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

Quality ManagerJob Title:Quality ManagerJob DescriptionConcentrix is a technology-enabled global business services company specializing in customer engagement and improving business performance. We partner with ambitious, progressive executives around the world to future-proof their business and stay ahead of the competition and customer expectations Role and Key Responsibilities:<ul><li>Supervise quality work group of clients with multiple programs or lines of businesses which can be across multiple sites/geos, including work assignment and attendance monitoring; providing input for selecting, training, developing, and completing performance appraisal of work group(s) in accordance with the organization’s policies and applicable legal requirements</li><li>Maintain accurate metrics of direct reports individual performance as well as overall team level performance</li><li>Evaluate levels of process and staff effectiveness and works with Business stakeholders to create and collaborate on execution of improvement action plans</li><li>Develop strong working relationships with key Business stakeholders, internal and external</li><li>Oversee audits of key support processes within each account and recommend changes</li></ul>Key skills and knowledge:<ul><li>Green Belt Six Sigma</li><li>Demonstrated ability to comprehend, analyze, and interpret.</li><li>Solid understanding of the organization's business operations and industry.</li><li>Demonstrated ability to foster customer service disposition and sense of professionalism for self and team.</li><li>Excellent attention to detail.</li><li>Demonstrated ability to take initiative and ownership with focus on continuous improvement.</li><li>Demonstrated ability to mentor, coach and provide direction to team members.</li><li>Demonstrated ability to lead team members - organizing and prioritizing projects in a fast-paced and deadline-oriented business environment.</li><li>Advanced Microsoft Office skills.</li><li>Demonstrated business acumen.</li></ul>Educational Qualification: Bachelor’s degreeDisclaimer: -'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities.'Location:IND Kolkata - Unitech Hitech, Blk A, Tower AI, 4th FlrLanguage Requirements:Time Type:Full timeIf you are a California resident, by submitting your information, you acknowledge that you have read and have access to the <a href="https://www.concentrix.com/resource/job-applicant-privacy-notice-for-california-residents/" rel="noopener noreferrer" target="_blank">Job Applicant Privacy Notice for California Residents</a><h4>Experience Level</h4>Mid Level

Concentrix

Quality Manager

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

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

Startek

Senior Executive, QA Validation & Engineering
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>Shall involve actively in the execution and act as a reviewer of validation and qualification documents in the validation section. Be a subject matter expert in the validation section and shall ensure compliance in all the activities performed.<h4>Job Responsibilities</h4><ul><li>General </li><li>Preparation of Validation Master Plan (VMP) and SOP’s related to validations section</li><li>Co-ordination, assessment and review of change control, notification, deviation in the quality management system related to validation activities.</li><li>Coordinate and participate in the quality risk management (QRM) exercise related to facility, utility, equipment and process carried out in the facility.</li><li>Shall carryout gap assessment against global procedures/regulatory requirements and address gaps ensuring compliance.</li><li>Act as coordinator for periodic self-inspection of validation section for evaluation of the effectiveness of the quality systems.</li><li>Maitaining adherence to regulatory requirements and ensure the validation section is ready for audit anytime.</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>All other duties as assigned. </li></ul><ul><li>Qualification</li><li>Act as Subject matter expert (SME) for qualification and validation protocols related to equipments, utilities</li><li>Review/approval of periodic requalification documents pertaining to equipment / system / utilities and instrument of various departments across ARPL.</li><li>Review/approval of annual schedules for calibration, qualification status review, qualification, AMC, cleaning &amp; sanitization, preventive maintenance and filter replacement etc.</li><li>Approval of layouts, yearly &amp; monthly schedules, to be added planners, New logbook request etc.</li><li>Cleaning Validation</li><li>Act as Subject matter expert (SME) for cleaning validation</li><li>Responsible for evaluation of products for cleaning validation, preparation of cleaning validation matrix, performing MACO calculation, preparation of Equipment Cleaning Process Design Document (ECPDD), .cleaning validation protocols and reports, Quarterly/Annual monitoring reports for cleaning validation</li><li>Responsible to carryout cleaning validation activities in eResidue Pro software application</li><li>Process Validation</li><li>Act as Subject matter expert (SME) for process validation</li><li>Responsible for review/approval of documents related to process validation for demonstration batch, Optimization batch, Technical Risk Assessment, Process Performance Qualification, packaging validation protocols and reports, Continuous process verification and hold time study protocols and reports.</li></ul> <h4>Job Requirements</h4><ul><li>Education :
<ul><li>Master degree in Pharmacy/ Science or any equivalent degree.</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Possess sound knowledge in Qualification of Equipment, facility and utilities.</li><li>Maintains good Interpersonal skills and communication skills.</li><li>Strives to drive projects related to Qualification effectively</li></ul></li><li>Experience
<ul><li>Minimum 6 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

