295 Technology Transfer Jobs

We are looking for a highly skilled and experienced Test Pilot (UAV) to join our team at Marvel Geospatial Solutions Pvt Ltd. The ideal candidate will have 7-8 years of experience in the IT Services & Consulting industry, with expertise in UAV technology. Roles and Responsibility Develop and implement test plans for UAV systems to ensure they meet required standards. Conduct thorough testing and evaluation of UAV systems to identify defects and areas for improvement. Collaborate with cross-functional teams to resolve issues and enhance system performance. Analyze data from tests and provide recommendations for process improvements. Stay up-to-date with industry trends and advancements in UAV technology. Participate in developing best practices and standards for testing UAV systems. Job Requirements Strong understanding of UAV technology and its applications. Experience with testing and evaluating complex systems. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills. Familiarity with industry standards and regulations related to UAVs.

As a Product Manager at Hyuman, you will play a crucial role in the end-to-end product development process, ensuring that our skincare products embody our commitment to self-care and innovation. You will lead the way from concept to commercial execution, driving technology transfer and liaising with vendors to deliver quality and intentional skincare solutions to empower women to feel confident in their skin. Your responsibilities will include managing the procurement of ingredients and materials, collaborating with internal teams for timely product launches, and ensuring consistency and quality throughout the product lifecycle. You will troubleshoot manufacturing issues, support lab testing, and assist Quality Control in upholding supply chain standards. Building strong relationships with vendors, suppliers, and R&D collaborators will be essential, along with identifying opportunities for innovation and efficiency within the vendor network. To excel in this role, you should have a Bachelor's degree in cosmetology, Chemistry, Pharmacy, or a related field, along with 2-3 years of experience in the personal care, cosmetics, or beauty industry. A strong understanding of product development and brand vision is crucial, as well as excellent communication and stakeholder management skills. You should be comfortable making agile decisions and multitasking across teams to drive the success of our skincare products at Hyuman.,

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. Your responsibilities will include developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines. You will be responsible for preparing and maintaining validation protocols, analytical reports, and ensuring compliance with Good Documentation Practices (GDP). Additionally, you will oversee method transfer to QC, provide training, and address any troubleshooting issues that may arise. Conducting stability studies, preparing data reports, and collaborating with cross-functional teams to support product development will also be part of your role. Furthermore, you will be expected to investigate and resolve analytical issues, including OOS, OOT, and deviations, and implement Corrective and Preventive Actions (CAPAs) as necessary. Maintaining up-to-date documentation and ensuring compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) will be integral to your responsibilities. You will also evaluate vendors and key starting materials (KSMs) and provide insights to management based on your findings. In terms of past experience, you should have a strong understanding of analytical chemistry principles and techniques, including HPLC, GC, Dissolution, and UV-Vis. Proven experience in method development, validation, and regulatory compliance is crucial for this role. Familiarity with global pharmaceutical regulations such as those from the FDA, EMA, WHO, and ICH guidelines is essential. You should also be skilled in handling regulatory submissions and documentation, possess excellent problem-solving abilities, and have experience mentoring R&D scientists. Familiarity with CAPA systems and good documentation practices will further strengthen your candidacy for this position.,

About Rubicon Research: Rubicon Research Limited is a fast-growing pharmaceutical formulation company dedicated to delivering value to customers and investors through the development, manufacturing, and marketing of branded specialty and generic prescription pharmaceutical products in regulated markets. With a product portfolio of over 250 SKUs across more than 70 product families, Rubicon Research has established a strong presence in the US market through its subsidiaries AdvaGen Pharma and Validus Pharmaceuticals. The company operates two US FDA-inspected R&D facilities in India and Canada, along with manufacturing facilities in Maharashtra, India, equipped with various drug development and manufacturing capabilities. Headquartered in Thane, India, Rubicon Research also maintains a sales and marketing office in New Jersey, USA. For more information, please visit www.rubicon.co.in. Position Title: Senior Executive-Formulation Development Type: Full-time Location: Thane, Maharashtra. Key Responsibilities: - Develop new products and optimize existing formulations for various dosage forms (Tablets, Capsules, Solutions, Suspensions, Pellets, MUPS) targeting regulated markets like the US, Europe, and ROW. - Conduct literature and patent searches, reviews, discussions, and documentation. - Perform API characterization, preformulation studies, and other related activities. - Plan and execute laboratory experiments on a daily basis. - Develop prototype formulas, optimize formulations and processes. - Prepare relevant documents such as MFC, BMR, STP, PDR, CPS, etc. - Collaborate with other departments including Stores, QA, RA, BD, IP sphere, CTS site, etc. - Coordinate with the Analytical Group for regular analysis of experimental samples. - Ensure effective execution of technology transfer activities at the manufacturing site. Qualifications & Pre-Requisites: - Master's in Pharmacy (Pharmaceutics). - Must-Have Skills: Formulation development experience in Solid & Liquid Oral products; experience with Pellets projects is preferred.,

