595 Technology Transfer Jobs - Page 6

Lead Software Engineer Responsibilities: Developing and owning C# .NET solutions for the organization. Development of applications in MRI Imaging domain independently. Debugging and maintaining written code. Reporting and resolving issues related to projects. Identifying and handling technical risks and issues Guiding team members for technical solutions and ramping them up Working in an agile team alongside other developers following SAFe agile principles. Reporting on project statuses and developments to senior team members. Participating in project meetings with management and other team members. Lead Software Engineer Requirements: Bachelor's degree in computer programming, computer science, or information technology. C#, .NET Core, and Microsoft Visual Studio experience (Certification is desirable) ... Minimum of 7-12 years of experience as a C# programmer or developer. Knowledge of other coding-languages (C++, Angular, HTML5 etc). Ability to write clean, easy to understand code. Outstanding analytical and problem-solving capabilities. Excellent written and verbal communication skills. Ability to work independently and complete projects with minimal supervision. Sound understanding of coding and development processes. Experience with working in an agile environment.

Wondering what's within Beckman Coulter Diagnostics Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Lead, Technical Project Management for Beckman Coulter Diagnostics is responsible for driving and implementing pivotal initiatives, running regional and/or global technical and non-technical projects, and giving to building the future Global Ops Project and Portfolio Management Office infrastructure and team. This position is part of the Global Operations PMO & Strategy Team and is a remote role. Travel will vary depending on the phases and needs of the program (40-50%) and will be global. At Global Ops PMO, our vision is to bring best in class project and portfolio management methodology and skills to support the achievement of our business goals. You will be a part of the Global Operations PMO and Strategy team, responsible for the management of a series of projects for outsourcing of contract manufacturing to India. If you thrive in a multifunctional, fast paced & supporting role and want to work in a global PMO-read on. In this role, you will have the opportunity to: Responsible for leading multi-phase and multi-year product transfer programs into third party contract manufacturing facilities initially in India. Provide project strategic direction and management of external manufacturing technical transfer activities, coordinating execution of cross-functional workstreams from Quality, Regulatory, Development, Technical Operations, Supply Chain, and Global Strategic Sourcing. Strong interpersonal skills as interactions will be both internal and external facing with Contract manufacturing teams. Take ownership of the full project life cycle - successful project delivery will include full implementation from initiation to deployment for one to two major or several minor/medium projects simultaneously. Establish and drive the achievement of Project and Portfolio KPIs through the adoption of Danaher Business Systems tools (Visual Project Management, Daily Management etc.) and Global Ops PMO Standard Work/Methodology. Demonstrate intuition for business to support how solutions will address project goals Ensure that projects/programs are proceeding according to scope, schedule, budget, and quality standards Work creatively and analytically in a problem-solving environment demonstrating collaboration, innovation, and excellence. Develop and deliver progress reports, proposals, requirements documentation, and presentations to various audiences, including project team, sponsors, steering team, and executive-level key partners. Participate in the development, implementation, and continuous improvement on standard methodologies and tools for project execution, portfolio management, and PM talent development. Establish and maintain technology transfer program / project budgets, cash flow analyses, and cost estimates related to the program. Establish and utilize effective risk management and mitigation practices through proper risk identification, assessment, tracking and communication. The essential requirements of the job include: Bachelor's degree in a relevant field with 14+ years experience OR Master's degree with 12+ years experience OR Doctoral degree with 9+ years experience Significant experience in an operations environment (manufacturing, supply chain, engineering or logistics and distribution) Strong Project Management experience leading large , sophisticated projects and Project management trained/qualified (e.g PMP certification or equivalent). Experience in Project Portfolio Management Proven experience leading all aspects of medium/large design changes, and all aspects of technology transfer programs/projects in the Medical Device or Diagnostics regulatory environment Excellent leadership, communication, and interpersonal skills, with the ability to influence and build relationships at all organizational levels. . Proven ability to mentor and facilitate PMs and project teams with varying levels of PM competence. Can take tough decisions around people and can quickly build effective teams in a global matrixed organization. Working with Contract Manufacturers & Understanding of contractual requirements It would be a plus if you also possess previous experience in: Experience managing and influencing in a matrix organization Change Management Certification desired (Prosci/ADKAR or Other) Lean /Six Sigma experience, certified Kaizen leaders in DBS and demonstrated capability in problem solving. Proficiency in Power BI/smartsheet, MIRO, excel and PM software. At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide. Travel will vary depending on the phases and needs of the program (40-50%) Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. 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About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : Java Standard Edition Good to have skills : C++ Programming LanguageMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Engineer, you will engage in a dynamic work environment where you will analyze, design, code, and test various components of application code for multiple clients. Your typical day will involve collaborating with team members to ensure the successful implementation of software solutions, addressing any challenges that arise, and contributing to the overall improvement of application performance and functionality. You will also participate in maintenance and enhancement activities, ensuring that existing systems remain efficient and effective. Job Responsibilities:Write high quality production code and configurations in Java that aggregates data for online travel pricingIntegrate with 3rd party providersWork directly with 3rd party providers and cross functional teams spread across multiple geographiesProduce high quality code and unit tests consistent with Google code standards. Conduct integration testing to validate implementationsIndependently troubleshoot issues with code and integrationUnderstand requirements and resolve ambiguity in order to develop solutionsReview production code and configurations that aggregates data for online travel pricing.Identify opportunities for improvements to development and support processesProvide mentoring and support to junior resources where appropriateAdditional development tasks as assigned Basic knowledge in C++ Skills/ QualificationsBachelor's degree in Computer Science or equivalent practical experience. Minimum 3-5 years of working experience in Java developmentAdvanced Java knowledge. Java 8+ experience is preferredSolid understanding of web technology and protocols (HTTP, SSL, JavaScript, HTML, Certificates etc)Solid understanding of JSON and other data representation and transfer technologies (XML, SOAP, DTD) Knowledge of Kotlin(Control Flow, Classes and Objects,Collections,Function,Null Safety, Coroutines) Should have expertise in application debugging.GUI development experience a plusImplementing third party APIs with existing systemsFamiliarity with source control systems such as Git, svn, or perforceStrong attention to detail, and ability to follow processesProven ability to manage conflicting priorities under guidanceShould be able to arrive at solutions independentlyBasic linux familiarityExperience working with teams in different timezones a plusVery strong communication skills for requirements clarification and troubleshooting via email/chatThis position is based at our Gurugram office.A 15 years full time education is required. Qualification 15 years full time education