Apotex Pharmachem India Pvt Ltd

Quality Assurance Associate

Manufacturing Quality Assurance Experienced ProfessionalLocation:Maneja, Gujarat, IndiaJob ID: R0108655Date Posted:2025-10-15Company Name:HITACHI ENERGY INDIA LIMITEDProfession (Job Category):Quality ManagementJob Schedule: Full timeRemote:NoJob Description:The opportunityManufacturing Quality Control work includes Auditing, monitoring, and determining the quality of manufacturing processes and/or outputs against defined internal and regulatory standards. Testing random samples of finished goods. Reporting manufacturing process deviations and defects in finished goods and liaising with Quality Assurance to troubleshoot and resolve problems An Experienced Professional (P2) applies practical knowledge of job area typically obtained through advanced education and work experience. May require the following proficiency: Works independently with general supervision. Problems faced are difficult but typically not complex. May influence others within the job area through explanation of facts, policies and practices.How you’ll make an impact<ul><li>Conduct thorough material inspections in accordance with approved drawings, technical specifications, and review test certificates. </li><li>Prepare and maintain comprehensive documentation related to quality, including inspection reports, calibration reports, NCR (Non-Conformance Reports), rejection data, QAP, and work instructions. </li><li>Perform Incoming Inspection of NPD part and provide the feedback to SQ &amp;SCM. </li><li>Develop checking fixtures, templates, and gauges to streamline the inspection process for parts. </li><li>Ensured quality clearance through SAP (QM Module), improving efficiency and consistency in product quality. </li><li>Conduct root cause analysis of non-conformance using problem reports and tools such as 4Q, DMAIC, 7QC, and 8D. </li><li>Preparing necessary IIPs (incoming inspection plan), checklist and CTQ (Critical to Quality) parameters to ensure best quality of material from supplier. Training quality third party employees in basic quality test routines to ensure quality process are followed as per standard. </li><li>Ensuring all quality tools and instruments are timely calibrated. Performing first article inspection (first out turn sample inspection) for new development. </li><li>Regular Quality Observation Tour (QOT) and drive improvement actions  </li><li>Regularly monitor production FPY data, identify repetitive failure modes and drive improvement actions </li><li>Review and monitor manufacturing non-conformance, deploy right problem-solving tool to drive improvement action. Ensure sustainable solution. Outgoing inspection.</li><li>Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines.</li><li>Living Hitachi Energy’s core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business</li></ul>Your background<ul><li>Degree/diploma in mechanical engineering with Lean Six Sigma certification. </li><li>Minimum 3 year of experience in quality background at IQC of mechanical / electrical components and related products. </li><li>Knowledge of Switchgear/Automotive Products and components manufacturing. </li><li>Deep understanding of various national and international standards such as ASME, ANSI, IS, DIN, ISO etc.  </li><li>knowledge of SAP QM module. Should be capable of SAP transactions like create inspection plan (IIP), create quality plan .</li><li>Handling and usage of quality tools and precise instruments such as CMM, bore gauge, surface roughness tester, etc. Basic knowledge of manufacturing process like casting, forging, welding &amp; machining parts would be added advantage. </li><li>Excellent collaboration and work within team skills will help you to succeed in this position. Willing to travel at supplier place. </li><li>Proficiency in both spoken &amp; written English language is required</li></ul><h4>Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a <a href="https://www.hitachienergy.com/contact-us/general-inquiry?type=I+have+a+General+question" rel="noopener noreferrer" target="_blank">general inquiry form</a> on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.</h4><h4>This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response. </h4>

