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Senior Executive, CL: RSU<h4>Job Description</h4>Senior Research Executive Gurugram/ Kolkata (preferably – Gurugram) • Full-time • Career Site Team: Retailer Vertical Customer Success ABOUT THIS JOB At Nielsen we autonomously contribute to analysis that resolves specific Client concerns; serves as a liaison between the Commercial team, Quality Assurance, Operations, Engineering, &amp; Data Science teams with regards to Internal and External Client Projects. Data science drives everything we do here at NielsenIQ. Our statistical research is at the forefront of an industry moving at the speed of light. In this role on the Digital Product team, your work on innovative methodologies and data optimization will directly impact our business and our clients. It is a Client servicing role; The FTE will be interacting with the CMI on a day-to-day basis. RESPONSIBILITIES • Maintain a client service orientation by managing the day-to-day administration of client service activities. • Working closely with the retailers – T&amp;D / FMCG – Getting timely data, solving queries, giving insights to the retailerClient Management: handle RMS related clients' queries • Working closely with hub team for reports, DB generation &amp; also in case of any adhoc queries • Technical: acquire knowledge of both RMS solutions by attending requisite training • Maintain accurate, complete, up-to-date, and insightful client business profiles• Serve as primary contact to assigned client contacts on ad-hoc analyses and understand and respond to questions on content, basic data,issues/questions, report generation, etc • Delivering quality services to clients and ensure the services provided to clients are timely and precise according to client business needs and specifications and at the same time meeting the company's quality standards • Be directly accountable for work conducted for their nominated clients in terms of analyses, charting, etc. and perform quality checks on all reports for alignment to request accuracy and correctness QUALIFICATIONS ● 2 to 4 years’ experience in Tech and Durable/ FMCG / Service / Retail industry ● Effective communication skills ● Strong Client Focus and Proactiveness ● Strong command on Microsoft Excel and PowerPoint ● Working knowledge of research techniques and methodologies ● Plus point: Working knowledge of statistic and multivariate analysis ● Knowledge of T&amp;D/ RMS is a plus A LITTLE BIT ABOUT YOU You’ve dabbled in research and analytics. And you have the communication chops to translate it all into conversation or presentations. While you’ve worked with global cross-functional teams, you can also put your head down and focus on independent projects. Seeing the big picture takes attention to detail. Keeping up with the fast-changing world of digital media measurement takes someone who recognizes that. You know what’s happening in big data and you’re ready to influence what’s next.<h4>Additional Information</h4>Our Benefits<ul><li>Flexible working environment</li><li>Volunteer time off</li><li>LinkedIn Learning</li><li>Employee-Assistance-Program (EAP)</li></ul>About NIQNIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state-of-the-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world’s population.For more information, visit NIQ.comWant to keep up with our latest updates?Follow us on: <a href="https://www.linkedin.com/company/nielseniq/mycompany/">LinkedIn</a> | <a href="https://www.instagram.com/nielseniq/">Instagram</a> | <a href="https://twitter.com/nielseniq">Twitter</a> | <a href="https://www.facebook.com/NielsenIQ.global/">Facebook</a>Our commitment to Diversity, Equity, and InclusionAt NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence.  All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the <a href="https://nam02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fnielseniq.com%2Fglobal%2Fen%2Fnews-center%2Fdiversity-inclusion&amp;data=05%7C02%7CJenny.Rebecca%40nielseniq.com%7C6e534cbe3eb041842d5f08dc6dca121e%7C6ac7a1f45fb14153bb4f12d2020a1f7d%7C0%7C0%7C638505961881417602%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&amp;sdata=B%2Fp40oNUpJOw1CNoc87EFXk%2BvxeO1jxYOSRCEKM%2Fz5Q%3D&amp;reserved=0">https://nielseniq.com/global/en/news-center/diversity-inclusion</a><h4>Experience Level</h4>Senior Level

