336 Technology Transfer Jobs - Page 3

As a bench scientist in our organization, you will be responsible for conducting experimentation and research in the area of formulation development, process development, regulatory affairs, and intellectual property for global markets. Your work will involve planning and executing experiments aligned with project milestones while applying scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be expected to analyze and interpret data from literature reviews effectively to support decision-making processes. Additionally, you will need to understand the intellectual property landscape, develop strategies, search for prior art, and establish proof of concept through experimentation. Collaboration with cross-functional teams including Manufacturing Science and Technology (MS&T), Quality Assurance (QA), Quality Control (QC), and production teams across different geographies will be crucial for technology transfer and timely execution of submission batches. Your role will also involve identifying challenges, bottlenecks in development, and providing mitigation proposals at various stages of product development. Furthermore, you will be responsible for problem-solving, prioritizing activities, conducting development trials, and ensuring alignment with established milestones. Clear communication with internal stakeholders, proactive identification of challenges or risks, and adherence to business unit Key Performance Indicators (KPIs) will be essential aspects of your role. On a day-to-day basis, you will work closely with the formulation development teams to achieve key milestones, conduct experiments following QbD principles, and prepare presentations at different stages of product development. Your tasks will include literature reviews, sourcing API and Excipients, conducting preformulation studies, executing development trials, interpreting analytical data, and preparing necessary documentation for regulatory submissions. To be successful in this role, you should hold a Ph.D. in Pharmaceutical Sciences with at least 1 year of experience or an M.Pharm in Pharmaceutical Sciences with a minimum of 3 years of experience from reputable universities. Prior experience in working with generic pharmaceuticals in regulated markets such as the US, EU, or Canada will be advantageous. Your commitment to personal accountability, effective work habits, continuous learning, and collaboration with internal teams will be instrumental in contributing to the success of our organization's mission to make good health more affordable and accessible globally.,

KPMG India is looking for Executive - Government Technology Executive - Government Technology to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

l Interaction with R&D department for new product development l Equipment mapping for kilo lab and kilo lab to pilot plant. l Responsible for preparing BPCR,PCOCR l Responsible for lab demonstration in R&D l Study of new product in R&D and plan batch in pilot scale l Planning for raw materials for batch trial. l Enquiry floating of equipment and technical clearance of equipment. l Responsible for scale up activities of new projects as well as cost reduction of product and waste reduction. l Able to lead subordinate technology transfer process engineer team l Planning and resource management for continuously pilot plant operation. l Equipment selection, Process mapping, Time cycle calculation, Volume calculations for new product . l Responsible for material balance and energy balance of product. l Utility calculation,hydraulic calculation and cost estimation of new products l Identify and analyze bottlenecks,implement best practice and continuous improvement for process optimization. l Optimize resource utilization,reduce waste for process efficiency. l Capacity calculation capacity enhancement for any new or existing products. l Plant development, Plant validation batches report preparation. l Detailed workout for equipment modification along with detailed job list & PFD for scale up purpose

Role & responsibilities To perform the Technology transfer of Product from R&D to Site receiving activities and QMS related activities at the manufacturing plant . To perform alternate vendor batch execution, process improvement, change in batch size, trouble shooting at shop floor, equipment change activities of product after technology transfer completion along with production team. To finalize batch sizes of scale up, exhibit and commercial batches to meet the equipment capacities and regulatory requirements with consent of R&D and production. To prepare/review relevant documents like SOP, Batch Manufacturing Record, Sampling Protocol, hold time study protocol/ report, stability study protocol/report, Process validation protocol and Report for the scale up, exhibit and validation batches. To provide technical support for change management, investigations of deviations or OOS, CAPA identification and QMS related activities at plant. Ensure cGMP and Regulatory compliance.

Develop tablet/capsule formulations for regulated markets (US/EU). Conduct pre-formulation, prototype trials, and scale-up. Execute lab, exhibit, and validation batches. Prepare technical documents for ANDA filings. Support tech transfer and respond to regulatory queries.

Specialized expertise in Inhaler Products including Metered Dose Inhalers (MDI) and Dry Powder Inhalers (DPI). Method development, validation, and forced degradation studies specific to inhalation dosage forms. Execution and support of technology transfer for analytical methods related to MDI/DPI. Ensure compliance with Quality Assurance systems and applicable regulatory guidelines (ICH, FDA, EMA). Lead analytical activities for ANDA and NDA projects for respiratory products. Coordinate with cross-functional teams for project planning, documentation , and timely regulatory submissions. Review and preparation of analytical method validation protocols, reports, and supporting documentation for regulatory filings. Active involvement in OOS/OOT investigations, troubleshooting, and CAPA implementation.

