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Experience Research Senior Associate - OperationsBring your industry trends and knowledge to our team and shape exceptional user experiences through cutting-edge research, influencing product design and functionality.As an Experience Research Senior Associate in Operations team, you will play a pivotal role in shaping user experiences across our products and services. Leveraging advanced proficiency in research methods, analysis, and both quantitative and qualitative techniques, identify customer needs and translate them into actionable insights and recommendations. You will act as a core contributor to aid in developing research studies that answer user needs. Your work will directly impact the design, architecture, and functionality of our offerings, collaborating with cross-functional teams to contribute to discussions on design and research, and leading the decision on which methods best suit key design questions.Job responsibilities<ul><li>Conduct and execute research studies using advanced research methods, such as surveys, interviews, ethnography, and quantitative and qualitative techniques, to gather customer insights</li><li>Analyze and interpret data, identify patterns and trends, and provide actionable recommendations to inform user experience design decisions and facilitate improvements in customer satisfaction and engagement</li><li>Collaborate with cross-functional teams to ensure the integration of user insights into product development processes based on research findings</li><li>Contribute to the creation and refinement of experience research strategies and connect craft work to business goals and success metrics, taking into consideration downstream implications</li><li>Stay current with industry trends and incorporate knowledge into team insights</li></ul>Required qualifications, capabilities, and skills<ul><li>3+ years of experience or equivalent expertise in generative and evaluative user experience research, employing advanced research methods and techniques</li><li>Demonstrated proficiency in both quantitative and qualitative research methods, including survey and interview design, ethnography, and data analysis</li><li>Advanced knowledge of user experience design principles and practices, with a focus on how ethnographic principles influence effective user experiences</li><li>Advanced understanding of current research methodologies, with the ability to review and understand how to apply current research practices to better inform experience designs</li></ul>Preferred qualifications, capabilities, and skills<ul><li>Project planning and management skills.</li><li>Understanding of Accessibility Guidelines and Inclusive Design practices.</li></ul>

JP Morgan Services India Pvt Ltd

Research Supervisor

R&D Data Engineering ExpertPosition Title: R&amp;D Data Engineering ExpertAbout the JobAt Sanofi, we’re committed to providing the next-gen healthcare that patients and customers need. It’s about harnessing data insights and leveraging AI responsibly to search deeper and solve sooner than ever before. Join our R&amp;D Data &amp; AI Products and Platforms Team as an R&amp;D Data Engineerand you can help make it happen.What you will be doing:Sanofi has recently embarked into a vast and ambitious digital transformation program. A cornerstone of this roadmap is the acceleration of its data transformation and of the adoption of artificial intelligence (AI) and machine learning (ML) solutions, to accelerate R&amp;D, manufacturing and commercial performance and bring better drugs and vaccines to patients faster, to improve health and save lives.The R&amp;D Data &amp; AI Products and Platforms Team is a key team within R&amp;D Digital, focused on developing and delivering Data and AI products for R&amp;D use cases. This team plays a critical role in pursuing broader democratization of data across R&amp;D and providing the foundation to scale AI/ML, advanced analytics, and operational analytics capabilities.As an R&amp;D Data Engineer, you will join this dynamic team committed to driving strategic and operational digital priorities and initiatives in R&amp;D. You will work as a part of a Data &amp; AI Product Delivery Pod, lead by a Product Owner, in an agile environment to deliver Data &amp; AI Products. As a part of this team, you will be responsible for the design and development of data pipelines and workflows to ingest, curate, process, and store large volumes of complex structured and unstructured data. You will have the ability to work on multiple data products serving multiple areas of the business.Our vision for digital, data analytics and AIJoin us on our journey in enabling Sanofi’s Digital Transformation through becoming an AI first organization. This means:<ul><li>AI Factory - Versatile Teams Operating in Cross Functional Pods: Utilizing digital and data resources to develop AI products, bringing data management, AI and product development skills to products, programs and projects to create an agile, fulfilling and meaningful work environment.</li><li>Leading Edge Tech Stack: Experience build products that will be deployed globally on a leading-edge tech stack.</li><li>World Class Mentorship and Training: Working with renown leaders and academics in machine learning to further develop your skillsets.</li></ul>We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?Main Responsibilities:Data Product Engineering:<ul><li>Provide input into the engineering feasibility of developing specific R&amp;D Data/AI Products</li><li>Provide input to Data/AI Product Owner and Scrum Master to support with planning, capacity, and resource estimates</li><li>Design, build, and maintain scalable and reusable ETL / ELT pipelines to ingest, transform, clean, and load data from sources into central platforms / repositories</li><li>Structure and provision data to support modelling and data discovery, including filtering, tagging, joining, parsing and normalizing data</li><li>Collaborate with Data/AI Product Owner and Scrum Master to share progress on engineering activities and inform of any delays, issues, bugs, or risks with proposed remediation plans</li><li>Design, develop, and deploy APIs, data feeds, or specific features required by product design and user stories</li><li>Optimize data workflows to drive high performance and reliability of implemented data products</li><li>Oversee and support junior engineer with Data/AI Product testing requirements and execution</li></ul>Innovation &amp; Team Collaboration:<ul><li>Stay current on industry trends, emerging technologies, and best practices in data product engineering</li><li>Contribute to a team culture of innovation, collaboration, and continuous learning within the product team</li></ul>About You:Key Functional Requirements &amp; Qualifications:<ul><li>Bachelor’s degree in software engineering or related field, or equivalent work experience</li><li>3-5 years of experience in data product engineering, software engineering, or other related field</li><li>Understanding of R&amp;D business and data environment preferred</li><li>Excellent communication and collaboration skills</li><li>Working knowledge and comfort working with Agile methodologies</li></ul>Key Technical Requirements &amp; Qualifications:<ul><li>Proficiency with data analytics and statistical software (incl. SQL, Python, Java, Excel, AWS, Snowflake, Informatica(IICS), Terraform, DBT, and Airflow)</li><li>Deep understanding and proven track record of developing data pipelines and workflows</li></ul>Why Choose Us?<ul><li>Bring the miracles of science to life alongside a supportive, future-focused team</li><li>Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally</li><li>Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact</li><li>Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs</li></ul>Pursue Progress. Discover Extraordinary.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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.At Sanofi, we provide equal opportunities to all regardless of race, color, 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>!<h4>Experience Level</h4>Senior Level

