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Advisor, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleAdvisor, Quality Assurance Engineering<h4>What does a successful Advisor, Software Development Engineering – Automation QA do?</h4>As a successful Automation QA Advisor, you will play a key role in ensuring the quality and reliability of Fiserv’s Digital Banking platform. You will design, develop, and execute automated tests for cloud-native Open APIs, working closely with development and business teams to understand user interactions and translate them into robust test scenarios. You will be responsible for driving quality initiatives, implementing best practices, and contributing to continuous improvement efforts across the QA team.<h4>What will you do:</h4><ul><li>Design and implement functional and integration tests for REST APIs using Postman and other tools.</li><li>Develop test automation frameworks and generate test data.</li><li>Perform performance testing and analyze results using tools like Splunk.</li><li>Collaborate with developers and stakeholders to ensure end-to-end test coverage.</li><li>Participate in agile ceremonies and contribute to sprint planning and retrospectives.</li><li>Work with Azure DevOps and JIRA for test management and tracking.</li><li>Contribute to containerization and deployment testing using Docker and Kubernetes.</li><li>Ensure compliance with industry standards and security best practices.</li></ul><h4>What you will need to have:</h4><ul><li>Minimum 8 years of experience in QA automation or software testing.</li><li>Strong programming and debugging skills in .NET Core and C#.</li><li>Expertise in functional testing using Postman.</li><li>Experience with REST APIs, Azure Services, and Cosmos DB.</li><li>Familiarity with performance testing and monitoring tools like Splunk.</li><li>Hands-on experience with Azure DevOps and JIRA.</li><li>Understanding of software-hardware interaction and documentation practices.</li></ul><h4>What would be great to have:</h4><ul><li>Exposure to Playwright for UI automation.</li><li>Experience with containerization platforms like Docker and Kubernetes.</li><li>Knowledge of US Banking industry standards and workflows.</li><li>Experience in agile development and a commitment to continuous improvement.</li><li>Ability to proactively identify and resolve quality and security issues.</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.<h4>Experience Level</h4>Senior Level

Fiserv India Pvt Ltd

Quality Assurance Officer

Professional, Quality Assurance EngineeringCalling all innovators – find your future at Fiserv.We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations, merchants, and consumers to one another millions of times a day – quickly, reliably, and securely. Any time you swipe your credit card, pay through a mobile app, or withdraw money from the bank, we’re involved. If you want to make an impact on a global scale, come make a difference at Fiserv.Job TitleProfessional, Quality Assurance EngineeringProfessional, Test Engineer (Manual + Automation )What does a Test engineer do at Fiserv?As an experienced member of our Payment Exchange Testing Team, you will own Requirement Analysis, Test Case Design and Manual Testing, Automation script preparation of our Product. What You Will Do:<ul><li>Your Primary responsibility would be to independently Test or prepare automated test scripts for the assignments and maintain highest degree of quality for all deliverables. </li><li>Provide estimations for analysis, design, manual testing, and automation script preparation of application functionality for the assignment.</li><li>Requirement Understanding through different source of information/documents available with the team.</li><li>Perform QA activities for manual as well as automation testing - execute, maintain &amp; enhance the existing and new automation test suite.</li><li>Conduct peer reviews of test conditions/test cases/test data requirement by testers and follow up to close the review comments.</li><li>Applying innovative concepts in testing to enhance the test coverage, improve quality and reliability.</li><li>Refine the requirements with BA during the grooming calls.</li><li>Learning the best practices and the methodology used in the program and adhere to the standards.</li><li>Provide L3 support as and when necessary for production issues. Analyze production issues, reproduce them in lower environments and provide data points and patterns to the technical team and help provide short-term and long-term fix and help the client support team in the whole process.</li><li>Mentor/train existing and new team members.</li><li>Identify and collaborate with all necessary stakeholders to reach agreement in accordance with defined project goals with little to no assistance.</li><li>Track progress against assigned tasks, report status, and proactively identify issues and report to the Product Owners, Architects and Management team.</li><li>Work successfully in a team environment and demonstrate a willingness to help team members in achieving their project goals if required.</li><li>Ownership and accountability for delivering assigned tasks and deliverables within the established schedule.</li></ul>What You Will Need to Have:<ul><li>Minimum of 4+ years of experience as a QA with minimum 2+ years of experience in automated testing.</li><li>Good understanding of Software Test Lifecycle including Test Strategy, Test Planning, Test Case Design, Test Data Setup, Defect Management and Test Log, Test results, Test Traceability Matrix and Test Metrics Screening and validation of application through database and system logs.</li><li>Technical Skillset required –<ul><li>Strong Knowledge on Selenium, TestNG, SQL Server</li><li>Knowledge of .Net or Java would help</li><li>Strong knowledge of Agile processes &amp; tools associated with it, such as – JIRA, Git hub, Jenkins.</li><li>Very good understanding of security aspect for an application or project.</li><li>Need to have good debugging and problem-solving skills.</li><li>Should have good understanding of Framework and able to understand complex Architectural aspects.</li><li>Experience in integrating to third party applications.</li></ul></li><li>Require minimal supervision, is a fast learner and a team player</li><li>Hands on experience on black box testing</li><li>Understanding of application interfaces, xml, security etc,</li><li>Must have good written and verbal communication skills. </li><li>Must have an experience in retail banking domain.</li><li>Creative thinking and good problem-solving skills</li></ul>What Would Be Great to Have:<ul><li>Handson experience on CI\CD tools like Jenkins/Harness and GitHub.</li><li>Hands on experience in coding Automation framework using programming language like C# or Java.</li><li>Knowledge of Payments domain.</li></ul>Thank you for considering employment with Fiserv.  Please:<ul><li>Apply using your legal name</li><li>Complete the step-by-step profile and attach your resume (either is acceptable, both are preferable).</li></ul>Our commitment to Diversity and Inclusion:Fiserv is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies:Fiserv does not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions.Warning about fake job posts:Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used by cyber criminals to target your personally identifiable information and/or to steal money or financial information. Any communications from a Fiserv representative will come from a legitimate Fiserv email address.<h4>Experience Level</h4>Mid Level