Hitachi India Pvt Ltd

Quality Assurance Officer

Executive, Quality Assurance
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

Quality Assurance Executive

Quality AnalystAbout 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

Quality Assurance EngineerWork Flexibility: HybridWhat you will do- <ul><li>Investigates &amp; document customer complaints according to applicable regulatory requirements and products.</li><li>Ensures timely investigation of and response to product complaints. This involves initiating and participating in investigations and corrective action arising from product complaints.</li><li>Proactive collaboration with cross functional team members to get resolution on customer complaints.</li><li>Timely closure of customer complaints; Collaborates effectively with cross functional and divisional partners to achieve goals</li><li>Effectively adapts style in global interactions accordingly.</li><li>Develop understanding of Stryker products and processes </li></ul>What you will need- Required- <ul><li>BE/BTech, ME/MTech in Bio Medical / Mechanical Engineering / Electrical Engineering or related field from premier institutes</li><li>experience- 2years to 6 years</li><li>At least 2+ years of experience in complaint handling or customer quality and TrackWise complaint handling tool or equivalent</li></ul>Preferred-<ul><li>Understanding of Post Market Surveillance requirement of Medical Devices under FDA &amp; EU MDR regulations; Medical Device Risk Management</li><li>Hands-on Experience on Complaint handling and Product investigations of medical devices; Experience on root cause analysis of field returned products and Knowledge of various quality tools.</li><li>Understanding on NC CAPA process</li></ul>Travel Percentage: None<h4>Experience Level</h4>Senior Level

Stryker India Private Limited

Quality Assurance Engineer

Team Lead - Process Quality Since our founding, IDEMIA has been on a mission to unlock the world and make it safer through our cutting-edge identity technologies. Our technology leadership makes us the partner of choice for hundreds of governments and thousands of enterprises in over 180 countries, including some of the biggest and most influential brands in the world. In applying our unique expertise in biometrics and cryptography, we enable our clients to unlock simpler and safer ways to pay, connect, access, identify, travel and protect public places – at scale and in total security. Our teams work from 5 continents and speak 100+ different languages. We strongly believe that our diversity is a key driver of innovation and performance. <h4>Purpose</h4>
This role is responsible for ensuring that all activities within the scope meet the required quality standards, minimize quality costs and maximise customer satisfaction by ensuring that procedures and processes are adhered to.<h4>Key Missions</h4>We are hiring a Team Lead - Process Quality based at NSEZ, Noida. Roles &amp; responsibilities:<ul><li>Leads or participates in regular reviews (with a quality focus) with relevant departments and teams (local and global) to improve business performance and consolidate customer feedback</li><li>Ensures KPIs are established and monitored to meet the business targets</li><li>Identifies opportunities to continually improve business performance supporting the continuous improvement efforts</li><li>Maintains accurate and relevant reporting or documentation as required to include inspection reports and documentations, central reports, customer reports, department reports, quality documents, templates and business presentations</li><li>Identifies and anticipates business risks</li><li>Manages through local register, host, lead or participation in audits from internal or external organizations in the delivery of successful scheme/customer accreditations (PCI, ISO9001, CQM etc)</li><li>Ensures that suitable inspections, audit and control activity is carried out by all levels of management and supervision in the delivery of business performance through use of the audit register</li><li>Manages the tracking and resolution of all relevant customer complaints and non-conformances</li><li>Supports the process owner in organizing cross-functional teams to investigate, identify root cause, implement and report on suitable corrective actions that will satisfy customer, third party or audit requirements</li><li>Communicates effectively with customer, suppliers and other external bodies as required Supports the business to ensure teams are appropriately trained, skilled and motivated to perform to a high standard of delivery in line with quality systems and processes</li><li>Owns responsibility for setting goals and objectives for team members for achievement of operational and inspection results</li><li>Faces problems that are occasionally complex</li><li>Ensures policies, practices and procedures are understood and followed by lower-level professionals, direct reports, customers and stakeholders</li><li>Manages projects or processes</li><li>Leads or hosts inspections, audits from external organizations and oversees the lower level quality employees in the delivery of successful scheme or customer accreditations</li><li>Undertakes some people management activities with the support of a manager including coaching and reviewing the work of lower-level professionals Works independently with limited supervision</li></ul>Industrial Experience (desired or essential): 6 to 10 years of experience in related mass production is an advantage. Personal qualities:<ul><li>Problem-solving capabilities to create meaningful strategies to improve support quality.</li><li>Excellent analytical and problem-solving skills with the ability to make data-driven decisions.</li><li>Strong communication, leadership, and team management abilities.</li><li>Knowledge of health, safety, and environmental regulations in the manufacturing industry</li></ul><h4>Profile &amp; Other Information</h4> By choosing to work at IDEMIA, you will join a unique tech company, offering a wide range of growth opportunities. You will contribute to a safer world, collaborating with an international and global community. We value the diversity of our teams and welcome people from all walks of life, regardless of how they look, where they come from, who they love, or what they think. We deliver cutting edge, future proof innovation that reach the highest technological standards and we’re transforming, fast, to stay a leader in a world that’s changing fast, too. At IDEMIA, people can develop their expertise and feel a sense of ownership and empowerment, in a global environment, as part of a company with the ambition and the ability to change the world. Visit our website to know more about the leader in Identity Technologies <a href="https://www.idemia.com">www.idemia.com</a><h4>Experience Level</h4>Senior Level