About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : Java Standard Edition Good to have skills : C++ Programming LanguageMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Software Development Engineer, you will engage in a dynamic work environment where you will analyze, design, code, and test various components of application code for multiple clients. Your typical day will involve collaborating with team members to ensure the successful implementation of software solutions, addressing any challenges that arise, and contributing to the overall improvement of application performance and functionality. You will also participate in maintenance and enhancement activities, ensuring that existing systems remain efficient and effective. Job Responsibilities:Write high quality production code and configurations in Java that aggregates data for online travel pricingIntegrate with 3rd party providersWork directly with 3rd party providers and cross functional teams spread across multiple geographiesProduce high quality code and unit tests consistent with Google code standards. Conduct integration testing to validate implementationsIndependently troubleshoot issues with code and integrationUnderstand requirements and resolve ambiguity in order to develop solutionsReview production code and configurations that aggregates data for online travel pricing.Identify opportunities for improvements to development and support processesProvide mentoring and support to junior resources where appropriateAdditional development tasks as assigned Basic knowledge in C++ Skills/ QualificationsBachelor's degree in Computer Science or equivalent practical experience. Minimum 3-5 years of working experience in Java developmentAdvanced Java knowledge. Java 8+ experience is preferredSolid understanding of web technology and protocols (HTTP, SSL, JavaScript, HTML, Certificates etc)Solid understanding of JSON and other data representation and transfer technologies (XML, SOAP, DTD) Knowledge of Kotlin(Control Flow, Classes and Objects,Collections,Function,Null Safety, Coroutines) Should have expertise in application debugging.GUI development experience a plusImplementing third party APIs with existing systemsFamiliarity with source control systems such as Git, svn, or perforceStrong attention to detail, and ability to follow processesProven ability to manage conflicting priorities under guidanceShould be able to arrive at solutions independentlyBasic linux familiarityExperience working with teams in different timezones a plusVery strong communication skills for requirements clarification and troubleshooting via email/chatThis position is based at our Gurugram office.A 15 years full time education is required. Qualification 15 years full time education

