215 Tech Transfer Jobs - Page 4

Walk In Drive For FR&D - Tech Transfer In Formulation Division @ Kothur Department:- FR&D - Tech Transfer Qualification :- M Pharmacy Division :- Formulation Interview Date: 08-11-2025 (Saturday) Interview Time :- 9.00AM TO 3.00PM Work Location:- MSN Formulations- Unit-II, Kothur | MSNF Unit-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded ...

As a Project Manager in the CDMO sector, your role involves managing and executing projects from initiation to delivery. You will be responsible for ensuring adherence to timelines, budgets, and quality standards throughout the project lifecycle. Your key responsibilities include: - Managing and executing CDMO projects, ensuring adherence to timelines, budgets, and quality standards. - Acting as the primary point of contact for internal stakeholders, ensuring smooth communication and alignment on project objectives. - Collaborating closely with various teams including R&D, Manufacturing, Quality, Supply Chain, and Regulatory to ensure project milestones are achieved. - Monitoring project pro...

Conduct NPD, process optimization, scale-up & value engineering. Develop synthetic routes, validate methods, identify raw material alternatives. Maintain documentation. Support validation & transfers. Coordinate with QA, QC & production.

Job Description Summary Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape! To serve as the primary technical interface between Sandoz Manufacturing sites and the Global MS&T Capability Hub, offering expert guidance on manufacturing process design, validation strategies, and resolution of complex technical issues. The Technical Expert ensures robust process performance, product quality, and regulatory compliance across...

Role & responsibilities 1. Develop and optimize cost-effective, scalable, and robust API processes suitable for GMP manufacturing 2. Conduct lab-scale and pilot-scale experiments to evaluate process parameters and critical quality attributes (CQAs) 3. Collaborate with R&D, Analytical, QA/QC, and Production teams for successful technology transfer 4. Prepare and review technology transfer documents 5. Provide on-site support during scale-up and commercial manufacturing, troubleshooting in case of any technical issues 6. Ensure compliance with regulatory guidelines (ICH, USFDA, EMA, etc.) during development and transfer 7. Identify and implement process improvements to enhance yield, purity an...

Role & responsibilities Responsible for upstream manufacturing process support, data acquisition, and trending. To manage statistical analysis of manufacturing batches data using statistical software like Minitab, etc. Lead the upstream team in troubleshooting and process related deviation investigations activities to identify the root cause followed by providing an effective CAPA. Plan, evaluate and manage the technology transfer of new / existing products from sending unit (R&D) to receiving unit (Manufacturing). To collaborate and communicate regularly with R&D teams in execution of experimental runs and any other scale down experiments to support manufacturing process changes/improvement...

Dear All, Greetings from Aizant Drug Research!! We're looking for experienced professionals to join with our Technology Transfer(TT) team. Responsibilities: This position requires experienced candidates with 4-7 years in Technology Transfer(Formulation). Co-ordinate for preparation of departmental SOPs/Guidelines/Operating instructions. To supervise transfer of batches from lab scale to Exhibit scale/commercial batches at the shop floor and to ensure quality system compliance. To prepare and review of Master Formula Card (MFC), Scale up protocol, Scale up BMR, process validation protocols (PVP), Stability protocols, Process validation report (PVR), Dissolution Profile Protocols (DPP) and Pil...

Should be from API background Currently working as AGM/DGM/GM level Candidate should be from a reputed pharma company Major Exposure - Tech Transfer, Detailed Engineering, basic Engineering , Scale Up Education :Btech Chemical Role & responsibilities

Use Your Power for Purpose As a Senior Associate, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives. What You Will Achieve In this role, you will: Handle Technology Transfer activities & New Product Introduction process Knowledge of validation and practices related to the manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems. Conversant with design & working principles ...

Preferred candidate profile Relevant experience in scale-up of processes from laboratory scale to pilot to plant scale, technology absorption from laboratory, preparation of BFD / PFD, mass balance, utility calculations E-mail - Deepanshu.bhatt1@piind.com Mobile - 8696900583

You will be joining the Formulation R&D team at Hetero Drugs as a Scientist II, focusing on the development of sterile injectable formulations, including aqueous, non-aqueous, lyophilized, and peptide-based oncology products. Your role will be crucial in advancing product development for regulated markets such as the US, Europe, and ROW. You will be responsible for comprehensive formulation design, process optimization, regulatory documentation, and coordination across departments. - Independently lead the development of sterile injectable products, including aqueous, non-aqueous, lyophilized, and peptide-based formulations. - Conduct formulation studies, process optimization, and scale-up a...

You will be joining UMEDICA, a vertically integrated company involved in manufacturing and exporting a wide range of finished formulations globally. The company's manufacturing facility in Vapi, Gujarat, is approved by global regulatory authorities. UMEDICA, established in 1983, operates in over 85 countries worldwide, including prominent markets like the USA, Canada, EU, UK, Australia, Middle East, and more. As part of our expansion plans, we are seeking an Assistant Manager / Manager with a strong background in Packaging to join our R&D center in Turbhe, Navi Mumbai. In this role, you will directly report to the Head of Formulation Development. Your responsibilities will include: - Develop...

As a Process & Manufacturing Chemist at our company, you will be responsible for translating high-performance, lab-scale exosome formulations into robust, GMP-compliant manufacturing processes. You will play a key role in optimizing small-batch and pilot production of luxury skincare (face serums, masks) and haircare (masks, serums), ensuring consistency, yield, and cost efficiency. - Develop pilot- and commercial-scale processes for creams, serums, gels, and masks infused with exosomes and advanced actives. - Define process parameters such as temperature, speed, and order of addition to preserve exosome integrity and product texture. - Conduct scale-up trials, identify bottlenecks, implemen...

