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Process R&D Scientist<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>We are seeking a highly skilled Process Scientist API (Active Pharmaceutical Ingredient) to join our team in Hyderabad, India. In this role, you will be responsible for developing, optimizing, and scaling up API manufacturing processes to ensure efficient and high-quality production of pharmaceutical ingredients.<ul><li>Design, develop, and optimize API manufacturing processes from laboratory scale to commercial production</li><li>Conduct experiments and analyze data to improve process efficiency, yield, and product quality</li><li>Troubleshoot process issues and implement solutions to enhance overall performance</li><li>Collaborate with cross-functional teams to ensure smooth technology transfer and scale-up of API processes</li><li>Prepare comprehensive technical reports and documentation for internal and regulatory purposes</li><li>Stay updated on current Good Manufacturing Practices (GMP) and regulatory requirements in the pharmaceutical industry</li><li>Participate in process validation activities and support regulatory filings</li><li>Mentor junior scientists and contribute to the continuous improvement of the department</li></ul><h4>Qualifications</h4><ul><li>Ph.D. or Master's degree in Chemistry, Chemical Engineering, or a related field</li><li>3-5 years of experience in API process development or a related field within the pharmaceutical industry</li><li>Extensive knowledge of API manufacturing processes and pharmaceutical industry regulations</li><li>Strong expertise in process development, optimization, and scale-up techniques</li><li>Proficiency in analytical techniques and instrumentation commonly used in API development</li><li>Excellent problem-solving and troubleshooting skills with a detail-oriented approach</li><li>Familiarity with Good Manufacturing Practices (GMP) and pharmaceutical industry standards</li><li>Strong data analysis and interpretation skills</li><li>Proficiency in using laboratory equipment and relevant software</li><li>Excellent written and verbal communication skills</li><li>Ability to work efficiently in a fast-paced, collaborative environment</li><li>Experience with tech transfer and process validation is preferred</li></ul><h4>Additional Information</h4>About the DepartmentIntegrated Product Development Organisation                                         We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/  <h4>Experience Level</h4>Mid Level

Dr Reddys Laboratories

Process Engineer

Analytical Specialist- Formulation AR&D<h4>Job Description</h4><ul><li>Analyze critical API, excipient, and FP methods in R&amp;D, and prepare verification reports to facilitate method transfer at the manufacturing site.</li><li>Core knowledge on Derma products, method development, and technology transfer is mandatory.</li><li>Perform elemental, genotoxic, and nitrosamine impurity assessments.</li><li>Develop and validate residue analytical methods.</li><li>Prepare technical justification reports in consultation with an expert.</li><li>Execute experiments to finalize critical methods and prepare method design and development reports.</li><li>Identify and ensure the availability of prerequisites like columns, chemicals, impurities, and standards for AMT at partner sites</li><li>Prepare specification, STPs, Justification and technical reports for the assigned products</li><li>Understand regulatory requirements specific to all regulated markets.</li><li>Knowledge on drafting the responses to regulatory queries.</li><li>Conversant with all pharmacopeias and guidelines.</li><li>Identify new technologies for project-specific challenges</li><li> </li></ul><h4>Additional Information</h4><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>

