Jobs

Quality Assurance

Anywhere in India

Agra

Ahmedabad

Ahmednagar

Ajmer

Aligarh

Amritsar

Asansol

Aurangabad

Bareilly

Belagavi

Bengaluru

Bhavnagar

Bhilai

Bhopal

Bhubaneswar

Bikaner

Chandigarh

Chennai

Coimbatore

Cuttack

Dehradun

Delhi-NCR

Dhanbad

Gorakhpur

Guntur

Guwahati

Gwalior

Hubli

Hyderabad

Indore

Jabalpur

Jaipur

Jalandhar

Jamnagar

Jamshedpur

Jodhpur

Kannur

Kanpur

Kochi

Kolhapur

Kolkata

Kota

Lucknow

Ludhiana

Madurai

Malappuram

Mangalore

Meerut

Mumbai

Mysuru

Nagpur

Nashik

Panipat

Patna

Prayagraj

Puducherry

Pune

Raipur

Rajkot

Ranchi

Saharanpur

Salem

Solapur

Surat

Thiruvananthapuram

Trichy

Udaipur

Ujjain

Vadodara

Varanasi

Vijayawada

Visakhapatnam

Warangal

Admin / Back Office / Computer Operator

Advertising / Communication

Aviation & Aerospace

Banking / Insurance / Financial Services

Beauty, Fitness & Personal Care

Construction & Site Engineering

Consulting

Content, Editorial & Journalism

CSR & Social Service

Customer Support

Data Science & Analytics

Delivery / Driver / Logistics

Domestic Worker

Energy & Mining

Engineering - Hardware & Networks

Environment Health & Safety

Facility Management

Finance & Accounting

Healthcare / Doctor / Hospital Staff

Human Resources

IT & Information Security

Legal & Regulatory

Maintenance Services

Marketing / Brand / Digital Marketing

Media Production & Entertainment

Operations

Production / Manufacturing / Engineering

Product Management

Project & Program Management

Purchase & Supply Chain

Research & Development

Restaurant / Hospitality / Tourism

Retail & eCommerce

Risk Management & Compliance

Sales & BD

Security Services

Shipping & Maritime

Software Engineering

Strategic & Top Management

Tailoring, Apparel & Home Furnishing

Teaching & Training

UX, Design & Architecture

Popular Job Localities

Popular Job Companies

Popular Job Departments

Jobs in Top Cities

Popular Job Type

Start Hiring

Senior Quality EngineerReq ID: 346829 NTT 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 seeking a Senior Quality Engineer to join our team in Pune, Mahārāshtra (IN-MH), India (IN). Once You Are Here, You Will: <ul><li>Design, develop and execute test automation frameworks and test automation suites.</li><li>Evaluate and maintain existing manual and automated test cases &amp; procedures.</li><li>Perform load and stress tests using enterprise level test automation tools.</li><li>Interpret test results and prepare comprehensive test reports.</li><li>Participate in project-wide reviews of requirements, system architecture and detailed design documents.</li><li>Act as key point of contact for other test engineers with automation needs.</li><li>Manage and maintain physical, virtualized and simulated test environments.</li><li>Identify and resolve issues that arise when integrating the application software with other software components.</li><li>Assist in reviewing and determining amount of code coverage of unit tests.</li></ul> Basic Qualifications:<ul><li>4+ years of experience using one or more of the following test automation tools or frameworks: Selenium, Tosca, Playwright, TestComplete, SpecFlow or similar.</li><li>4+ years of experience in software testing and writing software testing automation in one or more of the following: Java, C# and/or JavaScript/TypeScript.</li><li>Extremely strong with performance testing using Jmeter, K6 etc,</li><li>Strong experience with tests automation</li><li>Strong ability to code test scripts preferable in .net</li><li>Strong experience with API Testing</li><li>Be able to understand application process and take lead in identifying and building test cases.</li><li>Take ownership of building test cases and test data</li><li>Be able to mentor/direct mid level QEs</li></ul> Preferred Skills:<ul><li>Deep level of knowledge in test automation design, frameworks, and iterative development.</li><li>Experience with and can explain what Behavior-Driven Design (BDD) is and how the Cucumber (or similar) testing framework is used.</li><li>Understanding of the Gherkin syntax.</li><li>Experience in leadership roles is a bonus.</li><li>Strong organizational skills.</li><li>Curious, resourceful and eager to tackle new challenges.</li><li>Experience planning, designing, and implementing testing strategies and automation infrastructure for large scale system software.