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Procurement SpecialistAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<h4>The Position</h4>Procurement Specialist - Research &amp; DevelopmentRoche India – Roche Services &amp; SolutionsHyderabadA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love.That’s what makes us Roche.Roche has defined an exciting 10-year ambition plan, requiring us to adapt and transform to our evolving ecosystem and challenges ahead of us. We have redesigned our Global Procurement (GP) organization to ensure we can succeed in this new environment and deliver on our mission for patients by building new capabilities and creating a more agile organization. Our goal is to improve our ability to deliver on our vision to “accelerate Roche’s goal to bring innovative solutions to patients quickly and efficiently through business and supplier partnerships.” If you are excited about driving this change and catalyzing the future in the R&amp;D procurement capability, the Procurement Specialist - Clinical role is for you.What is the Delivery capability?The Delivery capability covers the core procurement activities from category management, strategic and operational sourcing, supplier management, content strategy definition, and execution. The Delivery capability comprises many communities grouping categories of the same value chain or having commonality. The communities are key enablers of strong category expertise while allowing flexibility in the procurement delivery response to the evolving needs of our customers.This position is part of the Indirect Procurement Delivery team reporting into the Procurement Delivery Operations Lead - R&amp;DAre you wondering what is in it for you?Are you interested in further developing and leveraging your market knowledge, business partnering, and influencing skills? Here is why we think the Procurement Specialist - Clinical role is a fantastic job to consider!As a Procurement Specialist, you will work in a dynamic global environment where you bring analytical thinking, planning, execution, and focus to the procurement sourcing and delivery capability area. Thanks to your strong problem-solving and core procurement skills, you will effectively collaborate with internal procurement (customer relationship management, contracting, solutions, etc.) and business stakeholders to translate business needs into sourcing, spend management activities, and content enhancement. Based on your general procurement and commodity expertise, you ensure the effective and efficient delivery of core procurement services and continuous improvement of automation and content availability. You will work closely with team members to support customer demand, improve the customer buying experience, deliver on day-to-day operational activities, and provide capacity and expertise to provide productivity and other customer-oriented projects/solutions.Your Opportunity:Your successful performance and contribution depend on the full embodiment and demonstration of core mindsets and behaviors, including an entrepreneurial spirit, enterprise thinking, inclusive collaboration, and desire for continuous learning that underpin our culture and ways of working.As a Procurement Specialist, you will play a variety of roles according to your experience, knowledge, and the general business/team requirements, such as:<ul><li>Sourcing and category subject matter specialist conducting market and internal analysis to develop and implement strategies and tactical plans for Roche to source and negotiate for third-party goods and services that satisfy stakeholder requirements.</li><li>Procurement practitioner delivering and executing sourcing strategies by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management, and project management skills to achieve objectives and key results.</li><li>Content and automation advocate translating sourcing outcomes and opportunities into content and automated buying channels that improve business adoption, satisfaction, and overall efficiency.</li></ul>You will work within the broader team and GP networks and squads to determine the various roles needed to deliver project and foundational work.Who you are: Skills <ul><li>You hold a university degree, with a business degree preferable. You also have 3+ years of experience in sourcing, contracting, operational efficiency projects, or relevant commodity experience, preferably in the Pharmaceutical industry</li><li>Knowledge in the Clinical Development and/or Clinical Technologies area (e.g. IxRS, Patient recruitment,  Patient questionnaires, licensing etc.)</li><li>The ability to explain general capability area information to others or collect/translate moderate complexity stakeholder requirements in straightforward situations</li><li>Knowledgeable in procurement systems and operational processes, such as contracting, e-Sourcing, and spot buying is desired</li><li>Proven capability in negotiating project budgets and contracts </li><li>You have knowledge and experience in supplier management, contract negotiations, cost optimization, market research &amp; analysis in R&amp;D categories, and understand the related R&amp;D regulations (e.g. GCP)</li><li>You have skills in project management</li><li>Business level fluency in English</li></ul>Mindset &amp; Behaviors<ul><li>You strive to act as an enterprise thinker and leverage knowledge and expertise to create solutions for business customers by proactively fostering collaboration, including across the procurement network</li><li>You are action-oriented and can make decisions and influence others to do the same; you repurpose work and ideas in favor of starting from scratch</li><li>You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement</li><li>You work with colleagues across procurement, business, and the broader Roche organization to broaden knowledge and expertise, better understand customer needs, and connect the dots</li><li>You are open-minded and inclusive, generously sharing ideas and knowledge while being receptive to ideas and feedback from others</li></ul><h4>Who we are</h4>A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together.Roche is an Equal Opportunity Employer.<h4>Experience Level</h4>Mid Level

