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Principal Applied ScientistAre you passionate about creating innovative solutions that empower users to achieve more with Office applications? Do you have a strong background in natural language processing, generative AI, and engineering? If so, we are looking for a Principal Applied Scientist to join our team of data and applied science engineers working at the intersection of generative AI and engineering for Office. In this role, you will drive cutting-edge projects, contribute to the Copilot ecosystem, and help shape the Agentic future with one of the most widely used software products in the world. Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.<h4>Responsibilities</h4><ul><li>Applied Research &amp; Development: Design and implement machine learning models and algorithms that improve search, summarization, and content understanding in Office applications. Stay current with advancements in NLP and generative AI to inform product innovation.</li><li>Model Development &amp; Deployment: Build and optimize ML/DL models using frameworks like PyTorch or TensorFlow. Contribute to the deployment of models in production environments, ensuring scalability and performance.</li><li>Cross-Functional Collaboration: Work closely with engineering, product, and research teams to define goals, align on priorities, and deliver impactful features. Translate business needs into technical solutions.</li><li>Experimentation &amp; Evaluation: Conduct experiments to evaluate model performance, analyze results, and iterate on solutions. Use data-driven insights to improve precision, recall, and user satisfaction.</li><li>Innovation &amp; Impact: Explore new signals, data sources, and modeling techniques to enhance intelligent systems. Contribute to the evolution of the Copilot ecosystem and agentic experiences in Office.</li></ul><h4>Qualifications</h4>Required Qualifications:<ul><li>Bachelor's Degree in Statistics, Econometrics, Computer Science, Electrical or Computer Engineering, or related field AND 6+ years related experience (e.g., statistics, predictive analytics, research) <ul><li>OR Master's Degree in Statistics, Econometrics, Computer Science, Electrical or Computer Engineering, or related field AND 4+ years related experience (e.g., statistics, predictive analytics, research) </li><li>OR Doctorate in Statistics, Econometrics, Computer Science, Electrical or Computer Engineering, or related field AND 3+ years related experience (e.g., statistics, predictive analytics, research) </li><li>OR equivalent experience.</li></ul></li><li>6+ years of industry experience in applied machine learning or data science roles.</li><li>Proficiency in Python and ML libraries (e.g., PyTorch, TensorFlow). Experience with NLP, generative models, or content understanding is highly desirable.</li><li>Demonstrated ability to tackle open-ended problems and deliver practical, scalable solutions.</li><li>Solid written and verbal communication skills. Ability to explain complex technical concepts to non-technical stakeholders.</li></ul>Preferred Qualifications:<ul><li>Master's Degree in Statistics, Econometrics, Computer Science, Electrical or Computer Engineering, or related field AND 9+ years related experience (e.g., statistics, predictive analytics, research) <ul><li>OR Doctorate in Statistics, Econometrics, Computer Science, Electrical or Computer Engineering, or related field AND 6+ years related experience (e.g., statistics, predictive analytics, research) </li><li>OR equivalent experience.</li></ul></li><li>5+ year(s) experience creating publications (e.g., patents, peer-reviewed academic papers).</li><li>Hands-on experience with modern LLM evaluation techniques, including LLM-as-a-Judge, agentic evaluations, and RAG assessments.</li><li>3+ years experience developing and deploying large language models (LLMs), including agentic systems, supervised fine-tuning, and Reinforcement Learning (RLHF)</li><li>3+ years experience designing, implementing, and optimizing Retrieval-Augmented Generation (RAG) pipelines and advanced context engineering.</li><li>Experience contributing to research publications, patents, or open-source projects.</li><li>Hands-on experience deploying ML models in production environments.</li><li>Familiarity with the full product lifecycle, from ideation to deployment and iteration.</li></ul>Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.  We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request via the <a href="https://careers.microsoft.com/us/en/accommodationrequest" rel="noopener" target="_blank">Accommodation request form</a>. Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work.<h4>Experience Level</h4>Senior Level

Microsoft Corporation India Pvt Ltd.