</li><li>Experience supporting and working with cross-functional teams in fast-growing environment.</li><li>Mobile test automation is a plus.</li></ul> Ideal Mindset:<ul><li>Lifelong Learner. You are always seeking to improve your technical and nontechnical skills.</li><li>Team Player. You are someone who wants to see everyone on the team succeed and is willing to go the extra mile to help a teammate in need.</li><li>Communicator. You know how to communicate your design ideas to both technical and nontechnical stakeholders, prioritizing critical information and leaving out extraneous details.</li></ul>  About NTT DATANTT DATA is a $30 billion business and technology services leader, serving 75% of the Fortune Global 100. We are committed to accelerating client success and positively impacting society through responsible innovation. We are one of the world's leading AI and digital infrastructure providers, with unmatched capabilities in enterprise-scale AI, cloud, security, connectivity, data centers and application services. our consulting and Industry solutions help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have experts in more than 50 countries. We also offer clients access to a robust ecosystem of innovation centers as well as established and start-up partners. NTT DATA is a part of NTT Group, which invests over $3 billion each year in R&amp;D.Whenever possible, we hire locally to NTT DATA offices or client sites. This ensures we can provide timely and effective support tailored to each client’s needs. While many positions offer remote or hybrid work options, these arrangements are subject to change based on client requirements. For employees near an NTT DATA office or client site, in-office attendance may be required for meetings or events, depending on business needs. At NTT DATA, we are committed to staying flexible and meeting the evolving needs of both our clients and employees. NTT DATA recruiters will never ask for payment or banking information and will only use @nttdata.com and @talent.nttdataservices.com email addresses. If you are requested to provide payment or disclose banking information, please submit a contact us form, <a href="https://us.nttdata.com/en/contact-us">https://us.nttdata.com/en/contact-us</a>.NTT DATA endeavors to make <a href="https://us.nttdata.com">https://us.nttdata.com</a> accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at <a href="https://us.nttdata.com/en/contact-us">https://us.nttdata.com/en/contact-us</a>. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click <a href="http://us.nttdata.com/en/compliance#eeos">here</a>. If you'd like more information on your EEO rights under the law, please click <a href="http://us.nttdata.com/en/compliance#know-your-rights">here</a>. For Pay Transparency information, please click<a href="http://us.nttdata.com/en/compliance#ppnp"> here</a>.<h4>Experience Level</h4>Senior Level

NTT DATA Global Delivery Services Ltd

Senior Quality Engineer

Quality Control 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>•    Detailed description of MAIN tasks and responsibilities:  •    Performing Stability analysis, Method transfer, Method Validation and review of analytical documents. •    Preparation and review of Method Transfer Protocols (MTP), Method transfer report (MTR), Method of analysis (MTH), Standard Testing Procedure, Test Data Sheet (TDS) for Stability Analysis, Method transfer and Method Validation, Stability Summary Reports and any document related to stability analysis, method transfer and method validation in compliance with current guidelines. Review and maintenance of  all logbooks of  the department •    Preparation of departmental SOP’s in compliance with current guidelines. Review of departmental SOP’s, training of analysts and other technical staff and review validation of data transfer, data management using computer systems. •    Preparation and review of validation protocols in compliance with current guidelines. •    Calibration and validation of all instruments / equipments.  •    Entry of stability sample results in LIMS &amp; SAP. •    Handling of LSCMS software •    Initiation of Quality Forms in Track wise Harmony, documents in Glorya EDMS and CAPA in Trackwise Harmony.<h4>Your experience and qualifications</h4>•    M. Pharmacy •    10 years and 7 months of experience<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.

