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Team Member - Analytical Quality Assurance<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>Job Summary Roles &amp; Responsibilities <ul><li>Review and approval of all analytical test data of Quality control.</li><li>Review and usage decision of analytical reports in LIMS, Empower and SAP.</li><li>Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments.</li><li>Review the Analytical test report in LIMS.</li><li>Review the reported results against specification and trends.</li><li>Review the method validation and method transfer documents.</li><li>Review the instrument calibrations and working standard qualification records.</li><li>Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure.</li><li>Monitoring of analytical activities in Quality control laboratory.</li><li>Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval.</li><li>Verification and review of the audit trails for Standalone, Empower and LIMS.</li><li>Ensure cGMP / cGLP compliance.</li><li>To follow Safety, Health and Environmental procedures and practices.</li><li>Review and approval of excel sheet validations.</li><li>Review results acceptance for API and Excipients and Packing material.</li><li>Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols.</li><li>Handling of Robotic Process Automation of Chromatography Data review (RPACD)</li><li>To carry any other activities assigned by upward reporting staff.</li></ul><h4>Qualifications</h4>Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience: 3 to 7 years of experience in QC or AQA department is mandatory. <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>Entry Level

Dr Reddys Laboratories

Quality Assurance Associate

QA-Officer     <h4>JOB DESCRIPTION:</h4><h4>Main Purpose of the Role</h4><ul><li>Summarize the main purpose of the roleAnalyze quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met.</li></ul><h4>Main Responsibilities</h4><ul><li>List the main responsibilities this role regularly performs.<ul><li>Apply quality principles, analyzes quality records, prepares reports and recommends improvements.</li><li>Conduct inspection, verification and validation of components or materials used in development processes.</li><li>Identify and address recurring problems either with the quality of the product or the reliability of testing procedures.</li><li>Document quality issues and performance measures for management review.</li><li>May liaise with external vendors.</li></ul></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>ANSC Nutrition Supply Chain        <h4>LOCATION:</h4>India &gt; Jhagadia : Operation Support     <h4>ADDITIONAL LOCATIONS:</h4>     <h4>WORK SHIFT:</h4>Standard     <h4>TRAVEL:</h4>Yes, 15 % of the Time     <h4>MEDICAL SURVEILLANCE:</h4>Not Applicable     <h4>SIGNIFICANT WORK ACTIVITIES:</h4>Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)               <h4>Experience Level</h4>Mid Level

Abbott India Ltd

Quality Assurance Officer

Quality Assurance Engineer - CareerEquifax is where you can power your possible. If you want to achieve your true potential, chart new paths, develop new skills, collaborate with bright minds,  and make a meaningful impact, we want to hear from you.What You’ll Do<ul><li>Lead complex testing efforts, estimating time and resources</li><li>Define test environment configuration</li><li>Define test cases outside of user-defined requirements and perform testing of applications, focusing on functional and end-to-end testing, validating that system response and output accurately reflect business requirements as outlined in requirements document</li><li>Recommend changes to existing testing methodologies</li><li>Collaborate with Product Owners and development team to plan and and assist with user acceptance testing</li><li>Identify and resolve test environment issues</li><li>Design, develop and execute automation scripts specifically targeted to test REST API integrations and services using Java and appropriate tools like REST Assured</li></ul>What Experience You Need <ul><li>BS degree in Computer Science or related technical field </li><li>5-7 years of software testing experience</li><li>Able to create and review test cases according to specifications</li><li>Created test strategies and plans</li><li>Led complex testing efforts or projects</li><li>Participated in Sprint Planning as the Test Lead</li><li>Collaborated with Product Owners, SREs, Technical Architects to define testing strategies and plans</li><li>Cloud Certification Strongly Preferred</li><li>Experience in developing automated testcases for web and API </li><li>Experience in performance testing using tools like jmeter </li></ul>What Could Set You ApartRequirements Analysis:Thoroughly review and analyze functional and non-functional requirements, user stories, and design specifications to gain a comprehensive understanding of the system under test.Participate in requirements review meetings and provide valuable feedback from a testing perspective.Identify ambiguities, inconsistencies, and potential testability issues in the requirements.Test Case Design and Development:Design, develop, and maintain well-structured, comprehensive, and reusable test cases and test scenarios based on the analyzed requirements.Create positive, negative, boundary value, and edge case test scenarios to ensure thorough test coverage.Organize and manage test cases effectively using test management tools.Automate the functional and regression test cases for UI /API and integrate with release pipelineTest Execution:Execute test cases meticulously and accurately according to the defined test plans and procedures.Perform various types of testing, including functional testing, integration testing, system testing, regression testing, and usability testing.Document test execution results clearly and concisely, indicating pass/fail status and any deviations from expected behavior.Defect Identification and Reporting:Identify, document, and track software defects with detailed steps to reproduce, expected results, actual results, severity, and priority using defect tracking tools.Participate in defect triage meetings to prioritize and manage the defect lifecycle.Test Bed &amp; Environment Setup:Assist in setting up and configuring test environments as needed.Ensure the test environments are stable and representative of the production environment.Troubleshoot any environment-related issues that may arise during testing. We offer a hybrid work setting, comprehensive compensation and healthcare packages, attractive paid time off, and organizational growth potential through our online learning platform with guided career tracks.Are you ready to power your possible?  Apply today, and get started on a path toward an exciting new career at Equifax, where you can make a difference!Primary Location: IND-Pune-Equifax Analytics-PECFunction: Function - Tech Dev and Client ServicesSchedule: Full time