Science Mentor

AI Applied Scientist 2Role Summary As a AI Applied Scientist for The Customer Service Applications Team, you will play a pivotal role in advancing Microsoft's mission to empower every individual and organization on the planet to achieve more. You will contribute to the development and integration of cutting-edge AI technologies into Microsoft products and services, ensuring they are inclusive, ethical, and impactful.    You will collaborate across product, research and engineering teams to bring innovative solutions to life, applying your expertise in machine learning, data science, and AI to solve complex problems. Your work will directly influence product direction and customer experience.  AI Mission and Impact We are in an era of unprecedented innovation and openness. As Microsoft continues to lead in AI, we are seeking individuals to help tackle some of the most exciting and meaningful challenges in the field. Our vision is to build a truly open architecture platform that enables users to summon tailored AI agents to drive real-world outcomes. We are looking for an (insert role/ external title) to join our team    This role will combine AI knowledge with applied science expertise and demonstrate a growth mindset and customer empathy. Join us in shaping the future of AI agents. Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.  <h4>Responsibilities</h4>Bringing the State of the Art to Products <ul><li>Build collaborative relationships with product and business groups to deliver AI-driven impact</li><li>Research and implement state-of-the-art using foundation models, prompt engineering, RAG, graphs, multi-agent architectures, as well as classical machine learning techniques.</li><li>Fine-tune foundation models using domain-specific datasets. - Evaluate model behavior on relevance, bias, hallucination, and response quality via offline evaluations, shadow experiments, online experiments, and ROI analysis.</li><li>Build rapid AI solution prototypes, contribute to production deployment of these solutions, debug production code, support MLOps/AIOps. Contribute to papers, patents, and conference presentations. - Translate research into production-ready solutions and measure their impact through A/B testing and telemetry that address customer needs.  </li><li>Ability to use data to identify gaps in AI quality, uncover insights and implement PoCs to show proof of concepts.</li></ul>Leveraging Research in real-world problems <ul><li>Demonstrate deep expertise in AI subfields (e.g., deep learning, Generative AI, NLP, muti-modal models) to translate cutting-edge research into practical, real-world solutions that drive product innovation and business impact.</li><li>Share insights on industry trends and applied technologies with engineering and product teams.</li><li>Formulate strategic plans that integrate state-of-the-art research to meet business goals.</li></ul>Documentation <ul><li>Maintain clear documentation of experiments, results, and methodologies.</li><li>Share findings through internal forums, newsletters, and demos to promote innovation and knowledge sharing </li></ul> Ethics, Privacy and Security Apply a deep understanding of fairness and bias in AI by proactively identifying and mitigating ethical and security risks—including XPIA (Cross-Prompt Injection Attack) unfairness, bias, and privacy concerns—to ensure equitable and responsible outcomes. <ul><li>Ensure responsible AI practices throughout the development lifecycle, from data collection to deployment and monitoring.</li><li>Contribute to internal ethics and privacy policies and ensure responsible AI practice throughout AI development cycle from data collection to model development, deployment, and monitoring. </li></ul>Specialty Responsibilities <ul><li>Design, develop, and integrate generative AI solutions using foundation models and more.</li><li>Deep understanding of small and large language models architecture, Deep learning, fine tuning techniques, multi-agent architectures, classical ML,  and optimization techniques to adapt out-of-the-box solutions to particular business problems</li><li>Prepare and analyze data for machine learning, identifying optimal features and addressing data gaps.</li><li>Develop, train, and evaluate machine learning models and algorithms to solve complex business problems, using modern frameworks and state-of-the-art models, open-source libraries, statistical tools, and rigorous metrics</li><li>Address scalability and performance issues using large-scale computing frameworks.</li><li>Monitor model behavior, , guide product monitoring and alerting, and adapt to changes in data streams.</li></ul><h4>Qualifications</h4><ul><li>Required Qualifications </li><li>Bachelor’s degree in computer science, Statistics, Electrical/Computer Engineering, Physics, Mathematics or related field AND 2+ years of experience in AI/ML, predictive analytics, or research OR Master’s degree AND 2+ years of experience OR equivalent experience </li><li>1+ years of experience with generative AI OR LLM/ML algorithms</li><li>Other Requirements: </li><li>Ability to meet Microsoft, customer and/or government security screening requirements are required for this role.</li><li> These requirements include but are not limited to the following specialized security screenings: </li><li>Microsoft Cloud Background Check: This position will be required to pass the Microsoft Cloud Background Check upon hire/transfer and every two years thereafter.</li><li>Preferred Qualifications: </li><li>Experience with MLOps Workflows, including CI/CD, monitoring, and retraining pipelines.</li><li>Familiarity with modern LLMOps frameworks (e.g., LangChain, PromptFlow)</li><li>Experience developing and deploying live production systemsone or more of the following: C#, Java, React/Angular, TypeScript.</li><li>Experience with design and implementation of enterprise-scale services </li><li>1+ years of experience publishing in peer-reviewed venues or filing patents</li><li>Experience presenting at conferences or industry events</li><li>1+ years of experience conducting research in academic or industry settings</li><li>1+ years of experience working with Generative AI models and ML stacks</li><li>Experience across the product lifecycle from ideation to shipping</li></ul> #BETJobs #CXAJobs #DVJobs #CXJobs #DYNAMICS365 #WEAREHIRING  #WEWANTTOTALKTOYOU! Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request via the <a href="https://careers.microsoft.com/us/en/accommodationrequest" rel="noopener" target="_blank">Accommodation request form</a>. Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work.<h4>Experience Level</h4>Mid Level

