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

Technical Auditor Eligibility:<ul><li><a rel="noopener noreferrer" href="\&quot;http://b.tech/B.E\&quot;" target="_blank">B.Tech/B.E</a>. (Food Tech, Dairy Tech, Biotech, Chemical, Textile &amp; Fibre, Agri, Petrochemical) OR <a rel="noopener noreferrer" href="\&quot;http://m.sc/\&quot;" target="_blank">M.Sc</a>. (Chemistry, Biochemistry, Microbiology)</li><li>Minimum 60% marks / 6.0 CGPA / First Division</li><li>2–5 years of relevant experience (Graduated before Feb 2023)</li></ul> Role Highlights:<ul><li>Conduct on-site factory inspections under BIS standards</li><li>Assess processes, raw materials &amp; lab facilities</li><li>Ensure compliance across Food, Chemical &amp; Textile sectors</li></ul> Share your resume now.

Quality Austria Central Asia

External Auditor

Senior Director, Quality AssuranceThe Senior Director, Quality Assurance is a strategic leader responsible for setting the vision, strategy, and execution of all test engineering activities across the large team. This role oversees the design and implementation of test processes for software or integrated systems to ensure products meet the highest standards of quality, reliability, and performance. The Senior Director will lead global teams, champion automation and innovation, and collaborate with cross-functional partners to deliver world-class products.About You (Skills &amp; Qualification Required)<ul><li>Bachelor’s or Master’s degree in Computer Science, Electrical Engineering, or a related technical field (advanced degree preferred).</li><li>18+ years of progressive experience in test engineering, with at least 5 years in a senior leadership role.</li><li>Deep expertise in test engineering for software, hardware, or integrated systems, including hands-on experience with modern test automation tools and frameworks.</li><li>Proven track record of building and scaling global test engineering teams.</li><li>Strong knowledge of Agile, DevOps, CI/CD, and modern software/hardware development practices.</li><li>Experience with cloud platforms, microservices, embedded systems, or AI/ML-driven testing is highly desirable.</li></ul>It would be great if you also have<ul><li>Demonstrated success in driving automation, efficiency, and cultural change within test engineering organizations.</li><li>Ability to thrive in a fast-paced, dynamic, and global environment.</li><li>Excellent analytical, problem-solving, and decision-making skills.</li><li>Outstanding communication, interpersonal, and organizational abilities.</li></ul>What will you be doing in this role? Strategic Leadership<ul><li>Define and execute the long-term vision and roadmap for test engineering in alignment with business objectives.</li><li>Serve as a thought leader and advisor to executive management on test engineering best practices and emerging trends.</li></ul>Test Engineering Management<ul><li>Oversee the planning, development, and execution of comprehensive test strategies, including manual, automated, performance, security, and system-level testing.</li><li>Drive the adoption of advanced test automation frameworks, tools, and methodologies.</li><li>Ensure rigorous validation of products throughout the development lifecycle, from early prototyping to post-release support.</li></ul>Team Leadership &amp; Development<ul><li>Build, mentor, and inspire high-performing global test engineering teams.</li><li>Establish clear goals and performance metrics, providing regular feedback and opportunities for professional growth.</li></ul>Process Optimization<ul><li>Identify and implement process improvements to increase test efficiency, coverage, and effectiveness.</li><li>Standardize best practices, metrics, and documentation across all test engineering teams.</li></ul>Collaboration &amp; Stakeholder Engagement<ul><li>Partner closely with Product Management, Development, DevOps, QA, and Support teams to integrate testing seamlessly into the software/tool development lifecycle.</li><li>Act as the primary representative for test engineering in cross-functional initiatives and with external partners.</li></ul>Risk &amp; Issue Management<ul><li>Proactively identify, assess, and mitigate risks related to product quality, delivery timelines, and customer satisfaction.</li><li>Lead root cause analysis and drive corrective and preventive actions for critical quality issues.</li></ul>Reporting &amp; Metrics<ul><li>Define, monitor, and report on key test engineering KPIs and quality metrics to senior leadership.</li><li>Present regular updates on test progress, quality trends, and continuous improvement initiatives.</li></ul>About the Team   The existing team is spread across India and includes Testers with strong technical and analytical skills. You would be part of large QA Group responsible for delivering world class products and innovative solutions in the field of IP.Hours of WorkThe role and employment will be of fulltime with Clarivate. You will be working in IST time zone. 9 hours of work per day including 1-hour lunch break. We have hybrid work model, flexible and employee friendly work environment.At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.<h4>Experience Level</h4>Senior Level