NielsenIQ

Research Intern

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

Biopharmaceutics 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 transparency Dr 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 person for the role of Scientist in Biopharmaceutical team to provide strategic guidance on assessment of product complexity, analysing data to identify critical attributes, and coordinating with regulatory agencies to ensure bioequivalence compliance. Provides strategic formulation support, conducts in-vitro-in-vivo correlation(IVIVC) development. Roles &amp; Responsibilities <ul><li>You will be responsible for the Assessment of complexity of products in terms of achieving bioequivalence.</li><li>You will be responsible to Analyse the data and Identify the critical material attributes (CMA) critical formulation components (CFC) and critical process parameters (CPP) that are expected to affect bio-availability and bio-equivalence.</li><li>You will be responsible for Identifying the appropriate tools and methodologies for formulation strategies and/or optimizing formulations to enhance success in bioequivalence studies. </li><li>You will be closely supporting the Formulation Development team for critical aspects of the drug while designing bioequivalence studies. </li><li>You will be involved in Development of in-vitro-in-vivo correlation (IVIVC).</li><li>You will be responsible for performing modelling &amp; simulations using tools like GastroPlus, Phoenix, Simcyp.</li><li>You will be responsible for coordinating with regulatory agencies related to dissolution and bioequivalence. </li></ul><h4>Qualifications</h4>Educational qualification: Masters in Pharmaceutics                                                                                                                            Minimum work experience: 3+ years’of experience in Biopharmaceutics, Formulation, Dissolution and understanding of in-vitro-in-vivo correlation IVIVC  Skills &amp; attributes: Technical Skills<ul><li>Deep knowledge in Bio-pharmaceutics and its processes.</li><li>Deep Knowledge on formulation and dissolution.</li><li>Experience in in-vitro-in-vivo correlation (IVIVC) and Mathematical Compartmental Modelling.  </li><li>Knowledge on critical material attributes (CMA) critical formulation components (CFC) and critical process parameters (CPP).</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 Regulatory and cross-functional teams. </li></ul><h4>Additional Information</h4>About the Department Integrated 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/#!/

Dr Reddys Laboratories

Chemical Analyst

HTAT 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 skilled Analytical Scientist to join our Analytical Research and Development team. The successful candidate will be responsible for routine testing of development/in process and stability samples. Apt knowledge in method development, method validations, and analysis of API and excipients as per pharmacopeial requirements is expected. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, data analysis and keen eye for detail and a commitment to ensuring the highest quality standards. Roles &amp; Responsibilities <ul><li>You will be responsible to perform real-time analysis of samples during product development stages including stability studies to ensure product quality and consistency.</li><li>You will be responsible for compilation of Stability Data to assess the stability profile of the products under various conditions.</li><li>You will be responsible to review relevant Literature and stay updated with the latest research and scientific literature relevant to the field.</li><li>You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department.</li><li>You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results.</li><li>You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy.</li><li>You will be responsible to maintain a clean and organized work area and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions.</li><li>You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. </li></ul><h4>Qualifications</h4>Educational qualification: Masters in Pharmaceutical Sciences/ Chemistry Minimum work experience:  4 - 7 years of experience in analytical method development Skills &amp; attributes: Technical Skills<ul><li>Have work experience in Oral solid products analysis.</li><li>Should be well versed handling of HPLC, Dissolution apparatus, KF instrument, pH meter, Gas Chromatography, to execute various tests like Assay, Related substances, Dissolution, pH, KF and other simple techniques.</li><li>Efficient in usage of analytical digital tools</li><li>Excellent knowledge of Good Laboratory Practices (GLP), Quality systems, Standard Operating Procedures, latest regulatory trends, and Global regulations as appropriate</li><li>Apt technical knowledge in HPLC method development/verifications/validations</li><li>Good understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis.</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 Department Global Generics India Global Generics India business journey began in 1986. In the last three decades, we have grown as a trusted name in the healthcare industry and rank as one of the top 10 Pharma Companies in the Indian Pharma Market (IPM) as per IQVIA MAT (November 2022). Our commitment to Lead Ahead has helped us move ranks from 16th position to 10th position (IPM) in the last four years. We are a fast-growing organisation with double-digit growth and significant market share in domestic markets. Currently, we rank among the top 5 in oncology, anti-allergy and gastrointestinal diseases and the top 10 in a few other therapy areas. Our focus is on leveraging our digital capabilities, collaborations, innovations and inorganic opportunities to become the top 5 companies in the Indian Pharma Market. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ <h4>Experience Level</h4>Senior Level