Quality Assurance Specialist

Quality Assurance Engineer, Aladdin Engineering, Vice PresidentAbout 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><li>Creative thinker: Analyze multiple solutions and deploy technologies in a flexible way.</li><li>Great teammate: Think and work collaboratively and communicate effectively.</li><li>Fast learner: Pick up new concepts and apply them quickly.</li></ul>Job Purpose / Background:AQE (Aladdin Quality Engineering) is a globally distributed team supporting Quality Engineering initiatives for Apps on Aladdin. AQE 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>Lead and manage a team of QA engineers, providing technical guidance, mentoring and performance feedback. Foster a culture of continuous improvement and accountability within the team.</li><li>Being hands-on and owning functional deliveries.</li><li>Responsible for managing comprehensive testing phases from planning to execution for functional and non-functional requirements including design, development, and delivery.</li><li>Collaborate with peers, product managers, developers, and other stakeholders to understand client requirements, provide input on design and ensure high quality deliverables.</li><li>Analyze and report on QA metrics, trends, and opportunities for improvement, presenting findings to senior management and recommending corrective actions.</li><li>Champion a culture of quality within the organization, driving awareness and adherence to Quality standards.</li><li>Prioritize and develop enhancements to continuously improve application stability and scalability.</li><li>Conduct reviews of applications and workflow processes to target automation effectiveness.</li><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</li><li>10+ 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 or a related field. Deep understanding of investment management processes, risk management methodologies, regulatory compliance requirements or Investment Accounting skills.</li><li>Proven track record of successfully leading and implementing QA programs that drive continuous improvement.</li><li>Deep understanding of software quality assurance and engineering processes, methodologies, and best practices. Solid understanding of Agile software development methodologies.</li><li>Excellent communication, interpersonal and leadership skills, with the ability to influence and collaborate effectively across diverse teams.</li><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><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><li>Problem-solving skills to identify and address complex issues.</li><li>Experience of working in Agile Development Team</li></ul>Nice to have and opportunities to learn:<ul><li>Strong knowledge of test automation frameworks, tools, and scripting languages along with strong analytical and</li><li>AZURE Dev Ops, CI/CD integration and associated tools and processes (Jenkins, Maven, SonarQube).</li><li>AI and Machine Learning (ChatGPT or GitHub CoPilot)</li><li>Cucumber and BDD</li><li>Cloud based testing.</li><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>Executive Level