R & D Biomedical Engineer- Biomedical Engineering, Medical Devices Manufacturing, or Clinical Trials An R & D Biomedical Engineer is a highly experienced professional specializing in the research and development of biomedical technologies. They are responsible for designing, developing, and optimizing medical devices and systems that enhance healthcare delivery. Their expertise ensures innovation in medical technologies, contributing to the advancement of patient care, while ensuring compliance with regulatory standards. By leading the development of cutting-edge solutions, they play a key role in improving the safety, functionality, and reliability of critical healthcare equipment. Primary Responsibilities & Authority: Key Responsibilities: Product Development: Lead and coordinate in research for the development of new medical devices, ensuring compliance with regulatory standards (CDSCO, FDA, ISO, CE). Clinical Research: Design and implement preclinical and clinical studies to validate new products and manufacturing processes. Manufacturing Collaboration: Collaborate closely with manufacturing teams to ensure research findings translate effectively into scalable and cost effective production. Data Analysis: Collect, analyse, and interpret scientific and clinical data to support product innovation and improvement. Regulatory Compliance: Ensure all research activities adhere to industry regulations and ethical standards. Technology Transfer: Facilitate the smooth transition of R&D prototypes to large-scale manufacturing by providing technical expertise and support. Documentation: Prepare comprehensive research reports, regulatory submissions, and patents as needed. Collaboration: Work closely with engineers, designers, quality assurance and back end teams to optimize product design and performance. Innovation: Stay updated on the latest advancements in biomedical technology and incorporate relevant innovations into product development. Bachelors or Masters degree in Biomedical Engineering with significant medical device industry experience and an aptitude for research will be considered.

R & D Biomedical Engineer- Biomedical Engineering, Medical Devices Manufacturing, or Clinical Trials An R & D Biomedical Engineer is a highly experienced professional specializing in the research and development of biomedical technologies. They are responsible for designing, developing, and optimizing medical devices and systems that enhance healthcare delivery. Their expertise ensures innovation in medical technologies, contributing to the advancement of patient care, while ensuring compliance with regulatory standards. By leading the development of cutting-edge solutions, they play a key role in improving the safety, functionality, and reliability of critical healthcare equipment. Primary Responsibilities & Authority: Key Responsibilities: Product Development: Lead and coordinate in research for the development of new medical devices, ensuring compliance with regulatory standards (CDSCO, FDA, ISO, CE). Clinical Research: Design and implement preclinical and clinical studies to validate new products and manufacturing processes. Manufacturing Collaboration: Collaborate closely with manufacturing teams to ensure research findings translate effectively into scalable and cost effective production. Data Analysis: Collect, analyse, and interpret scientific and clinical data to support product innovation and improvement. Regulatory Compliance: Ensure all research activities adhere to industry regulations and ethical standards. Technology Transfer: Facilitate the smooth transition of R&D prototypes to large-scale manufacturing by providing technical expertise and support. Documentation: Prepare comprehensive research reports, regulatory submissions, and patents as needed. Collaboration: Work closely with engineers, designers, quality assurance and back end teams to optimize product design and performance. Innovation: Stay updated on the latest advancements in biomedical technology and incorporate relevant innovations into product development. Bachelors or Masters degree in Biomedical Engineering with significant medical device industry experience and an aptitude for research will be considered.

Developer leads the cloud application development/deployment for client based on AWS development methodology, tools and best practices. A developer responsibility is to lead the execution of a project by working with a senior level resource on assigned development/deployment activities and design, build, and maintain cloud environments focusing on uptime, access, control, and network security using automation and configuration management tools. Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise Strong exp in Java 11 and above, Springboot, Micorservices, react js. Extensive experience in developing enterprise scale applications. SQL and relational database exp DB2/Sybase. Crystal clear Core Java concepts – types of classes, class loading, collections, writing code in multi-threading env, lambdas, functional interfaces etc. Experience 5-8+ yrs Preferred technical and professional experience None

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)