Analytical Chemist

Senior Research Executive-RV CS<h4>Job Description</h4>Senior Research Executive – Industry Insights (Retail Vertical)Location: Mumbai Employment Type: Full-time Team: Industry Insights – Retail VerticalAbout the RoleAs a Senior Research Executive within NielsenIQ’s Retail Insights team, you will play a pivotal role in supporting leading FMCG and Tech-Durables retailers across Modern Trade and E-commerce channels. This client-facing position involves delivering strategic insights through monthly and quarterly industry reviews to senior leadership at partner organizations. You will collaborate closely with cross-functional teams including Commercial, Operations, and Data Science to ensure high-quality, data-driven insights &amp; solutions.Key Responsibilities<ul><li>Client Engagement &amp; Servicing<ul><li>Act as the primary point of contact for assigned retail clients, managing day-to-day interactions and ensuring timely delivery of insights.</li><li>Present industry reviews and strategic recommendations to senior stakeholders at client organizations.</li><li>Support client onboarding and training on NielsenIQ tools and RMS methodologies.</li></ul></li><li>Internal Collaboration &amp; Analysis<ul><li>Coordinate and execute product / Market feasibility assessments and provide inputs during contract discussions.</li><li>Collaborate with internal Ops / BI teams for database generation, report creation, and ad-hoc analysis.</li><li>Maintain comprehensive and up-to-date client business profiles for internal use.   </li></ul></li></ul> <ul><li>Technical Expertise<ul><li>Acquire and apply knowledge of NielsenIQ’s RMS solutions through structured training.</li><li>Conduct quality checks on reports and analyses to ensure accuracy and alignment with client expectations.</li><li>Provide analytical and operational support to senior team members.</li></ul></li></ul>Qualifications &amp; Skills<ul><li>2–4 years of experience in FMCG, Retail, or Service industries.</li><li>Strong client orientation with excellent communication and presentation skills.</li><li>Proficiency in Microsoft Excel and PowerPoint.</li><li>Working knowledge of research methodologies; familiarity with statistics and multivariate analysis is a plus.</li><li>Prior experience with RMS tools is advantageous.</li><li>Ability to manage multiple stakeholders and deliver under tight timelines.</li></ul>What You BringYou are analytical, detail-oriented, and passionate about transforming data into actionable insights. You thrive in a fast-paced environment, balancing independent work with cross-functional collaboration. Your ability to communicate complex findings in a clear and compelling manner makes you a trusted advisor to clients. <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