Clarivate

Senior Quality Assurance Engineer

Quality AnalystJoin us as a Quality Analyst<ul><li>If you have a keen eye for detail, then this could be the role for you as you make sure that only well designed and built work packages get through quality testing</li><li>You’ll be the quality conscience of the team, assisting them to write and maintain automated tests as a standard way of working</li><li>Joining us in this fast paced role, you'll have excellent opportunities for progression and developing your analyst capabilities</li><li>We're offering this role at associate level</li></ul><h4>What you'll do</h4>As a Quality Analyst, you’ll be assisting the feature team to define testable work that is technically robust, high performing, stable and secure and ensures excellent customer experiences and outcomes. Promoting continuous improvement, you’ll identify opportunities to maximise the customer experience and reduce the test cycle time by improving techniques, tooling, eliminating waste and creating a collaborative, proactive approach to quality in the feature team.As well as this, you’ll be:<ul><li>Supporting the Quality Manager and the team in executing against the test strategy and quality by determining and advising which tests should be automated at which layer</li><li>Making sure that test plans are adequately covered by test scenarios</li><li>Creating different test and automation suites, such as smoke tests, full regression and progression tests, and end-to-end system regression tests</li><li>Analysing the results of automated tests</li><li>Providing data to the business and the team that focuses on quality and quality improvement</li></ul><h4>The skills you'll need</h4>We’re looking for someone with an extensive understanding of all stages of the product or service life cycle. This will include in-depth and hands on experience in areas such as product testing, static testing, systems testing, systems integration testing, user acceptance testing, compliance testing and operational readiness testing.Along with this, you’ll have experience of applying a wide range of testing automation tooling, as well as testing methodologies, including a range of Agile testing methods such as test driven development and behaviour driven development.We’ll also expect:<ul><li>Experience of manual, ETL and database testing with hands on experience in writing SQL queries</li><li>Experience in functional and non-functional testing such as system, system integration, user, load, volume, stress, security, accessibility, compatibility, penetration and back-out</li><li>Demonstrable knowledge of Agile methodologies with experience of working in an Agile team</li><li>A very capable communicator with the ability to communicate complex technical concepts clearly to your peers and management level colleagues</li><li>Good collaboration and stakeholder management skills</li></ul>Hours45Job Posting Closing Date:27/10/2025<h4>Experience Level</h4>Mid Level