Teva Pharmaceuticals

Quality Control Assistant

Quality Control Analyst I<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>To perform Stability analysis.</li><li>Maintenance of operating instruments / equipment.</li><li>To maintain the assigned Laboratory workplace, instruments and equipment etc.</li><li>To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP),  relevant regulatory guidelines and PAL procedure.</li><li>Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance.</li><li>Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP),  relevant regulatory guidelines and PAL procedure.</li><li>Performing stability testing (Assay, RS &amp; Dissolution) of all formulations by HPLC and UV techniques.</li><li>Preparing samples and executing the same as per the Method of Analysis and Verification of sample set sequence in applicable software’s.</li><li>Interpreting chromatographic data and ensuring proper documentation of all analytical activities in compliance with GLP / GDP requirements</li><li>Reporting of interpreted data in line with specification, compliance and regulatory standards and maintaining data integrity throughout the analytical lifecycle.</li><li>Evaluation of reported results and reporting of any abnormal results to the supervisor ontime.</li><li>Handling of laboratory software's.</li><li>Ensure to use safety apparels and PPEs while working in the laboratory.</li><li>Ensure timely completion of assigned training.</li></ul><h4>Your experience and qualifications</h4><ul><li>M.Sc., Chemistry</li><li>7+ years of experience</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.<h4>Experience Level</h4>Senior Level

Quality Analyst-7About TaskUs: TaskUs is a provider of outsourced digital services and next-generation customer experience to fast-growing technology companies, helping its clients represent, protect and grow their brands. Leveraging a cloud-based infrastructure, TaskUs serves clients in the fastest-growing sectors, including social media, e-commerce, gaming, streaming media, food delivery, ride-sharing, HiTech, FinTech, and HealthTech. The People First culture at TaskUs has enabled the company to expand its workforce to approximately 45,000 employees globally. Presently, we have a presence in twenty-three locations across twelve countries, which include the Philippines, India, and the United States.It started with one ridiculously good idea to create a different breed of Business Processing Outsourcing (BPO)! We at TaskUs understand that achieving growth for our partners requires a culture of constant motion, exploring new technologies, being ready to handle any challenge at a moment’s notice, and mastering consistency in an ever-changing world.What We Offer: At TaskUs, we prioritize our employees' well-being by offering competitive industry salaries and comprehensive benefits packages. Our commitment to a People First culture is reflected in the various departments we have established, including Total Rewards, Wellness, HR, and Diversity. We take pride in our inclusive environment and positive impact on the community. Moreover, we actively encourage internal mobility and professional growth at all stages of an employee's career within TaskUs. Join our team today and experience firsthand our dedication to supporting People First.As per JDHow We Partner To Protect You: TaskUs will neither solicit money from you during your application process nor require any form of payment in order to proceed with your application. Kindly ensure that you are always in communication with only authorized recruiters of TaskUs. DEI: In TaskUs we believe that innovation and higher performance are brought by people from all walks of life. We welcome applicants of different backgrounds, demographics, and circumstances. Inclusive and equitable practices are our responsibility as a business. TaskUs is committed to providing equal access to opportunities. If you need reasonable accommodations in any part of the hiring process, please let us know.We invite you to explore all TaskUs career opportunities and apply through the provided URL <a href="https://www.taskus.com/careers/" rel="noopener noreferrer" target="_blank">https://www.taskus.com/careers/</a>.<h4>Experience Level</h4>Senior Level

Taskus India Private Limited

Quality Analyst

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>IPQA activities.</li><li>Warehouse QA activities</li><li>MMaR’ S / MPaR’s Review.</li></ul><h4>Job Responsibilities</h4><ul><li>Line clearance of Various in process stage such as Dispensing, Granulation, Compression, Coating, Packaging and Sampling.</li><li>Routine monitoring of all functional area to ensure adherence to the SOPs.</li><li>Co-ordination &amp; Ensuring timely execution of Sampling activity of Raw and Packing materials.</li><li>Co-ordination of daily activities in Manufacturing and packaging areas.</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>Co-ordination &amp; ensuring timely execution of in-process activities for manufacturing and Packaging.</li><li>Coordination for implementation of CAPA.</li><li>In-process checks during manufacturing &amp; packaging stage, Performance of AQL, collection of samples as applicable and trending of AQL.</li><li>Sampling of validation &amp; commercial batch, Shelf life expiration date (SLED), Bulk completion date (BCD), sampling, Hold time study sample, In-process samples/Finished product samples, Collection, storage, and disposal of Reserve Sample.</li><li>Preparation, Review and updating of standard operating procedure.</li><li>Planning, co-ordination, and sampling of Raw and Packaging materials.</li><li>Co-ordination for Process validation &amp; cleaning validation execution.</li><li>Approved/ Rejected labels affixing for API, Excipients, Primary and Secondary packaging materials.</li><li>Swab/Rinse sampling for the cleaning verification &amp; validation programme, cleaning &amp; verification of sampling thief’s &amp; accessories.</li><li>Co-ordination for in-house and external calibration.</li><li>Review of Master Manufacturing Records &amp; Master Packing records &amp; logbooks.</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>Preparation for regulatory audits and making the compliance for the same.</li><li>To ensure that the impact of any risk reduction measures is not detrimental to the systems, facilities, utilities, equipment, or processes.</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>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></ul></li><li>Experience:<ul><li>Minimum 02 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 Assurance Executive