MGR I R&D/PRODUCT DVL ENGINEERINGAt 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 / FUNCTION DESCRIPTION Digital Data &amp; Networks (DDN) Business Unit at 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 power interconnection solution products which are used in hyperscale computers, AI, Datacenter, Cloud server, and other IT systems, including connector and cable assembly. We engineer and manufacture cutting-edge interconnect solutions that support high-speed data transmission, signal integrity, and power efficiency.ROLE OBJECTIVE As MGR R&amp;D/PRODUCT DVL ENGINEERING in TE Connectivity’s Digital Data &amp; Networks (DDN) Business Unit, you will lead a sustaining engineering team responsible for the continued support and evolution of production parts and products throughout their lifecycle. This includes driving product lifecycle management, product extensions, rapid NPIs, VAVE initiatives, sustainability improvements, material and process changes, and manufacturing location transfers. The role also involves providing technical support to plants, suppliers, and customers to ensure continuity, quality, and cost optimization. <h4>Job Responsibilities</h4>RESPONSIBILITIES  •    Lead, and manage a engineering team responsible for sustaining activities of board to bord and I/O product line. •    Serve as a strong technical partner to cross-functional teams, including Program Management, Sales, Field Application Engineering, Operations, Procurement, and Compliance. •    Lead team to execute critical engineering projects, including manufacturing transfers, sustaining, product extensions, cost reduction (VAVE), sustainability and rapid New Product Introduction (NPI) initiatives. •    Represent engineering in customer meetings, project meetings and site visits, providing technical support and insights as needed. •    Champion continuous improvement by enhancing product designs and engineering processes to drive efficiency, cost optimization, and sustainability.<h4>Job Requirements</h4>•    Bachelor’s degree in mechanical / electrical, or a related Engineering discipline; advanced degree preferred. •    10+ years of relevant engineering experience, including a minimum of 2 years in a leadership or management role. •    Strong foundation in mechanical and electrical engineering principles with proven application in product development. •    Demonstrated technical leadership in problem-solving, root cause analysis, and conflict resolution. •    Prior experience in board to board and high-speed connectors are highly preferred.  •    Proven expertise in sustaining engineering and product lifecycle support, including design enhancements, prototyping, testing, and cost/productivity improvements (VAVE). •    Hands-on experience with modern design and analysis tools including 3D CAD, modeling, Geometric Dimensioning &amp; Tolerancing (GD&amp;T), and simulation tools. •    Knowledge of manufacturing processes such as machining, molding, stamping, and plating. •    Knowledge of material properties (metal/plastics) and their application in products.  •    Familiarity with quality tools and methodologies such as FMEA, Six Sigma, DOE, 8D, etc. •    Proven capability to recruit, develop, and lead engineering teams. •    Effective communicator with the ability to collaborate across teams, cultures, and organizational levels. •    Highly organized, self-driven, and able to manage multiple competing priorities with minimal supervision. COMPETENCIES •    Technical Expertise: Deep functional and domain knowledge in mechanical/electrical engineering, with a strong foundation in connector and cable assembly technologies. •    Cross-Functional Engineering Leadership: Skilled in leading cross-functional teams across product management, design, manufacturing, quality, procurement and supply chain to drive product lifecycle support. •    Global Collaboration: Demonstrated success in working with global teams across regions and cultures, ensuring alignment and shared ownership of engineering deliverables. •    Talent Development: Committed to building organizational capability through mentoring, training, workforce planning, and succession development. •    Problem Solving: Strong analytical skills with a hands-on approach to root cause analysis, risk assessment, and implementing effective corrective/preventive actions. •    Execution Mindset: Results-driven and action-oriented, with a track record of delivering high-impact outcomes under tight timelines and shifting priorities.<h4>Competencies</h4>
SET : Strategy, Execution, Talent (for managers)<h4>Experience Level</h4>Executive Level

