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R&D Senior Member of Technical Staff, Product TestAVEVA is creating software trusted by over 90% of leading industrial companies.Job Title:  R&amp;D Senior Member of Technical Staff, Product TestLocation:  HyderabadEmployment Type: Full Time, regular, hybrid work arrangement About the RoleAs a part of this function, the R&amp;D Technology and Execution team designs, develops, and maintains software products and solutions, including the underlying systems and architecture. Responsible for delivering world-class products and solutions using established standards and processes in collaboration with other R&amp;D functions.We are looking for a seasoned Tester with the skills and passion to successfully test and validate the AI enabled products developed by the team.Main responsibilities<ul><li>Work with the Product Owner, Stakeholders, Dev Manager in addition to the Scrum Team to understand, define and implement test roadmap.</li><li>Participate in Scrum meetings with other team members including sprint planning and estimating; backlog refinement; daily Scrum meetings; sprint retrospectives and sprint reviews.</li><li>Work collaboratively with scrum colleagues to identify, implement and execute functional and non-functional test scenarios to validate the functionality of software.</li><li>Be responsible for defining stories, test strategy, test ideas and translating those into automated and manual tests as part of a cross-functional development team.</li><li>Use tools including test automation frameworks and data to make testing efficient and easily repeatable for regression purposes.</li><li>You may be required to update existing frameworks or modify them or build new ones depending on the need.</li><li>Contribute to decisions on how testing is conducted, share opinions on the right tools to use and the right methods to achieve the goals.</li><li>You may be required to mentor junior team-members.</li><li>Handle large amounts of data, as is normally the case with AI models.</li></ul>Qualifications<ul><li>You have minimum of 10+ years of Functional/Domain testing experience within Engineering domain or related industry.</li><li>Experience on Non-functional requirement gathering, identifying critical business scenarios</li><li>Hands-on experience of application/functional testing</li><li>Good hands-on experience CI/CD Tools, GIT, TFS, MS Test etc. and processes in Azure DevOps &amp; experience of using Agile methodologies</li><li>Automation Experience and Knowledge of popular scripting languages (Selenium-C#/Java Script, etc...)  will be required</li><li>Good understanding of Machine learning life cycle</li><li>Design and implement unit and integrations tests covering machine learning models with variety of data sets</li><li>Exceptional communication skills, working with a broad range of people, including Product Owners, System Testers &amp; Product Support across sites</li><li>Positive approach to problem solving with a ‘can do’ attitude</li></ul>Nice to have:<ul><li>Knowledge of .NET Framework &amp; .NET Core</li><li>Knowledge of working Microsoft Azure Platform</li><li>Knowledge of Restful services, Web API</li><li>Skills with multiple software development languages including Typescript, JavaScript, HTML5 and CSS3</li><li>Experience on creating self-contained, reusable, and testable modules and components</li><li>Experience with Industrial automation domain knowledge</li></ul>R&amp;D at AVEVA Our global team of 2000+ developers work on an incredibly diverse portfolio of over 75 industrial automation and engineering products, which cover everything from data management to 3D design. AI and cloud are at the centre of our strategy, and we have over 150 patents to our name.Our track record of innovation is no fluke – it’s the result of a structured and deliberate focus on learning, collaboration and inclusivity. If you want to build applications that solve big problems, join us.Find out more: <a href="https://aveva.com/en/about/careers/r-and-d-careers/" rel="noopener noreferrer" target="_blank">aveva.com/en/about/careers/r-and-d-careers/</a>Why Join AVEVA?At AVEVA, we are unlocking the power of industrial intelligence to create a more sustainable and efficient world. AVEVA Connect platform is at the heart of that transformation. As a leader in Core AI Services, you will help shape how AI is delivered at scale across industries. Join us in driving the next wave of industrial innovation.India Benefits include:  Gratuity, Medical and accidental insurance, very attractive leave entitlement, emergency leave days, childcare support, maternity, paternity and adoption leaves, education assistance program, home office set up support (for hybrid roles), well-being supportIt’s possible we’re hiring for this position in multiple countries, in which case the above benefits apply to the primary location. Specific benefits vary by country, but our packages are similarly comprehensive.Find out more: aveva.com/en/about/careers/benefits/Hybrid workingBy default, employees are expected to be in their local AVEVA office three days a week, but some positions are fully office-based. Roles supporting particular customers or markets are sometimes remote.Hiring processInterested? Great! Get started by submitting your cover letter and CV through our application portal. AVEVA is committed to recruiting and retaining people with disabilities. Please let us know in advance if you need reasonable support during your application process.Find out more: aveva.com/en/about/careers/hiring-processAbout AVEVAAVEVA is a global leader in industrial software with more than 6,500 employees in over 40 countries. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals, and minerals – safely, efficiently, and more sustainably.We are committed to embedding sustainability and inclusion into our operations, our culture, and our core business strategy. Learn more about how we are progressing against our ambitious 2030 targets: sustainability-report.aveva.com/Find out more: aveva.com/en/about/careers/AVEVA requires all successful applicants to undergo and pass a drug screening and comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may, subject to those laws, include proof of educational attainment, employment history verification, proof of work authorization, criminal records, identity verification, credit check.  Certain positions dealing with sensitive and/or third-party personal data may involve additional background check criteria.AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business.  AVEVA provides reasonable accommodation to applicants with disabilities where appropriate. If you need reasonable accommodation for any part of the application and hiring process, please notify your recruiter. Determinations on requests for reasonable accommodation will be made on a case-by-case basis.<h4>Experience Level</h4>Senior Level