Lead formulation and process development of HFA-based MDI products for regulated markets (US, EU, etc.). Manage drug-device combination product development , including coordination with device vendors for CMC and regulatory compliance. Coordinate cross-functionally with analytical, regulatory, clinical, and manufacturing teams to ensure timely project execution. Drive process optimization at the lab scale using QbD principles; establish control strategies for successful scale-up. Design and define product specifications in compliance with current global regulatory guidelines. Review Product Development Reports, Technology Transfer Reports , and Deviation/Investigation Reports for technical accuracy. Support regulatory query responses related to product development and manufacturing in collaboration with relevant departments. Lead technology transfer of HFA-based MDIs to contract manufacturing organizations (CMOs) for domestic and international markets. Provide technical and regulatory support for submissions including NDA, ANDA, and 505(b)(2) applications. Troubleshoot formulation-related issues during manufacturing to ensure smooth and compliant commercial production.

We are looking for a Chief Technology Officer (CTO) to provide sound technical leadership in all aspects of our business. You will communicate with employees, stakeholders and customers to ensure our companys technologies are used appropriately. Strategic thinking and strong business acumen are essential in this role. We expect you to be well-versed in current technological trends and familiar with a variety of business concepts. If you are also an excellent communicator and public speaker, wed like to meet you. Responsibilities Develop technical aspects of the companys strategy to ensure alignment with its business goals Discover and implement new technologies that yield competitive advantage Help departments use technology profitably Supervise system infrastructure to ensure functionality and efficiency Build quality assurance and data protection processes Monitor KPIs and IT budgets to assess technological performance Use stakeholders feedback to inform necessary improvements and adjustments to technology Communicate technology strategy to partners and investors Requirements and skills Proven experience as a CTO or similar leadership role Knowledge of technological trends to build strategy Understanding of budgets and business-planning Ability to conduct technological analyses and research Excellent communication skills Leadership and organizational abilities Strategic thinking Problem-solving aptitude BSc/BA in Computer Science, Engineering or a related field; MBA or other relevant graduate degree is a plus

Role & responsibilities Lead and execute technology transfer projects in alignment with Centre of Competency (CoC) guidelines and local regulatory requirements, ensuring seamless integration of friction material technologies. Develop and manage comprehensive project plans, schedules, and resource allocations to ensure timely and cost-effective delivery. Collaborate with cross-functional teamsincluding R&D, procurement, quality, and productionto support the localization and industrialization of friction materials, with a focus on organic chemistry and material performance. Identify and mitigate project risks while proactively managing opportunities to enhance profitability and technical outcomes. Coordinate technical communication with internal and external stakeholders, ensuring clarity on scope, deliverables, and timelines. Support financial planning and control by evaluating the commercial impact of technical decisions, including tooling, test benches, and critical equipment. Maintain key documentation such as gap analyses, risk registers, validation reports, and technology transfer plans to ensure traceability and compliance. Ensure successful handover of new processes and products to production, meeting quality, cost, and delivery (QCD) targets. Drive localization initiatives to reduce Total Manufacturing Cost (TMC) and improve contract margins, while monitoring phase-in/phase-out transitions. Integrate digital tools and processes to support traceability, paperless workflows, and real-time data collection, especially in serial number tracking and ERP systems. Facilitate business process alignment by coordinating with IT and functional teams to resolve system gaps and support digital transformation. Preferred candidate profile 12+ years of proven experience in technology transfer, project management, and digitalization initiatives, preferably in a manufacturing or industrial setting. Strong Project Management Skills. PMP certification will be an added value. Six Sigma Certification. Exposure to Industry 4.0, Digitalization. Preferred: Experience in friction material development, including organic chemistry of brake pad compounds, resin systems, and performance testing.