BlackRock Services India Pvt Ltd

Quality Engineer

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

Teva Pharmaceuticals

Quality Analyst

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

Quality Austria Central Asia

External Auditor

Manager Quality AssuranceJob Description - QA Function Key Responsibilities:<ol><li>Quality System Documentation as per ISO 9001:2015 which includes maintaining and upgradation of QMS Manual, Operating Procedures &amp; relevant other controlled documentation.</li><li>Maintain correspondence with M/s LRQA Certification body for External Audits. </li><li>Co-ordinate with Nominated Representatives (NR’s) and Internal Auditors for ensuring effective implementation of QMS in the organisation.</li><li>Undertake Internal Audits as per 9001 &amp; Prepare Audit Plan as per QMS cycle. </li><li>Prepare Quality Assurance Plan (QAP) for New Build and Repair/Refit vessels.</li><li>Monitor Ship Delivery Documentations (SDD) status and provide support to ensure the documents are produced as per the requirement of Client.</li><li>Support for External Audits wrt ISO 3834 : 2021 &amp; ISO 17025 : 2017.</li><li>Timely Review of Vendor QAP’s &amp; GRAQ’s submitted by Vendor and Design dept.</li><li>Timely input to BD Team wrt RFP/Build Specification Requirement’s. </li><li>Timely Analysis and Improvement wrt Inspection Remarks/Reworks/GD Defects. </li><li>Support for Implementation of Business Excellence Model (EFQM) &amp; CMMI L3.</li><li>Maintain / upgrade Shipyard Quality Standard and Critical tech. documentation.</li><li>Undertake Vendor Evaluation/Supplier Evaluation as per requirement.</li><li>Review of Statement of Technical Requirements (SOTR’s) provided by Design.</li><li>Prepare Measurement Plans &amp; Protocols as per project requirements.</li><li>Ensure timely Calibration of Yard instruments registered with QA.</li><li>Digitalize QA processes in consultation with IT/ERP team.</li><li>Collate learnings from each project and assist in conduct Lessons Learnt (LL) workshop as per requirements.</li><li>Conduct of MRM as per ISO 9001:2015 requirements.</li><li>Preparation of various presentations on process performances for periodic review with Management.</li><li>Monthly follow-up for monitoring of trends for DPP/KPI’s to identify the gaps in Product conformity and Process performance and provide regular feedback to Management.</li><li>ISO Awareness training to employees/Internal auditors.</li><li>Prepare Annual budget for Quality function. </li><li>Assist in CAS Audit &amp; Inter Business Audit </li><li>Assistance in providing input for Quality Council Meeting &amp; maintain MOM.</li><li>Assistance in providing input for Q4 Zine (IC Level) &amp; Quality Bulletin (Quality Council)</li><li>Maintain Technical Library in Yard.</li><li>Conduct Quality Month Celebration on November month involving all stakeholders.</li></ol>

Larsen & Toubro Ltd

Document Control Specialist<ul><li>Attend and complete Foundational Training, acquire process skills and meet qualification requirements.</li><li>Understand UL file structure, terminology and systems needed for Processing backend work.</li><li>Utilize system software and tools (internal and customer facing) to manage certification documents and correspondence while following appropriate Work Instructions/ SOPs.</li><li>Receive projects for processing/ fulfilling backend work from various functions and Industries.</li><li>Review project details to ensure readiness of information to process and determine further hand-off to subsequent function/ processes as applicable at the end of project completion.</li><li>Demonstrate ability to analyze data post certification for discrepancies then proactively communicate with appropriate function/departments to resolve issues within a project, if any, in order to complete assigned task/project in a timely manner.</li><li>While processing backend work, documents project status as needed.</li><li>Resolves problems in an expedient, professional and courteous manner.</li><li>Expediently manages and maintains personal request queues and email box.</li><li>Attends to emails from stakeholders with sense of urgency and seeks the direction from leadership to resolve issues requiring additional help.</li><li>Be a change agent, support Business Transformation efforts and continuous improvement initiatives that drives quality and efficiency.</li><li>Ability to work effectively with a diverse team.</li><li>Read and follow the Underwriters Laboratories Code of Conduct and follow all physical and digital security practices.</li><li>Perform other duties as directed.</li></ul><ul><li>1–2 years of experience in a similar role; freshers are welcome to apply.</li><li>Minimum of a 3-year university degree.</li><li>Basic computer proficiency.</li><li>Strong command of MS Word and good typing skills.</li><li>Excellent communication, critical thinking, and interpretation skills.</li><li>IT or computer knowledge is an added advantage.</li><li>Ability to handle repetitive tasks without compromising quality.</li><li>Capable of working independently.</li><li>Actively participates in team discussions and provides constructive feedback when needed.</li></ul>A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.<h4>Experience Level</h4>Mid Level