Roche Diagnostics India Pvt Ltd

Procurement Manager

QMS/CAPA Engineer<h4>Job Title</h4>QMS/CAPA Engineer<h4>Job Description</h4>Job title: QMS/CAPA Engineer Responsible for supervising the QMS team, ensuring efficient execution of quality management system (QMS) activities in compliance with company policies. The role monitors key quality performance indicators, analyzing data to identify trends and areas for improvement, and reporting to higher management. The role ensures timely process implementation and deployment, tracking progress and verifying effectiveness. The role conducts risk assessments and manages mitigation activities, developing strategies to minimize impact and facilitates cross-functional collaboration to resolve quality issues. The role drives continuous improvement initiatives within the QMS, proposing enhancements to processes, tools, and systems, guiding the QMS team to achieve operational goals. additionally, an active participation in CAPA facilitation is required Your role:<ul><li>Supervises day-to-day operations of the QMS team, ensuring all quality processes are executed efficiently and in compliance with company policies and other necessary requirements.</li><li>Manages the deployment and maintenance of QMS processes in the assigned area/ areas such as document control, training, and internal audits, ensuring they are effective, compliant, and aligned with both regulatory requirements and business needs.</li><li>Monitors and reports on the effectiveness of QMS processes by analyzing performance metrics, identifying trends, and developing action plans to address gaps, enhance compliance, and improve overall quality.</li><li>Prepares for and supports external audits and inspections by ensuring all necessary documentation is available and providing detailed responses to audit findings.</li><li>Facilitates cross-functional collaboration to resolve quality-related issues, working closely with other departments to ensure alignment and effective problem-solving.</li><li>Manages the documentation and resolution of non-conformance reports (NCRs), ensuring systematic tracking, effective resolution, and implementation of preventive measures to avoid recurrence.</li><li>Conducts risk assessments and manages risk mitigation activities, identifying potential risks to product quality and QMS integrity, and developing strategies to minimize their impact.</li><li>Drives continuous improvement initiatives within the QMS, proposing and implementing enhancements to processes, tools, and systems to improve overall quality performance and operational efficiency.</li><li>Addresses difficult to moderately complex issues or problems, requiring the evaluation of identifiable factors, following established processes and operational policies in selecting methods and techniques for obtaining solutions.</li><li>Guides and mentors the QMS team, actively contributing to employee selection, performance management, compensation management, career development, and overseeing operational processes.</li><li>Participates in training sessions to stay updated on quality standards and QMS procedures, actively engaging in learning opportunities to enhance understanding of industry regulations and best practices.</li><li>Manages CAPAs as CAPA engineer</li></ul> You're the right fit if: (4 x bullets max) 1. Experience- 10+yrs of experience in Medtech industry. 2. Skills-* German writing/speaking - preferred* English writing/speaking skills - must • Regulatory Requirements • Quality Management Systems (QMS) • Project Management • Data Analysis &amp; Interpretation • Process Improvements • Technical Writing • Training Content Development3. Education- Bachelor's / master’s degree, in engineering/science field or equivalent. 4. Anything else- Master's in areas such as Quality Management Systems, Quality Audits or equivalent in highly regulated environments/industries such as MD, Pharma, Automotive. 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>.#LI-PHILIN