Sanofi India Ltd

Data Engineer

Senior Data Programmer CPQP ProgrammingJob Title: Senior Data Programmer CPQP ProgrammingGlobal Career Level: DSkillsets Required: PKPD / Pharmacometrics / NONMEM / SAS ProgrammerIntroduction to role:Are you interested in shaping the future of drug development? We are looking for a Senior Data Programmer CPQP Programming to join our Clinical Pharmacology and Quantitative Pharmacology Data Programming team. In this position, you will be responsible for preparing, programming, validating, and diagnosing data to support Pharmacometrics and Clinical Pharmacology analyses. Your work will span all phases of drug development at both the study and compound levels.Accountabilities: As a Senior Data Programmer CPQP Programming, you will be responsible for data cleaning, manipulation, transformation, and integration at both the study and compound level. You will apply advanced data integration techniques that directly contribute to the value of each study and compound. Key responsibilities include pooling data from study and compound-level SDTM/ADaM datasets to prepare analysis-ready data for Pharmacometrics Modeling and Simulation (M&amp;S) software, such as NONMEM. This work will play a critical role in informing study design, dose selection, dose justification and guiding go/no-go decisions. Additionally, you will contribute to internal initiatives that advance the Pharmacometrics discipline and ensure compliance with Good Clinical Practice (GCP) regulations.Essential Skills/Experience:<ul><li>Proficient oral and written English communication skills</li><li>Strong SAS/R programming skills</li><li>Bachelor’s degree MS preferred with 6 to 8 years relevant experience required</li><li>Expert knowledge of data preparation and programming practices (CDISC, SDTM, ADaM)</li><li>Demonstrated data programming and clinical development expertise</li><li>Good knowledge of global regulatory, compliance, processes, standards</li><li>Varied programming languages (SAS, R, Python)</li><li>Experience in early and late-stage drug development</li><li>Quantitative/Scientific background (Statistics, Engineering, Biological Science)</li></ul>Desirable Skills/Experience:<ul><li>Demonstrated expertise in data preparation and programming to support Pharmacometrics Modeling and Simulation (M&amp;S) software (e.g. NONMEM, Monolix, R, Matlab) </li><li>Knowledge in pharmacology, drug targets and core Therapy areas (e.g. Oncology, Respiratory, Renal Metabolism etc.)</li><li>Relevant regulatory experience</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.At AstraZeneca, we are committed to making a difference by fusing data and technology with scientific innovation to achieve breakthroughs in healthcare. Our dynamic environment encourages creativity and bold decision-making as we strive to treat, prevent, modify, and even cure complex diseases. With a focus on collaboration and inclusivity, we unite diverse global knowledge to create impactful solutions for patients worldwide. Here, curiosity thrives as we explore new ways to handle diseases and push the boundaries of science.Ready to make an impact? Apply now and be part of a team that is transforming the future of healthcare!Date Posted08-Oct-2025Closing Date19-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

