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SR R&D/PRODUCT DVL ENGINEERAt TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. <h4>About TE:</h4>TE Connectivity Ltd. is a $16 billion global technology and manufacturing leader creating a safer, sustainable, productive, and connected future. For more than 75 years, our connectivity and sensor solutions, proven in the harshest environments, have enabled advancements in transportation, industrial applications, medical technology, energy, data communications, and the home. With 80,000 employees, including more than 8,000 engineers, working alongside customers in approximately 140 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at <a href="https://www.te.com">www.te.com</a> 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 connectors, cable assemblies, bus bars and sockets. We engineer and manufacture cutting-edge interconnect solutions that support high-speed data transmission, signal integrity, and power efficiency.<h4>Role Objective and Responsibilities:</h4>A PCB Simulation Engineer in PCB Simulation Team, Digital Data Networks (DDN) business in TE Connectivity, validates electronic designs by conducting electrical, signal integrity, power integrity, EMC, RF and thermal simulations to ensure optimal performance, reliability, and manufacturability. The responsibilities include analysing circuit designs, utilizing specialized simulation software, troubleshooting issues through modelling, and collaborating with cross-functional teams to meet project specifications before physical prototyping. Key Responsibilities• Circuit Simulation: Perform electrical, signal integrity (SI), power integrity (PI), EMC, RF and thermal simulations to predict and validate circuit behaviour and identify potential performance issues.• Design Optimization: Use simulation results to optimize component placement, routing, and overall design for performance, reliability, and manufacturability (DFM) in collaboration with PCB Design Team.• Analysis and Validation: Coordinate design validation activities with PCB Design Team for design rule checks (DRC) and performance evaluations to ensure designs meet requirements.• Software Proficiency: Utilize high speed PCB simulation tools (e.g. SIwave/HFSS, Pathwave ADS, SIPro, HyperLyx, Sigrity, CST Studio Suite, EMC Plus, Microwave Office, ICEPAK/FLOTHERM/CELSIUS etc.) to simulate and analyse designs.• Collaboration: Work with cross-functional teams, including electrical, mechanical, and manufacturing engineers, to define requirements and resolve design challenges.• Documentation: Prepare and maintain detailed documentation, including simulation reports, test procedures, and specifications, for project records.• Problem-Solving: Troubleshoot design issues and recommend improvements based on simulation and testing feedback.• Research and Development: Stay updated on industry trends, emerging technologies, and best practices in high-speed PCB simulation and design to enhance design processes. <h4>What your background should look like</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. Consistent performance throughout entire academics (e.g. STD-X onwards).Experience:• Around 4-6 years of extensive hands-on experience in high-speed PCB simulation, with a proven track record of successfully delivering complex projects with deadlines.• Proficient and foundational knowledge on printed circuit board layout, libraries and schematics, routing, manufacturability and testing.Technical Skills:• Expertise with simulation tools for high-speed 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.• Expertise with high-speed electronic circuit design principles, signal integrity (SI), power integrity (PI), electromagnetic compatibility (EMC), radio frequency interference (RFI) and thermal incidents.• Good understanding of PCB design and layout tools such as Cadence Allegro, Altium Designer, or Siemens PADS.• Good knowledge of industry standards (IPC, JEDEC, PCIe, USB, Ethernet) and PCB manufacturing processes, including design for manufacturability (DFM) and design for testing (DFT). Soft Skills:• Passion for Technology and scientific/engineering excellence.• Excellent problem-solving and analytical skills to resolve complex technical issues.• Strong in Technical Documentations and Report preparation.• Strong verbal and written communication skills to articulate complex technical concepts to both technical and non-technical stakeholders.• Ability to work effectively in a fast-paced, collaborative global environment and global time zones.• A team player and self-starter and works independently with minimal supervision and instructions.• Able to prioritise work, take self-care and manage personal well-being.<h4>Experience Level</h4>Senior Level