Automation Developer

Process R&D Scientist<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 seeking a highly skilled Process Scientist API (Active Pharmaceutical Ingredient) to join our team in Hyderabad, India. In this role, you will be responsible for developing, optimizing, and scaling up API manufacturing processes to ensure efficient and high-quality production of pharmaceutical ingredients.<ul><li>Design, develop, and optimize API manufacturing processes from laboratory scale to commercial production</li><li>Conduct experiments and analyze data to improve process efficiency, yield, and product quality</li><li>Troubleshoot process issues and implement solutions to enhance overall performance</li><li>Collaborate with cross-functional teams to ensure smooth technology transfer and scale-up of API processes</li><li>Prepare comprehensive technical reports and documentation for internal and regulatory purposes</li><li>Stay updated on current Good Manufacturing Practices (GMP) and regulatory requirements in the pharmaceutical industry</li><li>Participate in process validation activities and support regulatory filings</li><li>Mentor junior scientists and contribute to the continuous improvement of the department</li></ul><h4>Qualifications</h4><ul><li>Ph.D. or Master's degree in Chemistry, Chemical Engineering, or a related field</li><li>3-5 years of experience in API process development or a related field within the pharmaceutical industry</li><li>Extensive knowledge of API manufacturing processes and pharmaceutical industry regulations</li><li>Strong expertise in process development, optimization, and scale-up techniques</li><li>Proficiency in analytical techniques and instrumentation commonly used in API development</li><li>Excellent problem-solving and troubleshooting skills with a detail-oriented approach</li><li>Familiarity with Good Manufacturing Practices (GMP) and pharmaceutical industry standards</li><li>Strong data analysis and interpretation skills</li><li>Proficiency in using laboratory equipment and relevant software</li><li>Excellent written and verbal communication skills</li><li>Ability to work efficiently in a fast-paced, collaborative environment</li><li>Experience with tech transfer and process validation is preferred</li></ul><h4>Additional Information</h4>About the DepartmentIntegrated Product Development Organisation                                         We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. 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>Mid Level

Dr Reddys Laboratories

Process Engineer

Analytical Scientist-Injectable<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. Roles &amp; Responsibilities <ul><li>You will be responsible Analytical method development and validation of injectable products. </li><li>You will be responsible to perform the Drug Master File/Literature review and procure the relevant columns and standards in order to initiate the analytical method development. Stay updated with the latest literature and industry developments in the field.</li><li>You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.</li><li>You will be responsible to execute analytical activities as per defined procedures, document the data and send the respective record of analysis to group leader/analytical expert for the review and release in order to provide the approved results to formulation team. </li><li>You will be responsible for analytical method development for drug products for various tests mentioned in the specification in order to analyse the product development batches for the prototype screening. </li><li>You will be responsible for analytical method validation activities at the manufacturing sites providing method development reports to verify the validation parameters and ensure the execution of method validation as per the regulatory requirement in order to provide the authentic analytical validation report for the regulatory filing. </li><li>You will be responsible for analytical method transfer to plant locations successfully in order to train the Quality Control (QC) team on the methods for the Exhibit and commercial batch analysis at plant.</li><li>You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.</li><li>You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.</li><li>You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.</li><li>You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. </li></ul><h4>Qualifications</h4>QualificationsEducational qualification: Masters in Science/ Organic chemistry/ Pharmaceutical SciencesMinimum work experience: 6-12 years of experience in analytical method developmentSkills &amp; attributes:Technical Skills<ul><li>Extensive work experience in analytical method development and validation of injectable products.</li><li>Proven experience with injectable, ophthalmic, peptide, and suspension products.</li><li>Demonstrated expertise in sameness and characterization studies for complex molecules.</li><li>Proficient understanding of various analytical techniques including HPLC, GC, UV, FTIR, KF, and mass spectrometry.</li><li>Advanced skills in troubleshooting analytical methods and instruments.</li><li>Comprehensive understanding of Abbreviated New Drug Application (ANDA) filing requirements.</li><li>Strong knowledge of regulatory guidelines and industry standards related to pharmaceutical product development and analysis.</li><li>Proven experience in method development, validation, transfer, and documentation in compliance with regulatory requirements.</li><li>Familiarity with Quality by Design (QbD) principles and their application in analytical method development.</li><li>Experience with stability testing and forced degradation studies for injectable products.</li><li>Knowledge of current Good Manufacturing Practices (cGMP) and ICH guidelines.</li></ul>Behavioral Skills<ul><li>Strong analytical and problem-solving abilities, with a keen attention to detail</li><li>Excellent communication and interpersonal skills, with the ability to effectively present complex analytical data to diverse audiences..</li><li>Ability to work collaboratively with own team and cross-functional teams in a fast-paced environment.</li><li>Demonstrated project management skills and ability to handle multiple projects simultaneously.</li><li>Adaptability and willingness to learn new techniques and methodologies.</li><li>Strong commitment to safety protocols and environmental regulations in laboratory settings.</li></ul> <h4>Additional Information</h4>About the DepartmentIntegrated Product Development Organisation                                         We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. 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