Philips

Quality Control Engineer

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

Taskus India Private Limited

Quality Analyst

Quality Assurance EngineerWe are looking for a Quality Assurance Engineer, testing to join our Quality Engineering team. This is an amazing opportunity to work on various Clarivate products and services which could include automation, manual and security aspects of testing. We have a great skill set in Test Automation using Selenium with Java, API Testing, Security Testing, Browser Stack, Performance Engineering using JMeter and many other latest technologies. We would love to speak with you if you have skills in Selenium, Java, Java Script, or Python.About You<ul><li>Bachelor’s degree in Engineering or master’s degree (BE, ME, B Tech, MTech, MCA, MS) </li><li>2+ years of experience in software automation, BDD framework, API automation and test frameworks.</li><li>Good programming skills in language like Java. Strong coding &amp; debugging skills in Selenium binding with Java.</li><li>Experience in version control system Git or bitbucket.</li><li>Understanding of test automation frameworks &amp; assisting/reviewing script creation </li><li>Familiarity of testing pyramid, understanding of functional and non-functional aspects of testing</li><li>Familiarity and clear understanding of Agile &amp; Kanban development approaches</li><li>Familiarity of working with test and defect management tools like JIRA and confluence.</li></ul>It would be great if you also have…<ul><li>Working familiarity with cloud tools like AWS</li></ul>What will you be doing in this role?<ul><li>This is hands on role with skill sets in automation engineering</li><li>The person will not have a dedicated team under him</li><li>Be prepared to evaluate, learn and use new tools</li><li>Work with team members in a supportive way which encourages team building and confidence with individual members </li><li>Work accurately sometimes even under pressure &amp; delivering as per the expectations </li><li>Prioritizing individual &amp; team’s workload </li></ul>Product you will be developingThis intellectual property–focused product enables comprehensive IP searches, taxonomy management, and AI-driven search capabilities, supporting clients in research, innovation, and patent filing through advanced analytical data.About the TeamThe existing team is spread across India and includes Testers with strong technical and analytical skills. We have a great skill set in Java, Selenium, Python, C#, HTML5, Web API, SQL and JavaScript, to name a few of the Tools and technologies. You would be part of large QA Group responsible for delivering world class products and innovative solutions in the field of IP.Hours of WorkThis is permanent position with Clarivate. You will be working in IST time zone. 9 hours of work per day including 1-hour lunch break.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>Mid Level

Clarivate

Quality Assurance Engineer

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

Quality Manager

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

Quality Control Chemist

Petroleum Engineer (QA Specialist)We are looking for the right people — people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and their careers. Experience the challenges, rewards and opportunity of working for one of the world’s largest providers of products and services to the global energy industry.<h4>Job Duties</h4>Under broad direction, mentors a team of Software Testers that can be comprised of Manual and Automated Test Engineers. Comprehensive understanding of all elements of a successful software development program. Including but not limited to Code Inspections, Manual Testing, Automated Testing, Functional Requirements, Design, Usability, Test plans and Results and Defect Management. Assists with secure architecture design reviews and supports preparing applications for security testing. Ensures security vulnerabilities have been mitigated. This role is an integral part of the planning of future releases including estimating efforts required in Testing and Documentation and advising on product improvements based on experience gained from previous releases and customer feedback. Usually works on projects of moderate to complex scope. Requires completion of an undergraduate degree in Computer Science, Geo-science, Petroleum Engineering or similar discipline, and 4+ years of related experience, including software testing and/or development experience. Completion of a masters degree is preferred.<h4>Qualifications &amp; Experience</h4>Key Responsibilities <ul><li>Lead quality assurance efforts across upstream Oil &amp; Gas applications, ensuring robust testing coverage and high software reliability.</li><li>Design, develop, and execute effective test cases for various testing types including functional, integration, performance, regression, and UAT.</li><li>Collaborate with cross-functional teams including developers and Product Owners to align testing strategies with business goals.</li><li>Manage defect tracking and resolution processes, ensuring timely and accurate reporting.</li><li>Contribute to test automation initiatives and framework enhancements to improve efficiency and scalability.</li></ul> Qualifications <ul><li>Bachelor’s degree in Petroleum Engineering or a related discipline is required</li><li>Minimum 4 years of relevant experience in upstream Ol &amp; Gas software environments, preferably in a quality assurance role</li><li>Solid understanding of drilling and completions workflows such as well construction, fluids management, and performance monitoring.</li><li>Experience with the EDT suit of application is a plus</li><li>ISTQB Foundation Level Certification is preferred but not mandatory.</li><li>Excellent communication, analytical and decision-making skills are required </li></ul> Technical Expertise <ul><li>Proficient in software testing methodologies: Smoke, Functional, Integration, Performance, Regression, and UAT.</li><li>Hands-on experience with Agile methodologies and ALM tools like Azure DevOps/TFS or JIRA.</li><li>Familiarity with engineering software such as WellCat, WellPlan, and Compass is a plus.</li><li>Working knowledge of automation tools and test framework design.</li><li>Strong communication and documentation skills with a collaborative mindset.</li></ul>Halliburton is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, disability, genetic information, pregnancy, citizenship, marital status, sex/gender, sexual preference/ orientation, gender identity, age, veteran status, national origin, or any other status protected by law or regulation. Location4th Floor, Gardenia 2D, Bengaluru, , 560103,  Job DetailsRequisition Number: 201580   Experience Level: Experienced Hire  Job Family: Engineering/Science/Technology  Product Service Line: Landmark Software &amp; Services    Full Time / Part Time: Full TimeAdditional Locations for this position:  Compensation Information Compensation is competitive and commensurate with experience.