Senior Associate Manager - QualityDate Posted:2025-10-30Country:IndiaLocation:Plot No:132 to 167, Aerospace SEZ sector, Hi-tech, Defense and Aerospace Park, DEVANAHALLI, Bangalore, Karnataka, 562110, IndiaPosition Role Type:UnspecifiedJob Title: Senior Associate Manager - QualityJob Responsibilities <ul><li>Lead and direct support activities such as methods and procedures, planning and revision, gage planning and review, quality and reliability engineering, review and disposition of material variances</li><li>Develop, deploy, enhance, drive and implement plant-wide quality improvement projects through in-depth analysis of defect trends, manufacturing yields and KPC, to ensure delighted customers and to build customer and employee confidence in the performance of our products</li><li>Drive a culture of continuous improvement through the use of ACE tools to implement change that sustains ACE performance and supports the Standard Factory Lean Transformation plan</li><li>Ensure compliance and adherence to QMS and Internal audit system to meet AS9100, ISO9001 &amp; UTAS Procedures.</li><li>Provide direction for inspection and quality control of manufactured parts and materials including all dimensional, special and vendor quality control, metallurgical/chemical analysis and laboratory control</li><li>Manage quality inspection technicians and quality engineers/supervisors to coordinate inspection, MRB, purge and non-conformance management activities as required. Ensure that all products conform to specifications and meet the customers’ needs and expectations.</li><li>Coordinate quality problems with ME, Production &amp; SQA for Internal Producibility issue till resolution.</li><li>Oversee the performance &amp; reporting of daily, weekly and monthly review of all quality KPI's.</li><li>Work with Engineering to resolve problems relative to product design, Specifications, materials, tooling and production operations affecting quality</li><li>Overall accountability for CAB, MRB, OMRB, Clinic activities and process robustness</li><li>Lead the implementation of new inspection technologies that achieve process, reliability and productivity improvements</li><li>Maintain regular communication with direct reports and ensure a high level of support and engagement within the team.</li><li>Delegate and assign responsibilities in any of the areas such as ACE, quality assurance engineering and planning, parts inspection, defect analysis, statistical process control, etc</li><li>Foster and maintain a cooperative and productive working partnership with internal and external customers and overseas sites.</li></ul>Technical Knowledge / Soft Skill<ul><li>Degree in Electrical and Electronics Engineering.</li><li>At least 6+ years’ experience in a electrical assemblies / Manufacturing environment with at least 5 years leading a team of Quality</li><li>Good analytical technical problem-solving skills.</li><li>Assertive yet tactful in approach.</li><li>AS9100D Aviation QMS Auditor &amp; EtQ.</li><li>APQP / PPAP / MPR / MFP / ZDP / CORE</li><li>Technical capability to support analysis on Electronics, PCBA and Molding process.</li><li>Understanding of various manufacturing processes and digitalization tools</li><li>Knowledge of RRCA, analytics.</li><li>FAI as per AS9102, Net inspect</li><li>Special process knowledge</li><li>Statistical analysis / Six Sigma is desirable</li></ul>Collins Aerospace, a Raytheon Technologies company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers’ toughest challenges and to meet the demands of a rapidly evolving global market.The next chapter of our future as an aerospace company is here, and we are excited about what this means for our employees and customers! Get onboard theCollins Aerospace Operations team and play a part in managing our innovative products from inception to delivery. The Operations team continues to grow and aims to strengthen the connection of Manufacturing Operations, Supply Chain and Environment, Health &amp; Safety (EH&amp;S) across Collins Aerospace. In this dynamic environment, you will have the opportunity to network across our businesses and functions, all while improving the productivity, quality and efficiency of our operations worldwide.WE ARE REDEFINING AEROSPACE.Some of our competitive benefits package includes:<ul><li>Transportation facility.</li><li>Group Term Life Insurance.</li><li>Group Health Insurance.</li><li>Group Personal Accident Insurance.</li><li>Employee scholar program</li><li>Work life balance.</li><li>Car lease program</li><li>National Pension Scheme</li><li>LTA</li><li>Fuel &amp; Maintenance /Driver wages</li><li>And more!</li></ul>Nothing matters more to Collins Aerospace than our strong ethical and safety commitments. As such, all India positions require a background check, which may include a drug screen.Note:<ul><li>Background check and drug screen required (every external new hire in the India)</li><li>Drug Screen only performed for Operations Positions </li></ul>At Collins, the paths we pave together lead to limitless possibility. And the bonds we form – with our customers and with each other -- propel us all higher, again and again.                                                                                                                Apply now and be part of the team that’s redefining aerospace, every day.RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law.   Privacy Policy and Terms:Click on this <a href="http://www.rtx.com/privacy/Job-Applicant-Privacy-Notice" rel="noopener noreferrer" target="_blank">link</a> to read the Policy and Terms<h4>Experience Level</h4>Mid Level