AVEVA

Project Officer

Applied Scientist III, Alexa AIThe Amazon Alexa AI team in India is seeking a talented, self-driven Applied Scientist to work on prototyping, optimizing, and deploying ML algorithms within the realm of Generative AI. The Applied Scientist will be in a team of exceptional scientists to develop novel algorithms and modeling techniques to advance the state of the art in Natural Language Processing (NLP) or Computer Vision (CV) related tasks. They will work in a hybrid, fast-paced organization where scientists, engineers, and product managers work together to build customer facing experiences. They will collaborate with and mentor other scientists to raise the bar of scientific research in Amazon. Their work will directly impact our customers in the form of products and services that make use of speech, language, and computer vision technologies. Key job responsibilities - Research, experiment and build Proof Of Concepts advancing the state of the art in AI &amp; ML for GenAI. - Collaborate with cross-functional teams to architect and execute technically rigorous AI projects. - Thrive in dynamic environments, adapting quickly to evolving technical requirements and deadlines. - Engage in effective technical communication (written &amp; spoken) with coordination across teams. - Conduct thorough documentation of algorithms, methodologies, and findings for transparency and reproducibility. - Publish research papers in internal and external venues of repute - Support on-call activities for critical issues A day in the life You will be working with a group of talented scientists on researching algorithm and running experiments to test scientific proposal/solutions to improve solutions powering customer experience on Alexa+. This will involve collaboration with partner teams including engineering, PMs, data annotators, and other scientists to discuss data quality, policy, and model development. You will mentor other scientists, review and guide their work, help develop roadmaps for the team. You work closely with partner teams across Alexa to deliver platform features that require cross-team leadership.<h4>Basic Qualifications</h4> - 8+ years of building machine learning models for business application experience - PhD, or Master's degree and 8+ years of applied research experience - Experience programming in Java, C++, Python or related language - Experience with neural deep learning methods and machine learning <h4>Preferred Qualifications</h4>- Experience with modeling tools such as R, scikit-learn, Spark MLLib, MxNet, Tensorflow, numpy, scipy etc. - Experience with large scale distributed systems such as Hadoop, Spark etc. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit <a href="https://amazon.jobs/content/en/how-we-hire/accommodations">https://amazon.jobs/content/en/how-we-hire/accommodations</a> for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner.<h4>Experience Level</h4>Senior Level

 Amazon India Limited 

Science Mentor

Senior Statistical Programmer<h4>Job Title: Senior Statistical Programmer</h4>Introduction to role:Do you have a passion for programming? Are you an expert in your field? Would you like to apply your skills to impact the drug development process and regulatory interactions in a company that follows the science and turns ideas into life-enhancing medicines? Then AstraZeneca might be the one for you! Join our team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. With multiple indications and high-quality molecules in all stages of our innovative pipeline, we keep pushing forward to conquer cancer through data, innovation, and evidence-based decisions.<h4>Accountabilities:</h4>As a Senior Statistical Programmer, you will work within the Oncology Biometrics Programming department, providing statistical programming support and leading activities related to the analysis and reporting process at project/study level. Your responsibilities will include clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are numerous career paths available for your development and progression.<h4>Essential Skills/Experience:</h4><ul><li>Bachelor’s or Master’s (or local equivalent) degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field</li><li>At least 3 years of Industry experience with Master’s or 5+ years with Bachelor’s degree</li><li>Ability to pay attention to detail and lead/work on concurrent studies and activities</li><li>Excellent verbal and written communication skills and ability to influence team members</li><li>Extensive SAS programming expertise to an advanced level within clinical drug development</li><li>Ability to work independently on the assigned programming tasks</li><li>Comprehensive knowledge of technical and regulatory requirements</li><li>Good knowledge of CDISC standards and industry procedures</li><li>Experience leading studies or activities in clinical trials</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.AstraZeneca is a place where courage, curiosity, and collaboration thrive. We make bold decisions driven by patient outcomes, empowering our team to lead at every level. With cutting-edge science and technology, we aim to deliver six new molecular entities by 2025. Our collaborative research environment unites academia and industry, expediting breakthroughs in some of the hardest-to-treat cancers. Here, you can build a rewarding career while improving the lives of millions with cancer.Ready to make a difference? Apply now and be part of our journey to pioneer new frontiers in oncology!Date Posted30-Sept-2025Closing Date07-Oct-2025AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Senior Level

Astrazeneca India Private Limited

Research Analyst

Senior Researcher Psychometric Assessments<h4>Company:</h4>Mercer<h4>Description:</h4>Formats and sanitizes presentations and documents by working with Research colleagues and the KM team to identify the requirements needed for consistent formatting and/or sanitizing.Reviews and researches specified materials on a regular basis, in order to continually gain knowledge in specified areas, on specified topics.Creates and maintains information as directed, using the appropriate requested software.Identifies and drafts summaries of articles related to key topic areas relevant to businesses and clients, in order to provide relevant content, as requested.Assists with report writing and research analysis by providing relevant materials.Responds to research inquiries from consultants, senior management and clients on assigned key topic areas.Expands and maintains resources on specific topic areas.Contributes to team by providing research support, including resource identification and evaluation, and expansion of global content and intellectual capital.Mercer, a business of Marsh McLennan (NYSE: MMC), is a global leader in helping clients realize their investment objectives, shape the future of work and enhance health and retirement outcomes for their people. Marsh McLennan is a global leader in risk, strategy and people, advising clients in 130 countries across four businesses: Marsh, Guy Carpenter, Mercer and Oliver Wyman. With annual revenue of $24 billion and more than 90,000 colleagues, Marsh McLennan helps build the confidence to thrive through the power of perspective. For more information, visit mercer.com, or follow on LinkedIn and X.Marsh McLennan is committed to embracing a diverse, inclusive and flexible work environment. We aim to attract and retain the best people and embrace diversity of age, background, caste, disability, ethnic origin, family duties, gender orientation or expression, gender reassignment, marital status, nationality, parental status, personal or social status, political affiliation, race, religion and beliefs, sex/gender, sexual orientation or expression, skin color, or any other characteristic protected by applicable law.Marsh McLennan is committed to hybrid work, which includes the flexibility of working remotely and the collaboration, connections and professional development benefits of working together in the office. All Marsh McLennan colleagues are expected to be in their local office or working onsite with clients at least three days per week. Office-based teams will identify at least one “anchor day” per week on which their full team will be together in person.<h4>Experience Level</h4>Senior Level

