>Analyze stability study data and control samples to ensure product quality over shelf life.</li><li>Provide recommendations for shelf life extensions or product improvements based on data trends.</li></ul></li><li>Performance Scorecard Tracking:<ul><li>Maintain and update performance scorecards for TPMs in the West Zone.</li><li>Use scorecards to monitor quality metrics, identify trends, and drive continuous improvement initiatives.</li></ul></li><li>Compendial Change Compliance:<ul><li>Track updates in pharmacopeial standards and ensure timely implementation across relevant products.</li><li>Liaise with regulatory and formulation teams to assess impact and ensure compliance.</li></ul></li><li>Shelf Life Extension Projects:<ul><li>Coordinate with formulation, regulatory, and quality teams to evaluate and implement shelf life extension strategies.</li><li>Ensure documentation and regulatory submissions are completed accurately.</li></ul></li><li>Artwork Review &amp; Approval:<ul><li>Review and approve product artworks for new and existing products, ensuring compliance with regulatory and branding guidelines.</li><li>Collaborate with PLM, I&amp;D, and global teams to manage artwork lifecycle and changes.</li></ul></li><li>Export Barcode &amp; Global Artwork Management:<ul><li>Review and approve export barcodes and artworks received from global teams for India region products.</li><li>Ensure accuracy and compliance with international packaging and labeling standards.</li><li>Ensure timely execution and documentation of all assigned tasks.</li></ul></li><li>Project Support &amp; Cross-Functional Collaboration:<ul><li>Support quality-related projects assigned by the Manager, including process improvements, system upgrades, and regulatory initiatives.</li><li>Collaborate with internal and external stakeholders to ensure project goals are met efficiently.</li></ul></li><li>New Product Introduction / Technology Transfer<ul><li>Knowledge Transfer: Receive and assimilate new products approved by Innovation &amp; Development (I&amp;D) or New Product Introduction (NPI) teams as part of the pre-commercialization process at TPM.</li><li>Product Lifecycle Understanding: Possess comprehensive knowledge of the product lifecycle—from development through to commercialization.</li><li>Post-Approval Change Management: Effectively manage and implement changes to products after regulatory or internal approval.</li></ul></li></ul>Skill, Education, Experience        Education:<ul><li>Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related scientific discipline.</li></ul>Experience:<ul><li>10 - 13 years of progressive experience in pharmaceutical quality assurance, preferably in TPM or contract manufacturing environments.</li><li>In-depth knowledge of Schedule M, GMP, ICH guidelines, regulatory requirements, and quality management systems.</li><li>Strong analytical, communication, and leadership skills with the ability to influence cross-functional teams and TPM’s.</li><li>Experience in handling audits, investigations, and QRM is highly desirable.</li></ul>Skill:<ul><li>Attention to Detail: Critical for reviewing documentation, artworks, and compliance data.</li><li>Analytical Thinking: Required for investigations, risk assessments, and CAPA closure.</li><li>Communication Skills: To coordinate with TPMs, internal teams, and global stakeholders.</li><li>Time Management: For handling multiple reviews, approvals, and project tasks efficiently.</li><li>Adaptability: To manage evolving regulatory requirements and internal process changes.</li><li>Excellent problem-solving skills.</li><li>Ability to handle multiple projects and changing priorities</li><li>Excellent communication skills</li></ul>     The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.     <h4>JOB FAMILY:</h4>Operations Quality     <h4>DIVISION:</h4>EPD Established Pharma        <h4>LOCATION:</h4>India &gt; Mumbai : BKC Building     <h4>ADDITIONAL LOCATIONS:</h4>     <h4>WORK SHIFT:</h4>Standard     <h4>TRAVEL:</h4>Not specified     <h4>MEDICAL SURVEILLANCE:</h4>Not Applicable     <h4>SIGNIFICANT WORK ACTIVITIES:</h4>Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)               <h4>Experience Level</h4>Mid Level

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