Analytical Chemist

Senior Research Executive - Ecom<h4>Job Description</h4>Join NielsenIQ as a  Senior Research Executive to support our e-commerce and food delivery data expansion in India. This role blends data analysis, product insights, and client collaboration to drive commercial success.RESPONSIBILITIES<ul><li>Analyze and interpret large datasets to generate actionable insights for sales and clients.</li><li>Lead Customer Engagement &amp; Value Creation: Build and nurture strong, foundational relationships with key e-commerce customers and stakeholders. Develop a deep understanding of their business priorities and how they connect to the adoption and use of our products</li><li>Utilize Python, R, Power BI, and Tableau for data processing and visualization.</li><li>Collaborate with global teams to refine data quality and mitigate biases.</li><li>Support product development by identifying key analyses and automation opportunities.</li><li>Partner with sales teams to provide data-driven recommendations and enhance client engagement.</li><li>Build compelling presentations by transforming data insights into clear, impactful stories.</li><li>Create marketing content to drive product awareness.</li></ul>ABOUT YOUYou have a strong analytical mindset, a passion for data, and the ability to translate insights into impactful client solutions. You thrive in a fast-paced, global environment and collaborate effectively across teams.QUALIFICATIONS<ul><li>3+ years of experience in e-commerce, market intelligence, or data analysis.</li><li>Excellent analytical, problem-solving, and logical thinking skills</li><li>Proficiency in Python, R, Power BI, and Tableau.</li><li>Strong problem-solving, time management, and storytelling skills.</li><li>Experience working with commercial teams and engaging with clients.</li><li>Fluent in English, comfortable in an international work environment.</li></ul><h4>Additional Information</h4>Our Benefits<ul><li>Flexible working environment</li><li>Volunteer time off</li><li>LinkedIn Learning</li><li>Employee-Assistance-Program (EAP)</li></ul>About NIQNIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state-of-the-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world’s population.For more information, visit NIQ.comWant to keep up with our latest updates?Follow us on: <a href="https://www.linkedin.com/company/nielseniq/mycompany/">LinkedIn</a> | <a href="https://www.instagram.com/nielseniq/">Instagram</a> | <a href="https://twitter.com/nielseniq">Twitter</a> | <a href="https://www.facebook.com/NielsenIQ.global/">Facebook</a>Our commitment to Diversity, Equity, and InclusionAt NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence.  All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the <a href="https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fnielseniq.com%2Fglobal%2Fen%2Fnews-center%2Fdiversity-inclusion&amp;data=05%7C02%7CJenny.Rebecca%40nielseniq.com%7C6e534cbe3eb041842d5f08dc6dca121e%7C6ac7a1f45fb14153bb4f12d2020a1f7d%7C0%7C0%7C638505961881417602%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=B%2Fp40oNUpJOw1CNoc87EFXk%2BvxeO1jxYOSRCEKM%2Fz5Q%3D&amp;reserved=0">https://nielseniq.com/global/en/news-center/diversity-inclusion</a><h4>Experience Level</h4>Senior Level

NielsenIQ

Research Intern

Senior Research Executive-Ecom CS<h4>Job Description</h4>Join NielsenIQ as a  Senior Research Executive to support our e-commerce and food delivery data expansion in India. This role blends data analysis, product insights, and client collaboration to drive commercial success.RESPONSIBILITIES<ul><li>Analyze and interpret large datasets to generate actionable insights for sales and clients.</li><li>Lead Customer Engagement &amp; Value Creation: Build and nurture strong, foundational relationships with key e-commerce customers and stakeholders. Develop a deep understanding of their business priorities and how they connect to the adoption and use of our products</li><li>Utilize Python, R, Power BI, and Tableau for data processing and visualization.</li><li>Collaborate with global teams to refine data quality and mitigate biases.</li><li>Support product development by identifying key analyses and automation opportunities.</li><li>Partner with sales teams to provide data-driven recommendations and enhance client engagement.</li><li>Build compelling presentations by transforming data insights into clear, impactful stories.</li><li>Create marketing content to drive product awareness.</li></ul>ABOUT YOUYou have a strong analytical mindset, a passion for data, and the ability to translate insights into impactful client solutions. You thrive in a fast-paced, global environment and collaborate effectively across teams.QUALIFICATIONS<ul><li>3+ years of experience in e-commerce, market intelligence, or data analysis.</li><li>Excellent analytical, problem-solving, and logical thinking skills</li><li>Proficiency in Python, R, Power BI, and Tableau.</li><li>Strong problem-solving, time management, and storytelling skills.</li><li>Experience working with commercial teams and engaging with clients.</li><li>Fluent in English, comfortable in an international work environment.</li></ul> <h4>Additional Information</h4>Our Benefits<ul><li>Flexible working environment</li><li>Volunteer time off</li><li>LinkedIn Learning</li><li>Employee-Assistance-Program (EAP)</li></ul>About NIQNIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state-of-the-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world’s population.For more information, visit NIQ.comWant to keep up with our latest updates?Follow us on: <a href="https://www.linkedin.com/company/nielseniq/mycompany/">LinkedIn</a> | <a href="https://www.instagram.com/nielseniq/">Instagram</a> | <a href="https://twitter.com/nielseniq">Twitter</a> | <a href="https://www.facebook.com/NielsenIQ.global/">Facebook</a>Our commitment to Diversity, Equity, and InclusionAt NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence.  All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the <a href="https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fnielseniq.com%2Fglobal%2Fen%2Fnews-center%2Fdiversity-inclusion&amp;data=05%7C02%7CJenny.Rebecca%40nielseniq.com%7C6e534cbe3eb041842d5f08dc6dca121e%7C6ac7a1f45fb14153bb4f12d2020a1f7d%7C0%7C0%7C638505961881417602%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=B%2Fp40oNUpJOw1CNoc87EFXk%2BvxeO1jxYOSRCEKM%2Fz5Q%3D&amp;reserved=0">https://nielseniq.com/global/en/news-center/diversity-inclusion</a><h4>Experience Level</h4>Senior Level

