336 Technology Transfer Jobs - Page 4

You will be responsible for identifying high impact New Product Development (NPD) opportunities associated with RFID Solutions/Technology, aimed at long-term revenue generation. This involves exploring and shortlisting new Joint Venture/Joint Development and Collaboration Opportunities after conducting thorough studies on NPD, Innovations, Digital Technology & Solutions related to RFID Solutions/Technology. Moreover, you will need to study industry's best practices, methodologies, technology, equipment implementation, and their impacts, pros, and cons. It is essential to stay updated on all relevant new technologies, products/processes, and materials being introduced. You will be required to conduct multiple trials, quality checks, crash tests, certifications, etc., to ensure that the product is foolproof with zero failure before introducing it to the market. Additionally, you will need to research Intellectual property and patenting for Technology and print solutions, as well as conduct competitors mapping and analysis. Continuous market scanning and evaluation of industry trends will be necessary to assess our standing against competitors. Analyzing both internal and external customer expectations is crucial, and you will need to develop brand value propositions accordingly. Communication and engagement with internal and external customers to understand their needs, satisfaction levels with our products and services, and expectations are essential. Building roadmaps for effective project execution based on market dynamics and scenario planning will be part of your responsibilities. Innovative ideas must be generated continuously to maintain the new product pipeline while assessing the feasibility aspect and its potential business impact. Researching journals, literature, magazines, and the internet on printing, packaging, and related events is also expected. Value re-engineering of existing products to enhance quality and reduce costs will be a key focus area. You will lead the design & development projects of new products in collaboration with cross-functional teams and oversee technology transfer activities from the development group or vendors to manufacturing. Identifying criticalities/challenges in projects and implementing corrective actions, as well as identifying new technologies, products, manufacturing possibilities, assessing feasibility, and preparing solutions will be part of your role. Coordinating with internal or external development teams, obtaining necessary certifications for product development, scouting for automated manufacturing equipment, analyzing trends, identifying growth areas, conducting feasibility studies, and quantifying opportunities for new product development are also part of the responsibilities.,

As a Senior Chemist in the Pharma Manufacturing Industry based in Vatva, Ahmedabad, you will be responsible for the synthesis of APIs and intermediates. Your role will involve conducting feasibility studies, selecting synthesis routes, and implementing multi-step synthesis processes to improve yield and reduce costs. You will utilize your expertise in conducting literature searches using platforms such as SciFinder, Chemical Abstracts, and Free Patent Online, as well as referring to various journals. Additionally, you will be involved in extraction, purification, and distillation processes, along with conducting lab validations. Strong documentation skills are essential for this role, including the preparation of technical reports, process safety reports, and cost sheets. You will also play a key role in technology transfer activities from the laboratory to kilo lab and plant scale. Collaboration with departments such as IPR, Regulatory Affairs, and QA will be crucial in ensuring compliance and quality standards are met. Proficiency in tools like Chemdraw and Chemsketch will be beneficial for this role. Please note that this position is open to male candidates with a background in the Pharma Manufacturing Industry. If you have a Master's degree in Organic Chemistry and possess 5 to 8 years of relevant experience in API and intermediates manufacturing within the Pharma industry, we encourage you to apply for this full-time, permanent position. For further details or to express your interest, please contact Himani (HR) at 9377165778. Thank you.,

You should have a minimum of 8 years of experience in Agrochemicals/chemicals in process engineering/technology transfer. Your responsibilities will include: - Process design engineering including basic, detailing, and improvement. - Preparation of Material balance, PFDs, heat balance, and capacity calculations for products. - Preparation of technical data sheets of reactors, heat exchangers, pumps, vessels, columns, etc., as per product-specific requirements and different standards. - Preparation and review of P&IDs as per standards. Generating documents for design projects such as Process Flow Diagrams (PFDs) and Piping & Instrumentation Diagrams (P&IDs). - Carrying out HAZOP as per PID and ensuring execution is done as per the finalized document. - Estimating batch size considering product parameters and equipment size. - Time cycle reduction and product setup. - Implementing cost-effective improvement projects related to raw material, yield, time cycle, equipment debottlenecking, and reduction of overhead & fixed costs. - Involvement in improving safety systems including fire hydrants, blanketing devices, relief devices, N2 system in clean rooms, and heat detector systems. Qualification required for this position is BE/ B.Tech Chemical. The job is open to male candidates with 5 to 11 years of experience. The salary offered is between 3 Lac to 6 Lac 50 Thousand P.A. The industry is Manufacturing / Production / Quality. Key skills include Process Engineer, Chemical Engineer, Design Engineer, Process Design Engineer, and Process Design. This is a walk-in role.,

