201 Tech Transfer Jobs - Page 3

Role Overview: As a member of the GMP Services department in the role of Tech Transfer, your main responsibility will be to perform Gap analysis of the existing facilities with the required regulatory requirements for API / Excipients / Packaging Material companies / Testing Laboratories. You will also be responsible for preparing reports and CAPA reviews in a timely manner and preparing technical documents as per regulatory expectations. Additionally, you will provide Validation / Qualification Services, impart training to employees/site team members, and participate in remediation projects allotted by the company. Key Responsibilities: - Perform Gap analysis of existing facilities with reg...

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other sup...

JOB DESCRIPTION: Primary Job Function: Lead and guide the team for LLM Operations and functionality on GMP aspects and Abbott policies and procedures. Monitor compliance of Loan license manufacturing sites and TPMs. Perform LLM site visits on scheduled basis and ensure compliance of LLM sites to cGMP, Abbott policies and Procedures. Ensure Pharmacopoeial compliance of Abbott products manufactured at LLMs. Review ongoing stability data and control samples of Abbott products. Ensure implementation of Abbott quality audit CAPA & closure at LLMs. Ensure timely investigation of the Market complaints within SLA, root cause analysis, CAPA implementation and effectiveness check. Coordinate with resp...

Opening for Process Technology Transfer. Location : Dahej Role & responsibilities : To observe lab experiments during lab demonstration at optimization stage and suggest Negative experiment based on plant equipment and feasibility. Preparation of process summary, volume calculation, Mass balance, utility load, effluent load and costing. To identify and propose new ideas & technology to improve process efficiency, smooth unit operation/unit processes and effective utilization of resources To identify recovery and reuse of solvents. Ensure right equipment selection as per process requirement. Suggest required modification in equipment as per process requirement. Support the external job work a...

Designation: Apprentice Department: Formulation Technology Transfer Preferred candidate profile: Candidates should have brief knowledge about the Formulation Technology Transfer department. Basic concepts should be cleared which you have studied during your qualification. Qualification: B. Pharma / M. Pharma Selection Criteria: Candidates should have 60% and above in 10th & 12th both. And in graduation or post graduation candidate should not have any kind of ATKT/Backlog in any of the semesters above 55% is required in both B. Pharma / M. Pharma. Stipend: Rs. 15,000 p/m Interested candidates please share your updated CV's on akshitsharma@torrentpharma.com .

As a Process Development Chemist in the R&D department, your role involves developing, optimizing, and executing processes for APIs to ensure timely implementation within budget. Your key responsibilities include: - Developing API processes in the lab through literature surveys and API intermediate characterization to ensure quality and timely implementation - Conducting literature surveys and route selection for assigned projects - Preparing and executing development strategies for assigned projects - Maintaining records of experiments and results, optimizing process parameters, and supporting the creation of new IP assets - Calibrating instruments in the lab, following safety procedures, a...

SUMMARY *Experience with multi customers & Projects handling *Team work & CFT drive - Able to handle internal team towards customer need - Able to align and get the things done with other process / departments *Good communication skill - Maturity - Clarity - Spontaneous *Awareness on Die casting , machining, Assembly and associated process *Basics of Alloys and metallurgy *Vendor base connect - Tooling - Facilities - technology *Reading Simulation result & Drawings *APQP awareness Requirements 1) Project management 2) Customer handling, Communication 3) Decision making 4) Die casting, Machining background 5) Experience in customer contacts 6) Team player Benefits On time project execution Me...

Job Summary: We are seeking a skilled and motivated Research Scientist to join our Formulation & Development (F&D) Oral Solid Dosage (OSD) team. The ideal candidate will be responsible for the design, development, and optimization of oral solid dosage forms (tablets, capsules, etc.) from concept to commercial scale. The role involves conducting pre-formulation studies, formulation trials, process optimization, and technology transfer to manufacturing sites while ensuring compliance with regulatory and quality standards. Key Responsibilities: Design and develop robust formulations for oral solid dosage (OSD) products, including tablets, capsules, and modified-release systems. Conduct pre-form...

Role Overview: You are applying for the position of Head of R&D at The Bland Company, a food and biotech startup focused on producing cost-efficient, highly functional ingredients through novel biochemical processes. As the Head of R&D, you will be responsible for leading scientific innovation and scaling manufacturing processes, particularly in the development of novel protein ingredients. Key Responsibilities: - Lead R&D efforts in protein chemistry, process optimization, and application science - Translate business objectives into clear technical goals and outcomes - Develop and execute the R&D roadmap, from refining the platform to validating client-facing applications - Identify and ass...

As a Junior Executive-Tech Transfer at a leading pharmaceutical company in Hosur, Tamil Nadu, your role will involve the following responsibilities: - Involving in the batch execution activities for tech transfer & site transfer products. - Reviewing documents as per the requirements for the execution of tech transfer & site transfer products. - Applying for Test license for tech transfer & site transfer products. - Preparing & ensuring availability of item codes for raw materials, primary packaging materials, filter & tubings for tech transfer & site transfer products. - Conducting product and equipment gap assessment for the tech transfer & site transfer products. - Preparing engineering b...

Handle end to end scale up activities from Lab to Pilot to Commercial Scale Select the equipments for scale up & discuss with R & D and Production and finalize it. Act as a tool between Production, QC, QA with R & D / PELAB to absorb the technology from Lab to Plant. Prepare the PFD, checklist for Documents submitted &To assist QA in preparing Validation protocol.

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