Halliburton

Team Member - Analytical 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

Dr Reddys Laboratories

Quality Assurance Associate

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 EngineeringAbout your role: As a Quality Assurance Engineering - Advisor I, you will play a critical role in ensuring the highest standards of quality and performance for our software products. Your in-depth expertise will help shape the quality assurance processes and frameworks, ensuring that our solutions are reliable and meet the needs of our clients. You will work closely with development and product teams, identifying issues and implementing best practices to drive continuous improvements in our QA operations. This role offers the opportunity to make a significant impact on the quality of our products and the overall user experience.What you'll do:<ul><li>Lead the execution of detailed quality assurance testing for complex software products.</li><li>Develop and implement comprehensive test strategies and plans.</li><li>Identify, report, and track software defects to resolution.</li><li>Collaborate with development and product teams to improve quality practices.</li><li>Mentor and guide junior QA team members to ensure adherence to best practices.</li><li>Participate in continuous improvement initiatives within the QA team.</li><li>Responsibilities listed are not intended to be all-inclusive and may be modified as necessary.</li></ul>Experience you'll need to have:<ul><li>6+ years of experience in software quality assurance</li><li>3+ years of experience in automation testing</li><li>3+ years of experience in performance testing</li><li>3+ years of experience in Agile methodologies</li><li>6+ years of an equivalent combination of educational background, related experience, and/or military experience</li></ul>Experience that would be great to have:<ul><li>Experience with automated testing tools</li><li>Knowledge of continuous integration and continuous deployment (CI/CD) tools</li><li>Familiarity with security testing practices</li><li>Understanding of software development lifecycles</li><li>Certification in software testing methodologies</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

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

Qualys Security Techservices Private Limited

Senior Quality Assurance Engineer

Sr. Executive Quality SystemsAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.<h4>A Day in the Life</h4>Responsibilities may include the following and other duties may be assigned.<ul><li>Provides oversight for the development and maintenance of quality programs, systems, processes and procedures that ensure compliance with policies and that the performance and quality of services conform to established internal and external standards and guidelines.</li><li>Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.</li><li>Works directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.</li><li>Leads audit and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits.</li><li>Prepares reports and/or necessary documentation (ex Corrective and Preventative Actions) and provides to applicable stakeholders, both internal and external.</li><li>Co-ordinates legal requests in support of government investigations or litigations.</li><li>Ensures the quality assurance programs and policies are maintained and modified regularly.</li><li>Facilitates uniform standards worldwide and enables best practice sharing, thereby fostering the achievement of company's mission globally.</li></ul>SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.DIFFERENTIATING FACTORSAutonomy: Entry-level individual contributor on a project or work team. Works with close supervision.Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities.Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems .Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information.Leadership and Talent Management: N / A – job at this level is focused on self-development .Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A), 0 years of experience required.Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. <h4>Benefits &amp; Compensation</h4>Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. <h4>About Medtronic</h4>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" rel="noopener noreferrer" target="_blank">here</a>   <h4>Experience Level</h4>Senior Level