TE Connectivity India Pvt Ltd

Engineering Manager

Associate Team LeadTitle: Associate Team Lead, MumbaiShift: UK/ AU ShiftLocation: Vashi, Navi MumbaiCompany: Morningstar is a leading provider of independent investment research in North America, Europe, Australia, and Asia. We offer a wide variety of products and solutions that serve market participants of all kinds, including individual and institutional investors in public and private capital markets, financial advisors, asset managers, retirement plan providers and sponsors, and issuers of securities. Morningstar India has been a Great Place to Work-certified company for the past eight consecutive years.Team: Morningstar’s Research group provides independent analysis on individual securities, managed investments, portfolios, and markets. The group also collects and maintains high-quality data on the equities, managed investments, and fixed-income investments we cover in our database, one of the largest investment databases in the world. Morningstar is one of the largest independent sources of manager, equity, and credit research in the world. We transform data into insights that investors can use to reach their financial goals.Role: The Data Team Lead oversees the management of the day-to-day activities for a sub-team of managed investment data (MID) that powers the Morningstar products and platforms. Typically, the Data Team Lead works closely with Global Process Owners, MID Data Leaders and Global Data Director, as well as with the global stakeholders to ensure that all the agreed deliverables from the team are met, and that the team is fully equipped in terms of training and documentation. He or she, together with MID Data Leaders and Global Data Director, will be accountable for ensuring and improving the performance, productivity and efficiency of the teams and the delivery of the operational performance KPIs, for team engagement, morale, and supporting the build for growth ladders of members. This role will functionally report to MID Data Leader, and matrix report to MID Data Director, based in Mumbai.Responsibilities:<ul><li>Assist in managing and developing a team of 10+ Data Research Analysts by providing clear direction, establishing SMART goals, and optimizing resource allocation for processes/projects.</li><li>Working closely with multiple global teams and across various functions. Participate regularly in global calls and meetings.</li><li>Assist the team to identify and eliminate roadblocks by partnering with technology teams and other database teams. </li><li>Should be able to research complex projects leading to actionable recommendations and solutions. </li><li>Fair product knowledge, both upstream and downstream.</li><li>Assist in promoting LEAN Six Sigma tools and methodologies as an analyst framework for assessing the root cause of issues and improving processes.</li><li>Ensure appropriate methods and techniques to improve and maintain the highest quality standards in the data collected by the team.</li><li>Acts as main point of contact/manager for his or her entire team for all questions, comments and concerns.</li><li>Tracks, measures and reports on agreed daily, monthly and quarterly metrics to all stakeholders.</li><li>Provides coaching and training to team members as appropriate and according to the specific needs of the individual and the group.</li><li>Identifies areas for improvement across the team and proactively takes steps to improve upon these weaknesses by offering ideas for individual and group training and conducting or arranging individual and group training sessions as appropriate.</li><li>Sets goals and priorities for the individuals in the team in consultation with the Global Process Owner, MID Data Leaders and Global Data Director.</li><li>Effectively motivates and rewards the team insuring good overall morale.</li><li>Conducts performance reviews of each team member and explains/sets career development paths and opportunities for team members.</li><li>Monitors Data Research Analysts availability to guarantee minimum staffing requirements are met/exceeded. </li></ul>Qualifications:<ul><li>Bachelor/master’s degree in finance/business with an exceptional academic record.</li><li>Professional degree (CA, CA-Inter, ICWA, ICWA-Inter) preferred.</li><li>4+ years of professional work experience at various levels of seniority.</li><li>Strong people and project management skills.</li><li>Ability to effectively communicate with local and international teams.</li><li>Proven experience optimizing processes.</li><li>Prior experience leading teams of 10+ people will be an additional advantage.</li><li>Demonstrated successful leadership in building a high-performing team and developing talents.</li><li>Experience in business analysis is preferred. SQL or Python skills would be a plus.</li><li>A bachelor’s degree is required; professional certificates like CFA or Certificate in lean, Six Sigma would be plus.</li></ul>Morningstar is an equal opportunity employerMorningstar’s hybrid work environment gives you the opportunity to work remotely and collaborate in-person each week. We’ve found that we’re at our best when we’re purposely together on a regular basis, at least three days each week. A range of other benefits are also available to enhance flexibility as needs change. No matter where you are, you’ll have tools and resources to engage meaningfully with your global colleagues.I10_MstarIndiaPvtLtd Morningstar India Private Ltd. (Delhi) Legal Entity<h4>Experience Level</h4>Mid Level