Chemical Analyst

SR MGR R&D/PRODUCT DVL ENGINEERING - PCB Design and Simulation At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. <h4>Job Overview</h4>BU / FunctionDigital Data &amp; Networks (DDN) Business Unit in TE Connectivity, where we enable high-speed connectivity solutions that power today’s and tomorrow’s data-driven world. Engineering team is responsible for development of innovative interconnect solution products which are used in hyperscale computers, AI, Datacenter, Cloud server, and other IT systems, including connector, cable assembly, bus bars and sockets. We engineer and manufacture cutting-edge interconnect solutions that support high-speed data transmission, signal integrity, and power efficiency. Role ObjectiveSr. Manager is a senior engineering leader for high-speed PCB Design and Simulations. They lead teams in designing, simulating, and validating high-performance high speed printed circuit boards for AI and Datacentre applications ensuring quality, performance, and manufacturability through strategic planning, technical guidance, and collaboration across cross-functional teams. Responsibilities include team development, design and simulation strategy, project management, and continuous process improvement to meet deadlines, budget targets, and project performance goals. <h4>Responsibilities:</h4><ul type="disc"><li>Team Leadership &amp; Development: Lead, mentor, and develop teams of high-speed PCB design and simulation managers and engineers, focusing on their career growth and skill development. </li><li>Strategic Design and Simulation: Define and implement high speed design and simulation roadmaps, methodologies and best practices for signal integrity, power integrity, electromagnetic compatibility (EMC), radio frequency interference (RFI) and thermal analysis. </li><li>Cross-Functional Collaboration: Work closely with hardware, firmware, mechanical, and manufacturing teams to translate requirements into viable designs and resolve issues. </li><li>Project &amp; Resource Management: Oversee the management of multiple complex PCB design and simulation projects, ensuring they meet deadlines, budget requirements, and performance targets. </li><li>Technical Oversight: Provide technical guidance on PCB layout, schematic creation, and component selection, staying current with new technologies and design standards. </li><li>Design review and verifications: Conduct design and simulation reviews, providing strategic recommendations to optimize PCB performance and reliability.</li><li>Continuous improvement: Drive innovation and improvement in high-speed PCB design and simulation process. Stay current with emerging technologies, design standards (e.g. IPC), and simulation tools to enhance efficiency and maintain a competitive edge.</li><li>Quality and Validation: lead and drive accuracy in design and simulations, conduct design of experiments (DoE), plausibility check and sensitivity study of simulations, validate simulation results with experimental data, and design optimizations for first time right manufacturability (prototypes and mass production).</li></ul><h4>Candidate Desired Profile:</h4>Education: A bachelor’s degree in electrical or electronics engineering from a premier institute/university. A master’s degree in a related field is preferred. Experience: 20 yrs extensive hands-on experience in high-speed PCB design and simulation with a proven track record of delivering complex projects. Leadership: 8-10 years progressive leadership or management experience in leading and developing high-performing engineering teams. Experience in customer engagement and stakeholder management is essential.Technical Skills:<ul><li>Deep understanding of engineering principles for high-speed PCB design, signal integrity (SI), power integrity (PI), electromagnetic compatibility (EMC), radio frequency interference (RFI) and thermal incidents.</li><li>Deep understanding of PCB layout, schematic creation, routing, and manufacturability. </li><li>Expertise in high-speed PCB design tools such as Altium Designer, Allegro or PADS. </li><li>Expertise in high-speed PCB simulation tools for electrical and thermal analysis - Ansys SIwave/HFSS, Keysight Pathwave ADS, Keysight SIPro, Siemens HyperLyx, Cadence Sigrity, Dassault CST Studio Suite, Ansys EMC Plus, Cadence Microwave Office, and Ansys ICEPAK/Siemens FLOTHERM/Cadence CELSIUS.</li><li>Strong knowledge of industry standards (IPC, JEDEC, PCIe, USB, Ethernet) and PCB manufacturing processes, including design for manufacturability (DFM). </li></ul>Soft Skills:<ul><li>Proven abilities on inspiring leadership, team management, prioritisation, strategy and execution.</li><li>Experience in organizational development, and talent attraction/management/retention.</li><li>Promote and manage employee wellbeing and work-life balance.</li><li>Passion for Technology and scientific/engineering excellence.</li><li>Excellent problem-solving and analytical skills to resolve complex technical issues.</li><li>Strong in Technical Documentations, Report preparation and presentation</li><li>Strong verbal and written communication skills to articulate complex technical concepts to both technical and non-technical stakeholders.</li><li>Ability to work effectively in a fast-paced, collaborative global environment and global time zones.</li><li>Proficient using MS office software (Word, Excel, PPT, Outlook, MS Teams, etc.).</li></ul><h4>What your background should look like</h4>Generally requires Bachelors degree in appropriate field with 12 or more years of experience; or Masters with 10 or more years of experience; or PhD level with 6 or more years of experience; or local equivalent<h4>Competencies</h4>
SET : Strategy, Execution, Talent (for managers)ABOUT TE CONNECTIVITY TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at <a href="http://www.te.com/" target="_blank">www.te.com</a> and on <a href="https://www.linkedin.com/company/te-connectivity/">LinkedIn</a>, <a href="https://www.facebook.com/teconnectivity/">Facebook</a>, <a href="http://www.te.com.cn/chn-zh/policies-agreements/wechat.html">WeChat,</a> <a href="https://www.instagram.com/teconnectivity/">Instagram</a> and <a href="https://twitter.com/TEConnectivity">X (formerly Twitter).</a> WHAT TE CONNECTIVITY OFFERS: We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!•    Competitive Salary Package •    Performance-Based Bonus Plans •    Health and Wellness Incentives •    Employee Stock Purchase Program •    Community Outreach Programs / Charity Events •    Employee Resource Group IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity never requests payment or fees from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come only from actual email addresses ending in @te.com. If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site. <h4>Experience Level</h4>Senior Level