Rtx India Private Limited

Chief Quality Officer

Quality Assurance AnalystSkill required: Quality Checks - Operational Audit &amp; Compliance Designation: Quality Assurance Analyst Qualifications:Any Graduation Years of Experience:3 to 5 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? Quality Analysts (QA) Leads are responsible for performing audits providing feedback root cause analysis in the event of a metric or service level miss and accuracy across the team and scorecards. What are we looking for? •	Conduct QA evaluations of the agents output in the form of a QA form or scorecard
•	2 years of work experience working within a QA capacity
•	Excellent communication and interpersonal skills
•	Strong organizational and administrative skills
•	Participating in calibration sessions
•	This will be based in Hyderabad client office
•	Must be flexible to work in Night shift between 8 PM (IST) – 4.00 AM (IST) including weekends and holidays (It’s a 5-day working day week which may include weekends) Roles and Responsibilities: •	Perform a deep dive on the accuracy of the incoming request which includes how the overall customer experience was handled
•	Conduct root cause analysis and other data calibration with the team the client and internal stakeholders
•	Conduct health checks on the team with areas for process refreshers based on errors and recommendations to the Training Team
•	Act as liaison with Managers and Team Leads to ensure consistent quality measurements throughout the operation
•	Participate as project team member in problem prevention and continuous improvement projects
•	Act as escalation point of contact for process questions issues and resolution
•	Provide QA progress reports to Team Leads
•	Conduct coaching sessions to assist team leads when required
•	Analyze Customer Satisfaction Survey results where applicable &amp; recommend improvement efforts
•	Administer the QA issue repository and ensure all escalations are properly addressed

Accenture India Private Limited

Quality Assurance Specialist

Quality Assurance PractitionerProject Role : Quality Assurance Practitioner Project Role Description : Provide general support to quality assurance (QA) directors, conduct in-depth quality assurance reviews, assist on recovery teams and with root cause analysis. Must have skills : Functional Test Planning Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary: 
As a Quality Assurance Practitioner, you will provide essential support to quality assurance directors, ensuring that all processes meet the highest standards. Your typical day will involve conducting thorough quality assurance reviews, collaborating with recovery teams, and engaging in root cause analysis to identify areas for improvement and enhance overall quality.
 
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 developing and implementing quality assurance strategies to enhance operational efficiency.
- Engage in continuous learning and development to stay updated with industry best practices.
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in Functional Test Planning.
- Good To Have Skills: Experience with test automation tools.
- Strong understanding of quality assurance methodologies and processes.
- Ability to analyze and interpret complex data to inform decision-making.
- Experience in collaborating with cross-functional teams to achieve quality objectives.
 
Additional Information: 
- The candidate should have minimum 3 years of experience in Functional Test Planning.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.

Quality AssuranceThe Quality Assurance role involves ensuring that products and services meet the established standards set by the company. Responsibilities include conducting tests, identifying defects, and providing feedback to the production team for improvements.