As an Assistant General Manager (AGM) Formulation Development specializing in Injectable dosage forms, you will be responsible for the development, scale-up, and validation of both simple and complex formulations for Injectable products. Your primary focus will be on creating dosage forms compliant with regulations in the US, EU, India, Canada, Brazil, and other markets. Your key responsibilities will include: - Developing Injectable dosage forms for various global markets - Scaling up and transferring technology for Injectable products across different regions - Designing formulation strategies and overseeing the drug product development roadmap - Reviewing stability data of products under development and during validation batches - Handling regulatory queries and conducting studies as necessary - Coordinating with internal departments and external vendors for drug product development - Troubleshooting product and process failures, particularly for US, EU, and other markets - Providing technical guidance to subordinates and ensuring compliance with laboratory practices and safety regulations - Following Good Documentation Practices and Data Integrity requirements during GxP operations - Ensuring understanding and adherence to Data Integrity requirements and consequences - Reviewing data for compliance with Data Integrity requirements in the context of job responsibilities Your role will be crucial in ensuring the successful development and validation of Injectable dosage forms for multiple markets, requiring strong technical expertise, regulatory knowledge, and attention to detail.,

Raynas Infra & Geomatics services is looking for Drone Operator / Pilot (DGCA Pilot License) to join our dynamic team and embark on a rewarding career journey Operate drones for various applications. Conduct pre-flight and post-flight inspections. Ensure compliance with safety and regulatory standards. Maintain and update drone equipment. Collaborate with team members on drone projects. We required Geomatics Engineer with minimum Qualification of (BE/BA/Bsc/B-COM/B-tech/M-tech in any Stream) Working knowledge of Mission Planner Software and DJI Phantom 4 Pro V2,Idear Forge Nijja Drone.

As a Senior Chemist in the Pharma Manufacturing Industry located in Vatva, Ahmedabad, your role will involve utilizing your M.Sc. in Organic Chemistry and 5 to 8 years of experience in API / Intermediates manufacturing within the pharmaceutical sector. Your responsibilities will include hands-on experience in the synthesis of APIs and intermediates, conducting literature searches using platforms such as SciFinder, Chemical Abstracts, Free Patent Online, and Journals. You will be involved in feasibility studies, route selection for synthesis, multi-step synthesis, yield improvement, and cost reduction strategies. Additionally, you will be responsible for tasks such as extraction, purification, distillation, lab validations, process development with strong documentation including Tech reports, process safety reports, and cost sheets. Furthermore, you will lead technology transfer from the laboratory to kilo lab and plant scale, while coordinating with IPR, Regulatory Affairs, and QA departments. Proficiency in tools like Chemdraw / Chemsketch is essential for this role. Please note that only male candidates from the Pharma Manufacturing Industry will be considered for this position. If you are seeking a challenging full-time, permanent role that requires your expertise in organic chemistry and pharmaceutical manufacturing, we look forward to receiving your application. With Regards, Himani(HR) 9377165778,

As a Manager-II in the MSTG department at Sun Pharmaceutical Industries Ltd, your primary responsibility will be to provide support for the execution and monitoring of trial, scale up, exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheet, master formula card, bill of material, master formula, risk assessment reports, sampling protocol, reports, exhibit batch manufacturing record, and exhibit protocols. Additionally, you will be required to prepare regulatory responses and share process knowledge with cross-functional departments through presentations for smooth technology transfer. You will play a key role in reviewing and evaluating product history and process parameters for technical remediation and improvement of product robustness. Your duties will also include preparing and submitting investigation reports for OOS, OOT, and any failure during exhibit/validation/commercial batch manufacturing and stability testing. Furthermore, you will be responsible for tracking activities related to change control, CAPA, planned deviations, unplanned deviations, and more. Your role will involve preparing and reviewing product containment approaches, risk assessment reports for new products, elemental impurities, Nitrosamine impurities, and residual solvent. You will also be tasked with arranging placebos for quality control testing, change part development, and evaluating the feasibility of products. Statistical evaluation for process assessment, preparation and review of standard operating procedures, training schedules, conducting training sessions, and participating in regulatory audits to support the plant will also be part of your responsibilities. Overall, as a Manager-II in the MSTG department, you will be at the forefront of ensuring the quality and compliance of processes and procedures while contributing to the continuous improvement and development of new products within the organization.,