Chemical Analyst

Associate STEM Content Analyst - ChemistryAbout You – experience, education, skills, and accomplishments   <ul><li>Years of Service - Fresher or less than 2 years of relevant experience. Education - M.Sc Chemistry / M.Sc Biochemistry/ B. Pharm / M. Pharm graduates. </li><li>Preferred Qualifications- Chemical drawing packages, e.g., ISIS Draw</li><li>Problem identification and solving skills, Good analytical skills.</li><li>Outstanding communication skills (written and oral) with ability to communicate clearly, concisely, and objectively in both written and spoken English.</li></ul>What will you be doing in this role?  <ul><li>Responsible for indexing/coding chemical compounds in patents.</li><li>Extract pharmaceutical, therapeutic, agrochemical activities, chemical reaction, drug information and draw Markush etc. from patents.</li><li>Achieving target volume deliverables with high efficiency and quality.</li><li>Play an active role in team and maintain awareness of current trends and new developments in Pharmaceutical/Chemistry areas.</li><li>In-depth knowledge of at least one structure handling tool.</li><li>IUPAC nomenclature skills is added asset.</li><li>Comprehensive knowledge of chemistry, incl., reactions, formulae, catalysts, additives, and their functions.</li><li>Responsible for tasks as requested by manager on a permanent or temporary basis.</li><li>Prioritize and complete the tasks based on situation.</li><li>Maintain a flexible and adaptable approach towards process change.</li><li>Collaboratively work within and other teams to carry out the tasks and to be accountable for assigned responsibility.</li><li>Trusted resource in achieving the customer delight.</li></ul>Summary:Scientific Editor - Junior/Entry level in IP Content Editing Team - Delivering value-add scientific information for DWPI™ (Derwent World Patent Index) which is a proprietary database to easily search and identify Pharma. compounds/compositions/Structures covered in patents.At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.<h4>Experience Level</h4>Mid Level

Clarivate

Science Tutor

Associate Scientist - Biotech R&D<h4>Job Description</h4>1. Review of Biotech R&amp;D Documents as per ALCOA++ requirements, metadata review,and data integrity checks.2. Review of Process Development Reports, Tech transfer documents, ProcessCharacterization Reports. Co-ordination from DOA end to support for Techtransfer activities. Review of Clone Development, Clone Characterization andPackaging Documents.3. QAMS review support for evaluation and approval of Quality Managementnotifications such as deviation, Change Control, CAPA and LIR.4. QAMS Management: Tracking of QAMS Notifications, co-ordination with R&amp;Dfor QAMS related activities, Periodic Review and Trending as per SOP andtroubleshooting of QAMS system .5. Co-ordination with CQA and HO-IT for implementation of Corporate SOPs atBiotech R&amp;D and Management of QAMS for R&amp;D Biotech site for CorporateChange controls.6. Conducting Internal Audit for R&amp;D for compliance checks.7. Support in implementing new systems at R&amp;D as part of system improvisation.8. Support in Archival, Issuance and destruction of R&amp;D documents.<h4>Work Experience</h4>6-10 Years <h4>Education</h4>
Post Graduation in Biotechnology or BiotechnologyB.Tech in Biotechnology or Biotechnology<h4>Competencies</h4>
CollaborationCustomer CentricityDeveloping TalentInnovation &amp; CreativityProcess ExcellenceResult OrientationStakeholder ManagementStrategic Agility<h4>Experience Level</h4>Mid Level

lupin ltd

Food Technology Specialist

Sr. Executive Skills :- Candidate should have a good knowledge of safety, conduct safety rounds, ensure work permit, coordinate proper function of installed emergency alarm system, conduct safety meet, conduct mock drills, ensure tool box talk, inspect safety equipments, implementation of ISO for environment management system,HAZOP study, Evaluation of Process Hazard.Overall having safety background Experience :- 8 to 12 yearsQualification :- Graduate in Chemical Engineering or B.E (Fire, Safety)/ADIS Share your updated resume now.

Sun Pharmaceutical Industries Ltd

Project Management Officer

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

Intern<h4>Job Title</h4>Intern<h4>Job Description</h4>Job title: You are responsible for  Detailing out the project scope, which is assigned by Philips DXR R&amp;D  Learn the product, process, tools associated with the project  Understanding of user and business requirements into product requirements, high-level product design, check and optimize integration and verification  Get exposure of Model-Based System Engg., System Integration, Automation, etc.  Periodic review of the project and ensuring timely completion To succeed in this role, you should have the following skills and experience  Strong foundation in technology Biomedical/Mechanical/Electronics/ Software/ Mechatronics/Data science/Embedded.  Fast learner and interested to learn new technologies/business/systems  Ability to present ideas and to convince project team members  Be structured and self-organized  Excellent communication skills  Mindset to simplify and reach solutions with speed In return, we offer you  Learning environment with high-end Technologies, Tools, Infrastructure, etc.  Interaction with Domain experts  Rich Industry experienc<h4>Experience Level</h4>Entry Level