Equifax Credit Information Services Pvt Ltd

Quality Assurance Engineer

QUALITY ANALYST IAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. <h4>Job Overview</h4>Supports the development and continuous improvement of business quality management systems and facilities.<h4>Job Requirements</h4><ul><li>Assisting in the development and maintenance of quality policies and processes; attending training sessions on quality concepts and tools.</li><li>Assisting in the development and implementation of quality plans, programs, and procedures using quality control statistics, lean manufacturing concepts, and six-sigma tools.</li><li>Working with various teams to facilitate internal and external quality issue resolution.• Working with suppliers to confirm understanding of inspection techniques, and reviewing, analyzing, and reporting on quality discrepancies.</li></ul><h4>What your background should look like</h4>Generally requires Bachelors degree in appropriate field or local equivalent.<h4>Competencies</h4>
Values: Integrity, Accountability, Inclusion, Innovation, TeamworkSkill Set and Profile:•    Hands-on experience in injection molding process, specifically in automotive industry •    Excellent problem solving and analytical Skills •    Knowledge of PPAP, Control plan, FMEA, MSA &amp; SPC •    Demonstrated experience of working in a fast paced and changing environment with tight deadlines •    Knowledge and practical experience of Six sigma Green Belt (Preferrable) •    Knowledge of IATF19649 &amp; ISO 9001 standard requirements •    Strong technical aptitude with willingness to explore &amp; learn new Technologies •    Good English communication along with hands on experience in MS Office tools Compensation   •    Competitive base salary commensurate with experience: $xxx – xxx (subject to change dependent on physical location) •    Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity What TE Connectivity Internship Program offers TE has a robust internship program that provides our interns with an abundance of resources to feel included as part of our Team.  Every summer we coordinate various educational and networking events for our interns. The TE University Relations team will be hosting virtual meetups, information sessions, tours, skill building presentations, and topping it off with National Intern Day celebration activities. A unique employee resource group we have is the Young Professionals Employee Resource Group (ERG). This group is committed to creating a highly engaged and empowered cross-functional network of young professionals by placing high value in Professional Development, Networking Opportunities and Community Involvement to drive the success of our interns. In addition to the ERG, we also provide our interns with complete access to our internal library of self-lead courses. These courses include academies like leadership to help the interns develop their development in becoming future leaders at our organization. To help with their professional growth, we provide access to Mentors via our NAVIGATE platform. Mentors serve as a guide to navigate the organization and provide additional support in their career endeavors at the company. Our program provides a holistic experience for interns that targets professional development and personal growth. Our internship program typically runs May thru August and gives students the opportunity to work on projects that contribute to the success of their team and build on their classroom experience. Throughout the 10–12-week program, interns will be provided with:•            Onboarding &amp; Orientation•            Professional Development Workshops•            Networking Opportunities•            Operations Experience•            Executive Exposur Timeline TE Connectivity recruits on campus between September and March for New Grad (FT), Rotational, Internship and Co-op positions beginning in May. Once you have applied to a position, your resume and application will be reviewed. If you are selected to move to the next step in the application process, you will be contacted by a recruiter. Once you accept an offer, the onboarding process will begin in January for interns who have committed to offers in the fall semester and upon acceptance for interns who have committed to offers in the spring semester.EOE, Including Disability/Vet Important Notice Regarding Recruitment Fraud TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity never requests payment or fees from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come only from actual email addresses ending in @te.com. If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities<h4>Experience Level</h4>Entry Level