Marsh McLennan

Research Intern

R&D Principal TechnologistAVEVA is creating software trusted by over 90% of leading industrial companies.Position: Principal TechnologistLocation: Hyderabad, IndiaType: Full Time, regular employment, Hybrid work arrangementsPath: Individual ContributorAbout the RoleAs a part of this function, the R&amp;D Technology and Execution team designs, develops, and maintains software products and solutions, including the underlying systems and architecture. Responsible for delivering world-class products and solutions using established standards and processes in collaboration with other R&amp;D functions.We are looking for a talented developer with the skills and passion to successfully implement complex technical solution to join our cloud platform Team.Main responsibilities<ul><li>You will be responsible for the Architecture, design and development of our fastest growing products in the cloud platform BU</li><li>You will need to demonstrate technical leadership with new feature development of highly complex software requirements as well as enhance existing applications.</li><li>You will need to analyze the customer problem and define a design that is optimum for our users.</li><li>You will need to be hands-on with variety of programming languages implementing new features, troubleshooting, leading discussions as well as assisting other team members.</li><li>You will collaborate with subject matter experts and stakeholders across programs, work with system architects and the chief technologist, and security team to ensure effective design and implementation for our product and our customers adhering to the security standards within the committed timelines.</li><li>You will provide technical perspective to the product owners and/or R&amp;D management on features and solutions, address concerns, and provide detailed updates in timely manner.</li><li>You will provide technical direction to the team, estimate and establish delivery timelines, as well as assists junior staff in providing their timeline recommendations.</li><li>You will also identify challenges and technical interdependencies and suggest solutions to address them.</li><li>We want talented individuals who enjoy learning and contributing in a fast-paced software development environment.</li></ul>Qualifications<ul><li>Bachelor’s Degree in Computer Science or Software Engineering or a related field.</li><li>Minimum 10 years of relevant experience in a professional software development role.</li><li>Full SDLC experience, including release to operations and production of cloud products</li><li>Expert in technical designs for cloud applications, complying patterns and principles, security aspects, and implementing, troubleshooting major portions of a production stack.</li><li>Experienced in leading teams technically.</li><li>Proficiency in multiple software development languages including C#, Java Script and .Net</li><li>Expertise in back-end development on Microsoft Azure with core infrastructure concepts including Microservices, worker services, AKS, SFC, Web Apps, REST Web API, VMs, Service Fabric, NoSQL databases, ARM based deployment and containers.</li><li>Experience and applicable knowledge on front end development with HTML 5, CSS3 and Angular, react etc</li><li>Expert in low level development and debugging of memory and performance issues. An expert to identify and analyze a situation or problem using pattern recognition or logical reasoning that results in appropriate and practical solutions</li><li>Have deep and broad knowledge of current and emerging technologies</li><li>Experience in Test Driven Development, Continuous Integration and Continuous Delivery</li><li>Experienced with ALM, Infrastructure Management tools and Dev Ops</li><li>Familiarity with test automation techniques</li><li>Work experience in Industry digitalization products would be an added advantage</li><li>Experience in working in an Agile or SCRUM team environment, and with remote team</li><li>An inclination towards communication, inclusion, visibility, and transparency</li><li>Ability to find requirements and break them down into an actionable execution plan for the team and proactively identify problems</li><li>Innovation and Creativity – to show a willingness to understand innovative ideas and to apply new insights to existing situations</li><li>Collaborative communication skills (written and oral) - Ability to convert technical concepts into non-technical</li><li>Understanding of Azure Powershell/Azure CLI   is an added advantage.</li><li>You have a solid understanding of Cloud Service Architecture in Azure, however any AWS knowledge is also beneficial</li><li>You have good foundation on industry standards for Cyber Security and have applied them to develop secure applications. Knowledge on ethical hacking, knowledge of Penetration testing etc highly desired</li><li>Experienced in using Agile methodologies.</li><li>Experience in UML.</li></ul>R&amp;D at AVEVA Our global team of 2000+ developers work on an incredibly diverse portfolio of over 75 industrial automation and engineering products, which cover everything from data management to 3D design. AI and cloud are at the centre of our strategy, and we have over 150 patents to our name.Our track record of innovation is no fluke – it’s the result of a structured and deliberate focus on learning, collaboration and inclusivity. If you want to build applications that solve big problems, join us.Find out more: <a href="https://aveva.com/en/about/careers/r-and-d-careers/" rel="noopener noreferrer" target="_blank">aveva.com/en/about/careers/r-and-d-careers/</a>Why Join AVEVA?At AVEVA, we are unlocking the power of industrial intelligence to create a more sustainable and efficient world. AVEVA Connect platform is at the heart of that transformation. As a leader in Core AI Services, you will help shape how AI is delivered at scale across industries. Join us in driving the next wave of industrial innovation.India Benefits include:  Gratuity, Medical and accidental insurance, very attractive leave entitlement, emergency leave days, childcare support, maternity, paternity and adoption leaves, education assistance program, home office set up support (for hybrid roles), well-being supportIt’s possible we’re hiring for this position in multiple countries, in which case the above benefits apply to the primary location. Specific benefits vary by country, but our packages are similarly comprehensive.Find out more: aveva.com/en/about/careers/benefits/Hybrid workingBy default, employees are expected to be in their local AVEVA office three days a week, but some positions are fully office-based. Roles supporting particular customers or markets are sometimes remote.Hiring processInterested? Great! Get started by submitting your cover letter and CV through our application portal. AVEVA is committed to recruiting and retaining people with disabilities. Please let us know in advance if you need reasonable support during your application process.Find out more: aveva.com/en/about/careers/hiring-processAbout AVEVAAVEVA is a global leader in industrial software with more than 6,500 employees in over 40 countries. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals, and minerals – safely, efficiently, and more sustainably.We are committed to embedding sustainability and inclusion into our operations, our culture, and our core business strategy. Learn more about how we are progressing against our ambitious 2030 targets: sustainability-report.aveva.com/Find out more: aveva.com/en/about/careers/AVEVA requires all successful applicants to undergo and pass a drug screening and comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may, subject to those laws, include proof of educational attainment, employment history verification, proof of work authorization, criminal records, identity verification, credit check.  Certain positions dealing with sensitive and/or third-party personal data may involve additional background check criteria.AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business.  AVEVA provides reasonable accommodation to applicants with disabilities where appropriate. If you need reasonable accommodation for any part of the application and hiring process, please notify your recruiter. Determinations on requests for reasonable accommodation will be made on a case-by-case basis.<h4>Experience Level</h4>Senior Level