As an R&D - M19 at PURE CHEMICALS CO in Chennai, Tamil Nadu, India, you will be responsible for conducting patent analysis, technical research, internet research, reaction and formulation work, and documentation. Your role will primarily involve product development, technology transfer, chemistry, and testing. You will work within the R&D department of the organization and collaborate with colleagues to contribute to the innovation and development of new products. The ability to analyze patents, conduct technical research, and document findings accurately will be crucial for success in this role. Proficiency in English and Tamil languages will be required to effectively communicate and collaborate with team members. A minimum qualification of MSC in chemistry or related field is necessary for this position. Join our team at PURE CHEMICALS CO and be a part of our innovative research and development projects in the chemical industry.,

You will be joining Honasa Consumer Limited (HCL), a rapidly growing Beauty & Personal Care conglomerate with a focus on honesty, natural ingredients, and safe care. HCL houses brands such as Mamaearth, The Derma Co., Aqualogica, and BBlunt, catering to consumers across 500 cities in India. The company's ethos revolves around innovative products, direct-to-consumer marketing, and e-commerce fulfillment, supported by investments from renowned firms like Sequoia Capital India and Sofina SA. As a key member of our team, you will need to possess a high level of technical proficiency and a proactive approach to working in the lab. This role demands expertise in leading cutting-edge technology and product development projects, particularly within the personal care industry, with a focus on skin and hair care. To excel in this position, you should hold a degree in B.Tech/M.Tech in Cosmetology, B.Sc./M.Sc. in Organic Chemistry, B.Pharm, or M.Pharm. Previous experience in the personal care sector, especially in skin and hair care, is crucial for this role. Your responsibilities will include overseeing all stages of product formulation, from concept development to final approval, and managing pilot and full-scale production batches. You will lead the creation of stable and effective formulations for manufacturing at third-party facilities and in-house labs, conduct research to support production processes, and develop new formulations in line with business needs and innovation targets. A deep understanding of skincare and hair care products is essential, along with hands-on experience in surfactant-based formulations and knowledge of surfactants, conditioning agents, and raw materials used in hair care products. You will be responsible for technology transfer activities, ensuring compliance with SOPs, cosmetic regulations, and safety standards, as well as identifying cost-effective raw material substitutes to enhance product quality. In this role, you will drive the development of new personal care products through scientific expertise and technical leadership. Your ability to navigate ambiguity, stay abreast of regulatory trends, and innovate within the industry will be instrumental in shaping our product portfolio and maintaining our competitive edge.,

As an R&D Executive at VTC R&D, you are responsible for performing and overseeing all activities related to formulation and filling process development. Your duties include having a strong understanding of optimizing vaccine formulations, selecting stabilizers and excipients, as well as preparing adjuvants such as aluminium salts, Oil-In-Water emulsions, Liposome-based adjuvants with TLR agonists and saponin, and LNP formulation. You will also be involved in aseptic filling and Lyophilization cycle designing for new vaccine products and troubleshooting existing vaccines. In this role, you will execute clinical drug product manufacturing for clinical batches, plan and carry out media fill activities, and maintain R&D lab documents, equipment, and area qualifications in compliance with GMP requirements. Additionally, you will be responsible for preparing process validation and technology transfer protocols as per GMP requirements and collaborating with QA, QC, and Engineering departments for viral vaccine development activities. Ensuring proper hygiene and entry exit procedures in the formulation and filling section, preparing adjuvants, buffer solutions, and other materials, as well as coordinating with the central warehouse department for materials receipt and entry are also part of your responsibilities. You will supervise the preparation of disinfectant solutions, cleaning solutions, integrity testing of filters, and sanitization and disinfection activities in the R&D formulation department. As part of the QMS, you will handle deviations, MDD, investigations, observations, and ensure their timely closure. You will be involved in preparing standard operating procedures, batch manufacturing records, QRM, and protocols related to the R&D formulation and filling section. Moreover, you will supervise the washing, drying, packing, and sterilization of materials required for R&D development and GMP clinical batch preparation. Your role as an R&D Executive will be crucial in advancing vaccine development and ensuring compliance with quality standards and procedures.,

