829 Technology Transfer Jobs - Page 13

As Service Associate -Payroll,you will be supporting the end-to-end payroll related activities while ensuring you are in adherence to the policies and processes. Your primary responsibilities include: Process any payroll data in accordance with legal, IBM and the customer requirements related to personal data protection Ensure the timeliness of payroll processing (sending inputs to payroll services providers, approving payrolls) Ensure the timeliness of payroll payments processing (requesting uploads and payments releases, uploading payroll payments into the bank system, monitoring the rejected payments) Carry out the validation of payroll inputs and the reconciliation of output files and pr...

As a Process Analyst –HR Contact Center, you are responsiblefor receiving calls, emails, or chats and resolving HR-related queries from employees.You should be flexible to work in shifts. Your primary responsibilities include: Educate and document enquirers on processes whenever necessary. Provide quality customer service in every interaction. Identify, investigate, analyse, and resolve issues identified within the process. Monitor and process tickets in the ticketing system. Provide floor support for escalation and query resolution. Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise Graduate with 1-2 years of experience in ...

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 applicatio...

Should have worked in Operation,Process engineering & Technical services dept, well exposed to chemical engg practices & Chemical engg process calculations. Well exposed to Technical audit of all inputs including Energy inputs & development in Energy conservation area. Conversant with Process Engg economics & exposed to all development related to industry. Should be able to handle. Maintenance Engg service, Environment related activities. CRP( Cost reduction programme) is a regular activity & would be able to identify the weak area & implement the same to reduce the cost. Exposed to Feasibility studies related to new project & modernisation of existing facilities. Benchmarking of norms & oth...

Develop methods of analysis for new products and ensure smooth yield transfer to production. Troubleshoot technical issues in plant operations and develop reprocessing methods when required. Monitor quality and yield trends for ongoing projects.

QA Manager OSD/Liquid formulation background.Must have experience in BMR, batch release,validations,qualifications,SOPs,GMP,audits,QMS(Deviation,OOS, OOT, CAPA), tech transfer. Analytical exposure is an added advantage Resume to hrd@stedmanpharma.com

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 ...

Job Purpose: Daily audit of plant performance. Analysis of deviations. Root cause analysis of failures. Troubleshooting. Identifying opportunities and need for process and plant up-gradation, in the areas of capacity enhancement, quality improvement, energy efficiency, material efficiency, by-product recoveries, emission reduction, reducing recurring failures & interruptions, increasing equipment life, manpower rationalization, improving safety, HAZOP studies, Energy Audit and Conservation, overall cost reduction etc. Providing innovative technical solutions to achieve operational excellence of the plants and processes. Preparing Plant and process up-gradation schemes, implementation, provid...

The Research & Development Manager will be a senior member of the management team responsible for leading and managing the Research & Development Team within the Research, Development, and Innovation function of the company. You will collaborate closely with various cross-functional departmental managers, particularly Scientific, Clinical & Medical Affairs, Regulatory Affairs, and Quality Departments. Your role will encompass overseeing the internal product development pipeline, managing project-specific implementation, and providing technical support to departments such as Regulatory Affairs and Quality. A key aspect of this position is the development project planning and strategy executio...

Dr. Reddys is looking for Manufacturing Scientists or senior scientists specialized in cell therapy (CAR-T) programs to join their Manufacturing facility team. As a Manufacturing Scientist, you will collaborate with Research and Product Development teams to support GMP Manufacturing operations, Technology transfer, quality assessments, and process validation of the CAR-T process for various Cell therapy programs. Your responsibilities will include designing and executing experiments to develop robust manufacturing processes for cell therapy products, leading and training a team of cell process scientists/engineers, managing T-cell culture and differentiation, documenting experimental procedu...

Exciting Opportunity for Research associate - Alternate Vendor Development in Formulation & Development(PDR) We are looking for a skilled professional with 3-5 years of experience in alternate vendor development for diverse markets like US, EU, ROW, Domestic, WHO. Key Requirements: - B.Pharm/M.Pharm qualification - 3-5 years of relevant experience - Familiarity with various market guidelines - Expertise in technology transfer - Exposure to shopfloor operations is advantageous - Worked in R&D Department /Formulation Department Planning and execution of Alternate Vendor batches for product development

Assist in formulation development of Solid Oral Dosage form. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Solid Oral- Share CV- stuti.naik@enaltec.com

Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com

Overview Leading seasoning development across multiple snack brands and products for the PepsiCo India region. The role includes flavor ideation, seasoning development or reformulation, ecosystem partnerships with flavor and ingredient houses, seasoning scale up and seasoning qualification. Responsibilities Lead innovations and seasoning reformulation to drive human sustainability, Productivity, Competitive Advantage for brand Kurkure and Premium Support Chef and culinary engagements to build a future pipeline Collaborate/Partner with Internal (PD, Marketing, Consumer insights, Sensory and consumer product insights, Quality etc.) and external stakeholders (Seasoning suppliers) to leverage th...