TE Connectivity India Pvt Ltd

Quality Analyst

Quality Analyst (TS2)Join us as a Quality Analyst<ul><li>This is an opportunity for a driven individual to take on an exciting new career challenge</li><li>You’ll be able to build and maintain a wide network of stakeholders of varying degrees of seniority</li><li>It’s a chance to have a tangible effect on our function, put your existing skills to the test and advance your career</li><li>We're offering this role at senior analyst level</li></ul><h4>What you'll do</h4>As a Quality Analyst, you'll make sure that only well designed and built work packages get through quality testing, and that the test plans are adequately covered by test scenarios. You'll automate repetitive tests where appropriate to eliminate wasted effort, cost and risk of manual error. You’ll train and knowledge share, and be the quality conscience of the team, assisting them to write and maintain automated tests as a standard way of working.You’ll also:<ul><li>Choose the right set of tools to help the testing and reuse existing tooling, adopting Quality centre of excellence tools where appropriate</li><li>Work in conjunction with quality automation specialists in writing automated tests and analyse the results of the automated tests</li><li>Execute tests on a continuous basis triggered automatically by change events</li><li>Minimise the execution time for the automated tests in order to obtain quick feedback</li><li>Provide metrics to the business and the team that focus on quality and quality improvement</li></ul><h4>The skills you'll need</h4>You'll need an understanding of our current organisation change framework, and proven application of testing methodologies, including a range of Agile testing methods such as test driven development and behaviour driven development. You should also have proven application of a wide range of testing automation tooling, and practical experience of testing ideas, products, designs, planning and execution.You’ll also need:<ul><li>Hands on experience in UI Path RPA Automation tool along with Credit Cards Domain Knowledge is an added Advantage</li><li>Should possess good knowledge in Automation frameworks like Test NG, Cucumber, Keyword Driven and Hybrid</li><li>Should have hands on Experience in Mainframe tools like CA-View, CA7, File AID, JCL, DB2, SQL, CICS, TSYS TS2 , Web &amp; Desktop applications</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>Experience of delivering testing activities in a technology or IT function</li><li>Demonstrable knowledge of Agile methodologies with experience of working in an Agile team</li></ul>Hours45Job Posting Closing Date:23/09/2025

NatWest Group

Executive, Quality Control
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation.<h4>Job Responsibilities</h4><ul><li>To ensure timely completion of analysis and data completion for the same.</li><li>To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems.</li><li>To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and cleaning validation.</li><li>To Prepare Stability Trend Reports for Laboratory samples.</li><li>To collect and maintain various laboratory samples.</li><li>To generate and maintain records related to laboratory samples.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Performs all work in accordance with all established regulatory and compliance and safety requirements.</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.</li><li>To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory.</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 duties as assigned.</li></ul><h4>Job Requirements</h4><ul><li>Education
<ul><li>M.Sc\BPham or any equivalent degree</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Effective command over verbal and written communication with good interpersonal skills.</li><li>Command on Microsoft-Office (Word, Excel).</li><li>Able to prioritize the tasks.</li><li>Best in effective planning of work activities to meet the time lines.</li></ul></li><li>Experience
<ul><li>Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Executive Level