Principal Applied ResearcherSecurity represents the most critical priorities for our customers in a world awash in digital threats, regulatory scrutiny, and estate complexity. Microsoft Security aspires to make the world a safer place for all. We want to reshape security and empower every user, customer, and developer with a security cloud that protects them with end to end, simplified solutions. The Microsoft Security organization accelerates Microsoft’s mission and bold ambitions to ensure that our company and industry is securing digital technology platforms, devices, and clouds in our customers’ heterogeneous environments, as well as ensuring the security of our own internal estate. Our culture is centered on embracing a growth mindset, a theme of inspiring excellence, and encouraging teams and leaders to bring their best each day. In doing so, we create life-changing innovations that impact billions of lives around the world. Our mission is to build agentic systems that generalise across tasks, tools, and domains—enabling secure, scalable, and intelligent automation. We thrive on rapid experimentation, lean execution, and deep technical ownership, crafting AI products that redefine how security is delivered and experienced. With a focus on agility, cross-functional collaboration, and bold problem-solving, we aim to pioneer the next wave of AI-driven transformation in cybersecurity. Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond. <h4>Responsibilities</h4><ul><li>Drive end-to-end development of AI-powered products, from ideation and prototyping to scalable deployment. </li><li>Mentor a high-performing applied research team focused on building agentic AI systems for security applications. </li><li>Foster a startup-like culture of agility, ownership, and rapid experimentation to accelerate product innovation. Cultivate an inclusive, growth-oriented team culture that values curiosity, bold thinking, and continuous learning. Collaborate across research, product, and engineering teams to integrate cutting-edge AI into real-world scenarios.</li></ul><h4>Qualifications</h4><ul><li>8+ years of hands-on experience in machine learning, deep learning, or agentic systems, with a strong track record of shipping AI solutions. </li><li>Bachelor’s or Master’s degree in Computer Science, Artificial Intelligence, or a related field, PhD preferred.</li><li> Proficiency in Python and frameworks such as PyTorch or TensorFlow; familiarity with agentic workflows and LLM integration. </li><li>Demonstrated ability to drive end-to-end product development in fast-paced, ambiguous settings with a bias for execution. Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request via the <a href="https://careers.microsoft.com/us/en/accommodationrequest" rel="noopener" target="_blank">Accommodation request form</a>.</li></ul> Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work.<h4>Experience Level</h4>Senior Level

Research Assistant

Formulation Scientist<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary We are seeking a dynamic and experienced Formulation Scientist in Injectable division for designing and development of formulation process, ensuring quality by design (QbD) implementation, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. Roles &amp; Responsibilities <ul><li>You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval.</li><li>You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. </li><li>You will be responsible to support in scale-up to pilot/plant scales for Injectable Products.</li><li>You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions.</li><li>You will be responsible for technology transfer and execution of the batches. </li><li>You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up).  </li><li>You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. </li><li>You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. </li></ul><h4>Qualifications</h4>Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products.  Skills &amp; attributes:   Technical Skills<ul><li>Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.</li><li>Experience in areas of product development for Generic Injectable</li><li>Experience in Quality by Design (QbD).</li><li>Experience in Process Optimization and scale up.</li><li>Experience in Operational Excellence.</li><li>Knowledge on Good Manufacturing Practice and Good Laboratory Practice.</li><li>Experience in Technology Transfer.  </li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills.</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 DepartmentIntegrated Product Development Organisation                                         We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. 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