Morningstar India Pvt Ltd

Team Leader

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

Aristocrat Technologies

Maths Tutor

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

Packaging Manager

Business Manager – ResearchJob Title:      Business Manager – Research Location: New DelhiAbout Springer NatureSpringer Nature is one of the leading publishers of research in the world. We publish the largest number of journals and books and are a pioneer in open research. Through our leading brands, trusted for more than 180 years, we provide technology-enabled products, platforms and services that help researchers to uncover new ideas and share their discoveries, health professionals to stay at the forefront of medical science, and educators to advance learning. We are proud to be part of progress, working together with the communities we serve to share knowledge and bring greater understanding to the world. For more information, please visit about.springernature.com and @SpringerNature.  About the Brand Springer is a leading global scientific, technical and medical portfolio, providing researchers in academia, scientific institutions and corporate R&amp;D departments with quality content through innovative information, products and services. Springer has one of the strongest STM and HSS eBook collections and archives, as well as a comprehensive range of hybrid and open access journals. Visit <a href="http://springer.com/" rel="noopener noreferrer" target="_blank">springer.com</a> and follow @Springer1842About the Role (what’s in it for the candidate) Business Manager – Research is responsible for developing a long-term engagement with key research institutes, funders and government stakeholders for growing Springer Nature’s research business to promote Springer Nature’s vision and thought leadership position, as well as monitor and influence key policy developments, from an advocacy and outreach standpoint.Role Responsibilities:1. Actively represent organization in external forums and events centric around academic publishing, open access, editorial and research centric engagements2. Actively support in driving operations and strategy related workloads in driving India Leadership Council3. Closely work with various state government, central government and ministries to build impact partnership centric around OA transition.4. Help and support our partners in the process of driving advocacy and adoption of Open Access Workloads5. Engaging with key stakeholders like publishing acquisition team, editorial and business team and drive measurement metrics, KPIs, business dashboards etc.6. Build, connect, grow research communities in India7. Engage with Policy makers/Think-tanks to build engagements around research and outreach8. Work closely with market research organizations and actively build competitive landscape and strategy for the organization.9. Actively drive SDG initiative engaging with various national and international bodies like UNICEF, UNESCO, WHO, UNDP, impact investing organizations/foundations10. Be the SPOC to integrate DEI – internally and externally in the organization from the Research and Editorial standpoint in strengthening our commitment to this space  This role can be in our New Delhi office on a hybrid working model.  Qualifications<ul><li>Minimum Master’s degree in any specialization (MBA or equivalent preferred).</li><li>Strong analytical, problem-solving, and decision-making skills.</li><li>Excellent communication and interpersonal skills.</li><li>Proven ability to manage multiple priorities and deliver results within deadlines.</li><li>High level of accountability, integrity, and attention to detail.</li><li>Ability to work independently as well as collaboratively in a team environment.</li><li>Proficiency in MS Office and familiarity with business management tools will be an advantage.</li></ul>At Springer Nature, we value the diversity of our teams and work to build an inclusive culture, where people are treated fairly and can bring their differences to work and thrive. We empower our colleagues and value their diverse perspectives as we strive to attract, nurture and develop the very best talent. Springer Nature was awarded Diversity Team of the Year at the 2022 British Diversity Awards. Find out more about our DEI work here <a href="https://group.springernature.com/gp/group/taking-responsibility/diversity-equity-inclusion#NOTE/_blank" rel="noopener noreferrer" target="_blank">https://group.springernature.com/gp/group/taking-responsibility/diversity-equity-inclusion</a> If you have any access needs related to disability, neurodivergence or a chronic condition, please contact us so we can make all necessary accommodations. For more information about career opportunities in Springer Nature please visit <a href="https://springernature.wd3.myworkdayjobs.com/SpringerNatureCareers" rel="noopener noreferrer" target="_blank">https://springernature.wd3.myworkdayjobs.com/SpringerNatureCareers</a> #LI-RT1Job Posting End Date:2-10-2025<h4>Experience Level</h4>Mid Level

Springer Nature India Pvt Ltd

Business Manager

Engineer IIJoin Aristocrat as a Game Mathematician II and be part of a hard-working team dedicated to crafting world-class gaming experiences! We emphasize collaboration and innovation to deliver flawless games globally.This role is perfect for ambitious mathematicians who are eager to successfully implement their skills in an exciting and dynamic industry. If you're ready to compete at the highest level and make an impact in the gaming world, we want to hear from you!<h4>What You'll Do</h4><ul><li>Collaborate with artistic, executive producer, and technical staff to align game vision and player experience.</li><li>Craft all aspects of game mechanics, including entertainment value, pacing, mathematical outcomes, and player communication.</li><li>Develop meticulous math models and combination sheets using Excel to ensure efficient gaming outcomes.</li><li>Test and verify mathematical outcomes to ensure quality and accuracy.</li><li>Develop and detail initial and final math models to support game development.</li><li>Deliver mathematical design documents for assigned projects and coordinate their implementation through to development.</li><li>Engage in on-the-job training opportunities to improve domain expertise in game mathematics.</li></ul><h4>What We're Looking For</h4><ul><li>Bachelor’s or Master’s degree in Mathematics or B.Tech in Mathematics &amp; Computing with 1+ years of relevant experience.</li><li>Proficiency in statistical modeling and advanced Excel skills.</li><li>Strong expertise in Probability Theory and statistics.</li><li>Excellent data analytics skills.</li><li>Experience with programming languages such as C, C++, or Python.</li><li>Demonstrates strong interpersonal skills within a team environment.</li><li>Fast learner, self-motivated, and capable of communicating effectively across engineering, art, production, and business teams.</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