TE Connectivity India Pvt Ltd

Design And Development Engineer

PK Study Support AssociateJob Description SummaryThe Pharmacokinetic Sciences (PKS) technical study support team enables efficient management of tactical and operational support for clinical studies at a project and program level. The group is responsible for studies across the globe and would be closely working with a matrix team in enabling regulatory compliance within the target study cycle time. The PK Study Support Associate will build a global center of excellence for managing clinical studies supporting PKS project team members (PTM) thus enabling management of active research projects by the PTMs. Job Description<h4>Major accountabilities: </h4><ul><li><h4>Serve as a single point of contact for global PKS clinical project team members (PTM) for execution or oversight of clinical study support, quality check (QC) and/or non-compartmental analysis (NCA) work of pharmacokinetic data from global clinical studies.</h4></li><li><h4>Connect regularly with global colleagues in maintaining an active list of legacy studies to be covered by the PKS technical study support team</h4></li><li><h4>Build and maintain the team by providing technical and process execution and guidance to enabling successful management of regulatory compliance.</h4></li><li><h4>Execute clinical project support or manage experts to support the clinical project from the global PTM and act as the PKS representative on the study working with the clinical study team (CTT) towards study completion and final clinical study report (CSR).</h4></li><li><h4>Manage the team performance and periodically assess the team members while working closely with line function management to sustain a high-performing team.</h4></li></ul><ul><li><h4>Balance efficiently both the management of a team of experts, as well as individual contributor role with same study management activities performed by rest of the team.</h4></li></ul><h4>Key performance indicators: </h4><ul><li><h4>Enabling and maintaining business impact through efficient turnaround time for studies while managing key study partners.</h4></li></ul><h4>Minimum Requirements: Work Experience: </h4><ul><li><h4>Managing Crises.</h4></li><li><h4>Collaborating across boundaries.</h4></li><li><h4>Project Management.</h4></li></ul><h4>Skills: </h4><ul><li><h4>Drug Development.</h4></li><li><h4>Employee Recruitment.</h4></li><li><h4>Flexibility.</h4></li><li><h4>Phoenix Winnonlin software</h4></li><li><h4>Teamwork.</h4></li></ul><h4>Languages :</h4><ul><li><h4>English.</h4></li></ul> Skills DesiredAdobe Photoshop, Chemistry, Collaboration, Compensations Management (Employees), Curiosity, Drug Development, Employee Recruitment, Flexibility, Oscilloscope, Patient Care, Pipeline (Software), Sales, Small Business, Teamwork

Novartis India

Student Services Registrar

Sr. Engineer- Lighting<h4>Function</h4>

Research &amp; Development - Jaipur<h4>Pay Band</h4>

E4 to M2<h4>Role</h4>

Sr Engineer- Lighting<h4>A purpose driven role for you</h4>

To work as a team player with the Electronics Design &amp; Development team &amp; Coordinating with the Testing of Light and Signalling devices like Head Light/ Tail Light / Winkers etc. Should understand on the New Technology/Innovation concept embedded in the Electronic design and development is in line with Vehicle configuration and as per Goals aligned on each fiscal year.<h4>A Day in the life</h4>

• Lighting Electronics Design Activities &amp; Processes. • Testing/validation &amp; regulations compliance at Electronic System &amp; Subsystem level • Technical Solution &amp; Innovation in the Design • Coordinate internal resources and third vendors for the flawless execution of projects<h4>Academic Qualification &amp; Experience</h4>

B.Tech /M. Tech- Electrical &amp; Electronics<h4>Technical Skills/Knowledge</h4>

The ideal candidate should have relevant experience in: a)Electronic Design &amp; Dev b) Altium, ORCAD c) M.S. Office d) Electronic Software Exposure in Design &amp; Dev Knowledge of Power Supply Topologies, Regulations, Integrated Circuits Inverter IC etc Knowledge of Hardware Design concept , Development Process all types of process used in Lighting. Knowledge &amp; Exposure of Microcontroller, PCB Design, EMI/EMC, Passive &amp; Active component selection etc Knowledge of Software Microcontroller platform Embedded C, C++ Code development for Renesas RL78/F13 Series etc Exposure in handling suppliers and internal/ external customers Knowledge of Debugger, JTAG Emulator, Simulation Tools , Protocols UART, I2C, SPI, CAN, LIN etc. Knowledge of Testing tools like Peak CAN, CAN analyser etc.<h4>Behavioural Skills</h4>

Excellent written and verbal communication skills Having the Interpersonal skill to work in a Team<h4>What will it be like to work for Hero</h4>

As the world’s largest manufacturer of motorcycles and scooters for the last 22 years, Hero is where you will get to work with the brightest innovators, passionate about being the best in what they do. You will become a part of India’s proudest legacy, a brand that is celebrated by 110 million Indians and is now taking over the world with its manufacturing superpower. If you are someone who dreams big and goes after their dreams with absolute conviction, Hero is your place to be. At Hero, we are building a cutting-edge future of mobility, pushing frontiers of innovation and aiming for the very best. Choose to be with the best, choose to be your best.<h4>About Hero</h4>Headquartered in New Delhi (India), <a href="https://www.heromotocorp.com/en-in.html" target="_blank">Hero MotoCorp</a> is the world's largest manufacturer of motorcycles and scooters for 22 consecutive years. We are at the forefront of developing modern, technologically superior and eco-friendly mobility solutions for its millions of customers around the world. Hero MotoCorp has rapidly transformed into a true multinational organization with a presence in 47 countries across Asia, Africa, Latin America and the Middle East. We have achieved the coveted milestone of 110 million cumulative production and sales since inception. Aligned with its Vision “Be the Future of Mobility”, Hero MotoCorp plans to achieve its next 100 million sales by 2030. We have a globally benchmarked manufacturing and Research &amp; Development (R&amp;D) ecosystem that is spread across global geographies. Its R&amp;D facilities are located in India and Germany - the Centre of Innovation and Technology (CIT) at Jaipur, India, and the Tech Centre Germany (TCG), near Munich. Hero MotoCorp’s eight ‘green’ manufacturing facilities are spread across India (6), Colombia (1) and Bangladesh (1). Hero MotoCorp is the pre-eminent leader in the Indian two-wheeler market. It is the only motorcycle manufacturing company listed in Dow Jones Sustainability Index. In 2022, Hero MotoCorp launched a separate brand for emerging mobility solutions, including Electric Vehicles (EV) - VIDA, Powered by Hero. VIDA has commenced sales of VIDA V1 – its first EV – in India and plans to launch the product in global markets. We are one of the largest global corporate promoters of multiple sporting disciplines. Hero is globally associated with golf, football, field hockey, cricket and motorsports. Hero MotoSports Team Rally is one of India’s flag-bearers in global rally racing. The iconic golfer Tiger Woods is Hero MotoCorp’s Global Corporate Partner. Read more <a href="https://www.heromotocorp.com/en-in.html" target="_blank">about us.</a> Be with the best. Be your best. Catch-up on all our <a href="https://jobs.heromotocorp.com/" target="_blank">latest openings</a>. Recruitment assessments – We at Hero are equal opportunity employer and committed to a policy of treating all its employees and job applications equally. Some of our roles use assessments to help us understand how suitable you are for the role you've applied to. If you are invited to take an assessment, this is great news. It means your application has progressed to an important stage of our recruitment process.<h4>Experience Level</h4>Senior Level