Sterlite Technologies Ltd

Transaction Quality Assurance AnalystThe Candidate should possess<ul><li>Minimum 5 years work experience as a Transactional Quality Auditor/MIS specialist/Quality associate involved in implementation of basic Quality framework elements for a Healthcare / Insurance processes</li><li>Expert knowledge in handling Excel and should have good exposure in analytics</li><li>Good knowledge in preparing power point presentations</li><li>Ability to collate data/information from different sources and work on Management reports without any error</li><li>Facilitate process improvement meetings along with respective team in a domain to achieve the desired results</li><li>Provides inputs based on data analysis for process improvements using Quality tools</li><li>Good communication skills with an ability to present during the routine Quality forums</li><li>Skills to perform as an individual player with ability to build rapport with the delivery stakeholders and work along with delivery team</li><li>Good knowledge in performing error analysis (RCA) and present insights. Implement corrective and preventive actions to control the causes</li><li>Working knowledge in basic Quality Framework elements like Risk Management/FMEA/ISO Audits etc would be a good value add skill</li><li>Should be a quick learner, should have capabilities in identifying improvement opportunities in process</li><li>Work experience on Lean / Six sigma methodology would be a value add</li></ul> Preference: Yellow belt trained and certified with background experience in Healthcare / Insurance processes<h4>Experience Level</h4>Mid Level

QA / QC Analyst

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

Senior Manager (Quality Control)<h4>Responsibilities</h4><ul><li>Implementation of Quality Assurance Plan</li><li>To finalize the mix design for various grades of concrete</li><li>To attend the third-party inspection for quality tests</li><li>To perform and witness the quality tests on routine basis.</li><li>To prepare and maintain reports and documentation related to quality tests, inspection etc.</li></ul><h4>Qualifications</h4><ul><li>B.E./ B.Tech- Civil Engineering. </li><li>15+ years of experience in Quality control in Hydro PSP projects.  </li></ul>

adani capital pvt ltd

Senior Manager

Quality Assurance Engineer III, Device Content and AdvertisementThis position is for Device Content &amp; Advertisement QA team working on products used by advertisers to get their Ads delivered to different devices like Fire TV, Tablets, etc. There are 100s of millions of devices customers use every day including 10s of millions of FireTV devices. Would you like to join &amp; help the team to get to the next level? We are building next gen Video, Display and Alexa Advertisement experience and infrastructure, which is a collection of content from several content providers of different categories ranging from News, Music Videos, Trailers, Sports, Entertainment, Lifestyle, Cooking, etc. You will help drive our new customer interactions with our popular and growing entertainment platform. Here you will drive key engineering and business decisions that impact Amazon’s long-term vision, which includes rapid expansion and innovation in the delivery of media and non-media entertainment. Come join us as we shape the future of what people watch on television Key job responsibilities As a QAE on Device Content &amp; Advertisement team, you will champion the quality of our features in our development pipeline using both automated and manual tests, status reporting, verifying defects, and signing-off on features and release candidates. You will own authoring and the execution of test plans and test cases. You will have a significant impact in the quality and delivery speed of our software, our business, and most importantly our customers. You will work closely with developers, product managers, and other QA in order to ensure the features we deliver to our customers have a high level of quality. In addition, you will also have the opportunity to propose improvements to our existing processes and automated tools in order to improve the team’s speed, quality and efficiency. A day in the life Your day would be filled with working on test strategies, test plans &amp; test cases. Part of the day would be engaged in several discussions working with PMs, TPMs &amp; developers in making requirements clear, bug triages &amp; reproducing issues seen by others. You will also be working with QA team in US. As these QA engineers help you run different projects, you would be working with them on a frequent basis to get status from them, providing knowledge sessions &amp; tracking their progress.<h4>Basic Qualifications</h4> - 6+ years of quality assurance engineering experience - 4+ years of delivering test frameworks, test tools, leading the QA projects and initiatives experience - Knowledge of QA methodology and tools, with demonstrated experience in an QAE role - Experience in automation testing - Experience in manual testing <h4>Preferred Qualifications</h4>- 2+ years of UI Automation (preferably on mobile platforms) experience - Knowledge of at least one modern object-oriented programming language such as C++, Java, Objective C Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit <a href="https://amazon.jobs/content/en/how-we-hire/accommodations">https://amazon.jobs/content/en/how-we-hire/accommodations</a> for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.<h4>Experience Level</h4>Senior Level

 Amazon India Limited 

Quality Assurance Engineer

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

AI Resume builder

AI Resume checker

AI Cover letter generator

Blog

Quality Assurance Jobs In Hassan - 323 Verified Vacancies

Senior Quality Engineer

Quality Control Assistant

Quality Control Assistant

Quality Analyst

Quality Assurance Executive

Chief Quality Officer

Quality Assurance Specialist

Quality Assurance Specialist