As a Senior Manager in API Production, you will be responsible for overseeing the production activities at the Panoli (Baroda) location. With a background in B.Pharma/M.Pharma and a significant work experience of 17 to 19 years, you will lead a team of 150 to 200 members and manage a production capacity of a minimum of 50 Cr. Your role would involve handling various aspects such as Production Planning, Resource Management, and Regulatory Compliance within an API plant setting. Your key responsibilities will include coordinating Production Planning and scheduling on a day-to-day basis, ensuring the availability of necessary resources like BMR, Raw Material, and Manpower. You will collaborate with departments such as QC/QA/STORE/Eng. Dept. to address troubleshooting problems effectively. Upholding GMP Standards and overseeing the implementation of technology transfer for new products will be crucial in this role. Continuous improvement in product processes, efficiency, and services will be under your purview, along with documentation tasks like Monthly Reports, data analysis, and root cause analysis. Managing consumable items, planning Raw Material requirements, and ensuring proper documentation related to processes and cleaning activities are essential responsibilities. You will also oversee the handling of solvents, process waste, and maintenance of plant equipment while providing training to subordinates. Your role will involve operating electronic systems like ONE HR portal, Metis Track Wise, Minitab, and Outlook for efficient plant operations. Additionally, you will review and revise BMR and SOP as needed, ensuring compliance with regulatory standards and maintaining a high level of operational efficiency in the API production facility.,

Job Description As a part of Dr. Reddys Laboratories Ltd., a leading multinational pharmaceutical company with a global presence, your role is pivotal in accelerating access to affordable and innovative medicines. With a team of over 24,000 employees worldwide, you will contribute towards the collective purpose of ensuring that Good Health Cant Wait. Since our inception in 1984, we have grown exponentially to establish research and development centers, manufacturing facilities, and commercial presence across 66 countries. Our commitment to access, affordability, and innovation is unwavering, driven by deep science, progressive people practices, and robust corporate governance. In the ever-evolving pharmaceutical industry, we are seizing the opportunity to strengthen our core operations and pave the way for future growth. The Next and the New strategy focuses on being purpose-driven, future-ready, and sustainable. By aiming to reach over 1.5 billion patients globally by 2030, we are aligning our core businesses with sustainability at the forefront of our purpose and strategy, emphasizing respect for people, planet, and purpose. About Biologics At Dr. Reddys, our Biologics division is committed to making advanced medicines accessible to millions worldwide. With two decades of experience in developing high-quality global biosimilars, we have established ourselves as leaders in the biosimilars segment. Our focus on creating affordable yet effective generic biosimilars has enabled us to market 6 products in multiple countries with a robust development pipeline. As the biosimilar industry is poised for an 8X growth in the next 3-4 years, your role as Manufacturing Head will be pivotal in driving the transformation and scale-up agenda for the Biologics organization. This includes expanding capacity, ensuring facility readiness for regulated markets, implementing digital advancements, streamlining production planning, and strengthening manufacturing capabilities. Responsibilities In this role, you will: - Evaluate the organization's readiness for scaling operations and design a strategic roadmap for expansion. - Lead cross-functional teams in executing transformation initiatives and strengthening manufacturing and R&D capabilities. - Drive the adoption of innovative technologies and process enhancements to optimize performance at scale. - Track project milestones, analyze key performance indicators, and ensure progress aligns with objectives. - Implement change management strategies for seamless transitions to new processes and systems. - Utilize data analytics to improve decision-making, streamline operations, and enhance overall efficiency. - Identify, evaluate, and mitigate risks to ensure business continuity and regulatory compliance. - Oversee biosimilars drug substance manufacturing, ensuring compliance with GMP and regulatory standards. - Manage manufacturing services and technology teams to optimize production processes and improve efficiency. - Develop and implement manufacturing strategies to meet production goals and timelines. - Drive transformation initiatives to enable scale-up to 8X, achieving best-in-class productivity. - Ensure audit readiness of manufacturing plants and maintain quality control standards throughout the process. - Collaborate with cross-functional teams to support product development and commercialization. - Drive continuous improvement initiatives to enhance manufacturing capabilities and reduce costs. - Manage the technology transfer process for new products and processes and ensure compliance with safety, health, and environmental regulations. - Develop and manage the manufacturing budget, mentor team members, and foster a culture of innovation and excellence. Qualifications, Experience, Skills & Attributes - Bachelor's degree in Biochemistry, Biotechnology, Chemical Engineering, or related field (Advanced degree preferred). - Minimum of 15 years of experience in biologics manufacturing, with at least 5 years in a leadership role. - Extensive knowledge of biosimilars manufacturing processes, GMP, regulatory requirements, and quality control standards. - Proven experience in managing large-scale manufacturing operations, leading cross-functional teams, clearing FDA audits, and introducing new technologies for performance improvement. - Experience with single-use bioreactor technology, continuous manufacturing processes, process development, and technology transfer. - Familiarity with regulatory submissions, inspections, and managing budgets effectively.,