Hero Motocorp Limited

Senior Electrical Engineer

Senior Staff, Applied ScienceAbout Tekion:Positively disrupting an industry that has not seen any innovation in over 50 years, Tekion has challenged the paradigm with the first and fastest cloud-native automotive platform that includes the revolutionary Automotive Retail Cloud (ARC) for retailers, Automotive Enterprise Cloud (AEC) for manufacturers and other large automotive enterprises and Automotive Partner Cloud (APC) for technology and industry partners. Tekion connects the entire spectrum of the automotive retail ecosystem through one seamless platform. The transformative platform uses cutting-edge technology, big data, machine learning, and AI to seamlessly bring together OEMs, retailers/dealers and consumers. With its highly configurable integration and greater customer engagement capabilities, Tekion is enabling the best automotive retail experiences ever. Tekion employs close to 3,000 people across North America, Asia and Europe.Core responsibilities:<ul><li>Work directly with application/product teams to define, develop and implement the right ML solution for the problem at hand.</li><li>Come up with new solutions for solving automotive industry business problems.</li><li>Define the correct evaluation metrics for offline and online evaluation. Creating and tracking accuracy and performance metrics.</li><li>Incorporating new data sources and implementing creative methodologies to improve model performance.</li><li>Helping build production systems that take inputs from multiple models and support decision making.</li><li>Should be equally comfortable with digging in to customer requirements as you are drilling into design with development teams and developing production ready learning models.</li><li>Should consistently bring strong, data-driven business and technical judgment to decisions.</li></ul>Required Qualifications:<ul><li>Masters, PhD in Data Science, Mathematics, Operations Research or related field.</li><li>The right candidate has a background in probability and statistics, applied mathematics, or computational science and a history of solving difficult problems with good business impact using a scientific approach.</li><li>Experience working with ML algorithms and frameworks.</li><li>Significant experience in Data Science and Machine Learning with a strong proven track record in delivering positive business impact.</li><li> 10+ years of hands-on experience with analytics, data science and big data experience in a business context.</li><li>Experience in programming in Python or similar languages and maintaining code repositories in git.</li><li>Experience with data visualization and presentation, turning complex analysis into insights.</li></ul>Preferred qualifications:<ul><li>Experience in Recommendation Engine, Natural Language Processing.</li><li>Domain knowledge of automotive industry.</li><li>Enjoys discovering and solving problems; proactively seeking clarification of requirements and direction; being a self-starter who takes responsibility when required.</li><li>Strong interpersonal, verbal, visual and presentation skills, ability to communicate complex findings in a simple manner to executives.</li><li>Ability to work collaboratively across multiple products and application teams.</li><li>A willingness to learn, share and improve.</li></ul>Tekion is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, victim of violence or having a family member who is a victim of violence, the intersectionality of two or more protected categories, or other applicable legally protected characteristics. For more information on our privacy practices, please refer to our Applicant Privacy Notice <a href="https://tekion.com/legal/privacy/applicant-and-candidate-privacy-notice">here</a>.<h4>Experience Level</h4>Senior Level