Process Development 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 Scientist in Process Development in the pharmaceutical development process, responsible for strategy evaluations, process design, optimization, scale-up calculations, and handling exhibit batches. This role involves working on oral solid formulations and technical documentation, as well as process validations, to ensure the successful development and scale-up of pharmaceutical products. Roles &amp; Responsibilities <ul><li>You will be responsible to Conduct strategy evaluations to design and optimize pharmaceutical processes, ensuring efficient and cost-effective development.</li><li>You will be responsible to Calculate batch sizes for both early development and commercial production, considering critical parameters and quality standards.</li><li>You will be responsible to Lead process development activities for oral solid formulations, from concept to commercialization, including the design of experiments and formulation strategies.</li><li>You will be responsible to Perform scale-up calculations and execute scale-up processes to ensure successful transition from lab-scale to production-scale.</li><li>You will be responsible to Handle exhibit batches, coordinating activities and documentation to meet regulatory requirements and project timelines.</li><li>You will be responsible to Prepare and maintain technical documentation, including development reports, process validation protocols, and regulatory filings.</li><li>You will be responsible to Collaborate with cross-functional teams to drive process improvements, troubleshoot issues, and ensure product quality and consistency.</li><li>You will be responsible to Stay updated with industry trends and regulatory guidelines, incorporating best practices and innovative technologies into the development process. </li></ul><h4>Qualifications</h4>Educational qualification: Masters in pharma/Biotechnology/Chemical Engineering Minimum work experience: 4 - 6 years  of Experience in Process Development/Manufacturing Skills &amp; attributes: Technical Skills <ul><li>Experience in process optimization, development and troubleshooting in relevant dosage forms or technologies </li><li>Hands-on experience in end-to-end scale up</li><li>Depth understanding of process techniques &amp; equipment knowledge </li><li>Knowledge on Deficiency management and product validations.</li><li>Experience in manufacturing process improvement.</li><li>Experience with oral solid formulations.</li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills.</li><li>Strong analytical and problem-solving abilities.</li><li>Performance oriented and good at building, leveraging relationship.</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

Process Engineer

Manager, Innovation Strategy and SolutionsWorking 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>.Description                                 At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.The Manager, Innovation Strategy and Solutions Lead supports the framing, assessment, recommendation, and implementation of innovative strategies and solutions to bring efficiencies and automation to the clinical development process, under the direction of the Head, Analysis Standards &amp; Innovation. The incumbent will focus on modernizing processes and technology implementation with the ultimate goal of enabling end-to-end solutioning and transformation.The role requires strong technical and analytical capabilities, particularly in R programming (including Shiny applications and R package development) and preferably Python, with working knowledge of CDISC standards and clinical development workflows. The successful candidate will demonstrate an ability to work independently and collaboratively, combining strategic thinking with technical execution to deliver high-value innovations.The Manager will partner across GBDS departments and cross-functionally, including but not limited to Global Data Management &amp; Centralized Monitoring, Clinical, Regulatory, Medical Writing, and Technology teams, to deliver scalable, user-focused solutions that align with operational and regulatory requirements.Key Responsibilities<ul><li>Support the framing, assessment, and prioritization of internal and external innovation initiatives in collaboration with stakeholders across GBDS, with a focus on delivering solutions that enhance efficiency and quality across clinical development activities.</li><li>Apply expertise in R—including Shiny dashboards and package development—to design and prototype advanced tools and applications to support analytics, automation, and decision-making across GBDS.</li><li>Leverage Python to support areas such as DevOps, data engineering, machine learning, or generative AI, where applicable. Familiarity with SAS is a plus for integration with legacy environments.</li><li>Provide strategic input on project direction and contribute to the technical architecture of solutions, ensuring they are scalable, maintainable, and aligned with GBDS’ data and analytics strategy.</li><li>Partner with GBDS teams to propose, develop, and implement innovative solutions that streamline process execution across biometrics and the broader Global Drug Development organization.</li><li>Ensure scientific validity and technical correctness of tools and platforms supporting clinical trial processes, ensuring fitness for regulatory submission and operational use.</li><li>Promote solution governance by aligning development with internal policies, stakeholder workflows, and regulatory expectations, including those from FDA, PMDA, and other authorities.</li><li>Serve as a departmental expert in CDISC standards, contributing to innovation in standards implementation for protocol development, statistical analysis, and reporting.</li><li>Foster a culture of continuous improvement and innovation, including support for the evaluation and integration of new technologies (e.g., automation tools, GenAI, metadata-driven workflows).</li><li>Take ownership of cross-functional innovation efforts, from concept development through to implementation, with a strong bias toward rapid prototyping and scaling viable solutions.</li><li>Collaborate with internal teams (e.g., IT, Procurement) and external vendors to identify and prioritize new technical capabilities that advance GBDS’ digital and data objectives.</li><li>Contribute to training, communications, and change management activities to promote adoption and user engagement for newly developed tools and platforms.</li><li>Maintain up-to-date knowledge of trends and best practices across data science, analytics, clinical technology, and regulatory science, and apply this knowledge to optimize internal practices.</li><li>Actively participate in external organizations such as CDISC, PhUSE, and similar forums to exchange insights and maintain alignment with emerging regulatory requirements and industry innovations.</li></ul>Degree Requirements<ul><li>Bachelor's Degree in Statistics, Mathematics, Computer science or any other scientific field.</li><li>Master's degree preferred.</li></ul>Experience Requirements<ul><li>Minimum of 5 years in pharmaceutical industry.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