Assistant Manager - Secondary Market Research<h4 id="job_meta">Location: Gurugram ,None,None </h4>Job Description:We are seeking a highly motivated and detail-oriented professional to join our Research and Insights team as a Senior Research Associate. In this role, you will be integral to conducting secondary research to support our research initiatives. You will collaborate closely with project managers and external clients to ensure the accuracy and quality of our deliverables, contributing to strategic decision-making and enhancing our understanding of market dynamics.Responsibilities:Research &amp; Insights:·       Analyze and synthesize information from articles, reports, and various sources to evaluate the competitive landscape and consumer preferences.·       Conduct thorough competitive analysis and consumer insights research, including the design and execution of surveys and focus groups.·       Synthesize insights from previous studies and reports to develop actionable recommendations for stakeholders.·       Present findings clearly and effectively, ensuring they are actionable and aligned with project objectives.·       Investigate key topics and areas of interest within the client’s prior research, providing deeper insights into their needs.·       Collaborate with internal teams to ensure alignment on findings and agree on next steps for research initiatives.·       Conduct thorough quality checks on deliverables produced by research associates to ensure accuracy and adherence to project standards.·       Provide guidance and mentorship to research associates throughout the research process, fostering skill development and best practices.·       Demonstrate strong project management skills by scoping projects effectively, defining objectives, and planning timelines to meet project deadlines.·       Collaborate with team members to facilitate smooth workflow and communication, ensuring alignment on project goals and expectations.·       Monitor project progress and provide regular updates to managers/stakeholders, identifying potential challenges and implementing solutions proactively.Social Media and Marketing Analytics:·       Demonstrate familiarity with key concepts such as Paid Media Spend, Positioning &amp; Messaging, Search Engine Optimization (SEO), and Customer Relationship Management (CRM).·       Exhibit a comprehensive understanding of various media channels and best practices in creative strategy, including targeting and segmentation.·       Evaluate and analyze paid media spend across multiple channels, including TV, Out-of-Home (OOH), social media, and Display Advertising.·       Perform thorough evaluations of current positioning and messaging strategies, including website assessments and marketing materials.·       Interpret data from SEO tools (e.g., Google Search Console, Moz) to inform and optimize marketing strategies.Qualifications:·       Bachelor’s degree in a relevant field (e.g., Market Research, Business Administration with a concentration in Marketing, or related disciplines).·       3-5 years of experience in secondary research.·       Familiarity with social media analytics platforms (e.g., Brandwatch, Google Analytics, Meltwater, Captiv8) is advantageous.·       Exceptional attention to detail and a meticulous approach to all tasks.·       Excellent verbal and written communication skills, with the ability to convey complex information clearly and concisely.·       Proven ability to work effectively in a collaborative, team-oriented environment with colleagues from diverse backgrounds.·       Strong organizational and time management skills, capable of prioritizing and managing multiple tasks simultaneously.·       Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and other relevant software applications.·       Prior experience in customer research or market research is preferred.<a href="https://srijantech.recruiterbox.com/jobs/fk0zwuj/?apply=true">Apply to this job</a><h4>Experience Level</h4>Mid Level

Srijan Technologies Pvt Ltd

Market Analyst

Scientist - Cathode Design<h4>Job Description Summary</h4>To work within the engineering team on designing new or improving designs of existing electron-beam cathodes for x-ray tubes. Position requires understanding of concepts, methods, procedures &amp; strategies for design &amp; development of x-ray tube cathode components &amp; sub-assemblies. Learn practical application of scientific &amp; engineering principles, achieve expertise in Physics of X Ray Generation &amp; X Ray Sub systems. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.tex<h4>Job Description</h4><h4>Roles &amp; Responsibilities</h4><div><div><div><div><div><div><div><div><div><ul><li>Activities will include development of new designs and/or supporting enhancements to existing designs of X Ray Generation Devices by specifying SW / Algo / HW requirements followed by characterization, product integration and manufacturing transfer</li><li>The candidate is expected to gain a detailed functional understanding of the entire product, act independently, devise and drive innovative analyses and solutions for complex problems.</li><li>Execute design using sound Physics principles &amp; scientific tools</li><li>Develop test plans &amp; perform testing &amp; verification of designs, perform design calculations to support design work and lead technical design reviews</li><li>Work as a part of a team including cross functional team members &amp; suppliers to deliver technical solutions</li><li>Work with customers and/or technical leadership to ensure that the technical deliverables are consistent with the goals of larger programs, projects or initiatives</li><li>Seeks mentoring to learn and solve problems</li><li>Lead development of new techniques &amp; methodologies for designing Electron Emission &amp; focusing sub systems</li><li>Engaging in all phases of new product development, including concept, architecture, documentation, design, prototype, test, supplier interfaces, manufacturing introduction and service support</li><li>Developing and maintaining X Ray Generation subsystem quality and engineering project funnel</li><li>Defining and executing component design verification</li><li>Maintain and develop competence required for the job</li></ul><h4>Basic Qualifications:</h4><ul><li>MS (Physics), PhD in Electron Optics / Experimental Physics / Nuclear Physics / Applied Physics</li><li>PhD in Charged Particle Beam Design and X-Ray Physics, with over 2+ years of hands-on experience in designing charged particle beam systems, electron optics, and laser optics</li></ul><h4>Desired Characteristics:</h4><ul><li>Demonstrated ability to Design Experiments &amp; analyze data</li><li>Demonstrated ability to find Physics based solutions to fundamental problems</li><li>Demonstrated ability to use simulation / modeling-based approach to understand physical phenomenon</li><li>Demonstrated ability to use Mathematical Physics to explain physical phenomenon</li><li>Strong oral and written communication skills.</li><li>Strong interpersonal skills.</li><li>Demonstrated ability to analyze and resolve problems.</li><li>Demonstrated ability to lead programs / projects.</li></ul><h4>Inclusion and Diversity</h4>GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.Disclaimer: GE HealthCare will never ask for payment to process documents, refer you to a third party to process applications or visas, or ask you to pay costs. Never send money to anyone suggesting they can provide employment with GE HealthCare.#LI-SB1#LI-Onsite</div></div></div></div></div></div></div></div></div>