Tekion India

Science Instructor

Principal Programmer - Statistical Programming<h4>Job Title: Principal Programmer - Statistical Programming</h4>Introduction to role:Are you ready to take on a pivotal role in statistical programming? As a Principal Statistical Programmer, you'll be at the forefront of developing and validating programs that create datasets conforming to Alexion and ADaM specifications. Your expertise will drive the creation of Tables, Listings, and Figures for efficacy data analysis, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. You'll lead programming efforts, represent Clinical and Statistical Programming in meetings, and mentor fellow programmers. This is your chance to integrate statistical concepts with SAS Programming efficiently and effectively!<h4>Accountabilities:</h4><ul><li>Develop and validate technical programming specifications for analysis datasets using Alexion or ADaM standards.</li><li>Independently develop and validate programs that generate analysis datasets based on Alexion or ADaM specifications.</li><li>Develop and validate technical programming specifications for protocol-specific efficacy tables, listings, figures/graphs based on Protocol SAP.</li><li>Independently develop and validate programs that generate efficacy tables, listings, figures/graphs using Alexion specifications.</li><li>Supervise/manage external vendors and contract programmers.</li><li>Oversee progress of programming activities.</li><li>Review, maintain, and approve protocol-specific documents as necessary.</li><li>Provide guidance and mentoring to peer and junior-level Programmers.</li><li>Act as the primary department contact, when necessary, to ensure that department standards are implemented in all studies.</li><li>Contribute ideas and thoughts towards the optimization of standard operating procedures.</li><li>Lead team meetings when appropriate.</li><li>Any other activities as required.</li></ul><h4>Essential Skills/Experience:</h4><ul><li>Bachelor’s Degree (Minimum) or Master’s Degree (Preferred) in Biostatistics, Statistics or another related discipline</li><li>Minimum of 7 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.</li><li>Proven ability to:</li><li>Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs.</li><li>Independently and collaboratively resolve problems</li><li>Clearly communicate processes and standards with management and team members</li><li>Expertise in using SAS/Base, SAS/Macro, SAS/STAT.</li><li>Knowledge of SAS/Graph, and SAS/SQL</li><li>Knowledge of:</li><li>SDTM and ADaM</li><li>Relational Databases.</li><li>Good Clinical Practices.</li><li>Good Programming Practices.</li><li>21CFR Part 11 Standards.</li><li>Integrated Summary Safety/Efficacy Analyses.</li><li>Safety data and Coding Dictionaries (MedDRA and WHODD).</li><li>ICH eCTD format.</li></ul>At AstraZeneca, we play an essential role in helping patients who need it the most. Our high exposure roles allow us to shape end deliverables while embracing global opportunities across all Therapy Areas. With a restless drive for improvement, we foster an inspiring learning environment where every setback is a chance to innovate. Our courageous team speaks up, shares opinions, and makes bold decisions that could change patients' lives. We combine specialist knowledge with curiosity, always searching for better ways to achieve the best results. Here, dedication and motivation are key as we navigate unknowns with resilience.Ready to make an impact? Apply now to join our dynamic team!Date Posted06-Oct-2025Closing Date08-Oct-2025Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact <a href="mailto:accommodations@Alexion.com" rel="noopener noreferrer" target="_blank">accommodations@Alexion.com</a>. Alexion participates in E-Verify.<h4>Experience Level</h4>Senior Level

Astrazeneca India Private Limited

Research Analyst

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

Research Associate: Pharma Research-Inhalation<h4>Job Description</h4>Essential Duties and Responsibilities · Provide device and primary packaging expertise in a broader cross-functional drug product development organization, leading and coordinating the development and manufacturing of clinical and commercial device components and assembled devices in compliance with the Corporate, government and relevant industry standards, regulations and best practices. · Provide recommendations on strategies to select device material, developing device design concepts and incorporated technologies, cost-reduction, high-volume manufacturing and streamlining processes. · Leading the collaboration with internal and external development partners including monitoring work progress according to plan. · Monitor, support and challenge technical development as well as test and verification work. · Leading the definition of product requirements for medical devices and drug/device combination products. · Design, plan, perform, interpret, report results of studies related to development and related processes and procedures of medical devices with a focus on reliability testing, quality and documentation. · Develop efficient and robust devices and processes for the manufacture and/or analysis of Medical Devices/Combination Products, risk management activities, evaluating and challenging technical solutions. · Leading and monitoring documentation work and the development of a high-quality Design History Files (DHF). · Leading and monitoring human factors studies and activities. · Support Regulatory Affairs to prepare Medical Device/Combination Product pre-registration documents and provide input to answer Health Authority questions. Lead or support interaction with Health Authorities and various medical device industry governing and accreditation bodies. · Support/coach of team members, participation in project(s) sub-teams and contribution to overall strategies and goals. Education and Experience · Minimum: relevant degree in Engineering and at least 8 - 10 years of experience in a similar area with continuing education (EU) or BSc or equivalent. · Highly Desirable: Advanced degree in a scientific or relevant discipline (MSc or equivalent) and at least 5 years’ experience in medical device industry and pharmaceutical development experience. · Successfully demonstrated expertise in medical devices area. · Mechanical Engineering in general, especially experience in product design, injection molding of plastic components, testing and verification tools, equipment building and qualification desirable.<h4>Work Experience</h4> 8 - 10 years <h4>Education</h4>
Masters in Medicinal Chemistry or Engineering<h4>Competencies</h4><h4>Experience Level</h4>Senior Level

lupin ltd

Research Associate

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

Senior Analyst – Trial Analytics, Insights & Planning (TAIP) Sr. Mgr levelWorking 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 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