Philips

Recruitment Intern

Vehicle Validation- Technical Support<h4>Function</h4>Research &amp; Development - Jaipur<h4>Pay Band</h4>

E3 &amp; below<h4>Role</h4>

Vehicle Validation- Technical Support<h4>A purpose driven role for you</h4>

The ideal candidate will oversee the timely vehicle preparation and execution of test activities at vehicle and system level, ensuring the Durability, Reliability, Performance and Safety of our vehicles throughout their development lifecycle. Primary responsibilities:  Conducting hands-on testing activities, both in laboratory and field environments, to validate vehicle performance, functionality and durability under various operating conditions.  Prepare the vehicles for tests ensuring functionality of all parts and systems as per specifications.  Periodic measurements of different vehicle parts to monitor and estimate the service life.  Investigating and troubleshooting issues encountered during testing, propose the solutions.  Periodic inspection and drivability evaluation of the test vehicles.  Instrumentation of test vehicles to record data from vehicle CAN and other sensors.  Analysing test data using data analysis softwares and preparing results to identify trends, anomalies, and performance metrics.  Report preparation and maintain the database systematically for test data, results, reports, etc.  Participate in the vehicle service and repair activities and guide the technicians at shop floor.  Contributing to the continuous improvement of testing methodologies, preparing new fixtures for tests to enhance efficiency, accuracy and reliability of testing activities.<h4>A Day in the life</h4>

~Durability monitoring Performance Evaluation Environmental testing Functionality Evaluation ~Test Vehicle Instrumentation &amp; Service Data compilation ~Data analysis, Report preparation, Database management ~Continuous improvement initiatives<h4>Academic Qualification &amp; Experience</h4>

Diploma or equivalent (with relevant experience) in Mechanical Engineering or Automobile Engineering<h4>Technical Skills/Knowledge</h4>

Proven Hands-on experience in two wheeler testing with knowledge of internal combustion engine, powertrain system, brakes, electrical systems and other vehicle safety systems. Good knowledge of different vehicle attributes, validation methods and industry trends. Hands on experience in monitoring projects for durability testing and service life evaluation Hands on experience in using different measurement tools and service equipments. Detail-oriented mindset with a commitment to quality and continuous improvement. Better to have proficiency in vehicle data logging and experienced in relevant software tools for test data analysis (Vbox, CANalyzer, DiaLog, etc) Knowledge of vehicle test standards and should be able to understand the guidelines in test standards.<h4>Behavioural Skills</h4>

Effective communication skills. Proficient in MS Excel and other MS Office tools<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.

Service Advisor

R&D Officer - Innovation Harpic/Lysol<h4>We are Reckitt</h4>
Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.
Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.<h4>​Research &amp; Development​</h4>
In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&amp;D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.<h4>About the role</h4>
As an R &amp; D Category Assistant at Reckitt, you will thrive in our fast-paced environment alongside a team of expert scientists dedicated to ensuring product safety and efficacy. Your meticulous attention to detail will be crucial in supporting technical dossier management and analytical lab compliance.<h4>Your responsibilities</h4>
- Knowledge or experience in sourcing, screening and selecting candidates is a bonus. - Capability to manage projects, large and small, with diligence and efficiency. - Strong communication skills, capable of providing advice and best practise guidance. - Aptitude for innovative thinking and an entrepreneurial attitude within scientific realms. - Experience working under pressure, prioritising quality while delivering on deadlines.<h4>The experience we're looking for</h4>
- Knowledge or experience in sourcing, screening and selecting candidates is a bonus. - Capability to manage projects, large and small, with diligence and efficiency. - Strong communication skills, capable of providing advice and best practise guidance. - Aptitude for innovative thinking and an entrepreneurial attitude within scientific realms. - Experience working under pressure, prioritising quality while delivering on deadlines.<h4>The skills for success</h4>
R&amp;D, Product Lifecycle Management, Commercial Awareness, Business Partnership, Collaboration, Partnership building, Collaborator, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Analytical, Formulation, Science, Chemistry.<h4>What we offer</h4>
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.

