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

Gopipura

Sachin INA

We are looking for a candidate who is interested in QA/QC work.


MC Coy Drugs

QA / QC Executive

Gandhi Nagar Mod

Jetpura

Conduct routine inspections of raw materials, in-process products, and finished goods.
Perform basic laboratory tests and record results accurately.
Assist in identifying and reporting non-conformities or deviations from specifications.
Maintain and update QC documentation, logs, and quality records.
Support calibration and maintenance of testing equipment.
Ensure compliance with company quality standards, SOPs, and regulatory requirements.
Collaborate with production and warehouse teams to address quality issues.
Prepare samples for testing and ensure proper labeling and traceability.
Assist in internal audits and continuous improvement initiatives.
Follow safety and hygiene procedures within the workplace.



Smart-Bond Chemicals Private Limited

Quality Assistant

Gopalpura

About Company:Axestrack is India's leading provider of Digital Logistics Solutions for Heavy Commercial Vehicles, and the only Indian company to be ever featured in Gartners Market Guide for Fleet Management. We are proud to hold a dominant position in the Indian market and are actively expanding across Africa, the Middle East, and the US. Our innovative approach and scalable platforms are transforming logistics for the modern world.Website: www.axestrack.com

Position: Data Quality Executive
Location: Jaipur, Rajasthan
Job Type: Full Time
Position Overview: As an Support Executive, you will be the first line of defense in ensuring smooth operation of IT systems and support for both internal teams and external clients. You will handle hardware/software issues, assist clients with product queries, and contribute to the efficiency of our technical infrastructure.
Key Responsibilities
Provide Level 1 support for users (internal/external) related to hardware, software, and applications.
Offer product support to clients by resolving functional or technical issues.
Troubleshoot and resolve hardware-level problems, including data-related concerns.
Respond promptly to support tickets and queries, ensuring timely resolution
Handle routine IT administrative tasks including password resets, user account updates, and access management.
Maintain documentation of all troubleshooting procedures and resolutions.


Skills & Qualifications:
Basic knowledge of computer hardware and peripherals.
Fluency in Hindi and ability to speak and write basic English.
Strong communication and interpersonal skills.
Ability to prioritize tasks and work independently.




Axestrack Software Solutions Private Limited

Data Quality Executive

Senior Quality Engineer<h4>Department</h4>Ratings<h4>Job Description</h4>The role is to support an agile team in analyzing, designing, building and testing high quality risk application suite. The SQA engineer will review functional requirements and user stories from LOB’s; design test plans, write test cases, oversee test strategies and perform testing for assigned applications. The role is to submit and verify defects, maintain documentation of test results to assist in debugging and modification of new applications, analyze test results to certify existing functionality and integrations and recommends corrective action plan failures. Testing will include functional and non-functional, integration, regression, system, smoke, SpecFlow and sanity testing.MUST HAVE <ul><li>knowledge of Capital Markets </li><li>experience/ knowledge of Python BDD testing approach and tools like “SpecFlow”, selenium based automated testing. Desirable to have React based UI testing experience.</li><li>have hands-on experience in defining overall testing approach and define the test plans, test automation</li><li>Enthusiastic strong-minded person able to work closely with the development team and help instill a testing culture. </li><li>Experience of setting up test frameworks for new projects.</li><li>Knowledge of  capital markets and regulatory programs is highly desirable</li><li>Practical experience of QA testing within investment banking.</li><li>Experience with UNIX, PERL and shell scripting.</li><li>The ideal candidate will also have experience with Jira and Confluence</li></ul>Competencies:Strategic Thinking: Business knowledge, Innovation &amp; CreativityBusiness Results: Client relationships, Analytical ability, Execution.Personal Effectiveness: Communication, decisiveness, Energy &amp; drive, courage, character. <h4>Open Positions</h4>2<h4>Mandatory Skills</h4>QA Automation, automation testing, selenium, bdd, Spec Flow, SpecFlow, Agile, Unix, Shell<h4>Education Qualification</h4>Bachelor's degree in STEM / Master's degree in STEM<h4>Experience</h4>6 to 15 years