Senior Analyst

Analytical Technical Steward - Small MoleculeAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Organization Overview At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better.The Analytical Technical Steward in API (Active Pharmaceutical Ingredient) External Manufacturing Quality Control is a technical position helping to ensure that the analytical testing of products at multiple sites meets both Lilly and external requirements and is executed consistently to predetermined standards. This position will be small molecule focused and may require in-person site visits to the contract manufacturer up to three times per week or as needed. The Analytical Technical Steward reviews data released by contract manufacturers according to API EM Risk Based Oversight Governance to ensure it meets internal integration and data integrity expectations, reviews deviations for trends, reviews and/or releases stability data, and leads resolution of laboratory related manufacturing issues by performing in-depth problem solving, proactively identifying opportunities for continuous improvement, and completing thorough investigations of aberrant data and results. They may perform non-routine lab work in support of this. Additionally, the Analytical Technical Steward represents the quality laboratories on cross-functional internal and joint process teams. The Analytical Technical Steward works closely with development counterparts and GQL (Global Quality Laboratories) to ensure robust analytical control strategies are established for molecules they support.  Responsibilities:<ul><li>Technical review, interpretation, and release of data including data released from CM (Contract Manufacturers), stability, process validation, and reference standard characterization.</li><li>Utilizes technical skills to lead or perform in-depth investigations for out of specification results and aberrant data. Draws conclusions and performs root cause analysis investigations and recommends solutions to prevent reoccurrence.</li><li>Develop investigational testing protocols and perform testing as required.</li><li>Contribute to APR, tech transfer, and process validation as required.</li><li>Communicate effectively in both written and oral formats within the API EM organization as well as with external customers and business partners.</li><li>Participate in internal/external audits as needed.</li><li>Develop and ensure execution of quality plan projects.</li><li>Coordinate testing needs across sites in support of batch release, stability, process validation, or single batch verification testing.</li><li>Performs method assessments, with deficiencies and areas for improvement noted within the assessments.</li><li>Ensure that method validation packages for marketed products are consistent with current regulatory expectations and compendial monographs. This includes evaluating existing method validation data and taking actions to facilitate updating packages as needed.</li><li>Participates in method validations according to Global Quality Standards (either to bring methods up to current regulatory requirements or to provide additional data to support method changes or changes in practices).</li><li>Review of analytical test method packages.</li><li>Approval of test method protocols.</li><li>Approval of new test methods or changes or deletions to existing test methods.</li><li>Provides laboratory support (e.g., method development, validation, and implementation of method improvements) for marketed products (including: laboratory work, training/transfer of new method to QC labs, change controls, and regulatory submissions).</li><li>Support technical agenda projects including the implementation of new technologies into QC labs and improvements to existing methodologies.</li><li>Improve assays in QC. These improvements include variability reduction, method optimization, and new method development.</li><li>Local and Global Method Change Control Ownership.</li><li>Oversight of reference standard evaluations per Global Quality Standards.</li><li>Selection of appropriate packaging materials.</li><li>Consult in the preparation of the characterization protocol for corporate reference standards.</li><li>Approve the characterization protocol before the initiation of laboratory testing of candidate materials for corporate reference standards.</li><li>Participate in the review of the reference standard profile and associated documentation for data integrity and technical assessment</li><li>Oversee transfer and validations of analytical methods for marketed products to CM laboratories or to designated third party QC labs.</li><li>Monograph review and implementation.</li><li>Ensures consistent practices between laboratories running the same methods.</li><li>Effective management of multiple projects.</li><li>Oversight of laboratory data integrity compliance at contract manufacturers, use of effective influence to ensure appropriate compliance.</li></ul>Basic Requirements:<ul><li>Bachelor degree in a science field related to the lab (e.g. Chemistry, Biochemistry, Pharmacy), Masters degree preferred</li><li>10+ years of industry related experience in pharmaceuticals in a GMP lab</li><li>Location of position: Hyderabad, India with routine travel to Visakhapatnam required</li><li>Proven ability to provide GMP compliant QC support and strategic direction for contract manufacturers of small molecule starting materials, intermediates and APIs</li><li>Must have experience with small molecule synthesis and associated analytical techniques</li></ul>Additional Skills/Preferences:<ul><li>Demonstrated proficiency in complex laboratory analysis including, but not limited to chromatographic (HPLC Reverse Phase and Normal Phase, GC-HS), spectroscopic, KF, particle size, LOD, appearance, ICP-MS, ICP-OES, Karl Fischer, LCMS, GCMS, compendial tests, etc.</li><li>Experience with characterization techniques strongly preferred, includes but not limited to XRPD, specific surface area, NMR, particle size, moisture sorption, SEM, thermal analysis, etc.</li><li>Experience with Spray Dried Dispersion analytical techniques preferred</li><li>Experience with NDA or equivalent submissions (including authorship) preferred</li><li>Ability to work in a lab environment, including wearing appropriate PPE and following safety guidelines.</li><li>Deep understanding of compliance requirements and regulatory expectations.</li><li>Demonstrated accuracy and proficiency in analytical skills.</li><li>Demonstrated strong problem-solving skills. Preferred training completion and demonstrated proficiency in Root Cause Analysis methodology.</li><li>Strong oral and written communication skills demonstrated through documentation and presentations.</li><li>Demonstrated strong interpersonal interaction skills.</li><li>Ability to work in cross functional teams as well as across networks.</li><li>Demonstrated analytical skills.</li><li>Demonstrated experience with method qualification, validation, and transfer.</li><li>Proficient in establishment and maintenance of GMP or CS mode analytical equipment, to include computer systems validation (CSV).</li><li>Proven ability to support maintenance of Corporate Reference Standards and manage testing and reporting of results from contract manufacturers.</li></ul>Additional Information:<ul><li>Position will be day shift, but may require some shift to support global operations</li><li>May require travel overseas, passport required</li><li>May require up to three days per week person in plant responsibilities for the laboratory in both Hyderabad and Visakhapatnam, India</li></ul>Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Senior Level