As a bench scientist in our organization, you will be responsible for conducting experimentation and research in the area of formulation development, process development, regulatory affairs, and intellectual property for global markets. Your work will involve planning and executing experiments aligned with project milestones while applying scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be expected to analyze and interpret data from literature reviews effectively to support decision-making processes. Additionally, you will need to understand the intellectual property landscape, develop strategies, search for prior art, and establish proof of concept through experimentation. Collaboration with cross-functional teams including Manufacturing Science and Technology (MS&T), Quality Assurance (QA), Quality Control (QC), and production teams across different geographies will be crucial for technology transfer and timely execution of submission batches. Your role will also involve identifying challenges, bottlenecks in development, and providing mitigation proposals at various stages of product development. Furthermore, you will be responsible for problem-solving, prioritizing activities, conducting development trials, and ensuring alignment with established milestones. Clear communication with internal stakeholders, proactive identification of challenges or risks, and adherence to business unit Key Performance Indicators (KPIs) will be essential aspects of your role. On a day-to-day basis, you will work closely with the formulation development teams to achieve key milestones, conduct experiments following QbD principles, and prepare presentations at different stages of product development. Your tasks will include literature reviews, sourcing API and Excipients, conducting preformulation studies, executing development trials, interpreting analytical data, and preparing necessary documentation for regulatory submissions. To be successful in this role, you should hold a Ph.D. in Pharmaceutical Sciences with at least 1 year of experience or an M.Pharm in Pharmaceutical Sciences with a minimum of 3 years of experience from reputable universities. Prior experience in working with generic pharmaceuticals in regulated markets such as the US, EU, or Canada will be advantageous. Your commitment to personal accountability, effective work habits, continuous learning, and collaboration with internal teams will be instrumental in contributing to the success of our organization's mission to make good health more affordable and accessible globally.,

KPMG India is looking for Executive - Government Technology Executive - Government Technology to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Develop tablet/capsule formulations for regulated markets (US/EU). Conduct pre-formulation, prototype trials, and scale-up. Execute lab, exhibit, and validation batches. Prepare technical documents for ANDA filings. Support tech transfer and respond to regulatory queries.

Specialized expertise in Inhaler Products including Metered Dose Inhalers (MDI) and Dry Powder Inhalers (DPI). Method development, validation, and forced degradation studies specific to inhalation dosage forms. Execution and support of technology transfer for analytical methods related to MDI/DPI. Ensure compliance with Quality Assurance systems and applicable regulatory guidelines (ICH, FDA, EMA). Lead analytical activities for ANDA and NDA projects for respiratory products. Coordinate with cross-functional teams for project planning, documentation , and timely regulatory submissions. Review and preparation of analytical method validation protocols, reports, and supporting documentation for regulatory filings. Active involvement in OOS/OOT investigations, troubleshooting, and CAPA implementation.

Lead formulation and process development of HFA-based MDI products for regulated markets (US, EU, etc.). Manage drug-device combination product development , including coordination with device vendors for CMC and regulatory compliance. Coordinate cross-functionally with analytical, regulatory, clinical, and manufacturing teams to ensure timely project execution. Drive process optimization at the lab scale using QbD principles; establish control strategies for successful scale-up. Design and define product specifications in compliance with current global regulatory guidelines. Review Product Development Reports, Technology Transfer Reports , and Deviation/Investigation Reports for technical accuracy. Support regulatory query responses related to product development and manufacturing in collaboration with relevant departments. Lead technology transfer of HFA-based MDIs to contract manufacturing organizations (CMOs) for domestic and international markets. Provide technical and regulatory support for submissions including NDA, ANDA, and 505(b)(2) applications. Troubleshoot formulation-related issues during manufacturing to ensure smooth and compliant commercial production.

