336 Technology Transfer Jobs

The role involves planning and resource allocation for routine operations within the analytical development function. You will be responsible for ensuring timely analysis of finished products and raw materials for various projects. Your duties will include reviewing analytical data, raw data, daily usage logbooks, and lab notebooks to support operations. You will also be involved in preparing and reviewing critical documents such as Analytical Method validation protocols, reports, method transfer protocols, and Standard Operating Procedures (SOPs). Additionally, you will conduct literature searches and provide guidance on new method development. Another key aspect of the role is to review data for stability studies and ensure timely analysis of samples. You will need to identify resource needs and initiate procurement to prevent delays in project deliverables. Supporting product technology transfers and ensuring compliance with safety measures will also be part of your responsibilities. In terms of quality management, you will be required to raise change controls, ensure data integrity, and adhere to Good Manufacturing Practices (GMP). You will also handle documentation related to Quality Management Systems (QMS), Environmental Management Systems (EMS), and Occupational Health & Safety Assessment standards. As part of your job authority, you will review analytical data, plan and allocate resources, prepare and review SOPs, and technology transfer documents. You will also review calibration data, logbooks, and lab notebooks, as well as identify and report any near misses, hazards, or unsafe conditions. Other responsibilities include implementing QEHS policies and objectives, ensuring the use of personal protective equipment (PPE) during operations, and managing incidents and non-conformities effectively. You will also oversee work permit systems during maintenance activities and ensure proper waste disposal procedures are followed.,

Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global health Novo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you'll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). Apply Now! As a Manufacturing Specialist (SME), you'll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top-tier quality with our Contract Manufacturing Organizations (CMO) partners. Your key responsibilities will include leading cross-functional teams, ensuring seamless collaboration between Novo Nordisk as the sending Unit and Contract Manufacturing Organizations (CMCOs) partners as the receiving Unit. You will also act as a mentor and support Contract Manufacturing Organizations (CMOs) to ensure Novo Nordisk products are manufactured to the highest quality standards. Providing training, sharing best practices, and reviewing and approving validation documents to safeguard compliance will be crucial aspects of your role. Additionally, you will offer oversight and support during the planning and execution of validation and qualification activities. You will define, manage, and deliver on complex projects in collaboration with CMOs, Quality Assurance, and project managers. Driving problem-solving initiatives and providing scientific and technical solutions within tight project timelines will be key responsibilities. Qualifications for this role include a Bachelors or Masters degree in engineering, 10+ years of experience, and relevant 5 years of manufacturing experience, especially in an international, multicultural environment. Expertise in aseptic manufacturing processes is non-negotiable. The ideal candidate should be capable of communicating naturally and effectively with stakeholders at all levels, adept at finding solutions, and motivating stakeholders to achieve ambitious goals. Possessing a strong mindset, a focus on continuous improvement, and keen attention to detail is essential. Demonstrating the ability to work independently with minimal supervision, a strong willingness to learn new skills, and the motivation and flexibility to thrive in a fast-paced, dynamic environment are also important qualities. The GCM DP RoW Projects department is dedicated to delivering life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department plays a pivotal role in improving the quality of life for patients living with diabetes and obesity. With a focus on Market Access initiatives, the team tailors projects to meet the unique requirements of each country, offering exciting growth opportunities. The department thrives on innovation and problem-solving, overcoming challenges and navigating complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Based in Hyderabad, India, you'll join a diverse and dynamic team committed to making a difference. Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Join us and be part of a collective effort to change lives and go further together. To submit your application, please upload your CV online. Apply now and join us in making a difference.,

Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients" lives Do you thrive in an international environment where cultural awareness is key to your success If so, this could be your dream role! Apply Now! As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organization (CMO) partners. You will ensure the seamless Technology Transfer and manufacturing of our commercial products, always upholding Novo Nordisk's stringent quality standards and adhering to cGMP and regulatory requirements. Your responsibilities will include leading and managing aseptic manufacturing projects, specifically leveraging your expertise in areas like Formulation/Compounding, Filling, Washing & Sterilizations, Environmental Monitoring, or Clean Utilities. Additionally, you will be developing and managing detailed project plans and timelines, and communicating effectively with steering groups and key stakeholders. Monitoring progress and proactively securing necessary resources, as well as developing project risk grids and identifying mitigation strategies with both Novo Nordisk and our Contract Manufacturing Organization (CMOs), will be vital aspects of your role. Qualifications required for this position include a Bachelors or Masters degree in engineering, 5-12 years of project management experience with a proven track record of successful project delivery in a highly regulated environment, especially internationally. Aseptic manufacturing experience is a must, and experience with Technology Transfer of biologics is a significant advantage. Professional experience balancing individual drive with effective stakeholder involvement, proficiency in project management software (e.g., MS Project, Smartsheet, Jira, or equivalent), and demonstrated fluency in written and spoken English is essential. GCM DP RoW Projects is a dedicated team committed to providing life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department strives to make a meaningful impact on the quality of life for patients living with diabetes and obesity. Our projects are tailored to meet the unique requirements of each country, offering exciting growth opportunities. With a steadfast commitment to innovation and problem-solving, we work to overcome challenges and navigate complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Join us in making a difference. Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognise the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we're working toward something bigger than ourselves, and it's a collective effort. Join us! Together, we go further. Together, we're life-changing. To submit your application, please upload your CV online (click on Apply and follow the instructions). Deadline for application submission: 8 August 2025. Please note that instances of fraudulent job offers have been reported, purporting to be from Novo Nordisk and/or its affiliate companies. Novo Nordisk does not extend unsolicited employment offers and does not charge prospective employees for any reason.,

You will be joining our team as a Deputy Manager/Manager, Analytical method transfer, responsible for delivering developed analytical assays from R&D scale to GMP-compliant commercial quality control labs. Your role will involve overseeing projects related to analytical method transfer, collaborating with cross-functional teams, and ensuring technology transfer and assays qualification activities are conducted in compliance with GLP and GMP standards. The ideal candidate will possess expertise in cGMP, regulatory requirements, technical troubleshooting, method transfer, method validation, technology transfer, and laboratory techniques to support routine testing and release of research and cGMP grade materials. You will be directly involved in drafting technology transfer documents, risk assessments, process FMEA, method validation protocols, facility fit assessments, and other related activities necessary for the release and testing of microbial and mammalian fermentation-based products. You should have familiarity with analytical assays such as HPLC, GC, SDS-PAGE, agarose gel electrophoresis, densitometry, dd-PCR, RT-PCR, ELISA, UV-Visible spectrophotometry, western-Blot, as well as microbiological techniques like BET, BioBioburdend Sterility testing. Additionally, the position may entail assisting in cell bank testing and release under cGMP regulations and coordinating with third-party collaborators for external testing as needed. Your responsibilities will also include authoring and reviewing research studies, compiling experimental data, and contributing to protocols, study reports, and publications with minimal supervision. You will work as part of the method transfer and method validation team, ensuring timely and successful completion of process transfers while addressing any unexpected technical challenges. We are looking for individuals who are enthusiastic, highly motivated, and capable of multitasking. The role requires working collaboratively within a team environment and independently across various aspects of projects related to microbial-derived products.,