Technology Analyst

Statistical Programming Associate Director<h4>Job Title: Statistical Programming Associate Director</h4>Introduction to role:Do you have a passion for programming? Are you an expert in your field? Would you like to apply your skills to impact the drug development process and regulatory interactions in a company that follows the science and turns ideas into life-enhancing medicines? Then AstraZeneca might be the one for you! Join our team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. With multiple indications and high-quality molecules in all stages of our innovative pipeline, we keep pushing forward to conquer cancer through data, innovation, and evidence-based decisions.<h4>Accountabilities:</h4>You will be working in the Oncology Biometrics Programming department, reporting to the Director of Statistical Programming. Your role will involve providing leadership and management of statistical programming activities at the project/study level related to the planning, execution, and delivery of the statistical programming aspects of clinical development. The scope of work includes clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are many career options that you can pursue for your development and progression<h4>Essential Skills/Experience:</h4><ul><li>Bachelor’s or Master’s (or local equivalent) degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field</li><li>At least 6 years of industry experience with Master's or 8+ years with Bachelor's degree</li><li>Diligence – attention to detail and ability to manage concurrent projects and activities</li><li>Excellent verbal and written communication skills with an ability to influence stakeholders</li><li>Extensive SAS programming expertise to an advanced level within clinical drug development</li><li>Comprehensive knowledge of technical and regulatory requirements</li><li>Wide-ranging knowledge of CDISC standards and industry best practices</li><li>Experience leading projects/studies</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.AstraZeneca is a place built on courage, curiosity, and collaboration. We make bold decisions driven by patient outcomes and empower our employees to lead at every level. With cutting-edge science and technology, we aim to deliver breakthroughs that improve the lives of millions with cancer. Our commitment to pioneering new approaches and fostering a collaborative research environment makes AstraZeneca an exciting place to build a rewarding career.Ready to make a difference? Apply now and join us on this incredible journey!Date Posted30-Sept-2025Closing Date12-Oct-2025AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Mid Level

eCOA Build ProgrammerAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the worldThe electronic Clinical Outcomes Assessment (eCOA) Build Programmer is responsible for designing, programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in depth understanding of data technology, data flow, data standards, database programming, normalization and testing. This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager, Statistician and other key partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.Portfolio Delivery:<ul><li>Gather and influence eCOA design specifications from Clinical Trial Protocol to enable successful trial design and implementation</li><li>As a Clinical database programmer, build, program and test Clinical trial data collection systems (eCOA database) and associated data repository mappings for a trial or set of trials within a program using data standards library components</li><li>Ensure Clinical data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives</li><li>Partner with translation vendors to implement localized data collection in country specific language</li><li>Partner with Clinical Build Programmer to ensure complete data build for trial data collection needs</li><li>Provide insights into study level deliverables (i.e., Data Management Plan, Project Plan, database, and observed datasets)</li><li>Support submission, inspection and regulatory response activities</li><li>Lead cross Business Unit/Therapeutic Area projects or programs with high complexity</li><li>Opportunity to develop and tests new ideas and/or applies innovative solutions that add new value to the portfolio</li></ul>Project Management:<ul><li>Increase speed, accuracy, and consistency in the development of systems solutions</li><li>Enable metrics reporting of study development timelines and pre and postproduction changes to database</li><li>Partner to deliver study database per business need and before first patient visit</li><li>Follow and influence data standard decisions and strategies for a study and/or program</li><li>Utilize therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial data</li><li>Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables</li><li>Integrates multi-functional and/or external information and applies technical knowledge to data-driven decision making.</li><li>Enterprise Leadership:</li><li>Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis</li><li>Represent Data and Analytics processes in multi-functional initiatives</li><li>Actively engage in shared learning across Data and Analytics organization</li><li>Work to Increase re-usability of screens and edits by improving the initial design</li><li>Work to reduce postproduction changes change control process</li><li>Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization</li><li>Interacts with regulators, business partners and outside stakeholders on business issues</li><li>Thinks with end to end in mind consistently managing risk to minimize impact on delivery</li><li>Builds a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and development</li><li>Focuses on defining database solutions and timelines in support of advancing the portfolio</li></ul> Basic Qualifications &amp; Requirements:<ul><li>Bachelor’s or Master’s degree in computer science, engineering, medical field, Informatics, Life Sciences, Statistics, Information Technology, with hands-on experience in database programming, or a combination of clinical data management, system validation and data analysis, experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors.</li><li>Working experience in eCOA (electronic Clinical Outcome Assessment) or eDC (electronic data capture), eSource or Direct Data Capture implementation</li><li>Design of electronic CRF screens to capture Clinical data and build on required validations</li><li>Understanding of Clinical Protocol and interpretation of the Clinical terminologies to create or design specifications</li><li>Familiarity with Clinical data tools, technologies, workflow for collecting patient data, testing and validation of system</li><li>Analyse the impact and implement post production changes the Study design</li><li>Data analytics and visualizations</li><li>Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions</li><li>Deciding the technology platform (system/database) for data acquisition and aggregation</li><li>Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e., Data Sciences, Statistics, PK, Operations, Medical)</li><li>Strong therapeutic/scientific knowledge in the field of research</li><li>Project management experience</li><li>Vendor management experience</li><li>Understanding and experience in using data standards</li><li>Knowledge of medical terminology</li><li>Ability to balance multiple activities, prioritize and manage ambiguity</li><li>Demonstrated exemplary teamwork/interpersonal skills</li><li>Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment.</li></ul>Additional Preferences:<ul><li>Programming experience with HTML, CSS, JAVASCRIPT, Node.js, JSON.</li><li>Experience with relational and non-relational database technologies utilizing SQL, Data Functions and Procedures.</li><li>Technical proficiency with HTML, Data Mapping, understanding of database structures, etc.</li><li>Experience handling GITLAB utilities</li><li>Quick learner to new trends in technology</li><li>Excellent leadership, communication (written and oral) and interpersonal skills</li><li>Demonstrated leadership in professional setting</li><li>Demonstrated teamwork and collaboration in a professional setting Other Information:</li></ul>Domestic and International travel may be requiredLilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Senior Level