We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.<h4>Equality</h4>
We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.

All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.<h4>Experience Level</h4>Entry Level

Reckitt Benckiser

Design And Development Engineer

Technical Reporting Associate IThe Technical Reporting Associate I is an entry level position in the Global Reporting Solutions group, learning and performing tasks supporting non-clinical studies and the production of non-clinical study reports with limited supervision. General Duties<ul><li>Learns to use software tools to efficiently and accurately complete job duties.  Types of software include word processing, spreadsheet, table generation, collaboration/sharing, and database applications</li><li>After completion of sufficient training, manages a full study workload with varying tasks and study designs.</li><li>After completion of sufficient training, may provide basic training and mentoring to new technical reporting associate staff members and provide peer review of colleague’s work.</li></ul> Data Table Preparation<ul><li>Learns to understand study design from the Protocol and uses that knowledge to accurately prepare data tables for study updates (including completing basic statistical analysis) in table generation programs (ToxReporting).</li><li>Learns to and reviews data tables for accuracy, ensuring attention to detail of own work.</li><li>Learns to and prepares CTD tabulated summaries, accurately incorporating information from the study report.</li><li>Learns to and undertakes the drafting and quality checking of data tables that were manually prepared.</li><li>Learns to and undertakes the manual inputting of study data into MS Excel and when necessary, transfer the MS Excel output to MS Word for inclusion in study reports.</li><li>Learns to and undertakes QC activities.</li><li>Learns and becomes proficient in other reporting related duties as assigned.</li></ul> Scheduling Responsibilities<ul><li>Learns to and ensures own work is scheduled and organized to deliver tasks on time.</li><li>Communicates with direct team, supervisor and Global Reporting Solutions and Study Direction team to highlight and resolve any delivery challenges.</li></ul>Qualification:  M.Sc, M.Pharm, B.Pharm, M. Tech (Bio Tech), B. Tech (Bio Tech)Experience: 0-6 MonthsLabcorp is proud to be an Equal Opportunity Employer:Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to applyIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a href="https://careers.labcorp.com/global/en/accessibility" rel="noopener noreferrer" target="_blank">accessibility site</a> or contact us at <a href="mailto:Disability_apply@LabCorp.com" rel="noopener noreferrer" target="_blank">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a href="https://www.labcorp.com/about/web-privacy-policy" rel="noopener noreferrer" target="_blank">Privacy Statement</a>.<h4>Experience Level</h4>Mid Level

LabCorp

Technical Analyst

Quantitative Research : Equities Core Development : AssociateQuantitative Research : Equities Core Development : AssociateJPMorganChase, one of the oldest financial institutions, offers innovative financial solutions to millions of consumers, small businesses and many of the world’s most prominent corporate, institutional and government clients under the J.P. Morgan and Chase brands. Our history spans over 200 years and today we are a leader in investment banking, consumer and small business banking, commercial banking, financial transaction processing and asset management. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as mental health or physical disability needs. Visit our <a href="https://careers.jpmorgan.com/us/en/how-we-hire/faqs" rel="nofollow" target="_blank">FAQs</a> for more information about requesting an accommodation.<h4>Experience Level</h4>Mid Level