UL India Pvt Ltd

Documentation Officer

Quality Assurance Engineer FTCWe serve the needs of online shoppers in all Arabic speaking and surrounding countries through our trusted, secure payment network that gives everyone the opportunity to shop online safely and easily. We build trust between buyers and online sellers by enabling consumers to transact online using the payment options they prefer with complete security and peace of mind while supporting the most popular payment methods available globally. ONAmazon team is responsible for Payment Experience in Middle East is launching deferred payment method - BNPL in Middle East . The QAE I will ensure the quality of payment features being launched . Key job responsibilities*: 1+ years of quality assurance engineering experience Experience in manual testing Experience in automation testing Knowledge of QA methodology and tools Demonstrated passions around software quality, and technology. Demonstrated ability to learn and develop technical skills<h4>Basic Qualifications</h4> - 1+ years of quality assurance engineering experience - Bachelor's degree - Experience in manual testing - Experience in automation testing - Experience in UI and API automation testing (Selenium/SOAPUI) <h4>Preferred Qualifications</h4>- Experience in API &amp; Mobile testing - Experience designing and planning test conditions, test scripts, and test data sets to ensure appropriate and adequate coverage and control Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit <a href="https://amazon.jobs/content/en/how-we-hire/accommodations">https://amazon.jobs/content/en/how-we-hire/accommodations</a> for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.<h4>Experience Level</h4>Entry Level

 Amazon India Limited 

Quality Assurance Engineer

QMS Specialist<h4>Job Title</h4>QMS Specialist<h4>Job Description</h4>Job title: QMS Specialist - responsible for keeping an oversight on the issuance and review of QMS documents, ensuring rigorous tracking and adherence to system integrity Your role:<ul><li>Provides oversight for issuance and review of QMS documents, ensuring meticulous tracking and documentation of all changes, upholding the highest standards of system integrity and accuracy, and aligning QMS practices with organizational goals.</li><li>Participates in the effective deployment and continuous improvement of QMS processes.</li><li>Collaborates with cross-functional teams and stakeholders to ensure effective communication and understanding of QMS processes, and provide basic guidance on compliance-related inquiries.</li><li>Updates and support update to QMS documents to maintain QMS integrity and consistency.</li><li>Develops professional expertise and applies comprehensive knowledge of QMS requirements to effectively address challenges and opportunities.</li><li>Participates in the enhancement of review and approval process for new and revised QMS documents, ensuring alignment with company standards and regulatory requirements.</li><li>Provides support during internal and external audits and inspections by assisting with the preparation of documentation, ensuring document compliance with quality standards, responding to basic audit queries, and coordinating the implementation of corrective actions related to QMS control.</li><li>Conducts assessments related to QMS control activities, identifying potential issues and implementing mitigation strategies to ensure the integrity and security of all records.</li><li>Implements and manages QMS control software updates and upgrades, ensuring minimal disruption and compliance with the latest standards.</li><li>Works under general supervision and established processes, utilizing independent judgment to navigate and adhere to operational procedures, ensuring compliance and optimal performance.</li><li>Resolves medium complexity requests efficiently, exercising judgment within defined procedures and practices to determine appropriate actions that align with organizational goals and objectives.</li><li>Establishes productive internal and external working relationships to resolve mutual problems, collaborating effectively to ensure smooth operations and achieve common goals.</li><li>Engages in ongoing training and development programs to expand knowledge and skills related to document control and quality management systems, staying abreast of industry standards and regulatory compliance.</li></ul> You're the right fit if: (4 x bullets max) 1. Experience- 5+yrs of experience in Medtech industry 2. Skills- Electronic Document Control and Management advantage for experience in Regulatory Requirements (design or production), Quality Management Systems (QMS), Troubleshooting, Process Improvements 3. Education- Bachelor's Degree in Mechanical/ Electrical Engineering, IT, Industrial Engineering, Science or equivalent 4. Anything else- Team work, work in multicultural environment, vigilance, diligence, Strong written and verbal communication skills. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. Indicate if this role is an office/field/onsite role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. • Learn more about <a href="https://www.philips.com/a-w/about.html" rel="noopener noreferrer" target="_blank">our business</a>. • Discover <a href="https://www.philips.com/a-w/about/our-history.html" rel="noopener noreferrer" target="_blank">our rich and exciting history</a>. • Learn more about <a href="https://www.philips.com/a-w/about/environmental-social-governance/our-purpose" rel="noopener noreferrer" target="_blank">our purpose</a>. If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care <a href="https://www.careers.philips.com/global/en/our-culture" rel="noopener noreferrer" target="_blank">here</a>.<h4>Experience Level</h4>Mid Level