CRISIL Ltd

Senior Quality Engineer

Quality Compliance Manager<h4>Career Category</h4>Quality<h4>Job Description</h4>HOW MIGHT YOU DEFY IMAGINATION?You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.What you will doThe Quality Compliance Manager is a global role and part of the Safety &amp; Medical Quality (SMQ) team for the R&amp;D Quality Organization.SMQ Team at Amgen implements the global R&amp;D Quality strategy across R&amp;D and other functional areas requiring pharmacovigilance (PV) oversight. The team monitors the audit universe to identify compliance risks, which inform PV audit program development. They lead or support inspection readiness and management, communicate audit and inspection outcomes to stakeholders, and advise on remediation. Additionally, the SMQ Team partners with stakeholders to provide compliance guidance, highlight trends and risks from various data sources to drive process improvement, and participates in service provider governance and due diligence activities.In this vital role, the Quality Compliance Manager will ensure excellence in R&amp;D Quality processes is maintained through oversight and improvements when compliance issues are identified. They will be an integral team member working globally with Business Process Owners to ensure compliance with GPvP regulations and other business requirements including the Global Safety database and associated systems. Additionally, the Quality Compliance Manager will provide proactive end to end quality support for the management of Quality Incidents/Quality Events, working closely with Quality Leads in approving investigations, including root cause analysis (RCA) and Corrective &amp; Preventive Action (CAPA) plans.Roles &amp; Responsibilities:The Quality Compliance Manager will work both independently and in a team environment to foster collaborative relationships within R&amp;D Quality. In this dynamic role, they will be responsible for supporting processes and operational activities related to overseeing Good Pharmacovigilance Practice (GPvP) deviations, preparation of audits and inspections across R&amp;D Quality. As part of strengthening and advancing Amgen’s R&amp;D QMS, this role provides end-to-end quality support to deviation owners, RCA owners, and CAPA owners within Global Patient Safety and other parts of the organization.<ul><li>Supports the intake, triage, and categorization of deviations, ensuring appropriate classification and documentation.</li><li>Facilitates timely and thorough deviation investigations in collaboration with functional area representatives and Quality Leads</li><li>Ensures consistent and compliant documentation of deviation records within the electronic quality management system (DQMS).</li><li>Monitors and ensures adherence to timelines, escalating delays and risks as needed.</li></ul><ul><li>Supports Global Patient Safety and Global Development teams in GxP inspection management activities and GxP audits from business partners</li><li>Identifies, leads, or contributes to continuous improvement initiatives to enhance CAPA management practices.</li><li>Collaborates with cross-functional partners to ensure processes remain effective, efficient, and aligned with industry best practices and evolving regulations.</li><li>Ensures the integrity, traceability, and quality of deviation and CAPA records in compliance with ALCOA+ principles.</li><li>Monitors quality metrics and key performance indicators (KPIs) related to deviation and CAPA management.</li><li>Analyses trends and perform root cause trending to identify systemic issues and opportunities for process improvement.</li><li>Manages, organizes and analyses data through different systems, tools, or platforms, including Excel and Smartsheet</li><li>Maintains knowledge of current regulatory and quality practices/issues</li><li>Maintains the Global R&amp;D CRQ and SMQ SharePoint sites</li><li>Manages the appropriate archival and retention of audit documentation.</li></ul>What we expect of youBasic Qualifications and Experience:<ul><li>Master’s degree and 8-13 years in Pharma and Biotechnology R&amp;D Quality</li></ul>Additional Competencies/Skills:<ul><li>Comprehensive expertise in Good Pharmacovigilance Practices (GPvP), with a strong command of operational standards and the quality frameworks governing drug safety.</li><li>Understand of regulatory requirements: Knowledge of global PV regulations (e.g., EMA GVP Modules, ICH E2E/E2F, FDA safety guidelines, MHRA expectations).</li><li>Solid understanding of end-to-end case management workflows, including upstream and downstream activities, and the related systems such as global safety databases (e.g., Argus, ArisG).</li><li>Demonstrated ability to leverage artificial intelligence (AI) tools and technologies to streamline workflows, drive process automation, and support data-driven decision-making. Must be adept at identifying opportunities to apply AI for operational efficiency and continuous improvement initiatives.</li><li>Proficiency in operating Quality Management Systems (QMS), particularly TrackWise and Veeva QMS, to manage quality events, documentation, and compliance workflows.</li><li>Exceptional attention to detail and accuracy in all deliverables.</li><li>Ability to work independently and proactively in a fast-paced environment.</li><li>Proficiency in Smartsheet, Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and virtual collaboration tools (e.g., Teams, WebEx)</li><li>Good team building skills and the ability to on-board new employees and develop them over time</li></ul><ul><li>Familiarity with project management tools and methodologies.</li><li>Experience working in a multinational environment with global teams.</li></ul><ul><li>Excellent verbal and written communication skills.</li><li>High degree of professionalism and interpersonal skills.</li><li>Strong problem-solving abilities and adaptability to changing priorities.</li><li>Collaborative attitude and ability to build positive relationships across diverse teams.</li><li>Resilience, discretion, and the ability to thrive under pressure</li></ul>.<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Quality Control Manager