India Medtronic Pvt. Ltd

Quality Control Executive

Process Excellence Specialist Are you full of new ideas? Do you have strong process orientation and understand the need for good rigor? Do you enjoy working with teams to bring about change and transformation?  We are offering an exciting opportunity to define and implement, simplified and strengthened practices for handling of the L&amp;H treaty life cycle – from onboarding to claims payments, leveraging technology to enable the delivery of exceptional services by Operations. Major responsibilities: <ul type="disc"><li>Support in the design and implementation of business process improvements and required capabilities through leveraging data and tooling solutions</li><li>Work with business networks to identify opportunities for improvement.  Leverage knowledge of and insight to the business challenges and market considerations.</li><li>Support in the execution of initiatives and projects, prioritising effectively to implement changes </li><li>Develop structured business cases with clear benefit realisation metrics</li><li>Enable adoption of changes by working closely with the Operations teams to support them</li><li>Work with stakeholders to ensure handoffs and dependencies are well addressed and work smoothly</li><li>Develop and measure process adherence and other key performance metrics</li><li>Work with colleagues across Business Architecture to leverage reporting and quality insights to steer process improvements</li><li>Represent Operations in organisational initiatives</li></ul> About the team  The team consists of 8+ members currently located in different offices across key Swiss Re offices globally, working closely with the Market Units, COO teams, Risk management and IT partners.You would be working as part of a wider CoE team, which also covers risk and quality and skills and capabilities pillars, and an integrated approach across these pillars is critical. About you <ul type="disc"><li>You have proven track record in delivery and execution.</li><li>You have deep knowledge of L&amp;H processes and bring an e2e mindset</li><li>You have demonstrable experience or previous exposure to either: process design/improvement, change management</li><li>You work effectively with various stakeholders across the value chain and can easily move between operational, technical and technology topics.  You adopt a partnership mindset.</li><li>You have an eye for improvement and a preference to work with simple and pragmatic approaches</li><li>You have excellent communication, interpersonal and influential skills</li><li>You have the ability and courage to constructively challenge the status quo</li><li>You bring a college degree or equivalent work experience as well as excellent command of spoken and written English</li></ul> About Swiss Re Swiss Re is one of the world’s leading providers of reinsurance, insurance and other forms of insurance-based risk transfer, working to make the world more resilient. We anticipate and manage a wide variety of risks, from natural catastrophes and climate change to cybercrime. We cover both Property &amp; Casualty and Life &amp; Health. Combining experience with creative thinking and cutting-edge expertise, we create new opportunities and solutions for our clients. This is possible thanks to the collaboration of more than 14,000 employees across the world. Our success depends on our ability to build an inclusive culture encouraging fresh perspectives and innovative thinking. We embrace a workplace where everyone has equal opportunities to thrive and develop professionally regardless of their age, gender, race, ethnicity, gender identity and/or expression, sexual orientation, physical or mental ability, skillset, thought or other characteristics. In our inclusive and flexible environment everyone can bring their authentic selves to work and their passion for sustainability. If you are an experienced professional returning to the workforce after a career break, we encourage you to apply for open positions that match your skills and experience.   Keywords:   Reference Code: 135364