NatWest Group

Quality Analyst

Quality AnalystWho we areJohnson Controls is the global leader for smart, healthy and sustainable buildings. At Johnson Controls, we’ve been making buildings smarter since 1885, and our capabilities, depth of innovation experience, and global reach have been growing ever since. Today, we offer the world’s largest portfolio of building products, technologies, software, and services; we put that portfolio to work to transform the environments where people live, work, learn and play. This is where Johnson Controls comes in, helping drive the outcomes that matter most. Through a full range of systems and digital solutions, we make your buildings smarter. Sustainability is a top priority for our company.We committed to invest 75 percent of new product development R&amp;D in climate-related innovation to develop sustainable products and services. We take sustainability seriously. Achieving net zero carbon emissions before 2040 is just one of our commitments to making the world a better place.What you will doResponsible for ensuring business services meet established quality standards across reliability, usability, and performance. This role supports strategic programs and drives continuous improvement initiatives, ensuring excellence in service delivery.How you will do it<ul><li>Assist in the development and execution of strategic programs and initiatives aligned with company goals.</li><li>Track program performance using appropriate tools and techniques; report on progress, risks, and issues.</li><li>Support the preparation of executive-level presentations, dashboards, and reports.</li><li>Conduct research and analysis to support strategic planning and decision-making.</li><li>Help identify process improvement opportunities and contribute to operational efficiency.</li><li>Maintain documentation and ensure knowledge sharing across teams.</li><li>Coordinate and drive Kaizen and Six Sigma activities across lines of business.</li><li>Continuously Monitor Project KPI’s to drive Continuous Improvement Initiatives.</li><li>Support in devising procedures and directions for recording and reporting quality data.</li><li>Compile quality control reports, create statistical process control metrics, manage non-conformity reports and recommend continuous improvement activities.</li><li>Implement &amp; Monitor quality control and inspection procedures.</li><li>Manage internal audits and other quality assurance activities.</li><li>Collaborate with Design and Operations Managers to resolve customer complaints through RCA.</li><li>Support risk management, failure mode and effects analysis (FMEA), and regulatory compliance.</li><li>Assist in the failure investigation of product complaint and CAPA activities.</li></ul>What we look for<ul><li>Bachelor’s degree in engineering, Quality, or related field.</li><li>3–6 years of experience in Quality Management.</li><li>Proven track record in delivering Quality Training Programs.</li><li>Proficient in Product and Process Audits.</li><li>Strong command of Six Sigma methodologies and Lean tools (e.g., VSM, Kaizen, RCA, Standard Work).</li><li>Certified Internal Auditor for ISO 9001:2015.</li><li>Skilled in problem-solving techniques (Fishbone, 8D, etc.).</li></ul>Key Skills<ul><li>Excellent verbal and written communication.</li><li>Strong presentation and stakeholder management capabilities.</li><li>Customer-focused mindset with a service-oriented approach.</li><li>Advanced proficiency in Microsoft Office Suite (Excel, PowerPoint, Visio, Outlook, Forms).</li></ul><h4>Experience Level</h4>Senior Level

Johnson Controls Ltd

Assistant Manager - LMM QualityThe Assistant Manager - LMM Quality will be responsible for ensuring the quality of products and processes in the Haridwar plant. They will work closely with the quality control team to maintain high standards and compliance with regulations. The role involves implementing quality improvement initiatives and conducting regular audits to identify areas for enhancement.

Mahindra And Mahindra Limited

Quality Manager

Quality Manager, VPJoin us as a Quality Manager<ul><li>We’ll look to you to provide direction and leadership on all quality matters across the platform or domain including adoption and compliance with the bank's standards and policies</li><li>This is an opportunity to act as a key contributor in making sure that work packages transition seamlessly from development into live environments</li><li>Hone your knowledge of quality best practices and collaboration and stakeholder management skills</li><li>We're offering this role at vice president level</li></ul><h4>What you'll do</h4>In this key role, you’ll be making sure that only well designed and built work packages get through quality testing. You’ll aim to get it right first time for our customers through innovative service and solutions, using automation as an accelerator and working closely with stakeholders in an Agile and collaborative environment. We’ll also look to you to produce comprehensive and robust quality strategies and detailed quality test plans, enabling the continual flow of work packages across the domain, platform value stream or programme.Additionally, you’ll be:<ul><li>Taking accountability for all aspects of quality across both run and change and business as usual activity within the assigned platform or domain</li><li>Overseeing the output quality from all testing phases owned and making sure it meets the requirements of each quality test strategy</li><li>Making sure defects are detected and prioritised, based on impact, and resolved at the earliest possible moment and before the last responsible moment</li><li>Undertaking end-to-end test management including planning, risk, issue, dependency management, lessons learnt and governance</li><li>Reviewing all key collateral relating to delivery and making sure it is of sufficient quality and with no gaps or duplication</li></ul><h4>The skills you'll need</h4>We’re looking for someone with strong knowledge and understanding of quality standards, quality best practices, and our risk and controls framework. You’ll also need high levels of knowledge and demonstrable application of modern testing and quality practices and techniques used with Agile methodologies.Additionally, we’ll be looking for:<ul><li>Practical experience of quality strategy and planning, testing design and execution</li><li>Experience in functional and non-functional testing such as system, system integration, user, load, volume, stress, security, accessibility, compatibility, penetration and back-out</li><li>Exposure to Automation tools would be preferred</li><li>The ability to communicate complex technical concepts clearly to peers and management</li><li>Exposure to Automation tools will be preferred</li></ul>Hours45Job Posting Closing Date:10/09/2025<h4>Experience Level</h4>Executive Level