TE Connectivity India Pvt Ltd

Design And Development Engineer

Associate STEM Content Analyst - GENESEQ IndexingAssociate STEM Content Analyst – GENESEQ  We are looking for an Associate STEM Content Analyst to join our GENESEQ process in Chennai. This is an amazing opportunity to work on GENESEQ process in IPG. We would love to speak with you if you have skills in Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry.   About You   <ul><li>Must be a master’s degree graduate in Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry  </li></ul><ul><li>Can be a fresher or candidate with around 1 year experience in working on patents, patent indexing with basic patent knowledge.  </li></ul><ul><li>If experienced, must have at least a year’s experience in patent indexing, disease indexing, abstract writing </li></ul> It would be great if you also had . . .     <ul><li>1 to 2 years of experience on patent indexing, gene sequencing, genetics, and disease indexing. </li></ul><ul><li>Good knowledge on computer including MS office, PDF or TIFF images; good exposure to publicly available databases like NCBI taxonomy database, PubMed, etc; and secondary research skills.  </li></ul> What will you be doing in this role?   <ul><li>You will Apply biotechnology, genetics, and molecular biology concepts to curate biological sequence related information from patent documents in line with editorial policies and conventions. </li></ul><ul><li>Indexers manually curate all biological sequences given in the specification, including those found within PDF or TIFF images, not just those given in the formal electronic sequence listing. </li></ul><ul><li>indexers also create additional sequences which are described in the specification, which often are not given in the sequence listing, but which are claimed. The team will also create individual records for mutated sequences and for claimed SEQ ID fragments where the whole sequence has not been claimed.  </li></ul><ul><li>Achieve weekly production volume and quality targets and to maintain the consistency. </li></ul><ul><li>To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices.  </li></ul> About the Team                  GENESEQ Team is one of the key knowledge-driven teams in Intellectual Property Group in Clarivate. The team consists of 37 colleagues, in various roles with different experience and skill set in various domains like Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry; are reporting to a Team Manager. GENESEQ product includes Nucleic Acid sequences of minimum 10 bases or 8 if claimed and Amino Acid sequences of minimum 4 residues.   Hours of Work    9 AM to 6 PM IST (includes 1 hour break), subject to slight changes based on business needs.  At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.<h4>Experience Level</h4>Mid Level

Clarivate

Subject Matter Expert

Senior Manager– Trial Analytics, Insights & Planning (TAIP)Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: <a href="https://careers.bms.com/working-with-us" rel="noopener noreferrer" target="_blank">careers.bms.com/working-with-us</a>.Position SummaryThe Senior Analyst role in Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) unit is an excellent opportunity for professionals with approximately 3–6 years of experience in consulting, life sciences analytics, or clinical trial operations to step into an internal consulting environment that directly accelerates drug development.Senior Analysts join one of two tracks based on their background and preference:<ul><li>The Analytical track focuses on forecasting, data modelling, dashboards, and site performance analytics.</li><li>The Scientific track focuses on protocol logic, patient population sizing, eligibility criteria, and feasibility planning.</li></ul>Regardless of track, you will gain exposure to both domains and are expected to develop strong, well-rounded expertise in scientific and analytical areas over time.As a Senior Analyst, you will be embedded in a specific clinical trial team and work under the guidance of more senior team members to deliver core analytics workstreams that support smarter, faster trial execution. This includes taking ownership of trial forecasting models, feasibility analyses, and protocol analytics — always with the goal of helping bring therapies to patients more effectively.You are not expected to be a therapeutic area or protocol expert on day one, but you will be expected to build domain knowledge over time, apply structured thinking to complex trial problems, and deliver high-quality, consistent outputs. You’ll also be part of a global, cross-functional team, working closely with peers across time zones to deliver with speed and precision.Key Responsibilities<ul><li>Own key trial-level analytics workstreams (e.g., enrollment forecasting, feasibility analysis, protocol input)</li><li>Translate structured study requirements into analytical deliverables in collaboration with more senior TAIP colleagues</li><li>Work within a specific clinical trial context, gaining exposure to operational strategy, protocol logic, and real-world trial planning challenges</li><li>Build therapeutic area knowledge over time, contributing to more targeted and scientifically grounded analyses</li><li>Ensure accuracy, consistency, and clarity in data models, dashboards, and insights shared with the study team</li><li>Collaborate across geographies, coordinating with other analysts and team members globally</li><li>Contribute to cost-related analyses, such as country mix optimization and study design trade-offs</li><li>Support study optimization by analyzing site and patient burden, competitor activity, and external data sources</li><li>Coordinate with field-based colleagues to integrate local insights into feasibility and planning analytics</li><li>Utilize trial analytics platforms and tools to generate, structure, and communicate data-driven insights</li><li>Support analytics that may inform clinical supply forecasting or site-level supply considerations</li><li>Applies critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations</li></ul>Qualifications &amp; Experience<ul><li>Education: Preferred advanced degree (e.g., MSc, MPH, PharmD, PhD, MBA) in a relevant field</li><li>Experience:<ul><li>3–6+ years of experience in consulting, healthcare analytics, life sciences strategy, or clinical trial planning and delivery is required</li><li>Proven ability to manage and deliver complex analytical projects in fast-paced environments</li></ul></li><li>Skills:<ul><li>Excellent communication and structured problem-solving skills</li><li>Strong MS Office (Excel, PowerPoint) skills required</li><li>Interest in developing deeper expertise in therapeutic areas and clinical trial analytics</li></ul></li></ul>Why Join This Team?<ul><li>Grow in a Learning Environment: Build your scientific, analytical, and strategic expertise over time</li><li>Be Part of an Internal Consulting Model: Operate in a pod-based team inspired by top-tier strategy firms</li><li>Progress Through a Clear Career Path: Advance through a structured path modeled on strategic consulting, with transparent expectations, ~2–3 years per role, and rapid progression based on ownership and impact</li><li>Pathway to Strategic Leadership at BMS: Career development is actively encouraged and expected, with opportunities to move into broader strategy and leadership roles within BMS in a short timeframe</li><li>Accelerate Therapies to Patients: Help drive clinical decisions that bring treatments to patients faster</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Senior Level