Process Profile -API

Role & responsibilities Review and provide technical inputs on Product Development Reports (PDR), Master Formula Cards (MFC), and Technology Transfer (TT) documents. Prepare product process-related risk assessments, protocols, and reports for feasibility trials and scale-up batches. Execute trial and scale-up batches, and prepare summary reports. Prepare and review Exhibit Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR). Support regulatory filing by providing intended commercial BMR, BPR, and stability evaluation summaries. Support regulatory in obtaining Test Licenses, Import Licenses, No Objection Certificates (NOC), and Manufacturing Licenses by providing the necessary...

You have a good technical background in Tech transfer and Scale up studies, process conceptualization in the T&D department. You should have at least 7 to 10 years of experience and hold a BE Chemical degree. - Receive & absorb new process technology from R & D. - Ensure feasibility of the process on an Industrial scale. - Observe lab demo to understand the process & generate data required for Pilot trials & conceptual design. - Identify process safety aspects of the process & collect/generate safety data. - Generate Material & energy balance. - Define process performance at lab scale (norms). - Map process steps in the Pilot system along with Pilot plant operations team. - Monitor Pilot pla...

Company overview: A diversified Indian group engaged in both pharma and confectionery machinery & manufacturing , offering end-to-end solutions from formulation to packaging. Alongside specialized confectionery systems, it provides large-scale pharmaceutical contract manufacturing with a strong focus on quality, compliance, and innovation. Its USP lies in delivering integrated, cost-efficient solutions across pharma and food sectors , trusted by global brands. Job Location: Hyderabad Position: R&D Officer / R&D Executive (Topical formulation experience must required) Key Responsibilities: Formulation development of semi-solid dosage forms (creams, gels, ointments) using QbD Literature & pate...

We required candidate for the position of AGM-Formulation Exp in OSD-Immediate Release (IR),Extended Release (ER),Powder for Suspension(PFOS) &Oral Liquid dosage forms for US,EU&Canada. T-Exp-15 + CTC-Upto 30.00Lacs Loc-Mumbai(Kandivali)

Role & responsibilities 1. Prepare detailed project timelines using tools such as Gantt charts and milestone trackers to monitor the end-to-end progress of API and intermediate projects. 2. Define critical path activities that determine the project delivery date and monitor them closely to ensure adherence to schedules. 3. Escalate risks or delays to senior management and stakeholders, and implement recovery plans to bring projects back on track. 4. Rebaseline timelines with proper approvals when there are changes in scope, resources, or regulatory requirements. 5. Coordinate with cross-functional teams including Process R&D, Production, Engineering, QA/QC, SCM, RA, and EHS to ensure timely ...

Devp & implement New Technologies, Process Optimization, R&D & Tech Transfer. Lead innovation & cross functional collaboration. Ensure compliance with global regulatory & EHS Drive efficient scale up from lab to plant, ensuring quality & consistency Required Candidate profile Expert in process devpt, scale-up & tech transfer in Aroma Chemicals, Agrochemicals & Pharma Intermediates Strong in reaction engineering & process safety Proven leadership & cross functional teamwork

Position: Executive TSD (Technology Support / Technology Transfer) Department: TSD Location: Ahmedabad Reports to: TSD Manager / Head of Department Experience: 510 Years Education: B.E / M.E Chemical / Chemical Engineering Key Responsibilities: Execute technology transfer from R&D to pilot and commercial production. Support process scale-up and optimization for cost, yield, and safety. Prepare and review tech transfer protocols, BMR/BPR, SOPs, and risk assessments . Troubleshoot and resolve issues during pilot and commercial batch production . Ensure compliance with cGMP, GLP, QbD, and regulatory guidelines . Liaise with R&D, QA, AR&D, Production, and Regulatory Affairs teams. Support audits...

Job Description: We are seeking a highly skilled and experienced professional for the role of Formulation Development OSD , focused on regulated markets including USFDA, MHRA, EMA, and other global regulatory agencies. The ideal candidate will have a proven track record in developing and optimizing solid oral dosage forms (tablets, capsules) for submission and commercial-scale manufacturing. Key Responsibilities: Lead and execute formulation development projects for oral solid dosage (OSD) forms targeted at regulated markets (US, EU, etc.). Design and execute pre-formulation and formulation trials, optimization, and scale-up. Develop robust formulations and manufacturing processes based on Q...

Qualification :- B. Pharm / M.Pharm Experience :- 4 to 6 years in Pharmaceutical manufacturing , R&D or Tech Transfer Salary :- up to 7 LPA Location :- Changodar GIDC (Ahmedabad) Solid understanding of formulation scaleup and tech transfer

Role & responsibilities 1.Lead and execute the development of upstream process, scale-up, scale down qualification, technology transfer and process characterization of biotherapeutics by applying scientific principles and documentation of the same. 2. Lead, design and manage experiments to achieve product quality and determine appropriate ranges of process parameters for drug substance. 3. Lead and design experiments related to yield improvement, process improvements, scale down model, process characterization and ensure successful execution and documentation of the same. 4. Detailed data analysis and determination of critical process parameters for upstream process, trending of in-process c...

Role & responsibilities 1. Develop and optimize cost-effective, scalable, and robust API processes suitable for GMP manufacturing 2. Conduct lab-scale and pilot-scale experiments to evaluate process parameters and critical quality attributes (CQAs) 3. Collaborate with R&D, Analytical, QA/QC, and Production teams for successful technology transfer 4. Prepare and review technology transfer documents 5. Provide on-site support during scale-up and commercial manufacturing, troubleshooting in case of any technical issues 6. Ensure compliance with regulatory guidelines (ICH, USFDA, EMA, etc.) during development and transfer 7. Identify and implement process improvements to enhance yield, purity an...