Team Member - SIT<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary We are looking for an individual for the SIT Team to oversee the investigations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS incident or SAP log, and providing support during regulatory inspections. Roles &amp; Responsibilities • You will be responsible for overseeing the investigations of deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. • Your role involves active participation in investigating valid OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing. • You will review level Minor(Investigation required), Major and Critical incidents, providing constructive feedback for improvement. • Your responsibilities include periodically assessing the trending of level deviations, highlighting or escalating key observations, regularly reviewing the DCMS log or SAP OOS log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports. • You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations.<h4>Qualifications</h4>Educational qualification: A Bachelor's or Master's degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline Minimum work experience: 5 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills &amp; attributes: Technical Skills • In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA). • Expertise in investigating valid OOS and other relevant cases. • Familiarity with reviewing deviations log and ability to perform classification of data. • Ability to craft comprehensive investigation reports. • Experience in providing necessary support for regulatory inspections related to investigations. • Knowledge of regulatory requirements pertaining to incident investigations. Behavioural Skills • Ability to collaborate closely with CFT members. • Analytical mind set for identifying root causes and developing effective solutions. • Strong problem-solving skills and attention to detail in reviewing incidents, reports, and trending data and implementing corrective actions. • Effective communication skills for report writing and escalation of key observations. • Commitment to ensuring compliance with regulatory requirements in investigations. • Ability to offer necessary support to the site in readiness for or during regulatory inspections.<h4>Additional Information</h4>About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Dr Reddys Laboratories

Crew Member

Manager, Annual Product Quality Review (APQR)Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Key ResponsibilitiesAs an Individual contributor:The Annual Product Review (APQR) Manager–Will primarily manage the Global BMS site APQR program by authoring and completing the APQRs for all BMS commercial Marketed Products.  The APQR manager will be responsible for the completion of this annual compliance expectation by partnering with the site to draft and compete document from final approval.The APQR specialist will be responsible for the following defined roles and responsibilities:  <ul><li>Responsible to provide oversight and completion of the site APQRs</li><li>Responsible for authoring through approval of APQRS assigned, per site APQRs per schedule</li><li>Responsible for ensuring any site or CMO APQR is created following the effective process and procedures</li><li>Responsible for updates to the APQR program requiring SOP, WI and/or training</li><li>Provide in depth quality and compliance oversight during report authoring and reviewing.</li><li>Responsible for ensuring all elements of the AQPR procedure are compliantly fulfilled.</li><li>Responsible for facilitating review and approval meetings, problem-solving key issues, and effectively managing communications with key stakeholders.</li><li>Responsible to escalate any deficiencies in the draft APQR which cannot be resolved with the working team </li><li>Responsible for projecting and communicating stakeholder actions and timing.</li><li>Responsible for escalation of risk to management if not meeting the completion date.</li><li>Responsible for providing opportunities for process improvement and standardization.</li><li>Supporting onboarding and training of more junior team members</li><li>Support, as required, the implementation and/or maintenance of additional QA Systems, which may include (but is not limited to) APQR program documentation, Change Control, Quality Risk Management, Product Quality Complaints and Annual Product Quality Reviews</li><li>Support, as required, Digitalization/automation/efforts for the APQR program</li></ul>Qualifications &amp; ExperienceSpecific Knowledge, Skills, Abilities:<ul><li>Demonstrated knowledge of Biologics, Pharmaceutical, and/or Cell Therapy operations and processes required. </li><li>Completes work with periodic check in with direct manager</li><li>Experience in a GMP Quality role required in a commercial operations setting </li><li>Demonstrated experience in authoring and completing site APQRs </li><li>Ability to drive consensus, performance and to lead strategically</li><li>Prior experience with navigating multiple Quality Management systems. </li><li>Demonstrated strategic and tactical thinking capability with strong project management skills and ability to focus on execution of strategic decisions. </li><li>Solid negotiating and influencing skills in a matrixed organization.</li><li>Ability to work in a global matrix environment.   </li><li>Ability to build strong relationships by being transparent, reliable, and delivering on commitments. </li><li>Effective communication skills. </li><li>Ability to provide innovative ideas, align and make decisions balancing speed, quality, and risk. </li><li>Fluent in English, with proven professional working proficiency in English for reading, writing and speaking.</li></ul>Education:<ul><li>Minimum 5 years of experience in a quality, and/or regulatory role within the biopharmaceutical industry with demonstrated expertise in Quality Compliance, or Operations preferred.</li></ul>Travel:<ul><li>Must have ability to travel to US required (specifically for training purposes)</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