Swiss Re

Process Specialist

Project Quality ManagerBe part of the solution at Technip Energies and embark on a one-of-a-kind journey. You will be helping to develop cutting-edge solutions to solve real-world energy problems.We are currently seeking a Project Quality manager reporting directly to Head of Quality – IOC to join our Quality team based in  Chennai &amp; Delhi Operating CentersAbout us:Technip Energies is a global technology and engineering powerhouse. With leadership positions in LNG, hydrogen, ethylene, sustainable chemistry, and CO2 management, we are contributing to the development of critical markets such as energy, energy derivatives, decarbonization, and circularity. Our complementary business segments, Technology, Products and Services (TPS) and Project Delivery, turn innovation into scalable and industrial reality.Through collaboration and excellence in execution, our 17,000+ employees across 34 countries are fully committed to bridging prosperity with sustainability for a world designed to last. About the mission we offer you:<ul><li>To manage and coordinate Project quality assurance and quality control activities providing leadership, expertise and direction.</li><li>To apply high level of competencies and capabilities (tools, procedures, organization and resources) in discharging quality assurance functions in the assigned projects (Engineering / EPC).</li><li>To define the quality assurance and quality control execution methodology for the project assigned </li><li>Represent project on quality matters with Client and  stakeholders </li></ul>Relationship Responsibilities:Reports to: Head Quality - IOCDirectly supervises (operationally): Nil Key Interactions:Internally: Project Managers, Other Department Managers/Project Leads (Engineering, Construction, QHSE, Procurement, P&amp;C, Proposals, Subcontract, Planning, IT, Administration Externally: Clients Quality Representatives, PMC, Subcontractors Quality team, Third Party Inspection Agencies , Certification agencies.Major Responsibility Areas:<ul><li>Define and implement Project Quality Plan.</li><li>Ensure implementation of Disciple Quality Plans where applicable. </li><li>Establishment of an approved Project Internal IMS audit plan and schedule. </li><li>Define and implement Project quality objectives / KPIs in liaison with Project management.</li><li>Plan, schedule, conduct / participate in project internal IMS audit as per project internal audit plan and schedule.</li><li>Follow up to ensure timely closure of audit findings ( internal / external).</li><li>Develop and conduct Project quality inductions, where mandated.</li><li>Facilitate Client / PMC audits in Projects and Home Offices. </li><li>Liaise and coordinate with other Operating Centers on quality matters where the scope of work is shared. </li><li>Conduct lesson learned workshops and quality awareness sessions.</li><li>Participate in non-conformity investigations, root cause analysis and validate corrective action proposals.</li><li>Review of Client / Contract quality assurance requirements and ensure collation, communication and maintenance of the same.</li><li>Review of Project Quality Plan and procedures in liaison with Project Manager. </li><li>Close coordination with Vendor performance Management and Site Quality Control on Quality performance</li><li>Document and facilitate investigation into quality incidents and non-conformities customer complaints. </li><li>Participate in Project quality reviews/ meetings. </li><li>Participate in CNQ review and root cause analysis as needed.</li></ul>Starting Date: Sept -Oct 2025About you:We love to hear from you and how you match this position. To be successful in this mission you should consider the following requirements:<ul><li> Bachelor’s degree in engineering</li><li>Minimum 7 years of experience including experience of handling FEED, Detailed Design and EPC projects of large and complex nature.</li><li>Familiarity with Project Life Cycle principles and significant project milestones </li><li>Conversant with Quality Management System standard ISO 9001:2018 and related guidelines with familiarity on ISO 45001:2018 and ISO 14001 :2015 standards.</li><li>Lead Auditor or Internal Auditor qualifications on ISO9001/ ISO45001/ ISO14001 desirable</li><li>Proficiency in writing plans, procedures, process flow mapping, etc.</li><li>Familiar with project / discipline objectives, targets, goals, KPIs and QHSE metrics </li><li>Possess an investigative and analytical mindset </li><li>Proficient in the use of root cause analysis methods (e.g. Fishbone, FMEA, FTA, ETA, 5 Whys…)</li><li>Project management knowledge in a multi discipline engineering project is desirable</li><li>Very good report writing skills  </li><li>Excellent management and leadership skills</li><li>Excellent interpersonal and influential skills</li><li>Knowledge on ASME/ API/ ASNT/ EN/ IS codes desirable </li><li>Fluency in professional English</li></ul> Your career with us:Working at Technip Energies is an inspiring journey, filled with groundbreaking projects and dynamic collaborations. Surrounded by diverse and talented individuals, you will feel welcomed, respected, and engaged. Enjoy a safe, caring environment where you can spark new ideas, reimagine the future, and lead change. As your career grows, you will benefit from learning opportunities at T.EN University, such as The Future Ready Program, and from the support of your manager through check-in moments like the Mid-Year Development Review, fostering continuous growth and development What’s next?Once receiving your application, our Talent Acquisition professionals will screen and match your profile against the role requirements. We ask for your patience as the team completes the volume of applications with a reasonable timeframe. Check your application progress periodically via personal account from created candidate profile during your application. We invite you to get to know more about our company by visiting  and follow us on LinkedIn, Instagram, Facebook, X and YouTube for company updates.#LI-MS2<h4>Experience Level</h4>Senior Level