Eli Lilly and Company India Pvt Ltd

Programmer Analyst

Packaging 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><ul><li>Preparation of design verification protocol and test reposts for combination products such as pen injectors, autoinjectors and prefilled syringes.</li><li>Author and/or participate in preparation of Design Controls (ISO 13485) and Risk Management (ISO 14971) for drug-device combination products</li><li>Support preparation of technical package for Notified Body Opinion submissions</li><li>Manage vendor interactions and communication for device suppliers, primary packaging component suppliers, artwork development, secondary packaging development, device assembly and testing</li><li>Preparation of packaging documents – Material code, FG code, Bill of Materials, MPC, test method development, test method verification, artworks, print proofs, transport study, transfer checklist, drawings, layout, trials reports, specifications, STP etc.</li><li>Develop device assembly and automation for manufacturing. Evaluate concepts, ensure development and participate in equipment qualification</li><li>Identify and plan for device testing for primary container as per relevant USP and Ph.Eur requirements</li><li>Device primary functions testing with respect to relevant ISO standards (ISO 11608, ISO 11040, ISO 6236 etc.)</li><li>Lead technical investigations of medical device and combination product</li><li>Facilitate technology transfer of medical device and combination products from development to commercialization</li><li>Application of statistical tools for data analysis</li><li>Supporting global and site-specific projects, including those related to combination products and drug delivery systems</li><li>Keep current with ISO and FDA regulations respective to combination products. Train new and existing employees on Combination Product Requirements, processes, and procedures</li><li>Keep stake-holders and team members informed with effective communication. The key stakeholders include Internal and External Manufacturing Sites, R&amp;D, Quality, Operations, Product Development groups, Regulatory Affairs, Procurement, and suppliers.</li></ul><h4>Qualifications</h4><ul><li>Bachelor’s or master’s degree in science, engineering, biomedical, packaging, or a closely related technical field, coupled with over 7 years of hands-on experience in the pharmaceutical or medical device industry, specifically focused on drug delivery systems like pen injectors and autoinjectors</li><li>Experience with design verification testing</li><li>Seven plus years of relevant experience in medical devices or combination products</li><li>Seven plus years in design control, risk analysis and change control management for medical device or combination products</li><li>Experience in combination product design verification (ISO 11608, ISO 11040), design controls (ISO 13485), risk management (ISO 14971)</li><li>Experience with medical device or combination product commercialization, operations support, and materials/components</li><li>Experience with pen injectors, autoinjectors or other complex drug-delivery systems and associated pre-filled syringe systems or cartridges.</li><li>Experience with device assembly and/or packaging equipment/automation and design for manufacturing</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

Dr Reddys Laboratories

Packaging Manager

Associate Economics Analyst, Global Growth and Operations-1Our PurposeMastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we’re helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential.Title and SummaryAssociate Economics Analyst, Global Growth and Operations-1Overview The Mastercard Economics Institute (MEI) is an economics lab powering scale at Mastercard by owning economic thought leadership in support of Mastercard’s efforts to build a more inclusive and sustainable digital economy MEI was launched in 2020 to analyze economic trends through the lens of the consumer to deliver tailored and actionable insights on economic issues for customers, partners and policymakers The Institute is composed of a team of economists and data scientists that utilize &amp; synthesize the anonymized and aggregated data from the Mastercard network together with public data to bring powerful insights to life, in the form of 1:1 presentation, global thought leadership, media participation, and commercial work through the company’s product suites ________________________________________________________________________________________________________ About the Role Mastercard’s Economics Institute is seeking a talented Economic Analyst with R or Python Programmer skills to join our Global Growth and Operations team. Reporting to the Director, Growth and Operations, this individual will blend advanced economic research with strong programming and data visualization skills. This is a unique opportunity for someone passionate about applying economic thinking and technical expertise to real-world questions at the intersection of economics, retail, and commerce. The role involves working on large-scale data analytics, developing innovative economic insights, and building compelling visualizations that help communicate these insights to diverse audiences. Support client and stakeholder engagements across MEI Collaborate with team economists, econometricians, developers, visualization experts and industry partners. Develop and test hypotheses at the intersection of economics, retail, and commerce. Structure work and manage small project streams, delivering impactful results. Identify creative analyses and develop proprietary diagnostic indices using large and complex datasets, including macroeconomic and big data sources. Generate insights, synthesize analyses into impactful storylines and interactive visuals, and help write reports and client presentations. Enhance existing products and partner with internal stakeholders to develop new economic solutions. Help create thought leadership and intellectual capital. Create and format analytical content using Jupyter Notebooks, R Markdown and/or Quarto. Work with databases and data platforms, including Databricks, SQL and Hadoop. Write clear, well-documented code that others can understand and maintain. Collaborate using Git for version control. ________________________________________________________________________________________________________ All About You Bachelor’s degree in Economics (preferred), Statistics, Mathematics, or a related field. Proficient in working with relational databases and writing SQL queries. Expertise in working with large-scale data processing frameworks and tools, including Hadoop, Apache Spark, Apache Hive, and Apache Impala. Proficient in R or Python with experience in data processing packages. Skilled in creating data visualizations to communicate complex economic insights to diverse audiences. Experience using data visualization tools such as Tableau or Power BI. Proficiency in machine learning, econometric and statistical techniques, including predictive modeling, survival analysis, time series modeling, classification, regression and clustering methods is desirable. Strong problem-solving skills and critical thinking abilities. Excellent communication skills, both written and verbal. Organized and able to prioritize work across multiple projects. Collaborative team player who can also work independently. Passionate about data, technology, and creating impactful economic insights.Corporate Security Responsibility All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must:<ul><li>Abide by Mastercard’s security policies and practices;</li><li>Ensure the confidentiality and integrity of the information being accessed;</li><li>Report any suspected information security violation or breach, and</li><li>Complete all periodic mandatory security trainings in accordance with Mastercard’s guidelines.</li></ul> <h4>Experience Level</h4>Mid Level