Philips

Quality Control Chemist

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

Lead - QA/QC (WET IC)Essential Qualification:<ul><li>•                     B.E./B.Tech in Mechanical, Civil, or Chemical Engineering</li><li>•                     Minimum 18 years of total experience, with at least 12 years in Quality Assurance/Quality Control, specifically in large-scale industrial desalination, water treatment, or Water infrastructure EPC projects.</li><li>•                     Must hold Lead Auditor Certification in ISO 9001:2015</li></ul>Desirable Qualifications:<ul><li>•                     ASNT Level II / Level III in Non-Destructive Testing (NDT)</li><li>•                     CSWIP / AWS-CWI Welding Inspector Certification</li><li>•                     Certification in Water Quality Management, Desalination Technology, or Reverse Osmosis Processes</li></ul>Additional Qualifications:<ul><li>•                     Six Sigma Certification</li><li>•                     Certified in 5S, Kaizen, EFQM, or equivalent Quality Excellence Programs</li><li>•                     Job Description:</li><li>•                     Develop, implement, and continuously improve a comprehensive QMS aligned with ISO 9001:2015 </li><li>•                     Prepare and approve quality documentation such as Project Quality Plan, Inspection and Test Plans, Method Statements, Material submittal logs, in alignment with client specifications, international codes, and industry best practices.</li><li>•                     Provide strategic oversight to QA/QC teams across multiple projects, ensuring timely inspections, audits, compliance, and close-out of Non-Conformances (NCRs).</li><li>•                     Interface with internal customers engineering, procurement, and construction teams to integrate quality requirements early in the project lifecycle.</li><li>•                     Establish and maintain vendor and subcontractor quality control systems for fabrication, assembly, and erection of water treatment equipment, pipelines, mechanical systems, and civil structural elements.</li><li>•                     Lead regular Quality Review Meetings with clients, contractors, and third-party inspection agencies to monitor KPIs, resolve quality issues, and ensure proactive control.</li><li>•                     Review and approve test reports, calibration records, and material traceability documentation for desalination components (RO membranes, pumps, pressure vessels, etc.).</li><li>•                     Conduct Internal &amp; External Quality Audits and provide strategic recommendations to align with evolving regulatory and compliance requirements.</li><li>•                     Ensure project-wide quality training, toolbox talks, and motivational programs for all levels of staff to maintain a quality-focused culture.</li><li>•                     Maintain accurate records of inspection reports, audits, and quality documentation to support project handover and warranty phases.</li><li>•                     Serve as a technical mentor to QA/QC Engineers and Inspectors, ensuring competency development and alignment with project goals.</li><li>•                     Act as a client-facing authority on all quality-related matters throughout the project lifecycle, from design review to commissioning.</li></ul>Key Competencies:<ul><li>•                     Proven leadership track record in driving quality systems, compliance, and operational excellence across large EPC projects in water treatment and desalination infrastructure.</li><li>•                     Excellent documentation, communication, and team leadership skills</li><li>•                     Thorough knowledge of codes &amp; standards</li></ul>