We are looking for a Chief Technology Officer (CTO) to provide sound technical leadership in all aspects of our business. You will communicate with employees, stakeholders and customers to ensure our companys technologies are used appropriately. Strategic thinking and strong business acumen are essential in this role. We expect you to be well-versed in current technological trends and familiar with a variety of business concepts. If you are also an excellent communicator and public speaker, wed like to meet you. Responsibilities Develop technical aspects of the companys strategy to ensure alignment with its business goals Discover and implement new technologies that yield competitive advantage Help departments use technology profitably Supervise system infrastructure to ensure functionality and efficiency Build quality assurance and data protection processes Monitor KPIs and IT budgets to assess technological performance Use stakeholders feedback to inform necessary improvements and adjustments to technology Communicate technology strategy to partners and investors Requirements and skills Proven experience as a CTO or similar leadership role Knowledge of technological trends to build strategy Understanding of budgets and business-planning Ability to conduct technological analyses and research Excellent communication skills Leadership and organizational abilities Strategic thinking Problem-solving aptitude BSc/BA in Computer Science, Engineering or a related field; MBA or other relevant graduate degree is a plus

Notice Period Immediate Primary Skills: Azure admin, Scale Sets, VM administration, Windows fileserver, Load Balancers, SQL server RDS, Azure Managed Disk, Basic networking, .NET Job Details Hand-on experience in Scale sets, .NET, Azure DNS, ALBs.Networking knowledge to understand the various components between cloud and on-prem infrastructure.Identify and resolving connectivity issue by opening ports, get through firewalls, NSG, whitelist ip addresses on both on-prem and Azure envs.Configure database connectionsConfigure VM image backups, Azure Managed Disk replication, Configure and Test DR solution.Configure SQL server RDS replication on DR site

Must have demonstrated experience and a track record of success as Cutover Manager / Lead on ERP transformations. Demonstrated through At least five years prior experience in having led SAP cutovers. Must have enterprise scale experience Develop and own the overall Deployment workplan. This should contain a list of deliverables and activities that will be executed by the Deployment workstream. Liaise with project teams to develop a detailed integrated cutover which include both technical and functional steps to be executed during the deployment phase. Identify risks, cross application dependencies and downstream impacts for each release. Manges risks and issues associated with the cutover and prepare appropriate mitigation plans Create and maintain a detailed Integrated Cutover Project Plan from inception, execution, and post-implementation. Determine go-live readiness criteria, socialize them with key stakeholders and obtain requisite approvals Plan and execute mock cutovers to help teams prepare for the final production cutover Responsible for ensuring successful planning and execution of integrated release cutover activities and associated systems' outages Leads cutover activities for Pre Go-Live, Go-Live and Post Go-Live Coordinates requirements for Go Live Monitor data and cutover progress and communicate to leadership team including status, progress. Manage the scope and schedule of cutover activities Provide detailed backout options for severe contingencies Ensure compliance with IT processes including proper documentation and securing approvals of requisite changes through our Change Advisory Board process Provide timely escalation to IT leadership where necessary. Liaise with the functional SAP experts and business teams in order to assist with the planning and execution of Deployment activities. Plans the resources, human and physical required for cut-over activities. Develops the communication and escalation plan. (policies, procedures, downtime processes etc Provides Cutover status reporting to the project leadership and key stakeholders. Ensures entry into and exit out of cutover stage gates are met including the final Go/No-Go meetings. Acts as the final point of escalation for all Cut-over issues, proactively bringing about appropriate interventions when the Cutovermay be jeopardized. Please Share below details and Updated Resume: MatchedYes/No:Full Name with Surname:DOB:Adhacard No(Mandatory):Alternate Contact Number:Total Experience:Relevant Experience:Current Location:Preferred Location:Current CTC :Expected CTC :Current Organization/ Contract with Current Org :Payroll Company:Notice period :Passport/ Expiry Date:Holding any offerYES/NO:

Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Temenos Transact Good to have skills : Temenos Transact DevelopmentMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your day will involve overseeing the application development process and ensuring seamless communication within the team and stakeholders. Roles & Responsibilities:- Must be able to understand the requirements, provide technical solutions and do development based on the requirements- Strong understanding of Retail/corporate/wealth banking/payment process - Prior experience of understanding and writing BRD, FSD, TSD IRD is must- Able to manage team members by allocating tasks on daily basis- Monitor & report completion status and issues to project manager Professional & Technical Skills: - Must Have Skills: Temenos Transact Development, Temenos Technical, AA, Java- Strong understanding of Core modules, Payments, SWIFT, TPH, Arrangement Architecture, Wealth, etc- Must have experience in AA, L3 customization (Version, Enquiry, COB, OFS, Info basic, Delivery module and packaging) IRIS, Java, Payment engine, Interface development, Integration Framework, Web-services, API Development- Ability to be flexible and work analytically in a problem-solving environment- Excellent communication written oral and interpersonal skills- Experience working in Agile environment- Ability to learn new client applications Additional Information:- The candidate should have a minimum of 5 years of experience in Temenos Transact- This position is based at our Hyderabad office- A 15 years full-time education is required Qualification 15 years full time education

As an R&D - M19 at PURE CHEMICALS CO in Chennai, Tamil Nadu, India, you will be responsible for conducting patent analysis, technical research, internet research, reaction and formulation work, and documentation. Your role will primarily involve product development, technology transfer, chemistry, and testing. You will work within the R&D department of the organization and collaborate with colleagues to contribute to the innovation and development of new products. The ability to analyze patents, conduct technical research, and document findings accurately will be crucial for success in this role. Proficiency in English and Tamil languages will be required to effectively communicate and collaborate with team members. A minimum qualification of MSC in chemistry or related field is necessary for this position. Join our team at PURE CHEMICALS CO and be a part of our innovative research and development projects in the chemical industry.,

You will be joining Honasa Consumer Limited (HCL), a rapidly growing Beauty & Personal Care conglomerate with a focus on honesty, natural ingredients, and safe care. HCL houses brands such as Mamaearth, The Derma Co., Aqualogica, and BBlunt, catering to consumers across 500 cities in India. The company's ethos revolves around innovative products, direct-to-consumer marketing, and e-commerce fulfillment, supported by investments from renowned firms like Sequoia Capital India and Sofina SA. As a key member of our team, you will need to possess a high level of technical proficiency and a proactive approach to working in the lab. This role demands expertise in leading cutting-edge technology and product development projects, particularly within the personal care industry, with a focus on skin and hair care. To excel in this position, you should hold a degree in B.Tech/M.Tech in Cosmetology, B.Sc./M.Sc. in Organic Chemistry, B.Pharm, or M.Pharm. Previous experience in the personal care sector, especially in skin and hair care, is crucial for this role. Your responsibilities will include overseeing all stages of product formulation, from concept development to final approval, and managing pilot and full-scale production batches. You will lead the creation of stable and effective formulations for manufacturing at third-party facilities and in-house labs, conduct research to support production processes, and develop new formulations in line with business needs and innovation targets. A deep understanding of skincare and hair care products is essential, along with hands-on experience in surfactant-based formulations and knowledge of surfactants, conditioning agents, and raw materials used in hair care products. You will be responsible for technology transfer activities, ensuring compliance with SOPs, cosmetic regulations, and safety standards, as well as identifying cost-effective raw material substitutes to enhance product quality. In this role, you will drive the development of new personal care products through scientific expertise and technical leadership. Your ability to navigate ambiguity, stay abreast of regulatory trends, and innovate within the industry will be instrumental in shaping our product portfolio and maintaining our competitive edge.,

As an R&D Executive at VTC R&D, you are responsible for performing and overseeing all activities related to formulation and filling process development. Your duties include having a strong understanding of optimizing vaccine formulations, selecting stabilizers and excipients, as well as preparing adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, and LNP formulation. You will also be involved in aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting existing vaccines. In this role, you will execute clinical drug product manufacturing for clinical batches, plan and carry out media fill activities, and maintain R&D lab documents, equipment, and area qualifications in compliance with GMP requirements. Additionally, you will be responsible for preparing process validation and technology transfer protocols as per GMP requirements and collaborating with QA, QC, and Engineering departments for viral vaccine development activities. Ensuring proper hygiene and entry exit procedures in the formulation and filling section, preparing adjuvants, buffer solutions, and other materials, as well as coordinating with the central warehouse department for materials receipt and entry are also part of your responsibilities. You will supervise the preparation of disinfectant solutions, cleaning solutions, integrity testing of filters, and sanitization and disinfection activities in the R&D formulation department. As part of the QMS, you will handle deviations, MDD, investigations, observations, and ensure their timely closure. You will be involved in preparing standard operating procedures, batch manufacturing records, QRM, and protocols related to the R&D formulation and filling section. Moreover, you will supervise the washing, drying, packing, and sterilization of materials required for R&D development and GMP clinical batch preparation. Your role as an R&D Executive will be crucial in advancing vaccine development and ensuring compliance with quality standards and procedures.,