Mastercard India Services Pvt Ltd

Financial Analyst

Associate Director Biostatistics<h4>Career Category</h4>Research<h4>Job Description</h4><h4>HOW MIGHT YOU DEFY IMAGINATION?</h4><h4>If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.</h4><h4>Associate Director Biostatistics</h4><h4>What you will do</h4><h4>Let’s do this. Let’s change the world.</h4><h4>Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leadership. As Associate Director, Biostatistics, you will contribute statistical strategy, operational execution, and scientific leadership across Amgen’s clinical programs. You will oversee statistical contributions to clinical trials, lead study teams, and support regulatory and reimbursement submissions, while mentoring and managing statisticians.</h4><h4>This role provides both hands-on technical leadership and managerial responsibility, ensuring quality, compliance, and innovation in biostatistical delivery aligned with Amgen’s global clinical development strategy.</h4><h4>Responsibilities:</h4><ul><li><h4>Provide sound statistical guidance to clinical development, reimbursement, and medical affairs.</h4></li><li><h4>Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents.</h4></li><li><h4>Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies.</h4></li><li><h4>Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings.</h4></li><li><h4>Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives.</h4></li><li><h4>Provide sound statistical guidance to clinical development, reimbursement, and medical affairs.</h4></li><li><h4>Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents.</h4></li><li><h4>Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies.</h4></li><li><h4>Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings.</h4></li><li><h4>Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives.</h4></li><li><h4>Execute biostatistical strategies across the product lifecycle, from early development through post-marketing.</h4></li><li><h4>Provide consultancy and training to colleagues across R&amp;D.</h4></li><li><h4>Support governance of outsourced statistical activities, ensuring adherence to Amgen standards and regulatory compliance.</h4></li><li><h4>Represent Biostatistics in cross-functional and external interactions (e.g., with regulatory agencies, investigators, or data monitoring committees).</h4></li><li><h4>Drive technology adoption leveraging AI capabilities to streamline statistician’s work</h4></li></ul><h4>This position is currently located at Amgen India (Hyderabad).</h4><h4>Win</h4><h4>What we expect of you</h4><h4>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strategic Biostatistics leader with a passion for tech-enabled transformation.</h4><h4>Basic Qualifications:</h4><ul><li><h4>Doctorate in Statistics/Biostatistics (or related subject with high statistical content) with at least 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research, OR</h4></li><li><h4>Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with at least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research.</h4></li></ul><h4>Preferred Skills:</h4><ul><li><h4>Doctorate in Statistics/Biostatistics (or related subject with high statistical content) with at least 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research, OR</h4></li><li><h4>Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with at least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research.</h4></li></ul><h4>Thrive</h4><h4>What you can expect of us</h4><h4>As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.</h4><ul><li><h4>Vast opportunities to learn and develop within our global organization</h4></li><li><h4>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</h4></li><li><h4>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</h4></li></ul>.<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Medical Coder

Senior Manager Biostatistics<h4>Career Category</h4>Research<h4>Job Description</h4><h4>HOW MIGHT YOU DEFY IMAGINATION?</h4><h4>If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission -to serve patients - drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together - researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.</h4><h4>Biostatistics Sr. Manager</h4><h4>What you will do</h4><h4>Let’s do this. Let’s change the world.</h4><h4>Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN) playing a key role in integrated delivery and functional leadership. As a Biostatistics Sr. Manager, you will lead study-level statistical deliverables with substantial independence. This role manages small teams, mentors staff and ensures the delivery of high-quality statistical outputs that meet CfDA and regulatory expectations.</h4><h4>Responsibilities:</h4><ul><li><h4>Utilizing knowledge and expertise to inform and provide sound statistical guidance to areas and teams in clinical development, reimbursement, and medical affairs.</h4></li><li><h4>Plan and execute statistical contributions to protocols, Flash Memos and Clinical Study Reports (CSRs)</h4></li><li><h4>Implement, manage and support standards, technical quality and consistent approaches in strategy, study design and statistical analysis.</h4></li><li><h4>Knowledgeable of developments in the field of statistics in drug development (innovative trial design) and Amgen’s statistical policies, procedures and strategies.</h4></li><li><h4>Understand, promote, and communicate innovative and standard statistical methodologies, trial design, data analysis, and medical / clinical understanding for product</h4></li><li><h4>Oversee statistical contributions to key design elements, protocols, randomization specifications, statistical analysis plans, tables, figures and listing shells, submission data file specifications, and other key study-related documentation</h4></li><li><h4>Collaborate cross-functionally to deliver robust, valid and scientifically rigorous analysis results in Table, Figure and Listings (TFLs), Flash Memos (FM), Clinical Study Reports (CSRs), clinical publications, and other communications</h4></li><li><h4>Serve as the GBS lead on the Clinical Study Team leadership team to execute clinical trials according to the protocol, performing risk assessments and ensuring quality data collection and alignment between data collection and study objectives</h4></li><li><h4>Contribute to clinical publications, regulatory filing documents, reimbursement documents and other communications for product or study</h4></li><li><h4>Provide statistical consultancy, training, and advice within Amgen</h4></li><li><h4>Contributing to process improvement initiatives and operational efficiencies.</h4></li><li><h4>Oversee FSP statisticians and check their contributions for quality</h4></li><li><h4>Ensure statistics sections of the TMF are maintained and up-to-date</h4></li><li><h4>Opportunity to manage staff, e.g. external contractors</h4></li><li><h4>Opportunity to serve as a GSL for a product program</h4></li><li><h4>Opportunity to serve as a product regional lead</h4></li><li><h4>Contribute to and lead technology adoption leveraging AI capabilities to streamline statistician’s work</h4></li></ul><h4>This position is currently located at Amgen India (Hyderabad).</h4><h4>Win</h4><h4>What we expect of you</h4><h4>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strategic Biostatistics leader with a passion for tech-enabled transformation.</h4><h4>Basic Qualifications:</h4><ul><li><h4>Doctorate degree in Statistics/Biostatistics or related subject with high statistical content and</h4></li><li><h4>At least 2 years of post-graduate statistical experience in the pharmaceutical industry or medical research</h4></li></ul><h4>Or</h4><ul><li><h4>Master’s degree in Statistics/Biostatistics or related subject with high statistical content and</h4></li><li><h4>At least 6 years of post-graduate statistical experience in the pharmaceutical industry or medical research</h4></li></ul><h4>Or</h4><ul><li><h4>Bachelor’s degree in Statistics/Biostatistics or related subject with high statistical content and</h4></li><li><h4>At least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research</h4></li></ul><h4>Preferred Skills:</h4><ul><li><h4>Doctorate degree in biostatistics and at least 4 years of post-graduate statistical experience in the pharmaceutical industry or medical research</h4></li></ul><h4>Or</h4><ul><li><h4>Master’s degree in biostatistics and at least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research</h4></li><li><h4>Life Cycle Drug Development Experience (Pre-clinical Development, Clinical Development, and Post-marketing)</h4></li><li><h4>Strong verbal and written communication combined with organizational skills and cross-cultural sensitivity</h4></li><li><h4>Statistical leadership and contribution to regulatory and reimbursement submissions. of regulatory guidelines.</h4></li><li><h4>Experience working effectively in a globally dispersed team environment with cross-cultural partners.</h4></li></ul><h4>Thrive</h4><h4>What you can expect of us</h4><h4>As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.</h4><ul><li><h4>Vast opportunities to learn and develop within our global organization</h4></li><li><h4>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</h4></li><li><h4>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</h4></li></ul>.<h4>Experience Level</h4>Senior Level