QA / QC Manager

Lead Operational Excellence (Commercial Excellence)<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>We are looking for seasoned Marketing professionals looking to pivot their career into Operational Excellence while leveraging their rich marketing and branding experience. Job Summary We are seeking a dynamic and experienced Leader in Operational Excellence for overseeing the implementation of an operational framework, optimizing organizational processes through data analysis, and fostering continuous improvement. The role involves identifying and resolving operational issues, implementing knowledge management strategies, and enhancing employee proficiency in operational methodologies. The primary goal is to drive efficiency, resilience, and cost-effectiveness while ensuring adherence to performance metrics and targets. Roles &amp; Responsibilities <ul><li>You will be responsible to strategize and deploy the Process Excellence framework, Lean Management System, benchmarking and continuous improvement to enhance productivity across functions and teams in the business unit.</li><li>KAIKAKU (Radical change) across functions and team in the business unit.</li><li>You will be responsible to drive the process simplification and process improvement through leading a structured ideation process to drive innovation, eliminating non-value-adding activities, removing redundancies, digitizing tasks, outsourcing non-core activities and create more time for scientific endeavors.</li><li>You will be responsible to drive and implement a Cost Optimization program via Product and Cycle-time Excellence (PACE) methodology, identifying cost-saving ideas with functional leads, setting baselines and targets, and reviewing progress regularly.</li><li>You will be responsible for Business Process Redesign (BPR) and Metric Improvement through Strategic Initiatives. Also, evaluate and optimize business processes for scalability and future needs, conducting thorough analysis and workshops with stakeholders. Implement standardized work instructions and modifications to enhance efficiency and effectiveness.</li><li>You will be responsible to establish and manage knowledge sharing practices, overseeing implementation and application of knowledge, and maintaining a comprehensive repository for future reference.</li><li>You will be responsible to build leadership skills and motivate team members for improved Operational Excellence (OE) skills, enhancing their potential and resolving organizational challenges.</li></ul><h4>Qualifications</h4>Educational qualification: B.E/B.Tech preferably with an MBA Minimum work experience: 12 -15 years of experience in Pharma/ FMCG with core experience in Sales/ Marketing/ Commercial Excellence roles.  Skills &amp; attributes: Technical Skills<ul><li>Master Black Belt/ Black Belt Certifications in Lean Six Sigma, Certification in Project Management and other improvement methodology.</li><li>Prior experiences in internal/external process consulting, Process Excellence Framework</li><li>Good knowledge of Lean Six Sigma Methodology &amp; Tools</li><li>Understanding of Strategic Planning and business processes</li><li>Good in Data Analytics, visualization, deriving insights and providing recommendations</li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills</li><li>Business Acumen &amp; Decision Making</li><li>Strong analytical and problem-solving abilities</li><li>Ability to work collaboratively with own team and cross-functional teams</li></ul><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>Senior Level