As an R&D Executive, you will play a crucial role in leading our product innovation initiatives within the food and beverage industry. Your primary responsibilities will include driving end-to-end R&D projects from ideation to commercialization, conducting market research to identify trends, and collaborating with cross-functional teams such as Marketing, Sales, Supply Chain, and QA. You will be tasked with optimizing product formulations for taste, nutrition, and cost-effectiveness while ensuring compliance with various regulations including FSSAI, HACCP, GMP, and ISO standards. Additionally, you will lead sensory analysis, product testing, and data-driven improvements, along with managing supplier relationships for raw material sourcing and quality assurance. To excel in this role, you should hold an M-Tech/B-Tech in Food Technology, Food Science, or a related field, along with at least 3 years of experience in Nutraceuticals product development. Strong project management skills, familiarity with Stage Gate processes, excellent communication abilities, and stakeholder management skills are essential for success in this position. Your expertise in areas such as New Product Development, Advanced Formulation Science, Regulatory Compliance, Technology Transfer, Market Trend Analysis, and Cross-Functional Leadership will be instrumental in developing and launching high-quality nutraceutical products that align with evolving health trends. This is a full-time position that offers benefits such as health insurance, a yearly bonus, and follows a day shift schedule. Your experience in product development, clinical research, FDA regulations, and food safety will be valued as you contribute to our innovative projects. The work location for this role is in person. If you are a proactive and innovative individual with a passion for driving product innovation and have the requisite qualifications and experience, we invite you to apply for this exciting opportunity to lead our R&D initiatives.,

You will be responsible for leading the Site Processing Engineering team in a Medium to large Generic API company. With a minimum of 10-15 years of experience, you should have a strong background in solvent recovery enhancement, troubleshooting scale-up issues, and continuous improvement of running molecules in the plant. Your expertise should include time cycle reduction, improving process economics, utility cost reduction, technology transfer, and a proven track record of leading operational excellence programs. As a Process Chemist, you will join our team with a focus on Plant based Process Development. With a minimum of 5-8 years of experience, you will work on Process Development, Yield Improvement, and Cost Reduction to meet industry benchmarks. Your responsibilities will include troubleshooting plant process issues, OOS investigation, CAPA development, and handling complex chemistry improvement projects.,

Job Description Having 7-12 yrs of exp in PHP Design, develop, unit testing and maintain high-quality web applications and services using PHP, symfony, MySQL, HTML, CSS, and jQuery, Collaborate with cross-functional teams to gather requirements, analyze technical specifications, and translate them into scalable solutions, Architect and implement efficient and reusable code, following best practices and coding standards, Perform code reviews, provide constructive feedback, and mentor junior developers to foster a culture of continuous improvement and knowledge sharing, Troubleshoot and debug complex issues, ensuring optimal performance, reliability, and security of applications, Work closely with stakeholders to understand business objectives, prioritize tasks, and deliver solutions that meet or exceed expectations, Participate in agile development methodologies, including sprint planning, daily stand-ups, and retrospective meetings, to deliver high-quality software on time and within budget, Contribute to the technical documentation, including system architecture diagrams, API documentation, and user guides, to facilitate seamless collaboration and knowledge transfer, Proactively identify opportunities for process improvements, automation, and optimization to streamline development workflows and increase productivity, Solid understanding of object-oriented programming principles, design patterns, and data structures, Experience with RESTful API development, integration, and consumption, Familiarity with version control systems (e g , Git), continuous integration/deployment tools, and agile methodologies, Excellent problem-solving skills, with a keen attention to detail and a passion for delivering high-quality software solutions, Strong communication skills, both written and verbal, with the ability to effectively collaborate with team members and stakeholders, Proven ability to work independently and manage multiple tasks/projects simultaneously in a fast-paced environment, Should lead a small team of 3-4 members, Additional Information At Tietoevry, we believe in the power of diversity, equity, and inclusion We encourage applicants of all backgrounds, genders (m/f/d), and walks of life to join our team, as we believe that this fosters an inspiring workplace and fuels innovation ?Our commitment to openness, trust, and diversity is at the heart of our mission to create digital futures that benefit businesses, societies, and humanity, Diversity,?equity and?inclusion (tietoevry)