Manager – Quality SolutionsRole Responsibilities:<ul><li>Develop and manage project plans, including spend, resourcing and deliverables to design, configure, and develop Quality solutions using technologies such as SAP standard configuration, SAP QM, PP ,WM and FIORI</li><li>Able to Configure, design, development and implementation of Digital projects leveraging enterprise core solutions including but not limited to SAP ECC (modules – MM, PP, QM, WM), SAP S/4.</li><li>Learn and gain expertise in Pfizer’s Plant network global model template focusing on product quality and batch management.  Also learn Pfizer’s Business Processes relevant to these solution areas.</li><li>Design solutions for Continuous Improvement Enhancement Requests (ERs) that are high quality, reflect the most optimal use of available funding, and are implemented in a way that does not adversely impact Pfizer’s global SAP footprint.</li><li>Communicate effectively with stakeholders at various locations globally to ensure that they are adequately informed about the status of requests submitted by them and are kept abreast on progress made and issues encountered.</li><li>Serve as a Project Manager for bigger projects and serve as a coach to the contractors on smaller projects. Take responsibility for the deliverables and ensure cost and timeline commitments made to the business are adhere.</li><li>Conduct business requirements gathering meetings and workshops in an efficient and productive manner and documents minutes, notes and requirements concisely.</li><li>Translate business requirements into technical specifications and liaise with technical development teams to develop and implement system solutions to satisfy business needs.</li><li>Develop cost estimates for projects, create spend forecast and maintain project financial details in Pfizer internal tools and project portfolio systems.</li><li>Stay abreast of new technology trends and look for ways to apply new technologies where it makes sense.</li><li>Learn and adopt internal working procedures and foster conformance and standardization. Also suggest way to improve procedures and practices.</li><li>Partner closely with other Solutions Teams for cross-functional projects, and with other work streams within the Supply Chain Solutions Team such as TechDev, Integration, Data, Business Adoption, Compliance, BI, Serialization, and Security.</li><li>Engage with in cross functional teams including key business stakeholders within Pfizer Global Supply (PGS) and Digital colleagues to contribute to the business process and system development life cycle.</li><li>Provide technical and functional guidance to key stakeholder within PGS</li><li>Assist in unit, cycle, and integration testing of developed programs including but not limited to SAP PP, QM, WM and SAP Fiori.</li><li>Ensure compliance to GMP, deployment standards and quality guidelines with regulatory related obligations are executed with the highest standards of compliance</li><li>Support testing and other activities necessary for SAP IDOC/File interfaces.</li><li>Develop ideas and lead complex projects within and across multiple business units / Digital delivery centers</li></ul><h4>Basic Qualifications:</h4><ul><li>Bachelor’s degree in computer science or Engineering degree and 5 years of relevant experience</li><li>8 years' experience in IT system design and/or delivery, 5+ years in Pharma or business process experience</li><li>At least 5 years of experience working on SAP Quality Management Module, plus very good knowledge in LIMS interface, IDOCS and integration points with Materials Management, Process Order Execution and Warehouse Management. Experience in S4 Hana will be preferable.</li><li>Demonstrable experience in software development lifecycles using agile principles and DevOps practices</li><li>A thorough understanding of system GMP /GDP requirements in detailed knowledge of IT system design and the maintenance lifecycle in GMP environments.  </li><li>Knowledge or familiarity with the production support process, including tasks, escalation routes, communications, and other related activities</li><li>Proven track record of a successful team lead and solution design.</li><li>Excellent written and verbal communication skills, with the ability to communicate with business and technical people alike</li><li>Excellent presentation and facilitation skills, with the ability to interact with various levels of management</li><li>Excellent organization and problem-solving skills</li><li>Excellent leadership and project management skills</li><li>Quick learner. Demonstrate initiative and ownership.</li><li>Ability to operate in a global multi-cultural environment of time zones and requirements </li><li>High degree of business process acumen understanding the life cycle of product creation (Plan, Source, Make, Deliver, Return).</li></ul>PREFERRED QUALIFICATIONS<ul><li>SAP Quality Management and industry experience</li></ul> Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. PHYSICAL/MENTAL REQUIREMENTS<ul><li>Able to manage contract resources if needed. Mentally strong, able to communicate well and work with Teams.</li></ul>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS <ul><li>Travel as needed</li></ul>  Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Information &amp; Business Tech<h4>Experience Level</h4>Mid Level