Bristol-Myers Squibb India Pvt Ltd

QA / QC Manager

Principal R&D EngineerAt 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>Help streamline and speed our time to market and build quality in at every step. You will be a member of the Global Operation and Supply Chain - Strategy and Network team that supports the VAVE program for Surgical and other business portfolios. This role involves collaboration with cross-functional partners such as R&amp;D, Quality, reliability, regulatory, operations, and sourcing colleagues to evaluate and implement VAVE changes. Represent the VAVE organization as a prime talent a wide variety of VAVE projects. You can grow your career with us; we hope you’ll consider joining our team!Help streamline and speed our time to market and build quality in at every step. You will be a member of the Global Operation and Supply Chain - Strategy and Network team that supports the VAVE program for Surgical and other business portfolios.This role involves collaboration with cross-functional partners such as R&amp;D, Quality, reliability, regulatory, operations, and sourcing colleagues to evaluate and implement VAVE changes. Represent the VAVE organization as a prime talent a wide variety of VAVE projects.You can grow your career with us; we hope you’ll consider joining our team!Interact with personnel on significant technical matters often requiring coordination between organizations<ul><li>Lead Change Development Process from start to finish and assess VAVE project deliverables and critical milestones, working in collaboration with multi-disciplinary functions and VAVE Program leads.</li><li>Drive technical discussions related to critical activities for VAVE project execution</li><li>Coordinate design technical reviews in collaboration with multi-disciplinary functions – Supplier Quality, Regulatory, R&amp;D , Manufacturing, Project Management,</li><li>Support on documentation and engineering change order creation in PLM System</li><li>Support on Design Verification and Validation activities , performed locally or at US Site.</li><li>Provides problem solving/trouble shooting support to manufacturing sites and key suppliers to increase yields, maintain process capability, and improve efficiency and cost.</li><li>Own PPAP process (As applicable) in support of VAVE project execution activities</li><li>Drive technical PPAP discussions at site and supplier levels</li><li>Conduct Design Verification and Validation assessment support related to PPAP</li><li>Conduct Risk Management file reviews and updates.</li></ul>Must Haves•   Bachelor's Degree and 15+ years of Mechanical or Equivalent Degree<ul><li>VAVE Experience</li></ul>•    Knowledge of medical device industry standards, regulations compliance requirements•    Strong knowledge of mechanical processes, materials, processes, manufacturing, PFMEA and DFMEA•    Demonstrates good judgment pertaining to issue escalation and consultation with other SME’s•    Results focused. Able to deliver consistent, high quality work to meet product performance, compliance, schedule, and budget requirements•    Able to provide solutions to a variety of technical problems of challenging scope and complexity•    Possesses working knowledge of statistical and data analysis tools. SPC, DOE, Gauge R&amp;R, CpK•    Demonstrates clear, factual, and effective oral and written communication with variety of cross functional colleagues, technical peers, and senior-level management•    Able to effectively prioritize and work on multiple assignments in parallel while keeping stakeholders updated•    Excellent time management skills with ability to manage multiple priorities and deliver on time•    Interpersonal skills including ability to effectively formulate and convey technical and cost/benefit/risk information with peers and senior leaders•    Strong verbal and written communication skills including ability to articulate complex ideas in easy to understand terms•    Working knowledge of Quality System Regulation (QSR 21 CFR 820), EU Medical Device Directive, and ISO (13485:2003)•    Knowledge of 6 Sigma (DFSS) principles•    Able to work well under pressure and maintain a positive, engaged, and enthusiastic attitudeNice to Have :<ul><li>PMP Certification</li><li>VAVE Certification</li></ul>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. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).<h4>About Medtronic</h4>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" rel="noopener noreferrer" target="_blank">here</a>   <h4>Experience Level</h4>Senior Level