QA / QC Manager

Sr Associate Quality Compliance (Inspection)<h4>Career Category</h4>Quality<h4>Job Description</h4>If you feel like you’re part of something bigger, it’s because you are. 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. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.R&amp;D Quality Senior AssociateLIVEWhat you will doIn this vital role the R&amp;D Quality Senior Associate will play a crucial part in ensuring our organization's compliance with regulatory standards and preparing and coordinating a cross-functional team for Regulatory Health Authority inspections globally. The role also involves supporting the development of inspection management plans for each identified Regulatory Health Authority inspection, managing the R&amp;D inspection framework, and ensuring appropriate inspection resourcing and alignment across time zones. Additionally, the individual will support Regulatory Inspection Intelligence processes and contribute to operational quality initiatives.Responsibilities:<ul><li>Manage the R&amp;D inspection Framework (Calendars, Distribution Lists, Inspection notifications, SharePoint Sites, MSTeams Sites/Channels, Training Content, etc…). </li><li>Ensures that a cross-functional team (e.g. Quality, Clinical Operations, other functional areas, PV/GPS, GRAAS, DTI, etc.) is fully informed and prepared to support any Regulatory Health Authority inspection, worldwide.    </li><li>Supports the development of inspection management plan for each assigned and identified Regulatory Health Authority inspection, in conjunction with the applicable Cross-Functional Team. </li><li>Organizes mock interviews and/or inspections in preparation of potential Sponsor inspections. </li></ul><ul><li>Liaise with R&amp;D Quality TA Leads to develop appropriate inspection resourcing/scaling and facilities across time-zones and align TA compliance risk identified contact (CT-RACT, specific risk management items e.g. imaging approaches). </li></ul><ul><li>Support Regulatory Inspection Intelligence processes and provide input into Operational Quality Initiatives. </li></ul>Be part of our teamThe Clinical Quality Inspection team is a diverse international team within the Global R&amp;D Quality organisation. We are in charge of strengthening and enhancing the R&amp;D Quality Inspection Management System, providing Quality oversight on R&amp;D processes, and leading activities related to GCP regulatory inspections.WINWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:<ul><li>Degree Educated</li><li>3-6 years of Experience in inspection management within the pharmaceutical or biotechnology industry preferred.</li><li>Knowledge of global regulatory requirements and inspection processes.</li><li>Excellent communication and presentation skills.</li><li>Proven ability to work effectively in a cross-functional team environment.</li><li>Strong organizational and project management skills.</li><li>Experience with SharePoint and other inspection management tools.</li><li>Strong problem-solving skills and the ability to escalate issues effectively.</li><li>Ability to travel domestically and/or internationally, depending on business needs, to attend inspections as needed.</li></ul>THRIVEWhat you can expect of usAs we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.<ul><li>Vast opportunities to learn and move up and across our global organization</li><li>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul>APPLY NOWfor a career that defies imaginationIn our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.careers.amgen.com.<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Quality Assurance Officer