Pfizer Ltd

Chief Quality Officer

Senior Manager, QACome work at a place where innovation and teamwork come together to support the most exciting missions in the world!<h4>Role Overview</h4>We are seeking a seasoned Senior Manager, Quality Assurance with over 15 years of experience in software quality engineering, functional validation, performance testing, and automation. This leader will define and drive the QA strategy across multiple product lines, ensuring that quality remains a core pillar of delivery. While deep expertise in automation frameworks and performance testing is expected, experience with Agentic AI in testing and test automation will be considered a valuable plus.<h4>Key Responsibilities</h4><ul><li>Leadership &amp; Strategy<ul><li>Lead QA Managers, Senior Engineers, and geographically distributed teams across multiple product lines.</li><li>Define the QA roadmap focusing on functional correctness, performance, scalability, and automation coverage.</li><li>Collaborate closely with Product Management, Development, and DevOps leaders to integrate quality into every stage of delivery.</li></ul></li><li>Functional &amp; Performance Testing<ul><li>Oversee comprehensive functional testing strategies ensuring correctness across web, API, and microservices platforms.</li><li>Build and scale performance testing practices, focusing on load, stress, scalability, and reliability metrics.</li><li>Drive the adoption of performance benchmarking and monitoring integrated into CI/CD pipelines.</li></ul></li><li>Automation &amp; Quality Engineering<ul><li>Enhance automation coverage using modern frameworks and tools (Selenium, Cypress, Playwright, RestAssured, JMeter, etc.).</li><li>Implement shift-left testing and integrate automation into CI/CD for continuous validation.</li><li>Explore AI-assisted defect detection, regression prioritization, and self-healing tests to complement standard automation.</li></ul></li><li>Operational Excellence<ul><li>Define and monitor QA KPIs, dashboards, and release quality metrics to drive accountability.</li><li>Ensure compliance and security testing are embedded into QA practices.</li><li>Foster a culture of innovation and ownership within the QA team.</li></ul></li></ul><h4>Qualifications</h4><ul><li>15+ years of progressive experience in Quality Engineering, Test Automation, and QA Leadership roles.</li><li>Proven track record in leading functional and performance testing strategies at scale.</li><li>Strong expertise in automation frameworks and performance testing tools.</li><li>Experience working with cloud-native applications, CI/CD pipelines, and DevOps environments.</li><li>Excellent stakeholder management, executive communication, and cross-functional collaboration skills.</li><li>Bachelor’s or Master’s degree in Computer Science, Engineering, or equivalent field.</li></ul><h4>Good to Have</h4><ul><li>Exposure to Agentic AI in testing and test automation, including use of AI-driven tools for test case generation, defect analysis, and autonomous regression.</li><li>Knowledge of cybersecurity testing, compliance validation, and risk-based QA.</li><li>Familiarity with cloud platforms (AWS, Azure, GCP) and containerized environments (Kubernetes, Docker).</li><li>Experience with RAG (Retrieval-Augmented Generation) validation, AI observability, and intelligent monitoring.</li></ul><h4>Why Join Us?</h4><ul><li>Lead and scale QA transformation with a focus on functional excellence and performance at scale.</li><li>Opportunity to work on next-generation testing practices, with exposure to Agentic AI advancements in QA.</li><li>Collaborate with global teams driving cutting-edge technology platforms.</li><li>Shape the future of automation and quality engineering at enterprise scale.</li></ul><h4>Experience Level</h4>Senior Level

Qualys Security Techservices Private Limited

Senior Quality Assurance Engineer

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

Accenture India Private Limited

Quality Assurance Associate

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

QA Leader We're looking for experienced QA professionals who can lead from the front and deliver excellence at scale.<ul><li>10–12 years in Testing, with recent experience in Project Delivery</li><li>Strong foundation in Selenium design &amp; automation</li><li>Proven ability to lead large teams</li><li>Experience working with global customers</li><li>Onsite opportunity – Mumbai &amp; Bangalore</li></ul> Share your updated resume now.

Test Yantra Software Solutions India Pvt Ltd

QA Lead

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

Abbott India Ltd

Quality Assurance Officer

Business Excellence . Looking for Candidate with 5+ years of experience.. Experience in Process improvement, Making Policies, and standard operating procedures (SOPs). . Working Environment: 5 Days. Immediate availability is a strong advantage.. Location - Sohini Tech Park, 6, 7, 10th Floors, Nanakramguda Village, Gachibowli, Hyderabad, Telangana, 500032 Share your CV with the position mentioned.