JP Morgan Services India Pvt Ltd

Research Analyst

Associate Manager - Market ResearchRazorpay was founded by<a href="https://www.linkedin.com/in/kumarshashank/" target="_blank"> Shashank Kumar</a> and<a href="https://www.linkedin.com/in/harshilmathur/" target="_blank"> Harshil Mathur</a> in 2014. Razorpay is building a new-age digital banking hub (Neobank) for businesses in India with the mission is to enable frictionless banking and payments experiences for businesses of all shapes and sizes. What started as a B2B payments company is processing billions of dollars of payments for lakhs of businesses across India. We are a full-stack financial services organisation, committed to helping Indian businesses with comprehensive and innovative payment and business banking solutions built over robust technology to address the entire length and breadth of the payment and banking journey for any business. Over the past year, we've disbursed loans worth millions of dollars in loans to thousands of businesses. In parallel, Razorpay is reimagining how businesses manage money by simplifying business banking (via<a href="https://razorpay.com/x/" target="_blank"> Razorpay X</a>) and enabling capital availability for businesses (via<a href="https://razorpay.com/capital/" target="_blank"> Razorpay Capital</a>). The Role: As an Associate Manager you should be able to understand the issues faced by the merchants in the Fintech ecosystem and solve these issues with data oriented insights. Role and Responsibilities :<ul><li>Taking briefs from various internal stakeholders and distilling problem statements that research can focus upon</li><li>Core competency -
<ul><li>Drafting research briefs, outlining key business and research objectives, selecting methodology for the objectives</li><li>Ability to draft questionnaires basis relevant study objectives for primary research</li><li>Insights - Drafting actionable insights to various stakeholders</li></ul></li><li>Coordination and management - External vendors, supervision of fieldwork, interviews with B2B merchants for various studies</li><li>Working with our internal data to cull out insights</li><li>Working with various stakeholders to implement key insights into our product/marketing/brand solutions</li></ul>Mandatory qualifications:<ul><li>Prior Work Experience - 4-5 years in a Market Research Agency like Kantar, Nielsen, Ipsos, Third Eye, Quantum or researchers who have moved from agency to working with a brand inhouse.</li><li>Exposure to both qualitative and quantitative research through their career</li><li>Experience working with technology/product focused brands</li><li>Inclination to work with B2B consumers on Fintech product/service oriented projects</li><li>Deriving insights from data (Should be able to work with Excel, SPSS or Google Data Studios)</li><li>Presentation Skills - Both verbal and written. Should be able to visualize insights in a user friendly, easy to consume manner using PPT, Google Slides or any form of dashboarding.</li></ul> Razorpay believes in and follows an equal employment opportunity policy that doesn't discriminate on gender, religion, sexual orientation, colour, nationality, age, etc. We welcome interests and applications from all groups and communities across the globe.  Follow us on <a href="https://www.linkedin.com/company/razorpay/mycompany/" target="_blank">LinkedIn</a> &amp; <a href="https://twitter.com/Razorpay" target="_blank">Twitter</a><h4>Experience Level</h4>Mid Level

Razorpay Software Pvt Ltd

Market Research Associate

Formulation Scientist<h4>Company Description</h4>Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable.  Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.<h4>Job Description</h4>Job Summary We are seeking a dynamic and experienced Formulation Scientist in Injectable division for designing and development of formulation process, ensuring quality by design (QbD) implementation, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. Roles &amp; Responsibilities <ul><li>You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval.</li><li>You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. </li><li>You will be responsible to support in scale-up to pilot/plant scales for Injectable Products.</li><li>You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions.</li><li>You will be responsible for technology transfer and execution of the batches. </li><li>You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up).  </li><li>You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. </li><li>You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. </li></ul><h4>Qualifications</h4>Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products.  Skills &amp; attributes:   Technical Skills<ul><li>Have work experience on Formulation Development and expertise in inhalation/injectable dosage form.</li><li>Experience in areas of product development for Generic Injectable</li><li>Experience in Quality by Design (QbD).</li><li>Experience in Process Optimization and scale up.</li><li>Experience in Operational Excellence.</li><li>Knowledge on Good Manufacturing Practice and Good Laboratory Practice.</li><li>Experience in Technology Transfer.  </li></ul>Behavioral Skills<ul><li>Excellent communication and interpersonal skills.</li><li>Strong analytical and problem-solving abilities.</li><li>Ability to work collaboratively with own team and cross-functional teams. </li></ul><h4>Additional Information</h4>About the DepartmentIntegrated Product Development Organisation                                         We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/  <h4>Experience Level</h4>Senior Level