Assistant Manager - QualityIngersoll Rand is committed to achieving workforce diversity reflective of our communities. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. Job Title  Assistant Manager – QualityLocation  Fulgaon, PuneAbout UsGardner Denver Nash part of Ingersoll Rand. We are into Vacuum and blower business, building customise solutions for major customers in oil and gas, refineries, thermal power plants, paper, mining, chemical plants etc.Job Summary<ul><li>This role is for inspection activities Rotary and Static Equipments. You will be responsible for Quality Control &amp; Assurance activities of Rotary components &amp; Skids. Position requires hands on experience of ASME, API codes and fabrication techniques and job execution with requirement such as IGC, NACE, HIC etc.  </li></ul>Responsibilities <ul><li>Preparation of Package Stage wise inspection plan for shop floor activities. </li><li>Carry out shop inspection of various stages of Visual Dimension check, Hydro test, Mechanical Run Test, Performance Test, Blasting, Painting, Pickling/Passivation etc.</li><li>Coordination &amp; conducting Non-Destructive Testing  </li><li>Preparation of Package Quality Dossier and get approved from customer.</li><li>Preparation of various audits such as customer audit, ISO 9001 audit &amp; EHS audit</li><li>Identifying gaps in good engineering practices and implementing corrective actions to maintain world class quality of Nash Products  </li><li>Work with the Engineering, Procurement and Operations team on time and defect free supply of customer orders</li><li>Coordination of post order customer site feedback on supplied material Quality Issues and work with Service and Engineering team for on time closure of customer feedback.  </li></ul> Basic QualificationsBE Mechanical, ASNT NDT Level- II in RT,PTTravel &amp; Work Arrangements/RequirementsThrough Office , Travelling occasionally. Key CompetenciesHands on exposure to ASME, API Code Requirement, Fabrication technology, NDT, Rotary Component Inspection.What we Offer<ul type="disc"><li>We are all owners of the company! Stock options (Employee Ownership Program) that align your interests with the company's success.</li><li>Yearly performance-based bonus, rewarding your hard work and dedication.</li><li>Leave Encashments</li><li>Employee Health covered under Medical, Group Term Life &amp; Accident Insurance</li><li>Employee Assistance Program</li><li>Employee development with LinkedIn Learning</li><li>Employee recognition via Awardco</li><li>Collaborative, multicultural work environment with a team of dedicated professionals, fostering innovation and teamwork. </li></ul>Ingersoll Rand Inc. (NYSE:IR), driven by an entrepreneurial spirit and ownership mindset, is dedicated to helping make life better for our employees, customers and communities. Customers lean on us for our technology-driven excellence in mission-critical flow creation and industrial solutions across 40+ respected brands where our products and services excel in the most complex and harsh conditions. Our employees develop customers for life through their daily commitment to expertise, productivity and efficiency. For more information, visit www.IRCO.com.<h4>Experience Level</h4>Mid Level

Ingersoll-Rand India Ltd

Team Member - Quality Assurance<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary Roles &amp; Responsibilities <ul><li>Review and approval of all analytical test data of Quality control.</li><li>Review and usage decision of analytical reports in LIMS, Empower and SAP.</li><li>Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments.</li><li>Review the Analytical test report in LIMS.</li><li>Review the reported results against specification and trends.</li><li>Review the method validation and method transfer documents.</li><li>Review the instrument calibrations and working standard qualification records.</li><li>Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure.</li><li>Monitoring of analytical activities in Quality control laboratory.</li><li>Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval.</li><li>Verification and review of the audit trails for Standalone, Empower and LIMS.</li><li>Ensure cGMP / cGLP compliance.</li><li>To follow Safety, Health and Environmental procedures and practices.</li><li>Review and approval of excel sheet validations.</li><li>Review results acceptance for API and Excipients and Packing material.</li><li>Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols.</li><li>Handling of Robotic Process Automation of Chromatography Data review (RPACD)</li><li>To carry any other activities assigned by upward reporting staff.</li></ul><h4>Qualifications</h4>Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience: 3 to 7 years of experience in QC or AQA department is mandatory. <h4>Additional Information</h4>About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ <h4>Experience Level</h4>Entry Level