Eli Lilly and Company India Pvt Ltd

Technical Executive

Analytical Technical Steward-PeptidesAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Job Description - Analytical Technical Steward-Peptide (Hyderabad, India)Organization Overview At Lilly, we serve an extraordinary purpose. For more than 140 years, we have worked tirelessly to discover medicines that make life better.The Analytical Technical Steward in API (Active Pharmaceutical Ingredient) External Manufacturing Quality Control is a technical position helping to ensure that the analytical testing of products at multiple sites meets both Lilly and external requirements and is executed consistently to predetermined standards. This position will be Peptide focused and will require in-person site visits to the contract manufacturer up to four times per week or as needed. The Analytical Technical Steward reviews data released by contract manufacturers according to API EM Risk Based Oversight Governance to ensure it meets internal integration and data integrity expectations, reviews deviations for trends, reviews and/or releases stability data, and leads resolution of laboratory related manufacturing issues by performing in-depth problem solving, proactively identifying opportunities for continuous improvement, and completing thorough investigations of aberrant data and results. They may perform non-routine lab work in support of this. Additionally, the Analytical Technical Steward represents the quality laboratories on cross-functional internal and joint process teams. The Analytical Technical Steward works closely with development counterparts and GQL (Global Quality Laboratories) to ensure robust analytical control strategies are established for molecules they support.  Responsibilities:<ul><li>Technical review, interpretation, and release of data including data released from CM (Contract Manufacturers), stability, process validation, and reference standard characterization.</li><li>Utilizes technical skills to lead or perform in-depth investigations for out of specification results and aberrant data. Draws conclusions and performs root cause analysis investigations and recommends solutions to prevent reoccurrence.</li><li>Develop investigational testing protocols and perform testing as required.</li><li>Contribute to APR, tech transfer, and process validation as required.</li><li>Communicate effectively in both written and oral formats within the API EM organization as well as with external customers and business partners.</li><li>Participate in internal/external audits as needed.</li><li>Develop and ensure execution of quality plan projects.</li><li>Coordinate testing needs across sites in support of batch release, stability, process validation, or single batch verification testing.</li><li>Performs method assessments, with deficiencies and areas for improvement noted within the assessments.</li><li>Ensure that method validation packages for marketed products are consistent with current regulatory expectations and compendial monographs. This includes evaluating existing method validation data and taking actions to facilitate updating packages as needed.</li><li>Participates in method validations according to Global Quality Standards (either to bring methods up to current regulatory requirements or to provide additional data to support method changes or changes in practices).</li><li>Review of analytical test method packages.</li><li>Approval of test method protocols.</li><li>Approval of new test methods or changes or deletions to existing test methods.</li><li>Provides laboratory support (e.g., method development, validation, and implementation of method improvements) for marketed products (including: laboratory work, training/transfer of new method to QC labs, change controls, and regulatory submissions).</li><li>Support technical agenda projects including the implementation of new technologies into QC labs and improvements to existing methodologies.</li><li>Improve assays in QC. These improvements include variability reduction, method optimization, and new method development.</li><li>Local and Global Method Change Control Ownership.</li><li>Oversight of reference standard evaluations per Global Quality Standards.</li><li>Selection of appropriate packaging materials.</li><li>Consult in the preparation of the characterization protocol for corporate reference standards.</li><li>Approve the characterization protocol before the initiation of laboratory testing of candidate materials for corporate reference standards.</li><li>Participate in the review of the reference standard profile and associated documentation for data integrity and technical assessment</li><li>Oversee transfer and validations of analytical methods for marketed products to CM laboratories or to designated third party QC labs.</li><li>Monograph review and implementation.</li><li>Ensures consistent practices between laboratories running the same methods.</li><li>Effective management of multiple projects.</li><li>Oversight of laboratory data integrity compliance at contract manufacturers, and uses effective influence to ensure appropriate compliance.</li></ul>Basic Requirements:<ul><li>Bachelor degree in a science field related to the lab (e.g. Chemistry, Biochemistry, Biology, Pharmacy), Masters degree preferred</li><li>10+ years of industry related experience in pharmaceuticals in a GMP lab</li><li>Location of position: Hyderabad, India with routine travel to Visakhapatnam required</li><li>Must have experience in GMP laboratory and experience with contract laboratories and/or contract manufacturers</li><li>Must have experience with either Peptide SPPS/LPPS synthesis or Large Molecule</li><li>Must have experience with characterization testing and comparability assessments</li><li>Must have experience with NDA submissions, authoring for laboratory section and/or review. Experience with both NDA and BLA preferred</li></ul>Additional Skills/Preferences:<ul><li>Demonstrated proficiency in complex laboratory analysis including, but not limited to chromatographic (both HPLC-RP, Normal Phase, and SEC and GC-HS), spectroscopic, KF, particle size, LOD, appearance, LCMS, GCMS, Bioassay, compendial tests, etc.</li><li>Experience with both NDA and BLA submission preferred (minimum NDA required)</li><li>Ability to work in a lab environment, including wearing appropriate PPE and following safety guidelines.</li><li>Deep understanding of compliance requirements and regulatory expectations.</li><li>Demonstrated accuracy and proficiency in analytical skills.</li><li>Demonstrated strong problem-solving skills. Preferred training completion and demonstrated proficiency in Root Cause Analysis methodology.</li><li>Strong oral and written communication skills demonstrated through documentation and presentations.</li><li>Demonstrated strong interpersonal interaction skills.</li><li>Ability to work in cross functional teams as well as across networks.</li><li>Demonstrated analytical skills.</li><li>Demonstrated experience with method qualification, validation, and transfer.</li><li>Proficient in establishment and maintenance of GMP or CS mode analytical equipment, to include computer systems validation (CSV).</li><li>Proven ability to support maintenance of Corporate Reference Standards and manage testing and reporting of results from contract manufacturers.</li></ul>Additional Information:<ul><li>Position will be day shift, but may require some shift to support global operations</li><li>May require travel overseas, passport required</li><li>May require up to four days per week person in plant responsibilities for the laboratory in both Hyderabad and Visakhapatnam, India</li></ul>Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Senior Level