Analytical Chemist

R&D Global Supply Study SupportJob Tittle: R&amp;D Global Supply Study SupportLocation - HyderabadAbout the jobAt Sanofi R&amp;D, we develop future medicines that improve patients' lives worldwide. Our Clinical Supply Chain Operation (CSCO) department is responsible for packaging and distributing Investigational Medical Products (IMPs) to patients globally for clinical testing. The Global Supply Study Support (GSSS) provides support - on activities that can be centralized - to a worldwide team of CSC SL (Clinical Supply Chain Study Leader) located mainly in USA, France and China in charge to coordinate the flow of our investigational products ensuring quality, timely delivery, regulatory compliance, and accurate tracking through our internal systems.The GSSS will report to the GSSS Team Leader (India) and interact with the Clinical Supply Chain stakeholders.Main responsibilities include:Common : Clinical Trial &amp; Supply Knowledge<ul><li>Understanding of clinical trial design, protocols, regulatory requirements (GxP)</li><li>Understanding of clinical endpoints, patient randomization processes, study arms, dosing regimens, cohort management, stratification factors</li><li>Understanding of investigational product management in clinical trial including kit types, shelf life,  IMP production plan, depot management, IMP distribution, IMP reconciliation, returns/destruction.</li></ul>Level 1 responsibilities:<ul><li>Create and manage transfers to depot in IRT, customize them in Sanofi supply tool and maintain the Inventory Product Stock Management (IPSM) tracker.</li><li>Manage destruction of expired IMP and AxMP throughout the study lifecycle, performing appropriate actions in related Sanofi tools (ERP, RAID…)</li><li>Monitor IRT interface failures with Sanofi supply tools and promptly alert the CSC SL. </li><li>Support CSC SL by accurately capturing supply plans in Sanofi Clinical Supplies tools (ERP)</li><li>Perform global reconciliation of studies in Sanofi supply tools and follow up discrepancy investigations with appropriate stakeholders (CSC SL, IPMs, CRA, Investigational sites)</li><li>Provide filing and archiving support for IMP-related documents, including uploading documents into eTMF to ensure inspection readiness.</li></ul>Level 2 responsibilities:<ul><li>Support the CSC SL in monitoring IMP and AxMP stock levels throughout the study. Alert Promptly CSC SL in case of shortage risk.</li><li>Assist the CSC SL in tracking shipments throughout the study duration.</li><li>Prepare and Maintain mandatory shipment documentation prior shipment preparation (value for custom, country-specific documentation, study pre-requisite documents)</li><li>Support the CSC SL in preparation for regulatory inspections.</li><li>Manage service provider purchase orders and invoices, ensuring regular financial tracking and compliance.</li></ul>About you<ul><li>Bachelor’s degree required (advanced degree preferred, scientific discipline preferred) with at least 2 years of operational experience in pharmaceutical production, Supply Chain, Quality and/or clinical trials.</li><li>Basic knowledge of clinical development, Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP).</li><li>Strong organizational skills with ability to manage multiple concurrent tasks efficiently.</li><li>Demonstrated ability to work autonomously with methodology approach to meet guidelines and deadlines.</li><li>Experience working in a global, multi-cultural, multidisciplinary environment.</li><li>Effective communication both written and verbal</li><li>Adaptability to changing and challenging work environments, including technical environments changes.</li><li>Near-native fluency written and spoken in English</li><li>Proficiency with MS Office applications (Word, Excel, SharePoint, PowerBI) and clinical trial digital applications (IRT, ERP, Veeva, etc.)</li><li>Pursue progress, discover extraordinary</li></ul><h4>Pursue progress, discover extraordinary</h4>Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our <a href="https://www.youtube.com/watch?v=SkpDBZ-CJKw&amp;t=67s" rel="noopener noreferrer" target="_blank">ALL IN video</a> and check out our Diversity Equity and Inclusion actions at <a href="https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness" rel="noopener noreferrer" target="_blank">sanofi.com</a>!<h4>Experience Level</h4>Mid Level

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