Quality Assurance Intern

QA Document Controller - RAK QA Document Controller - RAK - RAS007VCompany: Worley<h4 xmlns:ftl="http://www.taleo.net/ftl" xmlns:htm="http://www.w3.org/1999/xhtml" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Primary Location</h4>:  SAU-EP-Ras Al-Khair<h4 xmlns:ftl="http://www.taleo.net/ftl" xmlns:htm="http://www.w3.org/1999/xhtml" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Job</h4>:  Quality Assurance<h4 xmlns:ftl="http://www.taleo.net/ftl" xmlns:htm="http://www.w3.org/1999/xhtml" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Schedule</h4>:  Full-timeEmployment Type:  EmployeeManagement Level:  Individual Contributor<h4 xmlns:ftl="http://www.taleo.net/ftl" xmlns:htm="http://www.w3.org/1999/xhtml" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Job Posting</h4>:  Aug 31, 2025<h4 xmlns:ftl="http://www.taleo.net/ftl" xmlns:htm="http://www.w3.org/1999/xhtml" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Unposting Date</h4>:  Sep 30, 2025Reporting Manager Title:  Project Director:   Building on our past. Ready for the futureWorley is a global professional services company of energy, chemicals and resources experts. We partner with customers to deliver projects and create value over the life of their assets. We’re bridging two worlds, moving towards more sustainable energy sources, while helping to provide the energy, chemicals and resources needed now.At Worley, we’re building a diverse, inclusive and respectful workplace. Creating a space where everyone feels they belong, can be themselves, and can thrive is essential to our mission of delivering sustainable change. We know that diverse and inclusive cultures are safer and more innovative. We encourage applications from candidates from all backgrounds and diversity characteristics and warmly encourage disabled or neuro divergent candidates to apply.<h4>Key Responsibilities:</h4><ul><li>Maintain and control all quality assurance and quality control documentation for the project.</li><li>Receive, review, register, distribute, and archive incoming and outgoing QA/QC documentation.</li><li>Ensure all documents comply with project and company standards, including document formatting and naming conventions.</li><li>Assist QA/QC engineers and site teams in compiling inspection and test records, method statements, ITPs, material approvals, and NCRs.</li><li>Maintain up-to-date records of drawings, submittals, transmittals, and quality documentation in both digital and physical formats.</li><li>Track document revisions and ensure only current versions are used on site.</li><li>Support the preparation of turnover/handover documentation and project close-out files.</li><li>Liaise with subcontractors and suppliers to ensure timely submission of quality-related documentation.</li><li>Perform regular audits to ensure document control procedures are followed on site.</li><li>Ensure secure and confidential handling of sensitive project data.</li></ul><h4>Qualifications and Experience:</h4><ul><li>Proven experience in document control or QA administration within the construction or engineering sector.</li><li>Familiarity with QA/QC processes, ISO standards, and construction documentation workflows.</li><li>Proficient in Microsoft Office Suite and document management systems (e.g., Aconex, Procore, EDMS, etc.).</li><li>Strong organizational and communication skills.</li><li>High attention to detail and ability to manage large volumes of documentation.</li><li>Ability to work independently and collaboratively in a fast-paced site environment.</li></ul> Moving forward togetherWe’re committed to building a diverse, inclusive and respectful workplace where everyone feels they belong, can bring themselves, and are heard. We provide equal employment opportunities to all qualified applicants and employees without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by law.We want our people to be energized and empowered to drive sustainable impact. So, our focus is on a values-inspired culture that unlocks brilliance through belonging, connection and innovation.And we're not just talking about it; we're doing it. We're reskilling our people, leveraging transferable skills, and supporting the transition of our workforce to become experts in today's low carbon energy infrastructure and technology.Whatever your ambition, there’s a path for you here. And there’s no barrier to your potential career success. Join us to broaden your horizons, explore diverse opportunities, and be part of delivering sustainable change.