India Medtronic Pvt. Ltd

Business Analyst (R&D)<h4>Career Category</h4>Information Systems<h4>Job Description</h4>Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. What you will do Let’s do this. Let’s change the world. In this vital role you will play a key role in successfully leading the engagement model between Amgen's Technology organization and Global Commercial Operations. <ul><li>Collaborate with R&amp;D Business SMEs, Data Engineers, Data Scientists and Product Managers to lead business analysis activities, ensuring alignment with engineering and product goals on the Data &amp; AI Product Teams </li></ul><ul><li>Become a R&amp;D domain authority in Data &amp; AI technology capabilities by researching, deploying, and sustaining features built according to Amgen’s Quality System </li></ul><ul><li>Lead the voice of the customer assessment to define business processes and product needs </li></ul><ul><li>Work with Product Managers and customers to define scope and value for new developments </li></ul><ul><li>Collaborate with Engineering and Product Management to prioritize release scopes and refine the Product backlog </li></ul><ul><li>Ensure non-functional requirements are included and prioritized in the Product and Release Backlogs </li></ul><ul><li>Facilitate the breakdown of Epics into Features and Sprint-Sized User Stories and participate in backlog reviews with the development team </li></ul><ul><li>Clearly express features in User Stories/requirements so all team members and partners understand how they fit into the product backlog </li></ul><ul><li>Ensure Acceptance Criteria and Definition of Done are well-defined </li></ul><ul><li>Work closely with Business SME’s, Data Scientists, ML Engineers to understand the requirements around Data product requirements, KPI’s etc. Analyzing the source systems and create the STTM documents. </li></ul><ul><li>Develop and implement effective product demonstrations for internal and external partners </li></ul><ul><li>Maintain accurate documentation of configurations, processes, and changes </li></ul><ul><li>Understand end-to-end data pipeline design and dataflow </li></ul><ul><li>Apply knowledge of data structures to diagnose data issues for resolution by data engineering team </li></ul>What we expect of you We are all different, yet we all use our unique contributions to serve patients. We are seeking a highly skilled and experienced Principal IS Business Analyst with a passion for innovation and a collaborative working style that partners effectively with business and technology leaders with these qualifications. Basic Qualifications: <ul><li>Master’s degree with 8 - 12 years of experience in R&amp;D Informatics </li></ul><ul><li>Bachelor’s degree with 10 - 14 years of experience in R&amp;D Informatics </li></ul><ul><li>Diploma with 14 - 18 years of experience in R&amp;D Informatics </li></ul><ul><li>Mandatory work experience in acting as a business analyst in DWH, Data product building, BI &amp; Analytics Applications. </li></ul><ul><li>Experience in Analyzing the requirements of BI, AI &amp; Analytics applications and working with Data Source SME, Data Owners to identify the data sources and data flows </li></ul><ul><li>Experience with writing user requirements and acceptance criteria </li></ul><ul><li>Affinity to work in a DevOps environment and Agile mind set </li></ul><ul><li>Ability to work in a team environment, effectively interacting with others </li></ul><ul><li>Ability to meet deadlines and schedules and be accountable </li></ul>Preferred Qualifications: Must-Have Skills <ul><li>Excellent problem-solving skills and a passion for solving complex challenges in for AI-driven technologies </li></ul><ul><li>Experience with Agile software development methodologies (Scrum) </li></ul><ul><li>Superb communication skills and the ability to work with senior leadership with confidence and clarity </li></ul><ul><li>Has experience with writing user requirements and acceptance criteria in agile project management systems such as JIRA </li></ul><ul><li>Experience in managing product features for PI planning and developing product roadmaps and user journeys </li></ul>Good-to-Have Skills: <ul><li>Demonstrated expertise in data and analytics and related technology concepts </li></ul><ul><li>Understanding of data and analytics software systems strategy, governance, and infrastructure </li></ul><ul><li>Familiarity with low-code, no-code test automation software </li></ul><ul><li>Technical thought leadership </li></ul><ul><li>Able to communicate technical or complex subject matters in business terms </li></ul><ul><li>Jira Align experience </li></ul><ul><li>Experience of DevOps, Continuous Integration, and Continuous Delivery methodology </li></ul>Soft Skills: <ul><li>Able to work under minimal supervision </li></ul><ul><li>Excellent analytical and gap/fit assessment skills </li></ul><ul><li>Strong verbal and written communication skills </li></ul><ul><li>Ability to work effectively with global, virtual teams </li></ul><ul><li>High degree of initiative and self-motivation </li></ul><ul><li>Ability to manage multiple priorities successfully </li></ul><ul><li>Team-oriented, with a focus on achieving team goals </li></ul><ul><li>Strong presentation and public speaking skills </li></ul>Technical Skills: <ul><li>Experience with cloud-based data technologies (e.g., Databricks, Redshift, S3 buckets) </li></ul><ul><li>AWS (similar cloud-based platforms) </li></ul><ul><li>Experience with design patterns, data structures, test-driven development </li></ul><ul><li>Knowledge of NLP techniques for text analysis and sentiment analysis </li></ul>What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.  careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.  .<h4>Experience Level</h4>Mid Level