Key Responsibilities: Handle end to end scale up activities from Lab to Pilot to Commercial Scale . Absorb the process from the PELAB / R & D and study the same and come out with queries considering the plant constraints and ask to modify the same if not feasible in the Plant. To observe the lab demo batches in PE Lab / R & D and identify Critical requirements of the process and provide the same. To select the equipment's for scale up & discuss with R & D and Production and finalize it. To act as a tool between Production, QC, QA with R & D / PELAB to absorb the technology from Lab to Plant. To observe the initial scale up batches critically & debottleneck the problems faced in the Plant. To...

Job Title: Dy Manager Technology Transfer Location : Mumbai Location Industry: Pharma Industry Experience: Minimum 2 years . Division: API Key Role & Responsibilities: Able to scale up technology from R&D to Kilo scale/ pilot scale/ commercial scale Coordination with R&D team for generating negative study data, concluding to optimize process parameters Observe R&D demo batches & preparation of demo batches report Identify & propose ideas/ technology to improve process efficiency, effective utilization for unit process & operations Preparation of BFD, PFD, P&ID, mass balance, energy balance sheets Skills: Technology Transfer, Process, Scale-up, optimization, validation, PFD, P&ID, BFD, troubl...

As a part of this role, you will be responsible for overseeing the scale-up and technology transfer of pharmaceutical processes. Your primary focus will be on ensuring the successful transition of processes from the laboratory to full-scale production. This will involve collaborating with cross-functional teams to optimize processes, troubleshoot any issues that may arise during scale-up, and ensure that all activities are carried out in compliance with regulatory requirements. Additionally, you will play a key role in identifying opportunities for process improvements and implementing solutions to enhance efficiency and productivity. The successful candidate will have a strong background in...

As a Consultant in Intellectual Property & Technology Transfer within the Lifesciences sector, you will be responsible for reviewing and drafting research collaboration agreements, IP licensing agreements, and other partnership documents. Your role will involve assessing the techno-commercial merit of IPR and invention disclosures, as well as conducting technology licensing, technology evaluation, and identifying potential partners. Additionally, you will be creating collaterals/technology briefs for outreach and managing reach-out for transaction closure. Furthermore, you will be tasked with organizing IP and technology transfer related trainings and programs, along with conducting patent c...

Job Purpose Culture Anchor:Work Hard - Consistently puts in effort. plans and tracks daily progress to achieve targetsExecute with Rigor - Takes responsibility for meeting targets with focus and effortOwn It - Maintains honesty and fairness in all interactions in line with organizations policiesAct with Integrity Duties and Responsibilities Implementation of Credit Policy and continuous evaluation to ensure adherence to the Policy and compliance with the Authority Matrix at branches in the area assigned.-Credit appraisal for BL & Doctor Loans files for the assigned location-Keeping delinquency under control-Compliance of policy and processes-Reporting of location metrics like Login, Approval...

Hiring for Principal Scientist for a leading Pharma MNC at Pune. Role & responsibilities Reporting to : Associate Director Job Summary : To develop synthesis processes of highly potent and/or cytotoxic ADC drug-linkers and transfer processes to internal/external clients and collaborate with manufacturing teams to deliver robust chemical processes that are suitable for commercial-scale manufacturing, while ensuring safety and regulatory compliance. Key Responsibilities: 1. Detailed technical evaluation of project enquiries received from the customers/ BD team. 2. Literature search, scouting the appropriate routes, and Drug-linker process optimization. 3. Execution of Bioconjugation Chemistry ...

Job Overview: The PDL Scientist - Injectable will be responsible for the development, optimization, and scale-up of sterile injectable formulations and manufacturing processes. The role demands expertise in injectable formulation science, process engineering, and compliance with regulatory and quality standards. Role & responsibilities Formulation Development: Design and optimize sterile injectable formulations, including solutions, emulsions, and suspensions. Perform compatibility and stability studies of active pharmaceutical ingredients (APIs) with excipients. Process Optimization: Develop robust, scalable manufacturing processes for injectable formulations. Define and optimize critical p...

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.

Lead end-to-end tech transfer of OSD products from R&D to commercial manufacturing sites, conduct scale-up and process validation activities, and provide technical support during regulatory audits and inspections.

Role & responsibilities 1. Capacity Planning of New / Existing Products 2. Solvent Recovery improvements 3. Process monitoring for yield improvement & failure investigation. 4. Process monitoring, process data collection, trend data preparation and discussion with concern department. 5. New product technology absorption 6. Trouble Shooting of Equipments & Processes 7. Utility calculation for cost reduction & Energy Conservation. 8. Plant Equipment modification as per Process requirement. 9. PFD, P&ID & Plant Layout Preparation 10. Material & Energy balance calculations 11. Equipment specification data sheet preparation, Techno-commercial preparation for procurement. 12. Equipment sizing, sel...

JOB DESCRIPTION: Pupose:Deliver formulations in defined timeframe to meet product delivery goals for I&D Development of different formulations either as generic or differentiated generics. To demonstrate successful stability and scale up at manufacturing site. Core Job Responsibilities . Development of formulation using scientific rationale in use of excipients to create a reproducible prototype formulation. . Ensure Proper documentation of every trial in the log note books and then using the information for creation of the Product Development Report for use in dossier for filing. . Use of QbD wherever required for Product and process optimization. . Ensure proper upkeep, maintenance and cal...