Role & responsibilities Responsible for formulation and process development (QbD approach) of following categories of Pharmaceutical products: Oral Immediate-Release Dosage Forms. Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology. Topical Semisolids (Creams, Ointment and Gels). Oral Liquid Dosage Forms Topical Liquid Dosage forms. Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications. Design and execute formulation trials and evaluate stability data to finalize formulation composition. Execution of technology transfer batches for manufacturing processes from laboratory scale to production scale. Oral Immediate-Release Dosage Forms. Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology. Topical Semisolids (Creams, Ointment and Gels). Oral Liquid Dosage Forms Topical Liquid Dosage forms. Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications. Knowledge of patent non infringing strategy based product development Knowledge of Bioequivalence study & clinical study protocol and criteria Independent contributor for batch planning, batch execution & technology transfer Develop manufacturing processes for R&D formulations so that the technical transfer is successful for large-scale batches. Responsible for all formulation/ process related CMC documents which will be part of regulatory filings. Write/review master formulas, manufacturing procedures, SOPs, stability protocols, process validation protocols, Product Development Reports etc. Prepare/review specifications for pharmaceutical products and packaging components, etc. Support the manufacturing of exhibit/submission batches per regulatory requirements. Work with Cross-functional teams (Analytical, Regulatory Affairs, Pharmacovigilance, Bioequivalence, Quality Control, Quality Assurance, Inventory Control, etc.) to expedite the development and approval of new products by different Agencies for Regulated and ROW Markets. Assure that all formulation and process development activities are documented in the notebook as per company procedures and cGLPs. Provide recommendations for continuous improvements in practices and systems to improve performance and enhance efficiency and quality. Communicate with outside vendors and laboratories. Preferred Skill Set: Thorough knowledge of the pharmaceutical industry, particularly drug delivery industry, and formulation and process development including guidelines. Knowledge for development of formulations comes under category of medical devices, Dietary Supplements and Cosmetics. Knowledge of ICH/GMP regulations. Behavioral /Managerial Skill Sets Skills building and maintaining productive relationships with organizational partners including teamwork. Skills related to develop and deliver products well with in specified timelines. Being a team player Appropriate communication with all stakeholders

Responsible For Design & Development, Optimization And implementation Of Chemical Processes within a Manufacturing Plant Lead Executives , Manage Projects, Ensure Safety And Quality Leading Role In Process Development, Innovation And Optimization Required Candidate profile BE - ME - Chemical From Reputed Institute Candidate Should Have Worked In Pilot Plant & Plant Deep Knowledge Of Troubleshooting And Problem-Solving Capable To Allocate Responsibility To Team Member

About The Role Job Title - GN -Health Japan Bilingual Consultant Management Level: 9-Team Lead/Consultant Location: Bengaluru, BDC7A Must-have skills: Positive Change Management Good to have skills: Ability to leverage design thinking, business process optimization, and stakeholder management skills. Job Summary : This role involves driving strategic initiatives, managing business transformations, and leveraging industry expertise to create value-driven solutions. Roles & Responsibilities: Provide strategic advisory services, conduct market research, and develop data-driven recommendations to enhance business performance. As a part of the Accenture Health & Public Services practice, our 4000+ practitioners across the globe, help our clients make a meaningful impact on patients lives through New Science, novel medical technologies and better collaboration. Together, lets deliver more effective, affordable, personalized patient outcomes. In this practice, youll help drive our Healthcare clients strategy and business planning efforts, with the following initiatives Support small to medium-size teams to deliver management consulting projects for global clients. Help define commercial strategy, strategy implementation, market scoping, customer journeys, go-to-market strategy and process improvement. Contribute as a part of pursuit teams, develop proposals and support efforts of the global sales team to win potential opportunities within the practice. Build the practice and track metrics. Also, develop assets and methodologies, point[1]of-view, research or white papers, internal tools or materials for use by larger community. Acquire skills that have utility across Health industry groups. Draw insights from complex financial and quantitative analysis and integrate these findings across work streams and come up with an overall plan to drive strategy and solution development. Structure and implement forecasting models and identify transformation opportunities. Identify companys key cost and value drivers and explain their priority and influence on business performance. Develop strategies and operating models focused on 1 or 2 business units and assess likely competitive responses. Also, assess implementation readiness and points of greatest impact. Manage proposals and business development efforts and coordinates with other colleagues to create consensus driven deliverables. Execute a transformational change plan aligned with clients business strategy. Engage stakeholders in the change journey and build commitment for change. Demonstrates good sales acumen, apply client knowledge, Accenture sales, opportunity management and contract processes to structure high impact solutions for clients. Lead presentations for the entire project with the client. Advocate a point of view and orchestrates, address difficult questions during presentations Bring your best skills forward to excel in the role: Health Industry expertise (optional) on how care delivery is managed across different settings and different channels Proven team handling skills with an ability to engage effectively with multiple stakeholders Ability to solve complex business problems and deliver client delight Strong writing skills to build point of views on current industry trends Good analytical and problem-solving skills with an aptitude to learn quickly Excellent communication, interpersonal and presentation skills Cross-cultural competence with an ability to thrive in a dynamic environment Professional & Technical Skills: - Relevant experience in the required domain. - Strong analytical, problem-solving, and communication skills. - Ability to work in a fast-paced, dynamic environment. Additional Information: - Opportunity to work on innovative projects. - Career growth and leadership exposure. About Our Company | Accenture Qualification Experience: 8-10Years Educational Qualification: Any Degree