Apotex Pharmachem India Pvt Ltd

Quality Control Executive

Senior Officer, Quality Con-ARPL-QFSA AR
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>Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation.<h4>Job Responsibilities</h4><ul><li>To ensure timely completion of analysis and data completion for the same.</li><li>To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems.</li><li>To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and Cleaning validation.</li><li>To Prepare Stability Trend Reports for Laboratory samples.</li><li>To collect and maintain various laboratory samples.</li><li>To generate and maintain records related to laboratory samples.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Performs all work in accordance with all established regulatory and compliance and safety requirements.</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.</li><li>To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory.</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 duties as assigned.</li></ul><h4>Job Requirements</h4><ul><li>Education
<ul><li>M.Sc\BPham or any equivalent degree</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Effective command over verbal and written communication with good interpersonal skills.</li><li>Command on Microsoft-Office (Word, Excel).</li><li>Able to prioritize the tasks.</li><li>Best in effective planning of work activities to meet the time lines.</li></ul></li><li>Experience
<ul><li>Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Senior Level

Quality Control Supervisor

Quality Assurance Engineer, Aladdin Quality 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.Team Overview<ul><li>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.</li><li>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!</li><li>Being a member of Aladdin Engineering, you will be:</li><li>Tenacious: Work in a fast paced and highly complex environment</li><li>Creative thinker: Analyse multiple solutions and deploy technologies in a flexible way.</li><li>Great teammate: Think and work collaboratively and communicate effectively.</li><li>Fast learner: Pick up new concepts and apply them quickly.</li></ul>Job Purpose / Background:<ul><li>AQE (Aladdin Quality Engineering) is a globally distributed team supporting Quality Engineering initiatives for Apps on Aladdin.</li><li>AQE employs use of industry-leading tools (Selenium, Java, 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.</li></ul>Responsibilities include:<ul><li>1-4 years of work experience in quality assurance/testing is preferred</li><li>Become a Subject Matter Expert on applications &amp; own Quality attestations for sign off on production releases.</li><li>Responsible for functional, non-functional and regression testing activities of a project.</li><li>Design and develop comprehensive test scenarios based on functional and non-functional requirements.</li><li>Apply expertise in Java, Selenium, or other test frameworks to design, develop and maintain automated test suites.</li><li>Identify, document, and track defects in a clear and concise manner.</li><li>Follow Agile model to track and manage sprint tasks using ADO which includes sprint planning, execution, and retrospectives.</li><li>Analyze production Incidents to identify action items for QA and Dev teams to drive Production stability.</li><li>Provide feedback to improve the product quality and contribute to the enhancement of testing processes.</li><li>Effectively communicate testing metrics, progress, schedules, and issues impacting delivery.</li><li>Troubleshoot Application, Environment or Data Issue</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

Dy. Manager / Manager - Quality (APU Quality Leader)Valeo is a tech global company, designing breakthrough solutions to reinvent the mobility. We are an automotive supplier partner to automakers and new mobility actors worldwide. Our vision? Invent a greener and more secured mobility, thanks to solutions focusing on intuitive driving and reducing CO2 emissions. We are leader on our businesses, and recognized as one of the largest global innovative companies.The APU Quality Leader position coordinate Quality members inside the APU, coordinate process and product audit, train and coach the Logical Thinking. This position cannot supersede Site Quality Manager authority. - Initiate the QRQC in QIM database – participate to the containment and validate the robustness of the containment - Support APU Managers / Site Manager in the analysis of issues assigned in the QRQC activities - Update the APU quality tracking charts : Customer Returns - Cost of Non Quality … - Perform audits on the line to detect non-respect of the Standard and identify with the APU the actions to be completed to therefore comply with the Standard - Participate in the eradication of Customer issues and Non Quality issues - Along the APU QRQC meeting ensure that rules are respected and “Stop at first disagree” and “Stop at first no” are applied - Perform the revision of the control plan after an issue - Verify 4M matrix respect with regards product or process changes and ensure customer awareness and approval of changes in accordance with the 4M matrix - Update the quality documents following a process related change - Verify the continuous conformance of the process to generate product to specification in accordance with the control plans (machine capability – yearly product audit …) - Has authority to stop a manufacturing / assembly line in any situation where Standards are not respected or a safety or quality risk for the operator or for the customer has been detected or following a LLC Stability audit demonstrating lower than 100% - Represent Customer within Valeo on Quality matters (communication/Escalation)Job:Quality - Operations OperationalOrganization:ProductionSchedule:Full timeEmployee Status:RegularJob Type:Permanent contractJob Posting Date:2025-08-05Join Us ! Being part of our team, you will join: - one of the largest global innovative companies, with more than 20,000 engineers working in Research &amp; Development - a multi-cultural environment that values diversity and international collaboration - more than 100,000 colleagues in 31 countries... which make a lot of opportunity for career growth - a business highly committed to limiting the environmental impact if its activities and ranked by Corporate Knights as the number one company in the automotive sector in terms of sustainable development More information on Valeo: <a href="https://www.valeo.com/" rel="noopener noreferrer" target="_blank">https://www.valeo.com</a><h4>Experience Level</h4>Senior Level