The Assistant Manager - Program / Project Management (Pharma) at Jubilant Generics Limited in Greater Noida will be responsible for managing Contract Manufacturers for different markets to ensure timely execution of identified Projects and uninterrupted supplies. Strong communication skills are essential for effective coordination with various teams. The candidate should have the ability to anticipate project-related issues and take timely actions to address them, ensuring availability of materials, timely completion of milestones, and launch of products in identified markets through constant stakeholder coordination. Responsibilities include leading end-to-end project lifecycle management for global regulatory and commercial projects, developing project timelines and risk mitigation plans, overseeing Analytical Method Transfer planning and execution, acting as a point of contact for international clients and internal teams, collaborating with cross-departmental teams, and ensuring deliverables meet regulatory standards of specific regions. Qualifications & Experience: - M.Pharm / B.Pharm from a reputed institution - PMP certification desired - 2 - 7 years of experience in program management in large / mid-sized Pharma Companies - Proficiency in Microsoft Office suite - Strong communication, organizational, analytical, and critical thinking skills Required Skills: - Microsoft Projects (MSP) - Project Plans and Charters - Technology Transfer Jubilant is an equal opportunity employer, committed to providing fair employment opportunities without discrimination based on various characteristics protected by local laws.,

Research In Agro Intermediate And Chemicals Doing Lab trials as per Instructions Analysis of results Follow safety rules and regulations Maintain data of all the Lab Experiments Preventive maintenance and improvement activities Statutory compliance Required Candidate profile M. Sc or Ph. D with Chemistry 2 to 9 years of Experience in Agro , Specialty Chemical , Fine chemical , Intermediate , Dyes , Pigment , Etc. Reporting to Local Unit Head - Research And Development

Summary Job Functions: Handling, supporting and executing all activities including training to subordinates for manufacturing process support and any late stage developmental work for process improvement related to Downstream process in MSAT. Key Responsibilities: - Execution of process scale up experiments, documentation and process improvements to support manufacturing. - Process transfer and execution of tech. transfer with help of BBM. - Planning and executing experiments of DSP for process improvement, demonstrating and recording the same in proper format / report. - Designing and execution of scale down experiments to support manufacturing for scale up. (Bag evaluation/Filter sizing/Alternate vendor evaluation etc.) - Drafting the process related reports, protocols and IOC as a part of documentation - Support of process transfers- Evaluation and support for implementation of new processes focusing on direct transfers - Preparation of Qualification /verification documents (Protocols and reports) of equipment Responsible for conducting experiments to support the manufacturing team in need for any issues or improvement in the process. Both for microbial and mammalian process - Responsible for providing shop floor support during scale up activities for engineering, CT and PPQ batches - Ensures corporate cGMP and GLP compliance of all activities performed. - To follow Good Documentation Practices and Data Integrity’ requirements during any GxP Operation and recording at site. - To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed. - To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to Job description.

Role & responsibilities Generate process engineering data for various products by carryout Material & Energy balance along with Reaction, Heat & Mass transfer & Separation studies, drive efficiencies. Carryout Technology transfer for In-house developed molecule / Externally acquired technology. R&D-Validate new process, Suggestion for plant suitability, Witness R&D demo batches. Preparing Variable cost, as per R&D Technical package and its validation during piloting. Support during Piloting. Guide/Support operations team during piloting & commercial plant commissioning/stabilization, at various plant locations, after handover from project execution team. Prepare Basic Engineering Package & Detail Engineering Package. Generate useful Process engineering data from Piloting batches for scale up & commercialization of the new process & improvement of existing process. Carryout process simulation in Aspen plus for process designing & equipment sizing. Carryout HAZOP studies. Prepare Capex for the designated project. Co-ordination & tracking with various disciplines such as process, mechanical, civil, electrical instrumentation, throughout the project execution phase. Highlight areas of concern coming in way of completion of project. Coordination with Detail Engineering Consultant during detail engineering phase. Experience in process simulation in ASPEN Plus / HYSYS / ASPEN EDR Carryout thermal design of heat exchangers, hydraulics, distillation columns design, chilled water and chilled brine systems, vacuum systems. Interact with Vendors for equipment procurement, technical queries. Should have experience in selection of instruments and DCS. Preferred candidate profile Have understanding on fluorine-based chemicals. Have process design exposure in handling AHF & Specialty chemicals. Generation of Process Engineering & Scale up data / documents. Understanding of Process safety w.r.t AHF. Understand process simulation & use of Aspen Plus simulation tool. Basic Engineering & Detail engineering documents. HAZOP study, PSSR. Procurement Till Technical Bid Analysis stage and GAD approvals Pre-Commissioning and Commissioning, Batch Validation for Repeatability and Reproducibility.