Responsible for software development projects involving design, development, testing, debugging and implementation of software applications and source code to support end users needs. This is an operational role, responsible for driving day-to-day operations. Responsibilities Participate in designing discussions, planning meetings. Developing the new application/software based on the business requirements. Translating designs into high quality code at all levels of SDLC Involve in defining infrastructure and deployment requirements. Build and maintain operational tools for testing, deployment, monitoring, and analysis. Integrate software components and third-party programs. Develop, test, troubleshoot, debug and upgrade software across a wide array of services and functional areas. Create technical documentation for reference and reporting. Involve with Product Owners and teams in story grooming, backlog maintenance and prioritization and planning. Prepare Test Strategies and Test Design Identify tools and approach for automated testing. Generate Test reports and based on the features, modules, severity, and releases based.Desired Skill sets Expert code/test case writing skills Ability to develop unit testing of code components or complete applications. Understand concepts of software engineering. Experience with software design, coding, testing and development. Knowledge and/or experience in scrum/Agile techniques.

* Process development, scale up and technology transfer of products from R&D to Pilot plant upto commercial batches to production department as per regulatory requirement * Day to day lab experiment planning & to ensure execution Required Candidate profile * To ensure requirement of raw materials as per experiment planned in R&D and pilot plant. *Complete literature search with IPR status study, ROS finalization, lab experiment planning.

-Conduct feasibility studies, scale up studies and technology transfer. -P&ID, BFD, heat balance & mass balance & HAZOP studies & provide technical inputs. -Design and calculate heat exchangers, utilities, pipe sizing, and for other equipment Required Candidate profile -Drive demo-commissioning scale-up in lab & pilot plant and to ensure successful transfer to commercial scale. -To do process improvements cost reduction and troubleshooting in plants.

One of India's fastest growing consumer health platforms -- Clinikally -- is seeking an ace Clinical Researcher to lead crucial areas of clinical research. As a Clinical Researcher at Clinikally, you will be responsible for conducting thorough and in-depth clinical research on the science supporting Clinikally's consumer health solutions. Your role will involve collaborating with clinical partners worldwide to carry out efficacy studies on various over-the-counter (OTC) and prescription-grade products focusing on dermatology and nutrition. Some of the solutions you will be investigating include the Hyaluronic acid serum, Vitamin C Serum, and a unique DMS technology-based moisturising lotion. The ideal candidate for this position should hold an MBBS + MD in Dermatology, or MBBS + DVD in Dermatology, PhD in life sciences, or an equivalent degree. Additionally, the candidate should possess a strong background in clinical research, with a preference for experience in clinical medicine, particularly dermatology, as evidenced by publications and participation in conferences. Proficiency in Technology Transfer and Research & Development (R&D) is essential, along with excellent teamwork and leadership skills. In this role, you will be expected to conduct robust, verifiable, and publishable research, including consumer pilots and clinical trials. You will also be required to provide research-based data to our Marketing & Branding Team to support the development and promotion of Clinikally's consumer health solutions.,