Bristol-Myers Squibb India Pvt Ltd

Senior Product Manager

Insights & Innovation Strategist – 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>.The Insights &amp; Innovation Strategist role within Bristol Myers Squibb’s TAIP Insights &amp; Innovation (I&amp;I) team offers an exciting opportunity to work at the forefront of clinical development transformation through analytics, tools, and innovation.As part of the centralized I&amp;I function in the Trial Analytics, Insights &amp; Planning (TAIP) organization, you will help design, test, and support implementation of portfolio-level analytics tools, AI/ML solutions, and workforce planning methods that accelerate trial delivery. Your work will focus on building repeatable, scalable solutions that are adopted by TAIP Trial Delivery teams across therapeutic areas.You will collaborate closely with TAIP colleagues, as well as stakeholders in GDO, IT, and Clinical, to translate business needs into impactful analytics deliverables. You’ll also contribute to the evolution of I&amp;I’s internal innovation model and help drive continuous improvement in how trials are planned, tracked, and resourced.This role is ideal for professionals with strong analytical, problem-solving, or life sciences experience who are passionate about enabling change through data and tools — and who want to make an enterprise-wide impact.Key Responsibilities<ul><li>Support design, testing, and implementation of analytics tools, templates, and AI/ML solutions</li><li>Conduct portfolio-level analytics to inform planning, performance tracking, and operational decision-making</li><li>Contribute to resource analytics, including forecasting, scenario modeling, and capacity planning</li><li>Apply established I&amp;I standards and toolkits to ensure consistent, high-quality analytics outputs</li><li>Partner with TAIP Trial Delivery teams to support adoption and enablement of tools and methods</li><li>Collaborate across functions including IT, Clinical, and GDO to ensure fit-for-purpose solutions</li><li>Contribute to the I&amp;I innovation pipeline, piloting new approaches and surfacing unmet needs</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>2–5+ years in analytics, consulting, clinical research, or operations is required</li><li>Prior experience in clinical development, data tools, or planning methods is a plus</li></ul></li><li>Skills:<ul><li>Strong analytical and structured problem-solving skills</li><li>Ability to translate complex questions into structured approaches and tools</li><li>Collaborative mindset and comfort working in cross-functional teams</li><li>Proficiency in Excel and PowerPoint; familiarity with BI or modeling tools (e.g., PowerBI, R, Python) a plus</li></ul></li></ul>Why Join This Team?<ul><li>Contribute to high-impact tools and analytics that shape global trial execution</li><li>Develop your capabilities in AI/ML, portfolio analytics, and innovation strategy</li><li>Join a dynamic, consulting-style environment where initiative and curiosity are valued</li><li>Work across a wide range of studies and functions, gaining broad exposure and visibility</li><li>Help bring therapies to patients faster by enabling smarter, data-driven clinical decisions</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" rel="noopener noreferrer" target="_blank">adastaffingsupport@bms.com</a>. Visit <a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">careers.bms.com/</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">eeo</a><a href="https://careers.bms.com/eeo-accessibility" rel="noopener noreferrer" target="_blank">-accessibility</a> to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: <a href="https://careers.bms.com/california-residents/" rel="noopener noreferrer" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<h4>Experience Level</h4>Mid Level

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