Valeo India Private Limited

Quality Manager

Test Manager We are currently looking for critical leadership role in our QA team: Test Manager (Hybrid)Experience: 9–12 years in Functional &amp; Automation Testing Key Responsibilities:<ul><li>Lead QA strategy for Agile projects with strong focus on delivery</li><li>Define and manage test plans for manual and automation testing</li><li>Drive automation using Selenium with Java</li><li>Own and execute API and SQL-based back-end testing</li><li>Leverage Python scripting for automation utilities and data handling</li><li>Ensure adoption of test frameworks and best practices</li><li>Integrate test suites into CI/CD (Jenkins, Git)</li><li>Mentor and guide QA teams, report on metrics, and flag risks</li></ul> Required Skills:<ul><li>Strong Selenium + Java automation experience</li><li>Advanced SQL and API testing skills</li><li>Hands-on Python for utilities/test data masking</li><li>Familiarity with Agile methodology and CI/CD tools</li><li>ISTQB Advanced / PMP certifications are a plus!</li></ul>

Ascendion Engineering Private Limited

Test Supervisor

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

Senior Executive – QualityJob Description :Job Title: Senior Executive – QualityAbout the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo’s 30,000+ people work in Supply Chain and Manufacturing. It’s an intricate and sophisticated operation that’s the product of logistical, manufacturing, and technical collaborations.Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We’re committed to realising our ‘Society 2030: Spirit of Progress’ goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we’ll help you to thrive in our inclusive culture.About the team: Description &amp; RequirementsJob Title: Senior Executive – QualityAbout the Function:Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo’s 30,000+ people work in Supply Chain and Manufacturing. It’s an intricate and sophisticated operation that’s the product of logistical, manufacturing, and technical collaborations.Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We’re committed to realising our ‘Society 2030: Spirit of Progress’ goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience, we’ll help you to thrive in our inclusive culture.About the team:Role Responsibilities:Desirable Qualification &amp; Work Experience:<ul><li>Post Graduate calibre or equivalent - preferably in Chemistry/Microbiology/Biochemistry/Biotechnology/Food technology/DIFAT</li><li>3-5 years of experience in the areas of Quality Assurance and Quality Systems on Food Processing / FMCG –Distillery, Brewery and Beverage Industry</li></ul>Good to have Knowledge/Skills/Exposure:<ul><li>Hands on experience and in-depth knowledge of quality management systems, developing quality related SOPs and its control</li><li>Experience in handling quality improvement projects</li><li>Knowledge of Microsoft Office package</li></ul>Best Suited for Someone Who:<ul><li>Excellent coaching, influencing and communication skills</li><li>Good Communication and Presentation skills</li></ul>Flexible Working Statement: Flexibility is key to our success. From part-time and compressed hours to different locations, our people work flexibly in ways to suit them. Talk to us about what flexibility means to you so that you’re supported from day one.Diversity statement: Our purpose is to celebrate life, every day, everywhere. And creating an inclusive culture, where everyone feels valued and that they can belong, is a crucial part of this.We embrace diversity in the broadest possible sense. This means that you’ll be welcomed and celebrated for who you are just by being you. You’ll be part of and help build and champion an inclusive culture that celebrates people of different gender, ethnicity, ability, age, sexual orientation, social class, educational backgrounds, experiences, mindsets, and more.Our ambition is to create the best performing, most trusted and respected consumer products companies in the world. Join us and help transform our business as we take our brands to the next level and build new ones as part of shaping the next generation of celebrations for consumers around the world.Feel inspired? Then this may be the opportunity for you. Worker Type :RegularPrimary Location:Kolkata Unit (Essencia)Additional Locations :Job Posting Start Date : 2025-09-17<h4>Experience Level</h4>Senior Level