Amgen Technology Private Limited

Business Analyst

R&D Executive - StatisticianABOUT UNILEVER With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people – we believe that when our people work with purpose, we will create a better business and a better world.Job Brief:The Clinical Biostatistics group is responsible for delivering leadership and expertise in the use of Statistics and Data Analytics across the Beauty &amp; Wellbeing and Personal Care (BW &amp; PC) Clinical Program. For Statistics this covers support in statistical design of clinical studies, statistical analysis, visualization of data and interpretation and reporting of results. Additionally, the group provides expertise in clinical data mining and modelling, and biostatistics support to the BWPC R&amp;D cross functional teams with respect to the clinical program and related areas. The group delivers via a highly skilled team that is aligned to specific program areas within BPC and works in close partnership with Clinical researchers as well as BWPC Science &amp; Technology (S&amp;T), Global Design, Category Design, and Cluster Design teams on a global level. Requirements &amp; Qualifications: The candidate should ideally have at least a master’s degree in Statistics/Biostatistics, with three to six years’ experience in research or the FMCG/Pharmaceutical industries, although applications from less experienced candidates will be considered. Proficiency in SAS and R is essential, including the ability to automate routine tasks, develop macros, and build applications. Strong written and verbal communication skills are also required. Responsibilities: • Engagement and collaboration with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies, analyse, visualise and interpret data. • Work in inter-disciplinary teams that includes clinical study experts, measurement scientists, bioinformaticians, and other statisticians, both within Unilever and with external partners. • Provision of statistical expertise across a range of R&amp;D disciplines to define and implement statistical solutions. • Deliver high quality statistical programming deliverables for all assignments that consistently meets study timelines, quality standards. • Responsibility for the quality and defensibility of study designs, statistical analyses, models and data interpretation. • Perform exploratory data analyses of clinical studies and reporting as required. • Follow all standard practices as per SOP’s and guidance documents. Key Accountabilities: • Works as a member of a team to design and/or review protocols, case report forms, and other key study documents • Write and review statistical sections and other relevant parts of study synopses and protocols • Performs relevant sample size calculations • Design randomization plans and generates random allocation lists • Develops statistical analysis plans including analysis files and data reporting specifications • Develops appropriate statistical methods for data analysis and ensures the accuracy and reproducibility of data sets and analyses of clinical study data • Follows relevant work practices and procedures and organizational SoPs • Working closely with mutli-disciplinary teams to ensure a complete review of the data, providing a thorough understanding of statistical processes and issues that may arise in analysis • Plan the statistical analyses, programming and execution of the analyses, instructing and reviewing statistical planning and analysis work • Perform hands-on data analysis and modeling of obtained data to provide outputs that will guide in decision making through various stages of project • Liaises with other statisticians and scientists in areas of expertise and experience and ensures continuous improvement for themselves and the broader team via sharing of approaches and best practices; • Provides statistical consultancy as required to the R&amp;D programme. • Engages and collaborates with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies. Teams may include clinicians, measurement scientists, bio scientists, product formulators, claims experts, and others; • Acts as secondary contact (supporting the Lead Statistician for the area) across multiple primary research areas (e.g. Skin Face Care, Microbiome, Skin cleansing, Hair Care, Oral, etc.);Our commitment to Equality, Diversity &amp; Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. "All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent—please verify before proceeding."<h4>Experience Level</h4>Executive Level

Hindustan Unilever Limited

Research Analyst

Stat Programmer 2Job Overview Provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.  Plan and lead the development of project-related solutions to the full scope of statistical programming tasks.  Provide technical expertise to the Statistical Programming department.Essential Functions • Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing summaries, (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks. • Program the integration of databases from multiple studies or sources. • Develop programming documentation including plans and specifications, as appropriate. • Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department. • Perform and plan the development, implementation and validation of new process technologies, macros and applications. • Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision. • Understand the Scope of Work, estimate the work completed, and manage Out of Scope for single studies. May manage budget and resource requirements and provide revenue and resource forecasts for single studies. May be required to understand budget and quote assumptions. • Provide training and guidance to lower level and new staff.Qualifications • Master's Degree Computer science or related field and 1 year relevant experience Req Or • Bachelor's Degree Computer science or related field and 2 years relevant experience Req • Equivalent combination of education, training and experience Req • Knowledge of statistics, programming and/or clinical drug development process • Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language • Good organizational, interpersonal, leadership and communication skills • Ability to effectively handle multiple tasks and projects • Excellent accuracy and attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clientsIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" rel="noopener noreferrer" target="_blank">https://jobs.iqvia.com</a><h4>Experience Level</h4>Mid Level

IQVIA

Data Analyst Intern

Principal Scientific WriterJob Description SummaryCreation of high-quality highly-complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery Job DescriptionPrincipal Scientific Writer Location – Hyderabad #LI Hybrid About the Role: Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts Key Responsibilities:<ul><li>Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards, including pivotal primary manuscripts, scientific communications platform and scientific lexicons, scientific writing for IEPs, meeting materials for satellite symposia, publication planning materials.</li><li>Initiates, implements and champions process improvement techniques.</li><li>Manages multiple projects across multiple brands and therapeutic areas.</li><li>Defines and implements customer management strategies and tactics.</li><li>Ideates and implements tactics to influence internal and external development environment.</li><li>Complies with and support group’s project management tool, standards, policies and initiatives.</li><li>Follows Novartis specifications for documentation, templates etc</li><li> Maintains records for all assigned projects including archiving.</li></ul>Commitment to Diversity &amp; Inclusion: :We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Essential Requirements: <ul><li>Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M.Pharm +10 years of clinical research (CR) experience</li><li>Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.</li></ul> Desired Requirements:• Thorough knowledge of Good Clinical practice. Demonstrated ability to establish effective working relationship in a matrix and multicultural environment. • Demonstrated presentation and diplomacy skills. Strong customer-oriented mindset. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networ Skills DesiredClinical Research, Clinical Trials, Detail-Oriented, Medical Writing, People Management, Regulatory Compliance, Safety, Waterfall Model<h4>Experience Level</h4>Senior Level