Senior Expert Science and TechnologyJob Description SummaryThe job purpose is to lead and manage all assigned project/network activities and apply scientific/technical expertise to address complex R&amp;D issues for the preparation and timely delivery of drug products (DP), processes and procedures; coach team members, participate in teams and contribute to overall Technical Research and Development strategies and goals. To develop our growing pipeline of products we are looking for experienced professionals in the area of pharmaceutical development. In this challenging position, you will play a key role in the development of oral solid and liquid dosage forms (including poorly soluble compounds). Job DescriptionMajor accountabilities: <ul><li>To ensure high quality products are developed applying risk analysis and QbD methodologies.</li><li>To work in multidisciplinary and international project teams and represent Pharmaceutical Development in external collaborations, resulting in a wide range of scientific and strategic tasks.</li><li>To develop and achieve robust formulations and processes through optimization, scale-up and validation work and provision of the re-quired documentation to allow worldwide registration.</li><li>To work in a GMP-role covering manufacturing, documentation, data management and quality management aspects.</li><li>To plan, supervise and report internal and external technical development campaigns as well as clinical supply campaigns.</li><li>To plan, supervise and to report internal and external technical transfer campaigns between Development sites and to production sites (internal and 3rd parties).</li><li>The development of new technologies and supervision of scientific projects are further options within this position.</li></ul>Key performance indicators: <ul><li>Adherence to costs, quality, quantity, and timelines for all assigned tasks.</li><li>Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.</li><li>Feedback from other team leaders and advisory boards.</li><li>Measurable contributions to the success, efficiency and productivity of the department and new programs/initiatives started and implemented.</li><li>Refer to annual individual and team objective setting.</li><li>Internal and external publications/presentations.</li><li>Successful and effective execution of assigned tasks within given timelines at expected quality; right the first time and on time; demonstrate initiative and strive for high level of quality.</li></ul>Minimum Requirements: <ul><li>PhD or M.Tech or M.Pharm in Pharmaceutical Technology/Pharmaceutics English PhD. with 8+years or M. Pharm with 12+ years of experience in the pharmaceutical industry.</li><li>Minimum 5-6 years of hands-on industry experience in the development of pharmaceutical formulations (ideally oral dosage forms, excellent understanding of QbD and biopharmaceuticals). </li><li>Awareness for safe handling of chemicals, potentially dangerous materials and equipment</li><li>Basic knowledge in scientific/technical areas of collaboration and good knowledge of laboratory and/or technical tools</li><li>Adequate knowledge of software and computer tools</li><li>Good presentation and Scientific writing skills.</li><li>Experience of working in international project teams (matrix organizations)</li></ul>Work Experience: <ul><li>People Challenges.</li><li>Managing Crises.</li><li>Functional Breadth.</li><li>Project Management.</li><li>Operations Management and Execution.</li><li>Collaborating across boundaries.</li></ul>Skills: <ul><li>Environment.</li><li>Experiments Design.</li><li>Health And Safety (Ehs).</li><li>Laboratory Equipment.</li><li>Manufacturing Process.</li><li>Materials Science.</li><li>Process Simulation.</li><li>Project Management.</li><li>Technical Writing.</li><li>Sop (Standard Operating Procedure).</li></ul>Languages:<ul><li>English.</li></ul> Skills DesiredCoaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Waterfall Model<h4>Experience Level</h4>Senior Level