Senior Quality Engineer (AI Platform Testing)At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.Lilly’s Purpose:At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 42,000+ employees across the globe work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work and put people first.Come build advanced software capabilities to accelerate our digital transformation and support Lilly’s evolution to be the leader in Pharma-tech!The Role:The Software Product Engineering (SPE) organization is actively looking for a Senior Quality Engineer with strong hands-on experience in AI platform testing, chatbot testing, AI model validation, agents testing, AI test automation, and API testing. This is a highly specialized role focused on validating complex AI and ML systems and ensuring scalable, safe, and effective deployment of AI-based solutions.UI automation experience using tools like Selenium, Cypress, or Playwright is desirable as a secondary skill.What You’ll Be Doing:You will drive quality engineering initiatives specifically focused on AI-powered platforms and solutions, including LLMs, chatbots, AI agents, and intelligent workflows. You’ll build robust test strategies and frameworks to validate data pipelines, model inference accuracy, prompt engineering, hallucination control, API contracts, and performance under real-world conditions.This role requires strong analytical and problem-solving skills, a deep understanding of AI systems testing, and the ability to collaborate across multidisciplinary teams such as SWE, SRE, ML Engineering, and Product.Key Responsibilities:<ul><li>AI Platform &amp; Model Testing (Primary Focus):<ul><li>Validate the behaviour and performance of AI/ML models, including LLMs, RAG pipelines, chatbots, and autonomous agents.</li><li>Design and execute prompt evaluation, response accuracy, toxicity detection, and hallucination control test scenarios.</li><li>Implement and enhance automated AI testing frameworks tailored to model versioning, retraining, and feedback loops.</li><li>Ensure quality in human-in-the-loop (HITL) and continuous learning pipelines.</li></ul></li><li>API Testing:<ul><li>Conduct thorough API validation using Postman, REST Assured, or GraphQL, with a focus on AI service endpoints, inference APIs, and orchestrators.</li><li>Build robust integration test suites to ensure seamless functionality between APIs and underlying AI systems.</li></ul></li><li>AI Test Automation:<ul><li>Build test harnesses to validate AI features through synthetic data, mock services, and model stubs.</li><li>Integrate test suites into CI/CD pipelines to ensure continuous validation of AI behaviors.</li></ul></li><li>UI and Functional Test Automation (Secondary Focus):<ul><li>Support end-to-end automation of AI-powered applications using tools such as Selenium, Cypress, Playwright, and WebdriverIO.</li><li>Automate critical user journeys involving AI-enabled decisions and interactions.</li></ul></li><li>Collaboration &amp; Test Strategy:<ul><li>Work closely with ML Engineers, SREs, and Product Managers to translate model design into testable components.</li><li>Monitor AI behavior in production using observability tools and adjust quality strategies based on live insights.</li><li>Drive discussions on fairness, bias, explainability, and model drift.</li></ul></li><li>Agile &amp; DevOps Integration:<ul><li>Participate in Agile ceremonies and actively contribute to sprint planning, test case reviews, and retrospectives.</li><li>Collaborate with DevOps teams to embed AI testing into CI/CD workflows using tools like GitHub, Jenkins, and Azure DevOps.</li></ul></li></ul>Required Technical Skills &amp; Qualifications:<ul><li>Bachelor’s or Master’s degree in Computer Science, Engineering, AI/ML, or a related field</li><li>6+ years of experience in Quality Engineering with at least 2 years in AI platform testing or model validation</li><li>Hands-on experience in AI model testing, chatbot testing, prompt tuning, or agent workflows</li><li>Proficiency in AI test automation and API testing tools (Postman, REST Assured, GraphQL)</li><li>Working knowledge of Python, JavaScript, or TypeScript</li><li>Experience integrating tests into CI/CD pipelines using GitHub, Jenkins, or Azure DevOps</li><li>Knowledge of OpenAI, Bedrock, Anthropic, LangChain, RAG, and vector stores</li><li>Understanding of LLM evaluation techniques, including metrics like BLEU, ROUGE, Toxicity Score, and RAGAs</li></ul>Preferred Qualifications:<ul><li>Experience testing AI applications hosted in multi-geographical and cloud-native environments (e.g., AWS, GCP, Azure)</li><li>Exposure to AI observability platforms such as Weights &amp; Biases, Arize AI, or WhyLabs</li><li>Understanding of prompt engineering, embedding quality, and tokenization behaviour</li><li>Familiarity with security, performance, or accessibility testing</li><li>Experience with AI governance frameworks and regulatory compliance (e.g., FDA, HIPAA in AI contexts)</li></ul>Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (<a href="https://careers.lilly.com/us/en/workplace-accommodation" rel="noopener noreferrer" target="_blank">https://careers.lilly.com/us/en/workplace-accommodation</a>) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.#WeAreLilly<h4>Experience Level</h4>Senior Level