IDEMIA

Senior Quality Analyst

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

Teva Pharmaceuticals

Quality Specialist

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

Quality ManagerAbout 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>Mid Level

Manager, QualityAirbnb was born in 2007 when two hosts welcomed three guests to their San Francisco home, and has since grown to over 5 million hosts who have welcomed over 2 billion guest arrivals in almost every country across the globe. Every day, hosts offer unique stays and experiences that make it possible for guests to connect with communities in a more authentic way.The Community You Will Join:You will work cross-functionally Supporting Trust initiatives, with the Support of Product, Service Managers, Regional Operations Managers, Operations Change Management, and Shared Services to deliver successful improvement projects with measurable positive impact and also transition these solutions to operations for sustained results.The Quality Manager is responsible for the day-to-day execution and management of the global Quality program in Airbnb Capability Center. This role will report directly to the Manager, Shared Services. The Quality Manager will execute on the designed quality strategy and help implement a world-class quality framework that will drive consistency in the support experience we deliver across the globe.The Difference You Will Make:<ul><li>Build problem solving skills and capability within the teams through workshops, learning forums, playbooks</li><li>Drive culture of continuous improvement within the teams</li><li>Socialize Continuous Improvement with the stakeholders, understand the Key business requirements and build the CI strategy around them. </li><li>Educate, build awareness and Program manage continuous improvement, FMEA framework. Identify risks &amp; opportunities, create controls and build plans for implementation, Support business in setting up risk free operations / mitigate risks.</li><li>People Management: Coach &amp; mentor team members for enhanced roles and responsibilities, career growth, and Overall Development</li><li>Streamline overall ways of working and identify opportunities for improvement</li><li>Identify high impact opportunities, problem solve through data and process re-design and lead them to delivery</li></ul>A Typical Day: Strategy &amp; Culture Building<ul><li>Develop and drive a culture of continuous improvement aligned with business objectives.</li><li>Lead the CI strategy by identifying key business requirements and embedding structured problem-solving frameworks.</li></ul><ul><li>Socialize the value of CI with stakeholders and establish it as a key lever for business growth. </li></ul>Capability Development<ul><li>Build CI capabilities within teams via learning forums, workshops, and playbooks.</li><li>Mentor and coach teams on RCA, Lean Six Sigma and FMEA frameworks.</li></ul>Project Leadership<ul><li>Lead high-impact initiatives from concept to implementation using data, stakeholder insights, and cross-functional collaboration.</li><li>Use project management methodologies to ensure timely and effective delivery of outcomes.</li></ul>Operations Excellence<ul><li>Identify process gaps and lead re-design efforts to streamline ways of working</li><li>Leverage large datasets for root cause analysis and influence business decisions with storytelling and insight-driven presentations.</li><li>Translate business strategy into executable, scalable process improvements. </li></ul>People Leadership<ul><li>Inspire and lead a team of Quality evaluators, driving their growth and readiness for future leadership roles.