GE Healthcare Private Limited

Electronic Service Engineer

Co-op/ApprenticeAt 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>This is a temporary position.</li><li>Responsible for performing and supporting research for teams operating within a service group, product group and/ or project group.</li><li>Assists with the development, monitoring, coordination and implementation of non-technical projects as assigned.</li><li>Provides analysis, reporting and internal communication services with team members.</li><li>Develops knowledge of industry and organizational processes.</li></ul>OFFICE SUPPORT CAREER STREAM: Individual contributors who provide organizational related support or service (administrative or clerical) for other members within the organization. The majority of time is spent in the delivery of support services or activities, typically under supervision.DIFFERENTIATING FACTORSAutonomy: Entry-level position typically requiring little to no prior experience. Works on well-defined administrative and clerical tasks. Work is routine or follows standard procedures and is closely supervised.Organizational Impact: Works to deliver on day-to-day objectives with some impact on achievement of results for the job area, including limited disruption or expense. Delivers job responsibilities following a defined standard output or set of procedures.Innovation and Complexity: Provides data and information when minor changes may be required based on review. Problems faced are routine and solutions clearly prescribed.Communication and Influence: Communicates with contacts typically within immediate job area. Obtains and provides information requiring little explanation or interpretation.Leadership and Talent Management: N/A – Job at this level are focused on self-development.Required Knowledge and Experience: Requires no or little job knowledge of systems and procedures. 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>

India Medtronic Pvt. Ltd

Apprentice

Principal Statistical ProgrammerAbout the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally.  Main responsibilities: The Principal Statistical Programmer will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans and provide QC’d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) ;The Principal Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques; The Principal Statistical Programmer will ensure SOPs are followed and timelines and quality are met; Collaboration of Local biostatistics and programming teams, Global Medical Affairs biostatisticians and Global Medical Affairs Scientific Communications personnel  <ul><li>People: 1) Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and/or programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. 2) Coach/mentor new team members to support efficient and quick onboarding. 3) Support graduate hiring program as needed </li></ul> <ul><li>Performance / Process:  1) Conduct appropriate post-hoc statistical analyses of clinical trial data and/or registry. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Remain current on advanced programming methods. 5) Work closely with the Global Medical Affairs biostatisticians and/or programmers to develop and implement project QC plans and timelines. </li></ul> <ul><li>Customer: 1) Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables. </li></ul> About you  <ul><li>Experience: Master's degree minimum 6 years/B.Sc. minimum 8 years of relevant experience required  </li></ul><ul><li>Soft skills: Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines </li></ul><ul><li>Technical skills: Advance SAS programming skills, SDTM &amp; ADaM (CDISC) and clinical data environment across multiple therapeutic areas </li></ul><ul><li>Education: Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field. </li></ul><ul><li>Languages: Excellent English language knowledge – written and spoken </li></ul>  Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.  At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.  Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!  <h4>Pursue progress, discover extraordinary</h4>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!