As an R&D Executive (Food Technologist) at our Mohali-based company, you will play a crucial role in leading New Product Development (NPD) and Technology Transfer projects with a specific focus on Nutraceuticals, Sports Nutrition, and Health Supplements. Your expertise in formulation, process innovation, and regulatory compliance will be vital in bringing science-backed products from the lab to the market. Your responsibilities will include managing NPD projects, ensuring compliance with FSSAI Nutraceutical Regulations, selecting ingredients based on scientific research, developing taste-masking strategies, conducting compatibility studies, validating nutritional information, and overseeing technology transfer to the production floor. Collaboration with cross-functional teams for cost optimization, process standardization, and sensory evaluation will be key aspects of your role. Preferred qualifications for this position include a B.Tech in Food Technology with a minimum of 3 years of industry experience in Sports Nutrition, Infant Nutrition, or Dietary Supplements. Proficiency in functional claim validation, regulatory documentation, and flavor optimization will be advantageous. This is a full-time position that offers health insurance, a yearly bonus, and requires fluency in Hindi. Your dedication to product innovation and commitment to quality will contribute significantly to our company's success.,

Job_Description":" Role : forward deployed engineer, to capture requirements, design and rapidy build/test and deploy to production. Multiple prototyping to production projects Skills: 10+ years experience .net development, co-pilot studio, AI integrations , SQL DB Strong communication skills Experience with large organizations /clients for atleast 2 years ","

1. Ensure QA oversight in product development lifecycle from pre-formulation to tech transfer 2.Review & approval of developmental protocols, reports & technical document 3. Readiness for audits and regulatory submissions - EU, USFDA, TGA Required Candidate profile 1. Work Location is Chengalpet 2. Qualified M.Pharm / M.Sc / B.Pharm 3. Minimum Exp of 7 to 10 yrs (in a DQA/QA role with pharma formulation R&D)

The Assistant General Manager - Nasal Spray Formulation Development will play a crucial role in leading the development of innovative nasal spray formulations within the Research & Development (R&D) department of a Pharmaceuticals company. Reporting to the Head of R&D, you will be responsible for driving projects from concept to commercial scale-up, ensuring regulatory compliance and meeting quality standards. Your primary focus will be on designing, developing, and optimizing nasal spray drug products for global markets. Key Responsibilities: - Develop and technology transfer Nasal Sprays, Dry Powder Inhalers, and Soft Mist Inhalers dosage forms for regulated markets like EU and US. - Conduct literature search reports for drug substances and products, design product development strategies, and propose different formulation strategies based on the review outcomes. - Guide executives in lab development batches, provide expert input into formulation and process studies, and ensure compliance with specifications. - Evaluate packaging material vendors, monitor stability studies, and prepare/review Technology Transfer documents. - Coordinate with internal stakeholders, follow GLP & GMP, participate in stability and validation batch manufacturing, and prepare PDR for regulatory submission. Qualifications & Skills: - M.Pharm or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field. - Specialization in drug delivery systems or formulation science preferred. Experience: - 8-10 years of formulation development experience, with a minimum of 5 years focused on nasal spray or inhalation formulations. - Proven experience in nasal spray product development from early-stage to commercial scale-up. Technical Expertise: - Strong understanding of nasal spray formulation techniques, drug-excipient interactions, and delivery systems. - Experience with device development and knowledge of regulatory requirements for nasal spray formulations. Project Management: - Strong project management skills, ability to manage multiple projects, work with cross-functional teams, and deliver results. Regulatory Knowledge: - Experience in preparing and reviewing regulatory submissions, familiarity with CMC requirements for nasal formulations. Leadership & Communication: - Ability to lead and develop a team, excellent communication and presentation skills for conveying complex scientific information. Problem-Solving & Innovation: - Strong analytical and problem-solving skills, ability to innovate and apply new technologies to improve drug delivery processes. Work Environment: - Primarily based at the R&D center with occasional travel to manufacturing sites, vendors, and regulatory meetings. Join us in this exciting role to contribute towards developing high-quality nasal spray formulations for global markets.,

Key responsibilities include literature reviews, pre-formulation, pellet formulation, stability studies, process validation, technology transfer, troubleshooting, and maintaining documentation like QAQN, MFR, FPS, and logbooks. Perks and benefits Accommodation, Transportation and Mediclaim.