Quality Engineer

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

Senior STEM Content AnalystWe are looking for a Senior STEM Content Analyst with strong expertise in CMC Biologics to join our Life Sciences team in India. The ideal candidate will have a solid background in pharmaceutical development or regulatory affairs, particularly in biologics and biopharmaceuticals, and will be passionate about delivering high-quality content that supports global health authority submissions. You will be responsible for monitoring regulatory changes, authoring detailed CMC reports, and supporting both internal teams and external customers. Your ability to work collaboratively across global teams, manage complex regulatory data, and contribute to product innovation will be key to your success in this role.   About You – experience, education, skills, and accomplishments   <ul><li>Minimum BS degree in Life Sciences.  </li></ul><ul><li>5+ years in pharmaceutical development, CMC manufacturing, or CMC regulatory affairs for Biologics/Biopharmaceuticals. </li></ul><ul><li>Experience managing BLA/MAA content and format. </li></ul><ul><li>Experience with FDA and EMA submissions, including responses to deficiency letters and communications with health authorities on quality aspects of the product. </li></ul><ul><li>Working knowledge/experience in regulatory submission and approval processes for new Biologics or biopharmaceutical products and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements </li></ul><ul><li>Strong knowledge of ICH requirements for quality aspects for Biologics and/or Biopharmaceutical products. </li></ul><ul><li>Understanding of scientific principles relevant to vaccine and biologics development. </li></ul><ul><li>Ability to work in global teams and remote environments with extended, multinational project teams on multiple tasks under pressure of time and workload. </li></ul><ul><li>Demonstrated ability to work collaboratively and resolve conflict across different functional areas in a highly matrixed organization. </li></ul><ul><li>Excellent communication, problem-solving, and decision-making skills. </li></ul><ul><li>Fluent in English; additional languages appreciated. </li></ul>It would be great if you also had . . .   <ul><li>Knowledge of biological entities. </li></ul><ul><li>Experience negotiating contracts and managing budgets/invoices. </li></ul><ul><li>Familiarity with copyright terms and local expert networks. </li></ul>What will you be doing in this role?  <ul><li>Author high-quality CMC reports for biologics to support regulatory submissions, facilitate the application of CMC global regulatory strategies, helping to assure technical congruency and regulatory compliance with customers. </li></ul><ul><li>Monitor and analyze global CMC regulatory changes. </li></ul><ul><li>Analyze changes in the CMC requirements and implement changes in the database capitalizing on internal expertise and the external network of consultants for local expertise and practice. </li></ul><ul><li>Act as internal CMC regulatory expert for assigned countries. </li></ul><ul><li>Support CMC Product Manager and provide customer expertise, acting as team representative for customers when required. </li></ul><ul><li>Collaborate with Product, Tech, Customer Care, and other stakeholders. </li></ul><ul><li>Participate in special projects and editorial/content operations. </li></ul>About the Team    As part of the Regulatory Market Access team, CMC is group of subject matter experts and is mainly responsible to curate content through monitoring and editing official worldwide guidelines and legislation related to the CMC area, for both pre- and post-approval content. It works closely with cross-functional teams including Product, Tech, Customer Care, supports internal and external stakeholders and contributes to Clarivate’s mission to improve innovation through curated content and technology. The team is spread across different locations: France, Malaysia, India, Serbia, Spain, US. Hours of Work   Hybrid (Monday - Friday) work mode. The work timing is 10 AM to 6 PM IST. 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>Senior Level

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