</li><li>Foster a high-performance culture by aligning individual goals with organizational outcomes.</li></ul>Your Expertise:<ul><li>A minimum of 6+ years of experience in call centre quality management, Continuous Improvement, Process Design, process re-engineering and/ or operations..</li><li>Any Post Graduate/graduate</li><li>Strong stakeholder management skills</li><li>Proven track-record of developing and delivering support with positive impact to business metrics</li><li>Experienced in project management and engaging with cross-functional teams to successfully achieve business goals</li><li>Comfortable with large data sets, able to derive insights and storytelling through presentations.</li><li>Excellent analytical capability &amp; ability to translate strategy into onground implementation</li><li>Self starter comfortable working in ambiguous situations</li><li>Excellent Storytelling capabilities</li><li>Certified Lean Six Sigma Black Belt/PMP preferred</li><li>Good understanding of the Industry relevant automation tools &amp; Technologies. - Preferred</li><li>Experience of working/ collaborating with product teams to bring improvements/ impact - preferred</li><li>Design Thinking Practitioner, Agile/Project Management certification is a plus</li></ul>Hybrid Work Requirements &amp; Expectations: To support productivity and maintain a professional hybrid work environment, employees are expected to adhere to the following:<ul><li>Workspace: A dedicated, quiet, and private workspace free from interruptions and external noise</li><li>Internet Connectivity: During the working hours, maintain a minimum and consistent internet speed of 10 Mbps on your official devices to ensure reliability for work-related tasks, including calls and virtual meetings</li><li>Professionalism: Employees must remain fully engaged, respectful, and maintain a professional presence during virtual meetings, with video participation required unless otherwise approved.</li><li>Confidentiality &amp; Security: Employees are responsible for protecting Airbnb’s Intellectual Property and Confidential Information. Work-related activities, including calls and meetings, must not be conducted in public places, while traveling, or in any setting that may compromise confidentiality or work quality.</li></ul>Our Commitment To Inclusion &amp; Belonging:Airbnb is committed to working with the broadest talent pool possible. We believe diverse ideas foster innovation and engagement, and allow us to attract creatively-led people, and to develop the best products, services and solutions. All qualified individuals are encouraged to apply.How We'll Take Care of You:Our job titles may span more than one career level. The actual base pay is dependent upon many factors, such as: training, transferable skills, work experience, business needs and market demands. The base pay range shown below is annualized, is inclusive of allowances and is subject to change and may be modified in the future. This role may also be eligible for bonus or incentives, one or more equity programs, benefits, and Employee Travel Credits.  India Pay Range₹2,380,000—₹3,400,000 INR<h4>Experience Level</h4>Mid Level

Airbnb India Private Limited

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

AI Resume builder

AI Resume checker

AI Cover letter generator

Blog

Quality Assurance Jobs - 336 Verified Vacancies

Quality Manager

External Auditor

Quality Manager

Quality Assurance Associate

Quality Assurance Officer

Quality Assurance Executive

Quality Analyst

Quality Assurance Engineer

Senior Quality Analyst

Quality Specialist

Quality Analyst

Quality Manager

Quality Manager

Quality Assurance Officer

Know more about Quality Assurance Jobs In Gurgaon Gurugram