201 Tech Transfer Jobs - Page 4

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...

Role - Process Engineering Key Responsibilities: To lead and support process development, scale-up, troubleshooting, and optimization of chemical processes from laboratory to commercial plant scale, ensuring safety, cost-efficiency, and robust performance. This role demands a technical expert with hands-on experience and expertise in process engineering, pilot plant trials, and production scale implementation, ensuring process safety, cost-efficiency, and robust performance. A. Process Development & Scale-Up Lead the design and execution of pilot plant and plant trials for new processes Translate lab-scale or kilo-lab processes to commercial scale protocols with minimal deviations Conduct ma...

Role & responsibilities Job Title: Sr. Executive/Executive ( 6 to 9 years of Experience ) Location : Baddi , Himachal Pradesh Key Responsibilities: 1. Technology transfer (NPD and site transfer), process validation, and continuous improvement/gross margin improvement projects. 2. Experience in product/process development for various dosage forms, including: - Solid Oral (Tablets/Capsules) - Semi- Solid dosage form - Topical (Creams/Lotions/Ointments) - Oral Liquids (Syrups/Suspensions) - Cosmetic formulation experience is a plus. Preferred candidate profile Preferred candidate profile from Solid Oral (Tablets/Capsules) - Semi- Solid dosage form - Topical (Creams/Lotions/Ointments) - Oral Liq...

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

Responsible to ensure Technology Transfer activities (From R&D to site, From Site to site). Manage the Scale-up, Process Optimization, submission batches, Process Validation, Process Improvements & Troubleshooting activities. Ensure timely execution of Feasibility, Assessment, Registration, New product launches and AVD projects by continuous co- ordination with unit Production, QC, ADL, RA and Project Management Team. Monitoring the progress of product status during stability study, responding the queries from various regulatory bodies. Review of Process Optimization reports. Review of gap analysis and define the action plan. To provide technical inputs for closure of OOS/OOT. Identification...

Greetings!!!! We are looking for a QA - Manger - OSD _Chennai Location Job Description: Responsible for BMR, batch release, validations, qualifications, SOPs, GMP compliance. Handle audits, QMS (Deviation, OOS, OOT, CAPA), and technology transfer. Exposure to analytical operations will be an added advantage. Strong experience in OSD / Liquid formulation QA required. Key Skills: QA, Quality Assurance, BMR, Batch Release, Validation, GMP, SOP, QMS, Audit, Deviation, OOS, OOT, CAPA, Pharma QA. Salary: As per market standards Note: Immediate joiners preferred. Interested Candidates Kindly share your updated cv to uma@bvrpc.com

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their busines...

As a Group Leader in the HP API Lab, you will be responsible for leading the end-to-end synthesis and scale-up of HP APIs. A Ph.D. in organic chemistry from reputable institutions in India or overseas, with post-doctoral experience being preferable, is required for this position. Your primary focus will be to ensure containment and EHS compliance throughout the process. In this role, you will drive cross-functional collaboration to facilitate successful technology transfer and scale-up processes. Your expertise and leadership will play a critical role in the advancement of the HP API Lab's objectives.,

Lead formulation R&D for OSD, external, and liquid preparations. Oversee pre-formulation, development, and scale-up, ensuring regulatory compliance. Manage tech transfer and mentor junior scientists. Required Candidate profile B.Pharm/ M.Pharm 6-10 Yrs

Lead formulation R&D for OSD, external, and liquid preparations. Oversee pre-formulation, development, and scale-up, ensuring regulatory compliance. Manage tech transfer and mentor junior scientists. Required Candidate profile B.Pharm/ M.Pharm 6-10 Yrs

The Manager of Competitive Intelligence R&D at Amgen will play a crucial role in leading intelligence gathering activities to support marketing teams across various business units. Reporting directly to the Director/Sr Director of Competitive Intelligence, you will work on-site at the Amgen India Hyderabad Office for a minimum of 4 days a week. Your primary responsibilities will include developing and presenting key Competitive Intelligence deliverables for internal stakeholders, leveraging various secondary research resources to generate competitive insights, working with R&D leads to conduct primary and secondary competitive intelligence research, and managing multiple CI vendors for hypot...

You will be responsible for the formulation development of Pharmaceutical and Nutraceutical products including tablets, capsules, effervescent tablets, sachets powders, and liquid formulations. This involves conducting literature search and patent search for the formulation, as well as developing cost-effective and fast production processes along with stable formulations. You will be required to create MFR and relevant specifications, facilitate tech transfer, and maintain documentation. Additionally, you will need to address any ongoing issues in the existing formulations. The ideal candidate should have 7 to 10 years of experience in this field. If you are interested in this opportunity, p...

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...

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...