Novartis India

Senior Writer

R&D Staff Scientist<h4>JD: Staff Scientist</h4><h4>Job Title : Staff Scientist</h4><h4>Department : Research &amp; Development – Food &amp; Beverage</h4><h4>Location : Mumbai</h4><h4>Role</h4><ul><li><h4>The individual in this role will independently lead the design &amp; development of new product / innovation project</h4></li><li><h4>Responsible for generating ideas, developing product, and executing customer validation trials for assigned projects and work for customer approval.</h4></li><li><h4>Demonstrates understanding of the basic principles and applications in their area of expertise.</h4></li><li><h4>Individual must apply and interpret standard scientific theories, concepts and techniques. </h4></li><li><h4>Provides creative solutions and patentable technologies for solving assigned innovation projects.</h4></li><li><h4>Can determine own approach to problems and devise solutions within scope of own ability. </h4></li><li><h4>Independently plans and performs laboratory experimentation, customer trials, and operates various machines and testing equipment in evaluation of products.    </h4></li><li><h4>Regularly communicates progress of and requirements to complete assigned work with manager and project teams.</h4></li><li><h4>Responsible to lead and influence all stakeholders’ meetings and project technical outcome.</h4></li><li><h4>Contributes to Innovation Idea Pipeline/Funnel through new Ideas and POCs for new exploratory projects.</h4></li></ul><h4>Key Result Areas</h4><ul><li><h4>Independently lead product Innovation for Ideation, Product development &amp; Validation stage.</h4></li><li><h4>Support in developing/improving and implementation of Global laboratory best practices.</h4></li><li><h4>Demonstrated ability to deliver projects within agreed time and budget</h4></li><li><h4>Demonstrated ability to work independently and focus on critical project parameters that determine success or failure.</h4></li><li><h4>Compliance of laboratory with company safety regulations</h4></li><li><h4>Identify potential Project technical risks and create and execute mitigation plan</h4></li><li><h4>Manage technical database and Document product design and performance specifications.to ensure ISO compliance.</h4></li><li><h4>Demonstrate Subject matter expertise in respective Project domain. Execute the Stage Gate process as per appropriate project management tools in the Ideation, Development and Validation Phase.</h4></li><li><h4>Responsible for all key tasks of new product introduction such as Development, planning, Design of experiments, Validations etc.</h4></li><li><h4>Conducts independent research and investigations to design and develop a product or process.</h4></li><li><h4>Execute project plans and schedules for timely completion of projects.</h4></li><li><h4>Independently plan and execute Feasibility study of diversifying product range and explore ideas/concepts for new business opportunities.</h4></li><li><h4>Independently develops test procedures and policies for evaluating raw materials, work in process and finished products.</h4></li><li><h4>Regularly Interact &amp; communicate with Global R&amp;D team and work in collaboration with multifunctional Teams (Marketing, Analytical, Regulatory etc.)</h4></li></ul><h4>Functional Knowledge / Skills</h4><ul><li><h4>Wide technical and business knowledge of the Cleaning &amp; Hygiene industry must be self-motivated, creative with a high-level of energy, customer focus, result oriented. Presentation Skills, - Drive for Results, Process Management, Decision Making, Planning &amp; Estimating, Monitoring &amp; Controlling"</h4></li></ul><ul><li><h4>Excellent Chemical and technical know – how, Formulation knowledge of specialty/FMCG chemicals, project management skills, R&amp;D tools and techniques, Stage gate process, Six Sigma, Cost analysis, Good conceptual &amp; problem solving skills essential</h4></li></ul><ul><li><h4>Must possess excellent communication and interpersonal skills, Result oriented, Ability to lead and drive execution of scientific projects with clear accountability, knowledge of analytical chemistry and cleaning formulation</h4></li></ul><h4>Qualification</h4><h4>M. Tech. / Ph.D (Chemical Engg, Chemistry, Chemical Technology, Microbiology, Biotechnology, Food Technology or equivalent)</h4><h4>Six Sigma: Black Belt or Green Belt / Stage gate process / Project Management preferred</h4><h4>Ph.D (5-8 yrs / MTech (7-9 yrs)</h4><h4>experience in chemical, Detergent, Surfactant / FMCG, specialty Industry, Dairy, Brewery, Beverage, Food Industry</h4><h4>Candidate experienced handling Global R&amp;D project are preferred.</h4><h4>Position reporting to Director R&amp;D - Global Food &amp; Beverage</h4><h4>Positions reporting to the Job Title : None</h4>

Solenis Chemicals India Pvt Ltd

Science Mentor

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

Dr Reddys Laboratories

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

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