Investigator Pyts Coordinator India, Chennai/Bangalore Hybrid, Office-Based ICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development, We are currently seeking an Investigator Payments Coordinator to join our diverse and dynamic team As an Investigator Payments Coordinator at ICON, you will play a key role in managing and processing payments to clinical trial investigators, ensuring accuracy and timeliness in financial transactions You will collaborate with internal teams and external partners to support the financial aspects of clinical trials, contributing to smooth operations and effective investigator engagement, What You Will Be Doing Coordinating the processing of investigator payments, including reviewing invoices, verifying accuracy, and ensuring compliance with contractual agreements and company policies, Working closely with clinical and finance teams to resolve payment-related queries and discrepancies in a timely manner, Maintaining accurate financial records and documentation for audit purposes and providing regular updates on payment status, Supporting the development and implementation of streamlined payment processes to enhance efficiency and investigator satisfaction, Communicating with investigators and sites to provide guidance on payment procedures and addressing any concerns or issues they may have, Your Profile Bachelors degree in finance, accounting, business administration, or a related field, 2+ years of experience in financial coordination, payments processing, or a related role, preferably within the clinical research or healthcare sectors, Strong attention to detail and organizational skills, with the ability to manage multiple tasks and deadlines effectively, Excellent communication and interpersonal skills, with a customer-focused approach to stakeholder engagement, Proficiency in financial software and tools, as well as Microsoft Office applications, particularly Excel, What ICON Can Offer You Our success depends on the quality of our people Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent, In addition to your competitive salary, ICON offers a range of additional benefits Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family, Our Benefits Examples Include Various annual leave entitlements A range of health insurance offerings to suit you and your familys needs, Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead, Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your familys well-being, Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others, Visit our careers site to read more about the benefits ICON offers, At ICON, inclusion & belonging are fundamental to our culture and values Were dedicated to providing an inclusive and accessible environment for all candidates ICON is committed to providing a workplace free of discrimination and harassment All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles, Are you a current ICON EmployeePlease click here to apply

Role & responsibilities Job Responsibilities: 1.Market samples receiving, entry and stock maintenance. 2.List updations, equipment and SOPs, Product code list updation 3.RM BOM preparation and checking of new product solid, liquid and semi-solid dosage form. 4.Preparation of MFR/MPR/PDR of solid, liquid and semi-solid, injectable dosage form. 5.Sample upkeep Withdrawal and Storage of Sample. 6.RA related mail communication, document follow ups, preparation and send as per urgency and priority of documents. 7.List updations (RM/PM/Stability samples)/ Innovator samples/ Equipments. 8.BOP preparation and corresponding mail correspondence. Responsible for QMS activity ,MFR preparation and corresponding change control documentation. 9.Document preparation as per regulatory requirement and commercial MFR preparation and revision with change control. 10.BMR/BPR filling as per dossier requirement/ Dossier related documentation 11.Filing of documents and list updation. 12.Commercial Work Order Request form entry & Clearance. 13.Audit related documentation 14.New item code creation 15.Change control initiation for new product development & tech transfer Preferred candidate profile Reputed Pharma background

Role & responsibilities Process Development: Conduct research and design experiments to develop and optimize synthetic routes for API molecules. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. Documentation: Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders. Design synthetic routes for the synthesis and isolation of impurities and reference standards. Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: Adhere to all safety protocols and ensure a safe working environment in the laboratory. Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques.Team Collaboration: Plan daily activities for team members, focusing on feasibility studies, process optimization, and laboratory validation. Work closely with the Analytical Research and Development (ARD) team on method development, in-process testing, and reference standards qualification. Qualifications: Education: MSc/BSc in Organic Chemistry, Experience: Fresher or 1-2 years experience in process development and optimization in the pharmaceutical or bulk drug industry. Skills: Strong knowledge of synthetic organic chemistry and process chemistry. Proficiency in using and interpreting data from analytical instruments. Excellent problem-solving skills and attention to detail. Effective communication and teamwork skills. Ability to work independently and manage multiple projects simultaneously. Preferred candidate profile We are looking for a talented and driven junior R&D Associate to join our team. The successful candidate will be responsible for developing and optimizing chemical processes for synthesizing active pharmaceutical ingredients (APIs). This role requires a strong background in synthetic organic chemistry, process development, and scale-up techniques. The R&D Chemist will collaborate with cross-functional teams to ensure the smooth transition of processes from the lab to full-scale production. Perks and benefits

Position Purpose : This position is responsible for daily overall functioning of the R & D laboratory, provide guidance perform experiments and prepare documentation for R & D and Pilot Plant. Role & Responsibilities: To Plan & perform Lab experiments for Process development as per Guideline To modify & optimise lab process for plant scale-up batches To keep record of all experiment taken To prepare & record the documents of R&D & Pilot plant batch work on day to day To execute and assist demo batches to plant chemist To Deliver the project/Product as per committed timeline To provide online support to production dept. for trouble shooting To look after glass wares, lab wares / instruments, calibration & maintenance. To Prepare the process write up with document team. To submit tech transfer document to QA along with PDR To follow the guideline and SOPs of R&D department To create healthy working atmosphere in R&D To train & guide trainee chemist Be always careful about chemical handling by following safety measures and also give training to juniors. To coordinate with ADL, Plant and maintenance. To take work as per allocation for officers and operators. To carry out literature search for better alternate safe process.