Technip Energies

Quality Head

Manager, Global Quality Complaint SurveillanceWorking 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 ResponsibilitiesResponsible for managing and reporting of accurate and on time Global Quality metrics for Product Quality Complaints (PQC) in a fast-paced environment that support Tier Councils, Product Quality Complaint compliance &amp; trending across the organization, internal &amp; regulatory audits. Expertise with data management and analysis using electronic software solutions, eg VEEVA, Tableau, SpotFire, and Microsoft Office, with focus on Excel, PowerPoint, and SharePoint.Responsible to maintain a high level of knowledge &amp; understanding of Pharmaceutical/Biologic Quality Assurance, Device Quality Assurance, cGood Manufacturing Practices as applicable in global GMP regulations (including FDA, EMA, MHRA, PMDA, ENVISA, TGA).Responsible to develop &amp; maintain tools and dashboards in support of PQC trending, data surveillance and PQC user support.Responsible to provide PQC data assessments, highlighting trends, signals and risks and business critical information related to Product Quality Complaint data to Quality leadership in a timely fashion. Data &amp; trend assessments will be communicated with stakeholders in a manner commensurate with risk, and enabling appropriate action taking to protect BMS and our patients. Responsible to complete required training and provide support for Product Complaints, Product Surety and Quality Serialization business process activities.You are accountable for other key activities that support the business such as:<ul><li>SharePoint design, data requests/analysis, and providing communication of trends, signals and risks in addition to business critical information to leadership</li><li>Maintain expertise on PQC data management at BMS, including data sources, data quality, data management, data users</li><li>Report at appropriate intervals (weekly, monthly, quarterly, year-on-year etc) metrics on key compliance indicators related to PQC performance and procedural compliance (for example on-time closure, increasing/decreasing trends by product/defect category/market etc).</li><li>Review signals and trends that may present a risk to the organization and/or to our patients. Engage with PQC management and appropriate stakeholders to identify corrective actions. Align with PQC management for escalations to Quality leadership.</li><li>Provide recommendations and communications based on output from analytical tools and visualizations.</li><li>Provide risk assessment support for PQC processes, data management and related activities</li><li>Continuously improve process for assessment and reporting PQC data to drive consistency and understanding of Quality compliance-focused metrics</li><li>Use Operational Excellence and similar approaches to support the design of metric tools that facilitate proactive discussion and provide visibility/transparency to drive continuous improvement, prioritization and product quality related decisions</li><li>Lead teams in the development of tools and reports to optimize and standardize metrics</li><li>Lead collection and review of PQC data in response to health authority requests</li><li>Lead collection and review of PQC data in support of audit requests (internal and external audits)</li><li>Lead metrics initiatives related to product quality complaint programs and processes</li><li>Facilitate and drive standards for communication, management and visibility of product quality support metrics</li><li>Implementation and timely update of information to ensure content is current and accurate</li><li>Establish appropriate procedural documents for product quality support metrics</li><li>Cross train in other areas of the Global Quality organization to assist the business in developing its employees</li><li>Develop and maintain high quality relationships with key stakeholders</li><li>Work on multiple projects at one time and manage priorities based on timelines</li><li>Work independently with a high degree of professional integrity, be highly organized, and be detail-oriented</li><li>Perform duties as aligned with PQC management</li></ul>Qualifications &amp; ExperienceDegree/Certification/LicensureBachelor of Science degree in data analytics/statistics/biostatistics, engineering, chemistry, biology, or other quantitative field.Advanced degree preferred.Required Competencies<ul><li>Fluent in English, with proven professional working proficiency in English for reading, writing and speaking</li><li>Excellent communication with management, peers, and other functional areas</li><li>Excellent ability to analyse data to extract useful information and trends, and to translate data to effective messaging to  stakeholders and leaders supporting effective decision-making</li><li>Ability to work well cross-functionally with stakeholders</li><li>Ability to influence positively in a matrix environment</li><li>Proven ability to understand complex processes/problems and propose alternate solutions</li><li>Customer and partner focus, including the ability to listen to and incorporate feedback from key stakeholders</li><li>Demonstrated Enterprise mindset to be able to think and act across functions and divisions</li><li>Demonstrated ability to work in a matrixed organization with a range of technically, culturally, and geographically diverse teams and to influence areas not under direct control to achieve objectives and effectively communicate challenging goals and objectives</li><li>Excellent teamwork, interpersonal, and communication skills, with the ability to communicate and collaborate with employees and management at all levels and through various formats</li><li>Demonstrated strategic thinking capability and ability to balance conflicting priorities</li><li>Ability to provide innovative ideas or alternatives that create value including seeking new information and external insights without compromising compliance</li><li>Ability to clearly articulate analytical needs to functional partners</li></ul>Experience – Responsibility and minimum number of years<ul><li>A minimum of 5 years of experience in a data analytical role, or in a Quality role where data analytics was a key component in the pharmaceutical/ biotech/ device industry</li><li>Strong working knowledge/experience with systems such as QMS, SAP/ERP, Veeva</li><li>Experience with understanding how to respond to trend signals within the context of quality surveillance</li><li>Strong problem solving skills are required</li><li>Strong program and project management</li><li>Ability to manage multiple, simultaneous projects</li><li>Thorough understanding of Quality Risk Management</li><li>Mastery of relevant Quality compliance processes and regulations</li><li>Understanding of technical areas related to pharmaceutical and/or biological manufacturing, chemical and/or biochemical analyses, microbiological</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

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