The role is responsible for software development /testing/deployment/debugging process. This is an operational role that may seek appropriate level of guidance and advice to ensure delivery of quality outcomes. Responsibilities Writing effective and scalable code/test case Debugging and deploying applications Providing support for production environment Preparing software development calendar Preparing reports and dashboards on project time deviations, rework time etc Conducting development testing and reports testing issues to supervisor Identifying and tracking bugs, assessing nature of bugs, and executing corrective actionsDesired Skill sets Good programming skills Familiar with software applications and tools Good Knowledge on coding/testing environment

As an Executive in MSTG at Sun Pharmaceutical Industries Ltd, your primary responsibility involves executing technology transfers to Sun/CMO sites, overseeing scale-up processes, exhibit batches planning, and process validation. This requires effective planning and efficient utilization of resources such as manpower, materials, and machinery. You will be responsible for various documentation tasks including the preparation of new production introduction forms, scale-up reports, reviewing Sun/CMO Batch Manufacturing Records (BMR), developing sampling plans, process validation (PV) protocols, User Requirement Specification (URS) preparation, and Dashboard preparation. It is essential to ensure that products are manufactured and stored in compliance with relevant documentation to achieve the desired quality standards. Additionally, your role includes reviewing and providing comments on Master Formulae (MF), Failure Mode and Effects Analysis (FMEA), Risk Assessments (RA), and protocols such as Sampling plans and Process Validation protocols to ensure regulatory compliance. You will also be involved in handling and supporting troubleshooting batches for data comparison and root cause investigation at Sun/CMO sites, investigating product troubleshooting, and overseeing timely packing operations. Furthermore, you are required to monitor and conduct pre-checks on equipment planned for use in scale-up, exhibit, and process validation batches, including equipment preparation, vial washing and dehydrogenation, Clean-in-Place/Sterilize-in-Place (CIP/SIP) systems, Programmable Logic Controllers (PLCs), and various instruments. Your role also involves supervising and conducting skid trials to enhance product development, improve processes, and address potential manufacturing constraints effectively.,

You have hands-on work experience in mammalian cell culture, microbial cell culture, and molecular biology areas. You are proficient in therapeutic protein expression and purification using E.coli or yeast expression systems. Your expertise includes molecular biology techniques such as molecular cloning, primer designing, expression vector generation, characterization, and related molecular biology techniques. You have a background in generating CHO-based stable monoclonal cell lines for mAb/therapeutic protein production. Your experience also covers single cell cloning, fed-batch study, cell bank preparation (RCB, MCB, WCB, EPCB), and characterization. You will collaborate with multiple teams, Contract Research Organizations (CRO), Contract Development and Manufacturing Organizations (CDMO) for technology transfer. You will work according to Standard Operating Procedures (SOP), design experiments, and troubleshoot any arising problems. It is crucial for you to maintain proper experimental documentation records in Laboratory Notebook (LNB) and Electronic Laboratory Notebook (ELN) specific formats.,

Educational Requirements Bachelor of Engineering Service Line Enterprise Package Application Services Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Preferred Skills: Technology-BPMI - IBM-IBM Integration Bus (IIB)

Educational Requirements Bachelor of Engineering Service Line Enterprise Package Application Services Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Preferred Skills: Technology-SAP Technical-SAP Process Integration/ SAP PI

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking-GPP Financial Services Domain-Payments-GPP Generic Skills: Banking