Worley India Private Limited

Junior Qa Tester

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

BlackRock Services India Pvt Ltd

Quality Assurance Engineer

Senior Specialist, Annual Product Quality Review (APQR)Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Key ResponsibilitiesAs an Individual contributor:The Annual Product Review (APQR) Specialist –Will primarily manage the Global BMS site APQR program by leading and generating the APQRs for all commercial Marketed Products.  The APQR specialist will be responsible for the completion of this annual compliance expectation by leading a team of Subject Matter Experts to draft and compete document from draft to final approval and delivery to the key stakeholders in alignment with the prescribed schedule.The APQR specialist will be responsible for the following defined roles and responsibilities:  <ul><li>Responsible to provide oversight and completion of the site APQRs</li><li>Responsible for authoring of APQRS assigned, per site APQRs per schedule</li><li>Responsible for ensuring any site or CMO APQR is created following the effective process and procedures</li><li>Provide in depth quality and compliance oversight during report authoring.</li><li>Responsible for ensuring all elements of the AQPR procedure are fulfilled accurately.</li><li>Responsible for facilitating review and approval meetings, problem-solving key issues, and effectively managing communications with key stakeholders. </li><li>Responsible for collecting review feedback and resolving comments and questions.</li><li>Responsible for projecting and communicating stakeholder actions and timing.</li><li>Responsible to escalate any deficiencies in the draft APQR which cannot be resolved with the working team</li><li>Responsible for escalation of risk to not meeting the completion date.</li><li>Responsible for providing opportunities for process improvement.</li><li>Accountable to adhere to GMPs and BMS Policies and Procedures </li><li>Support as may be required, the implementation and/or maintenance of additional QA Systems, which may include (but is not limited to) APQR program documentation, Change Control, Quality Risk Management, Product Quality Complaints and Annual Product Quality Reviews</li><li>Support as required Digitalization/automation/efforts for the APQR program</li></ul>Qualifications &amp; ExperienceSpecific Knowledge, Skills, Abilities:<ul><li>Understanding of Biologics, Pharmaceutical, and/or Cell Therapy operations and processes required. </li><li>Works with the routine oversight on direct manager.</li><li>Experience in a GMP Quality role required </li><li>Experience in authoring APQRs </li><li>Prior experience with navigating Quality Management systems. </li><li>Demonstrated tactical thinking capability with strong project management skills.</li><li>Ability to work in a global environment.   </li><li>Demonstrated negotiating and influencing skills in a matrixed organization. </li><li>Ability to build strong relationships by being transparent, reliable, and delivering on commitments. </li><li>Effective communication skills. </li><li>Ability to provide innovative ideas, align and make decisions balancing speed, quality, and risk. </li><li>Fluent in English, with proven professional working proficiency in English for reading, writing and speaking.</li></ul>Education:<ul><li>Minimum 3 years of experience in a technical, quality, and/or regulatory role within the biopharmaceutical industry with demonstrated acumen in Quality Compliance or Operations preferred.</li></ul>Travel:<ul><li>Must have ability to travel to US required (specifically for training purposes)</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Senior Level

AI Resume builder

AI Resume checker

AI Cover letter generator

Blog

Quality Assurance Jobs - 309 Verified Vacancies

External Auditor

Senior Quality Assurance Engineer

Quality Analyst

Quality Analyst

Quality Manager

Quality Manager

Crew Member

QA / QC Manager

Quality Assurance Officer

Quality Manager

Quality Assurance Intern

Junior Qa Tester

Quality Assurance Engineer

QA / QC Manager

Know more about Quality Assurance Jobs In Bengaluru Bangalore Region