Novartis India

Science Instructor

Architect- Custom design and Standard Cell Design methodologies<h4>
 
 General Information
 </h4>






 Job Title
 

 Architect- Custom design and Standard Cell Design methodologies
 



 Job ID
 

 12493
 



 Country
 

 India
 



 City
 

 Bengaluru
 



 Date Posted
 

 06-Aug-2025
 



 Job Category
 

 Engineering
 



 Job Subcategory
 

 R&amp;D Engineering
 



 Hire Type
 

 Employee
 



 Remote Eligible
 

 No
 






<h4>
 
 Descriptions &amp; Requirements
 </h4>






 Job Description and Requirements
 

<h4 id="isPasted">We Are: At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation. You Are: You are an experienced and initiative-taking individual with a strong technical background in custom design and Standard Cell Design methodologies. You thrive in collaborative environments and possess a passion for creating innovative technology. Your expertise lies in working with advanced finfet and GAA process challenges, and you have a proactive analytical approach with a keen eye for detail. Your dedication to delivering high-quality results is complemented by excellent communication and people skills, allowing you to effectively collaborate with both internal teams and external customers. Driven by a desire to innovate, you are eager to contribute to the success of our cutting-edge technology products. What You’ll Be Doing: * Conceptualizing, designing, and productizing state-of-the-art circuit components for SLM monitors realized through ASIC design flow.  * Designing on-chip Process, Voltage, Temperature, glitch, and Droop monitors for monitoring silicon biometrics.  * Developing statistical simulation methodologies and collaborating with the layout team to achieve optimal design solutions. * Characterizing designed custom cells and deploying new circuits into test chips for post-silicon characterization.  * Creating new cells and updating existing ones through collaboration with architects and Physical Design engineers. * Conducting pre and post-layout simulations and characterizations across various design corners to ensure reliability and aging requirements. The Impact You Will Have: * Accelerating the integration of next-generation intelligent in-chip sensors and analytics into technology products.  * Optimizing performance, power, area, schedule, and yield of semiconductor lifecycle stages. * Enhancing the reliability and differentiation of products in the market with reduced risk.  * Driving innovation in custom circuit design methodologies and tools. * Contributing to the development of industry-leading SLM monitors and silicon biometrics solutions. * Collaborating with cross-functional teams to ensure the successful deployment of advanced technologies. What You’ll Need:  * BS or MS degree in Electrical Engineering with 8+ years of relevant industry experience. * Strong custom design experience, including specification, circuit design description, and schematics.  * Proficiency with circuit design and simulation tools, IC design CAD packages from any EDA vendor.  * Sound understanding of SPICE simulator concepts and simulation methods.  * Experience with statistical design methodologies like generating and analyzing Monte-Carlo results. Who You Are: * Proactive and detail-oriented with excellent problem-solving skills.  * Adept at working independently and providing circuit solutions.  * Excellent communicator and team player, capable of collaborating effectively with diverse teams.  * Innovative thinker with a passion for technology and continuous improvement.  * Committed to delivering high-quality results and achieving project goals. The Team You’ll Be A Part Of: You will be part of the SLM Monitors group, a team dedicated to building next-generation intelligent in-chip sensors, hardware/software capabilities, and analytics. Our team focuses on developing and integrating solutions that manage and improve each semiconductor lifecycle stage, enabling customers to bring differentiated products to market quickly with reduced risk. Rewards and Benefits:  We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non-monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process.</h4>At Synopsys, we want talented people of every background to feel valued and supported to do their best work. Synopsys considers all applicants for employment without regard to race, color, religion, national origin, gender, sexual orientation, age, military veteran status, or disability.<h4>Experience Level</h4>Senior Level

Synopsys India Pvt Ltd

CAD Engineer

Game Mathematician IIAt Aristocrat, we are driven by a single goal: to bring happiness to life through the power of play. As a Game Mathematician II, you will play a pivotal role in crafting the player experience and the mathematical models that make our games exciting and engaging. Join us and be part of a team that thrives on innovation and collaboration, working together to build flawless, world-class gaming experiences. This role offers an outstanding opportunity to combine creative vision with technical expertise, making a significant impact on our diverse portfolio of games!<h4>What You'll Do</h4><ul><li>Participate in crafting all aspects of a game design, including entertainment, pacing, mathematical outcomes, and player communication.</li><li>Achieve efficient math models with meticulous attention to detail.</li><li>Generate initial and final Excel-based math models and combination sheets.</li><li>Test mathematical outcomes to ensure quality and accurate calculations through Excel.</li><li>Understand game design concepts for multiple products in our games portfolio.</li><li>Coordinate the delivery of mathematical design documents for assigned projects and lead all aspects of their full implementation through the development process.</li><li>Work on crafting great games by crafting player experiences and mathematics models for multiple games.</li><li>Participate in on-the-job training opportunities to improve domain expertise.</li></ul><h4>What We're Looking For</h4><ul><li>1-3 years of experience with a Bachelor’s or Master’s in Mathematics or B.Tech in Mathematics &amp; Computing.</li><li>Proficiency in statistical models and Excel.</li><li>Strong expertise in Probability Theory and statistics.</li><li>Robust data analytics skills.</li><li>Experience in one of the programming languages: C, C++, Python.</li><li>A great teammate with effective communication skills.</li><li>A self-motivated, fast learner who can communicate effectively with engineering, art, production, and business personnel.</li></ul>Why Aristocrat?Aristocrat is a world leader in gaming content and technology, and a top-tier publisher of free-to-play mobile games. We deliver great performance for our B2B customers and bring joy to the lives of the millions of people who love to play our casino and mobile games. And while we focus on fun, we never forget our responsibilities. We strive to lead the way in responsible gameplay, and to lift the bar in company governance, employee wellbeing and sustainability. We’re a diverse business united by shared values and an inspiring mission to bring joy to life through the power of play.We aim to create an environment where individual differences are valued, and all employees have the opportunity to realize their potential. We welcome and encourage applications from all people regardless of age, gender, race, ethnicity, cultural background, disability status or LGBTQ+ identity. EEO M/F/D/V<ul><li>World Leader in Gaming Entertainment</li><li>Robust benefits package</li><li>Global career opportunities</li></ul>Our Values<ul><li>All about the Player</li><li>Talent Unleashed</li><li>Collective Brilliance</li><li>Good Business Good Citizen</li></ul>Travel ExpectationsNoneAdditional InformationAt this time, we are unable to sponsor work visas for this position. Candidates must be authorized to work in the job posting location for this position on a full-time basis without the need for current or future visa sponsorship. <h4>Experience Level</h4>Entry Level

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