Job Description Summary: We are seeking a motivated and detail-oriented Patent Content Analyst to join our team. In this role, you will be responsible for coding and indexing patent documents related to Polymer Chemistry, ensuring compliance with editorial policies and conventions. Your work will directly contribute to achieving production volume and quality targets while maintaining high standards of accuracy and efficiency. Key Responsibilities: Apply coding and indexing to patent documents in line with editorial policies and conventions. Meet production volume and quality targets while maintaining a focus on accuracy and consistency. Track and record performance against established targets. Take an active role within the team to ensure targets are met. Stay informed on current developments in Polymer Chemistry and related technology areas. Consistently maintain high-quality standards in all work. Practice effective personal planning and time management to meet deadlines. Maintain flexibility and adaptability in response to process changes. Deputize for team members as required, supporting a collaborative environment. Continuously identify personal technology training and development needs, and take responsibility for self-improvement. Promote a safe working environment by adhering to safety protocols and best practices. Perform any other reasonable duties as assigned by the line manager or director. Required Qualifications: Comprehensive knowledge of Polymer Chemistry, including chemical nomenclature, reactions, formulae, catalysts, and additives. Proficiency in chemical drawing packages such as ISIS Draw. Strong technical skills related to Polymer Chemistry. Problem-solving abilities and analytical thinking. Good numerical skills and attention to detail. Computer and internet literacy with strong keyboard skills. Excellent written and verbal communication skills in English. Strong interpersonal skills and a team player with the ability to work independently. Well-organized with a disciplined approach to policy, procedure, and standards. Ability to prioritize and manage time effectively in a fast-paced environment. Self-motivated, able to consistently meet performance targets and handle complex issues. Preferred Qualifications: Experience in patent document analysis or related fields. Ability to deal with complex and demanding issues in a dynamic environment.

As an individual with hands-on work experience in mammalian cell culture, microbial cell culture, and molecular biology, you will be responsible for various tasks related to therapeutic protein expression and purification utilizing E.coli and yeast expression systems. Your expertise should encompass molecular biology techniques such as molecular cloning, primer designing, generation of expression vectors, and characterization of related molecular processes. Moreover, your role will entail working on the development of CHO-based stable monoclonal cell lines dedicated to mAb/therapeutic protein production. Proficiency in single cell cloning, conducting fed-batch studies, preparing cell banks (RCB, MCB, WCB, EPCB), and their subsequent characterization will be highly valued. Collaboration with multiple teams, Contract Research Organizations (CROs), and Contract Development and Manufacturing Organizations (CDMOs) for technology transfer will be a crucial aspect of your responsibilities. Adhering to standard operating procedures (SOPs), designing experiments, troubleshooting issues as they arise, and ensuring meticulous maintenance of experimental documentation records in LNB and ELN specific formats will also be expected from you.,

As a Process/Project Engineer at GFCL EV Products Limited in the Technical Services department, your primary responsibility will be to assist in process/project engineering and front-end engineering for the commercialization of in-house and licensed processes. You will be instrumental in generating Technology Transfer Data from R&D Kilo Lab Scale and Pilot Plant scale to facilitate the transfer of technology to the Commercial Plant. Your duties will include generating and reviewing various engineering documents such as mass balance, energy balance, process engineering calculations, PFDs, P&IDs, layouts, isometric drawings, project cost estimates, and project schedules. Working closely with the R&D team, you will plan Design of Experiments and organize studies on material compatibility, effluent minimization, solvent recovery, and more. In addition, you will be responsible for selecting appropriate equipment and agitation patterns for scaled-up plant operations, preparing proposals for trial and validation batches in the Pilot Plant, and conducting Process HAZOP and Risk Assessment. Your role will also involve collaborating with the Process Engineering Team to finalize the scaled-up version of the commercial plant and arranging trials at vendors" shops for various operations as per process requirements. Furthermore, you will assist the ADL team in transferring analytical methods to the Plant, support the commissioning of new plants, and collect data for process improvements and modifications. Troubleshooting process problems, ensuring equipment works to specifications, and providing information throughout project phases will be essential aspects of your job. To excel in this role, you must have a minimum qualification of B.E./B. Tech in Chemical Engineering along with at least 5 years of relevant experience in process/project engineering, technology transfer, scale-up, and technical services. Your expertise will be crucial in developing methods for upgrading operational techniques, improving yield, efficiency, and cost-effectiveness of processes, and training Process Engineers on newly developed technologies. Join us at GFCL EV Products Limited and contribute to the continuous improvement and success of our technology transfer and commercialization processes.,