As a Senior Manager in API Production, you will be responsible for overseeing the production activities at the Panoli (Baroda) location. With a background in B.Pharma/M.Pharma and a significant work experience of 17 to 19 years, you will lead a team of 150 to 200 members and manage a production capacity of a minimum of 50 Cr. Your role would involve handling various aspects such as Production Planning, Resource Management, and Regulatory Compliance within an API plant setting. Your key responsibilities will include coordinating Production Planning and scheduling on a day-to-day basis, ensuring the availability of necessary resources like BMR, Raw Material, and Manpower. You will collaborate with departments such as QC/QA/STORE/Eng. Dept. to address troubleshooting problems effectively. Upholding GMP Standards and overseeing the implementation of technology transfer for new products will be crucial in this role. Continuous improvement in product processes, efficiency, and services will be under your purview, along with documentation tasks like Monthly Reports, data analysis, and root cause analysis. Managing consumable items, planning Raw Material requirements, and ensuring proper documentation related to processes and cleaning activities are essential responsibilities. You will also oversee the handling of solvents, process waste, and maintenance of plant equipment while providing training to subordinates. Your role will involve operating electronic systems like ONE HR portal, Metis Track Wise, Minitab, and Outlook for efficient plant operations. Additionally, you will review and revise BMR and SOP as needed, ensuring compliance with regulatory standards and maintaining a high level of operational efficiency in the API production facility.,

Job Description As a part of Dr. Reddys Laboratories Ltd., a leading multinational pharmaceutical company with a global presence, your role is pivotal in accelerating access to affordable and innovative medicines. With a team of over 24,000 employees worldwide, you will contribute towards the collective purpose of ensuring that Good Health Cant Wait. Since our inception in 1984, we have grown exponentially to establish research and development centers, manufacturing facilities, and commercial presence across 66 countries. Our commitment to access, affordability, and innovation is unwavering, driven by deep science, progressive people practices, and robust corporate governance. In the ever-evolving pharmaceutical industry, we are seizing the opportunity to strengthen our core operations and pave the way for future growth. The Next and the New strategy focuses on being purpose-driven, future-ready, and sustainable. By aiming to reach over 1.5 billion patients globally by 2030, we are aligning our core businesses with sustainability at the forefront of our purpose and strategy, emphasizing respect for people, planet, and purpose. About Biologics At Dr. Reddys, our Biologics division is committed to making advanced medicines accessible to millions worldwide. With two decades of experience in developing high-quality global biosimilars, we have established ourselves as leaders in the biosimilars segment. Our focus on creating affordable yet effective generic biosimilars has enabled us to market 6 products in multiple countries with a robust development pipeline. As the biosimilar industry is poised for an 8X growth in the next 3-4 years, your role as Manufacturing Head will be pivotal in driving the transformation and scale-up agenda for the Biologics organization. This includes expanding capacity, ensuring facility readiness for regulated markets, implementing digital advancements, streamlining production planning, and strengthening manufacturing capabilities. Responsibilities In this role, you will: - Evaluate the organization's readiness for scaling operations and design a strategic roadmap for expansion. - Lead cross-functional teams in executing transformation initiatives and strengthening manufacturing and R&D capabilities. - Drive the adoption of innovative technologies and process enhancements to optimize performance at scale. - Track project milestones, analyze key performance indicators, and ensure progress aligns with objectives. - Implement change management strategies for seamless transitions to new processes and systems. - Utilize data analytics to improve decision-making, streamline operations, and enhance overall efficiency. - Identify, evaluate, and mitigate risks to ensure business continuity and regulatory compliance. - Oversee biosimilars drug substance manufacturing, ensuring compliance with GMP and regulatory standards. - Manage manufacturing services and technology teams to optimize production processes and improve efficiency. - Develop and implement manufacturing strategies to meet production goals and timelines. - Drive transformation initiatives to enable scale-up to 8X, achieving best-in-class productivity. - Ensure audit readiness of manufacturing plants and maintain quality control standards throughout the process. - Collaborate with cross-functional teams to support product development and commercialization. - Drive continuous improvement initiatives to enhance manufacturing capabilities and reduce costs. - Manage the technology transfer process for new products and processes and ensure compliance with safety, health, and environmental regulations. - Develop and manage the manufacturing budget, mentor team members, and foster a culture of innovation and excellence. Qualifications, Experience, Skills & Attributes - Bachelor's degree in Biochemistry, Biotechnology, Chemical Engineering, or related field (Advanced degree preferred). - Minimum of 15 years of experience in biologics manufacturing, with at least 5 years in a leadership role. - Extensive knowledge of biosimilars manufacturing processes, GMP, regulatory requirements, and quality control standards. - Proven experience in managing large-scale manufacturing operations, leading cross-functional teams, clearing FDA audits, and introducing new technologies for performance improvement. - Experience with single-use bioreactor technology, continuous manufacturing processes, process development, and technology transfer. - Familiarity with regulatory submissions, inspections, and managing budgets effectively.,