Role & responsibilities Responsible for Pre-formulation studies for lab formulation development trials of solid orals, Oral Liquid, injectable, products, and Nutraceuticals product. To design strategy for projects through literature surveys. Respective API characterization, excipients characterization, drug and excipient study and its ratio. Worked on different manufacturing strategies for the development of products. To evaluate product for stability in manufacturing, monitor and review the stabilized batches. To study on existing formulations. Responsible for co-ordination, execution and monitoring of scale up activity, Responsible for Trial batches, Scale up batches, Optimization batches, Exhibit batches. Co- ordination with all cross-functional teams. TT sites and LL Sites To design/assist/support/ review for documents such as SOP, LNB, QQ, Risk assessment, PDR, MFR, Scale up BMR, stability protocol, qualification, validation documents, change controls, deviations, investigations and CAPAs etc. Preferred candidate profile pharma THANKS YOU REGARDS MILAP RATHOD (7486829377) any time call me or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

You should have a minimum of 8 years of experience in Agrochemicals/chemicals in process engineering/technology transfer or related fields. As a Process Design Engineer, your responsibilities will include: - Performing process design engineering tasks such as basic, detailing, and improvement. - Creating material balance, Process Flow Diagrams (PFDs), heat balance, and capacity calculations for products. - Developing technical data sheets for various equipment such as reactors, heat exchangers, pumps, vessels, and columns. - Reviewing and preparing Piping & Instrumentation Diagrams (P&IDs) according to standards. - Conducting HAZOP studies based on P&IDs and ensuring execution aligns with finalized documents. - Estimating batch sizes considering product parameters and equipment specifications. - Identifying opportunities for time cycle reduction and product setup improvements. - Implementing cost-effective projects to enhance raw material utilization, yield, time efficiency, and cost reduction. - Contributing to safety system enhancements including fire hydrants, blanketing devices, relief devices, N2 systems, and heat detector systems. Qualifications: - Bachelor's degree in Chemical Engineering (BE/ B.Tech Chemical) Additional Details: - Gender: Male - Experience: 5 - 11 Years - Salary: INR 3 Lac To 6 Lac 50 Thousand P.A. - Industry: Manufacturing / Production / Quality Key Skills: - Process Engineer - Chemical Engineer - Design Engineer - Process Design Engineer - Process Design If you meet the specified qualifications and experience requirements, you are encouraged to attend the walk-in interview.,

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

Manage product lifecycle from concept to launch ensuring compliance with regulations Manage budgets/resources for cost-effective product delivery Review documentation/protocols Ensure regulatory/safety standards (e.g., FDA, CE) Required Candidate profile 15+ yrs exp in IVD NPD/research. B.tech in mechanical/electrical/biomedical Proficient in CAD software/other design tools. Knowledge of IVD regulations Job location is Kochi, Kerala

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, selection & Design calculation. 13. Capex & OPEX preparation 14. Should take active participation in equipment qualification activities such as DQ, IQ & OQ

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation R&D Department (OSD) Position : Executive or Sr Executive Experience : 4 - 9 Yrs Job Description: 1) Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3)Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. 7) Good Communication Skills. Ref to Friends or colleagues. Please Share me update resume: careers@biophore.com Total Exp: Current CTC: Exp CTC : Notice Period: Designation:

Looking for experienced and licensed DGCA drone pilots to join our team. We are a leading provider of aerial surveying, mapping, and inspection services in the region, and we are looking for motivated and skilled professionals to help us continue our growth. Key Responsibilities: Operate SnapM, F90+, or Q6 drones for LiDAR and aerial m apping projects. Conduct pre/post-flight checks and maintain detailed flight logs. Coordinate with survey and DGPS teams for seamless field operations. Ensure data quality and compliance with DGCA and Digital Sky regulations. Handle routine drone maintenance and safety procedures during missions. Requirements: 0-4 years of drone piloting experience with relevant platforms. DGCA Certified Drone Pilot (mandatory). Strong understanding of flight software, mapping sensors, and field logistics. Willingness to travel and work in remote locations