Diageo India Pvt Ltd

Quality Specialist

Intern - Controlled Docs CoordinatorFollow applicable departmental Standard Operating Procedures and Work Instructions.  Complete required trainings according to required timelines.  Complete day-to-day tasks ensuring quality and productivity.  Administer controlled documents ensuring availability to the end user.  Maintain inventory of controlled documents.  Perform checks to ensure quality of work completed.  Ensure timely escalation of issues and resolution management impacting controlled document release.  Ensure Regulatory Compliance and Quality Assurance (RC&amp;QA) responsibilities, as indicated in applicable controlled documents, are followed.  Other duties as assigned by management.Labcorp is proud to be an Equal Opportunity Employer:Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to applyIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a href="https://careers.labcorp.com/global/en/accessibility" rel="noopener noreferrer" target="_blank">accessibility site</a> or contact us at <a href="mailto:Disability_apply@LabCorp.com" rel="noopener noreferrer" target="_blank">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a href="https://www.labcorp.com/about/web-privacy-policy" rel="noopener noreferrer" target="_blank">Privacy Statement</a>.<h4>Experience Level</h4>Entry Level

LabCorp

Documentation Officer

Senior Executive, Quality Assurance Operations
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><ul><li>Sampling activity.</li><li>IPQA activities.</li><li>CCR initiation, QA assessment in QMS Track wise.</li><li>SME for Raw material sampling Packing material sampling, Liquid sampler and Tuscan operation.</li></ul> <h4>Job Responsibilities</h4><ul><li>Co-ordination &amp; Ensuring timely execution of Sampling activity of Raw and Packing materials.</li><li>Preparation, Review and updating of standard operating procedure.</li><li>To ensure line clearance for dispensing, sampling and packing activity.</li><li>Routine monitoring of all functional area to ensure adherence to the SOPs.</li><li>Create signature and methods for raw materials by using Truscan RM analyzer.</li><li>Approved / Rejected labels affixing for API, Excipients, Primary packing and secondary packing materials finished goods and operation supplies.</li><li>Verification of Temperature and Relative Humidity reports generated from TESTO software.</li><li>To perform the QMS (change control) activities as per access approvals.</li><li>To perform necessary SAP transaction as per access approvals.</li><li>Review and co-ordination for in-house and external calibration.</li><li>Imparting training &amp; co-ordination for implementation of training activities.</li><li>In-process checks during packing.</li><li>Sampling of Finished products.</li><li>To ensure training completion as required.</li><li>Review of executed batch packing records &amp; logbooks.</li><li>Issuance and verification of packing batch documents.</li><li>Collection of swab sample as applicable.</li><li>Co-ordination for Process validation / cleaning validation.</li><li>Co-ordination for Qualification activities as applicable.</li><li>Preparation for regulatory audits and making the compliance for the same.</li><li>Participate and lead performance conversations with employees, including monthly one on ones, to connect on performance; check in on employee’s progress toward achieving Objectives, offer support and remove barriers; and communicate and revisit performance expectations to reinforce and encourage high performance culture and a safe working environment for all employees.</li><li>Utilize open, honest, two-way communication to build trust-based relationships with employees, business partners and direct leader while continuously improving leadership capabilities by personally seeking feedback and development.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>Utilize your networks to attract and hire talent in a comprehensive, differentiated and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.</li><li>Ensure adherence of team members (direct reports) with all compliance programs and company policies and procedures.</li><li>All other duties as assigned.</li></ul> <h4>Job Requirements</h4><ul><li>Education:
<ul><li>Minimum Bachelor of Pharmacy/ Science or any equivalent degree.</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Should possess good communication and interpersonal skills along with Computer efficacy in MS-Office and Internet.</li><li>Preparation and review of SOP.</li></ul></li><li>Experience
<ul><li>Minimum 6 years’ experience in GMP Regulated Pharmaceutical industry.</li><li>4 to 6 years</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>Senior Level

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Quality Assurance Jobs - 324 Verified Vacancies

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Documentation Officer

Quality Assurance Officer

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