Accountabilities: Participate in witnessing / Technology absorption of process & operations during batches at Lab / Kilo Lab / Pilot Plant and accordingly implement it for smooth transfer of technical knowhow for scale up batches at Plant scale. Lead the CFT during technology transfer at plant scale. Planning and executing the plant campaign to meet the delivery as per time and quality commitment. Job Descriptions:- Technology Transfer of products (APIs & Intermediates) from R&D, One site to another site. This includes Facility evaluation and retro fitment of new products and cost reduction products for exhibit campaign at In house as well as at Contract manufacturing facilities & accordingly arranging for modification costing and facilitate approval of budget, follow-up for modifications & plant readiness. Preparation of all documents related to project and coordination with all CFT members to expedite work to meet delivery timelines. Involvement during Pilot scale-up of new products for identification and optimization of critical operations to ensure smooth operations and proper hardware identification during Scale-up/exhibit batches. Complete planning of RMs for required API quantity and facilitate in procurement activities. Plan for analysis on receiving at the locations Leads HAZOP study and implementation of its recommendations for specific process requirements with respect to safety, during the plant campaign. Exhibit campaign planning, scheduling and execution of development and exhibit batches at both in house and contract manufacturing locations to meet the delivery timelines with desired yield and quality. Coordination with respective CFT members including CRD, TD, AD, DRA, GMS, Production, QA and QC before and during the course of campaign so as to minimize delays and ensure that product delivery timelines are met. Assist in resolution of unexpected issues that crop up during technology transfer. Process improvement (Cost reduction, Quality improvement; Capacity debottlenecking, troubleshooting of APIs / Intermediates). This includes the Identification of projects & coordination with all stake holders for project scale up. To study the unit operations in plant for identifying the improvement areas (Power, Energy, EHS, waste minimization, Efficiency Improvement etc.) and giving solutions for the same. To ensure GMP and EHS compliance in the area of work.

As an R&D Executive at PTC - SIGMA, you will be responsible for a wide range of activities related to documentation, product development, collaboration & coordination, and team training. Your primary responsibilities will include preparing various Technology Transfer documents such as LIF, PIF, PBOM, BOM for VAQ review, FBOM, and MFC. You will also be initiating AIF and Change control in the portal and handling SAP related activities including BOM loading, New SAP code generation, and Code extension. Additionally, you will be involved in LnB Issuance, PDR review, LnB and Project Files Archival, SOP preparation, review, and training, as well as Form 29, Form-11 application activities. In terms of product development, you will be conducting literature searches, monitoring raw material availability, aligning formulation development activities, preparing project presentations, loading products in stability studies, and analyzing stability data. You will also be responsible for preparing regulatory submission documents and ensuring compliance with SOPs during practical work. Collaboration and coordination with other departments such as ADL, PKG, RA, GDSO, and CQA will be crucial for the successful execution of day-to-day activities. Additionally, you will be expected to deliver presentations on assigned topics and share execution learnings within the team. Overall, as an R&D Executive at PTC - SIGMA, you will play a key role in driving the successful development and documentation of products, ensuring regulatory compliance, and fostering effective collaboration within the organization.,

As an experienced professional with over 15 years of expertise, you will be responsible for providing assistance in the project Crop Area estimation and loss assessment utilizing Remote Sensing and Geospatial technology. Your role will involve contributing to the preparation of various models for yield estimation based on environmental factors. You will also be expected to share information on different models and statistical tools utilized for forecasting pests and diseases. Furthermore, you will play a key role in project execution and management, ensuring that information and results are delivered in accordance with project requirements. Your responsibilities will also include the development of weather-based efficient farm operations and studying the crop weather relationship across major crops to forecast yield. Additionally, you will be involved in creating weather-based agro advisories to support crop production by leveraging weather forecasts and climatic predictions. Moreover, you will be tasked with developing a crop growth simulation model to assess potential yield in different agro-climatic zones within the Gujarat state. Your role will also involve monitoring droughts on a crop-wise and area-wise basis to facilitate effective drought management. Additionally, you will be responsible for preparing crop weather calendars to assist farmers. Lastly, you will be involved in delineating agro-climatic zones to define agro-climatic analogues, enabling the efficient and rapid transfer of technology for the sustainable development of agriculture.,