The Assistant Manager - Program / Project Management (Pharma) at Jubilant Generics Limited in Greater Noida will be responsible for managing Contract Manufacturers for different markets to ensure timely execution of identified Projects and uninterrupted supplies. Strong communication skills are essential for effective coordination with various teams. The candidate should have the ability to anticipate project-related issues and take timely actions to address them, ensuring availability of materials, timely completion of milestones, and launch of products in identified markets through constant stakeholder coordination. Responsibilities include leading end-to-end project lifecycle management for global regulatory and commercial projects, developing project timelines and risk mitigation plans, overseeing Analytical Method Transfer planning and execution, acting as a point of contact for international clients and internal teams, collaborating with cross-departmental teams, and ensuring deliverables meet regulatory standards of specific regions. Qualifications & Experience: - M.Pharm / B.Pharm from a reputed institution - PMP certification desired - 2 - 7 years of experience in program management in large / mid-sized Pharma Companies - Proficiency in Microsoft Office suite - Strong communication, organizational, analytical, and critical thinking skills Required Skills: - Microsoft Projects (MSP) - Project Plans and Charters - Technology Transfer Jubilant is an equal opportunity employer, committed to providing fair employment opportunities without discrimination based on various characteristics protected by local laws.,

About The Role Job description Job title: Data, Personal Loan Location: Head Office Mumbai Grade M3 Number of Position 1 Job Responsibilities: Monitor portfolio delinquencies at micro level, identification of segments, locations, channels, profiles and proposing policies/ strategies to enable business and control risk Proficient in coding and working experience in creating risk monitoring dashboards like vintage charts, KPIs, business trends, etc. Managing portfolio with data driven insights using Demog and Bureau data and recommend necessary alteration in policy when required Experience on creating features using bureau/demog/banking variables and creating insights Handled cross functional projects to develop new product/program Knowledge about policy framework pertaining to personal loan product/Unsecured product Monitoring loss in the business in different segments and highlight the reason for breach in threshold if any. Automating crucial reports, testing and verifying the correctness of the same. Co-ordinating with different stockholder for risk and policy related data and recommendation. Job Requirements: Minimum 3-8 year of experience Work experience with MNC on risk/data analytics field is preferable Proficiency in SAS/Python/DEX for risk management and policy implementation. Ability to debug, troubleshoot and resolve issues related to risk and policy. Use analytical skill to identify root causes of problem and recommend effective solution. Experience in creating features and running decision tree/cluster analysis to identify segments will be an added advantage. Good problem solving skills and clear communicator. Education qualification: Btech or Grad/Post Grad in statistics - Preferred Certification in coding languages like SAS/SQL/Python Preferred

Research In Agro Intermediate And Chemicals Doing Lab trials as per Instructions Analysis of results Follow safety rules and regulations Maintain data of all the Lab Experiments Preventive maintenance and improvement activities Statutory compliance Required Candidate profile M. Sc or Ph. D with Chemistry 2 to 9 years of Experience in Agro , Specialty Chemical , Fine chemical , Intermediate , Dyes , Pigment , Etc. Reporting to Local Unit Head - Research And Development