Sanofi India Ltd

Research Analyst

Global Trial Acceleration AssociateWorking 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>.Position SummaryThis individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials. This may also include review of all the Site Monitoring Visit reports, issue escalation, resolution and follow up tasks.Key Responsibilities<ul><li>The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.</li><li>The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies).</li><li>As the main point of contact for essential document management, ethical and regulatory submission-related activities, develops and maintains collaborative working relationships with relevant stakeholders.</li><li>Support outsourcing activities by interfacing with operational teams, support groups and service providers for successful selection, contracting and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, BMS outsourcing and procurement policies and procedures.</li><li>Initiate and manage start-up documentation activities for global clinical trials.</li><li>Submission of potential investigators to CTSS for debarment review and tracking of decisions.</li><li>Responsible for country/Site Activation for clinical trials as applicable per region; this includes the final review of applicable documents, final sign-off of the country/site activation checklist. The incumbent may also be responsible for activating the site in accordance with all applicable global / local study procedures.</li><li>May provide a level of quality control of start-up activity.</li><li>Update and review of various study-related clinical systems to determine and report status of clinical trial documents for insourced studies (i.e., CTMS, eTMF, etc. or corresponding vendor systems)</li><li>May arrange certified translation of study level documentation from translators as requested (i.e., ICF, Protocol, IB)</li><li>May assist with the coordination or creation of other study specific materials such as pharmacy or Investigator site file to ensure that these are available on site for site initiation visits/prior to first patient visit.</li><li>May act as single point of contact for the study team for centralized activities during study start-up.</li><li>Ongoing maintenance and tracking of essential documentation and collection of updated/outstanding documentation and submission as required during all phases of clinical trial.</li><li>Ongoing communication with study teams regarding centralized study activities.</li><li>Maybe responsible for creation and management of standardized document templates.</li><li>Assist with CSR distribution</li><li>Country and site level ICF adaptation.</li><li>Essential document collection, review and approval of country and site level documents.</li><li>Centrally reviewing all the Site Monitoring Visit reports, issue escalation, resolution and follow up tasks.</li><li>Other duties as assigned to support Clinical Trials.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

Business Development Intern

Associate STEM Content AnalystJob DescriptionWe are looking for an Associate STEM Content Analyst to join our CDDI Chemistry team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 17 members based across Chennai, Hyderabad, Bangalore and Barcelona (Spain) and this role reports to the Chemistry Team Manager. We have a great skill set in Chemistry, Pharamacology, Medicinal chemistry, Synthesis and complementary skill sets to address challenges in drug discovery, including new chemical drugs identification, curation of drugs and formulations. We would love to speak with you if you have an understanding of chemical drug products.About You – experience, education, skills, and accomplishments  <ul><li>M.Sc, Chemistry/B.Pharm/M.Pharm(Medicinal Chemistry, Pharmaceutics or Pharmacology) related degree</li><li>Knowledge in content analysis and editing</li><li>Ability to draw chemical molecules in drawing tools</li><li>Strong background in drug development processes</li><li>Proficiency in English</li><li>Good scientific and analytical skills, with attention to details</li><li>High ability to interpret and explain scientific data</li><li>Ability to work independently and within a multidisciplinary team of diverse collaborators</li><li>General computer proficiency (MS Office) and ability to quickly learn new software tools</li></ul>It would be great if you also had . . .  <ul><li>Good interpersonal skills</li><li>Effective time management skills</li><li>Excellent English written and verbal communication skills</li><li>High motivation with a strong work ethic and ability to thrive in a fast-paced environment</li><li>Adherence to SOP and Policies</li><li>Experience with AI tools</li></ul>What will you be doing in this role?<ul><li>To select and analyse relevant drug-focused articles and/or patents</li><li>Drawing chemical compounds of the selected drugs from the articles and patents.</li><li>Ability to understand and interpret complex and detailed Pharma and Chemical related information from Patents/Articles</li><li>Achieve production volume and quality targets</li><li>Recording of performance against target</li><li>Taking an active role within the team to ensure targets are met</li><li>Maintain awareness of current developments in own technology areas</li><li>Achieve and maintain consistent quality standards effective personal planning and time management</li><li>Maintain a flexible and adaptable approach towards process change</li><li>To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis</li><li>To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.</li><li>Actively participate to team activities and work towards the process improvement by raising, discussing, and resolving subject matter and production issues</li><li>Collaborate with ROW &amp; Cross BU groups when needed</li></ul>ProductCortellis Drug Discovery Intelligence focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, and pharmacological data from disparate sources into a single platform. Users will benefit from the broadest, deepest, most accurate source of R&amp;D intelligence that has been manually curated, validated, and shared using a solution built by scientists for scientists.About the Team  <ul><li>We are a global, high-performing synergistic team of members including associate content editors, content editors and senior content editors, based across India and Barcelona (Spain).</li><li>Our main goal is to analyse journals, patents and meeting abstracts to provide content to CDDI product, including details like Drug Chemical Structure ,Description, Mechanisms of Action, Product Categories, Drug Phase, Developmental Stage, Therapeutic activity, and all related retrospective articles and patents reported for the drug.</li><li>Hybrid working system (working from office and digital workplace)</li></ul>Hours of Work  This is a full-time permanent position, with flexible 8 working hours/day in core time of 9:00am-6:00pm (IST). Workdays - Monday to Friday.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

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