Roles and Responsibilities Develop new polymer products through formulation development, process development, and technology transfer. Conduct consumer trials to test product performance and provide technical support to sales teams. Clarify customer requirements and develop solutions using analytical skills. Provide technical expertise on polymer products to internal stakeholders. Desired Candidate Profile MS/M.Sc(Science) degree from a recognized university. Minimum 7-9 years of experience in R&D, in the polymers industry. Strong understanding of formulation development, process development, and technology transfer processes. Excellent analytical skills with ability to clarify complex issues.

Project Role : Cloud Migration Engineer Project Role Description : Provides assessment of existing solutions and infrastructure to migrate to the cloud. Plan, deliver, and implement application and data migration with scalable, high-performance solutions using private and public cloud technologies driving next-generation business outcomes. Must have skills : Cloud Migration Planning Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time educationAbout The Role :Accenture is looking Application Assessment Lead who will conduct Cloud application discovery and assessment services, by assessing the current application landscape and accelerate the Cloud adoption by providing treatment, remediation & transformation approach. Key Technical Skills requirementsExperience of working with Public cloud provider solutions like AWS, Azure, GCP etc. including highly available and disaster recovery architecturesShould have awareness and opinion on the latest industry trends and its adoptions in the enterpriseShould be aware of enterprise applications and Cloud adoption trends and challenges (Ex:SAP, Oracle EBS, Vertical Applications, Database, and Middleware)Evaluation of cloud deployment models and recommending the most suitable model (like for e.g. IaaS vs PaaS vs SaaS)Good understanding of Assessment methodologiesExperience on Cloud readiness & Application assessment Experience on migration planning, grouping Applications for phased migration and migration schedule managementCandidate will be required to Lead, and conduct customer workshops with application teams to understand application footprint, interdependency and migration strategy Deep technical knowledge on migrating custom applications to PaaSDeep technical knowledge about assessment and migration of COTS applications to cloudOverview of compliance and regulations pertaining to Cloud adoptionDeep knowledge of application modernization strategies - re-host, re-platform or re-architectThe candidate should have good understanding of Application portfolio in at least two industry verticals.Understanding of Enterprise service bus/iPaaS, Stateless and Micro service-based architecture.Possess experience with container services like Docker, Kubernetes etc.Good understanding of 12 factor application and implementationHigh-level understanding of SDLC and AgileGood knowledge on application tiers and its functionalityCloud operating model design, Business case development, TCO and vendor evaluationKnowledge of enterprise architecture, Datacenter technologies & Application architecture (high level)Good analytical skills to understanding infrastructure and application data and interpret in meaningful way for cloud assessment Certifications/Accreditations:AWS/Azure/GCP/IBM certificationsTOGAFEducation Qualifications:Bachelors degreeMBA Degree from Tier-1 College (Preferable)Minimum of 12-16 years large scale consulting experienceA 15 Years full time education is required. Qualification 15 years full time education

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.