Dr Reddys Laboratories

Team Leader - Operations

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

Valeo India Private Limited

Quality Manager

Senior Manager, CorpQualAud-ARPL-CQA AR
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>Responsible for auditing Apotex Enterprise sites, Apotex and Apotex Pharmachem Group of Companies’ suppliers encompassing audit scheduling, execution, reporting, follow-up and closure of the audits. Accountable for adhering to the requirements of the Apotex’s Quality Manual, policies, procedures; and applying all regulatory standards such as ISO, Health Canada, FDA, EU/EMEA, MHRA, PIC/s, ANVISA and TGA, when conducting audits. Responsible for recommending audit system enhancements based on the learnings leveraging the existing system/field experience and collaborating with management to ensure continuous compliance, development &amp; improvement of the Corporate Quality Audit program.<h4>Job Responsibilities</h4><ul><li>Execute Corporate and supplier audits such as first GMP, routine, Targeted Technical Assessment (TTA) and For-Cause audits in accordance with Apotex’s SOPs and current GMP regulations</li><li>Adopt the best practices of Excellence in Partnership to develop and sustain effective relationships with Apotex sites, suppliers, contractors, and business partners</li><li>Perform Due Diligence audits of potential new Apotex suppliers, generate reports and provide recommendations pertinent to suitability and sustainability of the quality and compliance of new suppliers. Propose remediation plans to mitigate risks that could be impeding the future stability of Apotex supply chain</li><li>Liaise with Apotex Enterprise sites to evaluate the leading indicators such as QPIs prior to conducting site audits to ensure high risk areas are included as part of the site audit scope. Communicate potential non-compliance aspects of the audit outcome with the applicable site leadership team and escalate to Apotex Escalation Committee (AEC) as appropriate</li><li>Research and compile all available supplier quality/procurement data such as complaints, investigations/deviations, recalls in Apotex systems (SAP, QMS TW, LIMS, etc.) and external systems (e.g. Health Canada, FDA, MHRA websites) to ensure high risk areas are included as part of the audit scope.</li><li>Perform Risk Profiling of Apotex suppliers for Predictive Analytics to determine the audit frequencies based on the risks</li><li>Compile precise, accurate and chronologically factual audit reports within the allotted time to enable meaningful review and approval of the audit reports</li><li>Communicate the identified deficiencies and compliance risks to appropriate business stakeholders such as Global Active Pharmaceutical Ingredients (GAPI), External Manufacturing Quality (EMQ), Supplier Quality (SQ), Business Development (BD), Apotex Site Heads and Global Supply &amp; Technical Operations (GSTO)</li><li>Support the sites with developing and executing remediation actions to drive sustainable compliance to regulatory and Apotex’s standards. Evaluate the appropriateness of proposed CAPAs and remediation plans, monitor the progress and evaluate the effectiveness of the CAPAs implemented</li><li>Provide authoritative technical and regulatory guidance/direction to internal and external stakeholders pertinent to regulatory compliance</li><li>Provide expert inspection and logistics support during inspections of Apotex sites by regulatory agencies and customers when requested</li><li>Prepare, update and review proposed changes to SOPs</li><li>Share knowledge, collaborate with auditors across the regions to enhance expertise in different disciplines and to mentor/coach new &amp; existing auditors</li><li>Review emerging/ever-changing regulatory landscape, standards &amp; inspection trends to stay a step ahead of the regulators in protecting Apotex’s interests internally and externally</li><li>Fiscally responsible for spending in accordance with company policy and to accomplish budget targets favourable to plan</li><li>Accountable for meeting individual and departmental monthly, quarterly and yearly audit metrics</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.</li><li>Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.</li><li>All other relevant duties as assigned.</li></ul> <h4>Job Requirements</h4><ul><li>Education<ul><li>University degree in science or Regulatory affairs related program</li><li>Background in pharmaceutical/chemical sector would be an asset</li></ul></li><li>Knowledge, Skills and Abilities<ul><li>Excellent knowledge in current good manufacturing regulations and standards as applicable to the pharmaceutical industry such as ISO, Health Canada, FDA, EU/EMEA, MHRA, PIC/s, ANVISA and TGA</li><li>Expertise in at least one specific area: non-sterile manufacturing, sterile manufacturing, biopharmaceuticals, medical devices, API, excipients and intermediates is preferred.</li><li>Ability to review and comprehend the requirements of ICH, WHO, EXCiPACT, ISO, IPEC, ISPE, etc. guidance documents</li><li>Clear and concise written and verbal communication in Apotex’ s language of business</li><li>Demonstrated organizational skills and strong attention to details</li><li>Demonstrated ability to effectively manage multiple priorities in a fast-paced environment</li><li>Demonstrated ability to exercise discretion, maturity, good judgement and maintain strict confidentiality when exposed to, and handling, sensitive and confidential information</li><li>Work independently or in a team setting to achieve individual, departmental and organizational goals</li><li>Advanced computer skills, including Microsoft Office Products</li><li>Working knowledge with electronic Enterprise systems such as Quality Management System TrackWise (QMS TW), Systems Applications and Products (SAP) and Laboratory Information Management System (LIMS) would be an asset</li></ul></li><li>Experience<ul><li>Minimum 10 years of relevant experience in the Pharmaceutical industry with a minimum of 5 years spent in Quality operations, Quality Assurance and Quality Audits</li><li>Working knowledge and/ or hands-on experience with the other Pharmaceutical Quality Systems would be an asset</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Senior Level

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External Auditor