Latinem Private Limited 

Business Development Specialist

Senior Manager - Quality Management<ul><li>Job Title: Senior Manager - Quality ManagementCareer Level - EIntroduction to roleProtecting AstraZeneca's license to operate through the delivery and maintenance of compliant innovation, projects, and services. This function comprises Quality Management professionals who understand AstraZeneca's business processes and are experts at integrating business-appropriate risk management techniques. This function will also consult and educate the business and the broader workforce on effectively integrating Compliance Requirements into all IT Lifecycle activities. The function is truly global in scale with resources in Asia, EU, North America, and South America.<h4>Accountabilities</h4><ul><li>Accountable for the application of Quality Management processes and services to assure that projects, systems, solutions, and services delivered by IT and their 3rd party suppliers meet AstraZeneca internal and external regulatory requirements.</li><li>Act upon risks and issues to raise compliance and quality levels within IT and the business.</li><li>Support the development and roll-out of training, education, and awareness campaigns for quality and compliance.</li><li>Contribute to the continuous improvement of IT Policies, standards, and procedures.</li><li>Collaborate with system/business process owners to complete or update the Risk Impact Determination (RID) as per the procedure to ensure an understanding of the Regulatory applicability (GxP, SOx, Data Privacy etc.), business, technical, software category, and regulatory risks.</li><li>Review System lifecycle deliverables including RID, specifications, protocols, reports, and the Test Closure Memo with a focus on cGMP impact, validation lifecycle requirements, and quality, and compliance requirements.</li><li>Participate in the review and approval of Exceptions, CAPA, Deviations, Changes, Incidents, and Problems ensuring timely completion and update of System Lifecycle deliverables.</li><li>Collaborate with the IT Project Manager to define the Quality Plan, processes, validation planning, and reporting processes.</li><li>Lead/Participate in the Supplier Assessment to ensure that IT Suppliers meet AstraZeneca Regulatory requirements.</li><li>Act as a QC point of contact for any potential internal and/or regulatory inspection.</li><li>Drive accountability for the completeness, accuracy, and currency of Quality-related data through effective monitoring, tracking, and reporting.</li><li>Process authoring, ownership, lead, quality review, and/or approval as appropriate.</li></ul><h4>Essential Skills/Experience</h4><ul><li>BA, BSc in Computer or Life Sciences or equivalent, with 3-5 years of experience in the pharmaceutical industry regulatory requirements</li><li>Experience of providing regulatory support including validation of laboratory and business applications</li><li>Knowledge of industry good practice and standards such as ISO 9000, ISO 27002, CMMI, GAMP, GxP, ITIL, S404 Sarbanes-Oxley</li><li>Experience of contributing to implementation of a Quality and/or Compliance strategy with the ability to prioritise and understand the impact of the decisions made</li><li>Experience of operating across business functions and geographies in large, complex and sometimes uncertain IT environments</li><li>Strong communication, influencing and relationship building skills, capable of discussing technical IT terms with a non-technical business audience</li><li>Strong change leadership and team working skills</li><li>Ability to make pragmatic decisions by analysing complex situations and assessing risks</li><li>Concern for impact, analytically minded and able to prioritise and plan using initiative</li><li>High levels of drive, energy, resilience and a desire for professional excellence</li><li>Ability to hold self and others accountable for actions</li></ul><h4>Desirable Skills/Experience</h4><ul><li>Broad IT management experience including project or service management</li><li>Familiarity with technical concepts in infrastructure or applications</li><li>External qualifications such as ISPE PCC CPIP and ISACA CISM</li><li>Understanding of Lean principles, tools and techniques</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca, our work has a direct impact on patients by transforming our ability to develop life-changing medicines. We empower the business to perform at its peak by combining cutting-edge science with leading digital technology platforms. Join us at this crucial stage of our journey in becoming a digital and data-led enterprise.Ready to make a difference? Apply today!</li><li>A</li></ul>Date Posted09-Sept-2025Closing DateAstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Senior Level

Astrazeneca India Private Limited

Quality Manager

QA Manager Looking for an experienced QA Manager (10–14 years) to lead a team of 8 QA engineers and drive testing excellence across projects. Key Skills:<ul><li>Manual &amp; Automation Testing (Selenium, JMeter, Postman, Cypress)</li><li>QA Strategy, Test Planning, CI/CD, Agile/Scrum</li><li>Strong leadership &amp; communication skills</li></ul> Share your updated resume now.

AI Resume builder

AI Resume checker

AI Cover letter generator

Blog

Quality Assurance Jobs In Hassan - 347 Verified Vacancies

QA / QC Executive

Quality Assistant

Data Quality Executive

Senior Quality Engineer

Quality Control Manager

Chief Quality Officer

Senior Quality Assurance Engineer

Quality Assurance Associate

External Auditor

QA Lead

Quality Assurance Officer

Business Development Specialist

Quality Manager

QA Lead