We are looking for a meticulous Officer Technology Transfer to champion process validation and technology transfer activities at Synnat Pharma Private Limited. As a key member of our team, you will be instrumental in monitoring process validation batches, meticulously recording observed data, and identifying opportunities for process improvements within our API Manufacturing Industry. Your responsibilities will extend to collecting, updating, and correlating data to identify variations, contributing to the preparation of process validation documents such as Batch Manufacturing Records (BMRs), protocols, and reports. This role demands a proactive individual capable of working in shifts and collaborating effectively with cross-functional teams. The ideal candidate will possess a strong foundation in chemical engineering principles and a keen eye for detail, ensuring adherence to quality standards and regulatory requirements. You will play a critical role in the seamless transfer of technology and the continuous improvement of our manufacturing processes, contributing directly to Synnat Pharma's commitment to global leadership in the API sector. Job Details Industry: API Manufacturing Industry Department: Technology Transfer Role: Officer Technology Transfer Location: Visakhapatnam Experience: 0 years Employment Type: Full-time Qualification: Bachelor's degree in Chemical Engineering or related field Responsibilities Process Validation and Monitoring Monitor process validation batches meticulously, ensuring adherence to established protocols and procedures. Record and document all observed data, both qualitative and quantitative, with accuracy and attention to detail. Identify deviations from expected results and report findings to the superior for further investigation. Collaborate with production and quality control teams to troubleshoot process-related issues during validation runs. Ensure compliance with all relevant regulatory requirements and internal quality standards throughout the validation process. Analyze process validation data to identify trends and areas for process optimization. Data Collection and Analysis Collect data from various sources, including batch records, laboratory analyses, and process monitoring systems. Update and correlate data with previous data sets to identify variations and potential process inconsistencies. Analyze data to determine the root cause of process deviations and propose corrective actions. Prepare reports summarizing data analysis findings and recommendations for process improvements. Maintain accurate and complete records of all data collected and analyzed. Present data and findings to relevant stakeholders in a clear and concise manner. Documentation and Reporting Prepare process validation documents, including Batch Manufacturing Records (BMRs), protocols, and reports, in accordance with established templates and guidelines. Ensure all documentation is accurate, complete, and compliant with regulatory requirements. Maintain a comprehensive library of process validation documents for easy access and retrieval. Assist in the preparation of regulatory submissions related to process validation. Contribute to the development and maintenance of standard operating procedures (SOPs) for process validation activities. Generate periodic reports on the status of process validation activities. Technology Transfer Activities Participate in the transfer of technology from research and development to manufacturing. Assist in the development and implementation of technology transfer protocols. Ensure that all necessary documentation is prepared and maintained during the technology transfer process. Provide training and support to manufacturing personnel on new technologies and processes. Collaborate with cross-functional teams to ensure a smooth and efficient technology transfer process. Troubleshoot technical issues that may arise during technology transfer. General Expectations and Past Experiences Bachelor's degree in Chemical Engineering or a related field is essential. Demonstrated ability to work effectively in a shift-based environment. Proven ability to meticulously monitor process validation batches and accurately record observed data. Strong understanding of existing processes and the ability to identify areas for improvement. Proficiency in collecting, updating, and correlating data to identify variations. Experience in preparing process validation documents such as BMRs, protocols, and reports. Excellent teamwork and collaboration skills to work effectively with cross-functional teams.

Key Responsibilities: Formulation Development: Design and develop formulations for injectable products such as solutions, suspensions, emulsions, lyophilized products, and pre-filled syringes. Conduct pre-formulation studies, compatibility studies, and stability testing. Process Optimization: Define and optimize manufacturing processes for sterile products. Work on scale-up and validation batches for tech transfer. Documentation & Compliance: Prepare and maintain development reports, batch manufacturing records (BMR), and related documentation as per cGMP. Ensure compliance with ICH, USFDA, EMA, and other regulatory guidelines. Technology Transfer: Support technology transfer activities from R&D to production. Assist in troubleshooting during exhibit and commercial batches. Cross-Functional Interaction: Collaborate with Analytical, Regulatory, QA, and Manufacturing teams. Required Skills & Competencies: In-depth knowledge of injectable dosage forms and aseptic processing. Hands-on experience in lyophilization, sterilization techniques, and formulation design. Familiarity with QbD principles and DoE approach. Strong understanding of regulatory guidelines (USFDA, EMA, WHO). Qualification & Experience: Education: M. Pharm / PhD in Pharmaceutics or related discipline. Experience: 10 to 15 years in sterile formulation development.

Responsible for Technology Transfer activities (From R&D to site, From Site to site). Responsible for Execution of Placebo, Scale Up & Trail Batches. Review of validation protocol/report, responsible for manufacturing of validation batches. Preparation of scale up and trail batch summary to support the commercialization of products. Coordination with quality control department & quality assurance department for getting analytical data with respect to process optimization batches & validation batches

Role & responsibilities Formulation Development (Solid Orals, Liquids, MUPS, Molten Mass, Roll Compaction) Technology Transfer & Scale Up. QbD & DoE Methodologies Regulatory Compliance (US, EU, Emerging Markets) Preferred candidate profile Leading Successful Technology Transfer of Multiple Site Transfer Products for US & EU Markets, Ensuring Zero Regulatory observations during Inspectoins.