Job Description: R&D Head (Cosmetics and Skincare) Job Title R&D Manager (Cosmetics and Skincare) Eligibility Criteria (Experience, Qualification, Skills)Qualification Advanced degree (Master's or Doctorate) in Ayurveda, Herbal Sciences, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field Experience Minimum 12 years of in research and development, with significant exposure to cosmetics, homecare, or FMCG industries. Proven track record of leading successful product development projects and teams. Skills required Expertise in cosmetic chemistry, formulation techniques, and product innovation. In depth Knowledge of Cosmetics and homecare products and properties Leadership and strategic planning abilities. Communication and stakeholder management skills. Problem-solving and decision-making capabilities. Project management and organizational skills. Ability to inspire and motivate a multidisciplinary team. Market knowledge Job Location Jaipur Key Responsibilities Provide strategic leadership for setting the R&D vision Provide technical expertise and guidance to the Cosmetics and homecare R&D team Oversee all aspects of cosmetics and homecare product development Collaborate with internal (cross functional team) and external stakeholders Manage R&D budgets and resources effectively Ensure regulatory compliance and quality standards Establish KPIs metrics and benchmarks Drive continuous improvement and innovation Job description Provide vision, direction, and strategic guidance for the company's R&D efforts in cosmetics and homecare products Develop and implement R&D strategies aligned with business objectives, to address market needs and capitalize on emerging opportunities Lead, mentor, and inspire a multidisciplinary team of scientists, researchers, and technicians, fostering a culture of excellence, innovation, and collaboration. Oversee the entire product development lifecycle, from conceptualization and formulation to testing, validation, and commercialization. Drive collaborative research initiatives, joint ventures, and technology transfer agreements to enhance the company's R&D capabilities and accelerate innovation Ensure that all R&D activities comply with applicable regulatory requirements, quality standards, and industry best practices. Develop and manage the R&D budget, allocating resources effectively and efficiently to support priority projects and initiatives. Establish key performance indicators (KPIs), metrics, and benchmarks to monitor and evaluate the performance and impact of R&D initiatives. Stay abreast of market trends, consumer preferences, competitor activities, and technological advancements in the cosmetics and homecare segment.

Role & responsibilities Process Development: Conduct research and design experiments to develop and optimize synthetic routes for API molecules. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. Documentation: Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders. Design synthetic routes for the synthesis and isolation of impurities and reference standards. Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: Adhere to all safety protocols and ensure a safe working environment in the laboratory. Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques.Team Collaboration: Plan daily activities for team members, focusing on feasibility studies, process optimization, and laboratory validation. Work closely with the Analytical Research and Development (ARD) team on method development, in-process testing, and reference standards qualification. Qualifications: Education: MSc/BSc in Organic Chemistry, Experience: Minimum of 3-5 years of experience in process development and optimization in the pharmaceutical or bulk drug industry. Skills: Strong knowledge of synthetic organic chemistry and process chemistry. Proficiency in using and interpreting data from analytical instruments. Excellent problem-solving skills and attention to detail. EZective communication and teamwork skills. Ability to work independently and manage multiple projects simultaneously. Preferred candidate profile We are looking for a talented and driven R&D Chemist to join our team. The successful candidate will be responsible for developing and optimizing chemical processes for synthesizing active pharmaceutical ingredients (APIs). This role requires a strong background in synthetic organic chemistry, process development, and scale-up techniques. The R&D Chemist will collaborate with cross-functional teams to ensure the smooth transition of processes from the lab to full-scale production. Perks and benefits

Technology transfer of new molecules from R&D to plants (in-house as well as outsourced locations) through Kilo lab and Pilot plant. Day-to-day operation management of tech-transfer activities. Review of basic engineering design package for Technology transfer. Review of critical and hazardous activities planned in tech-transfer campaign. Close batch monitoring wherever critical operations are involved. Plant troubleshooting, capacity enhancement and provide technical support in repeat campaigns. New products Production planning, monitoring and delivering on time. Provide training to team members. Ensuring personal safety in place. Ensuring GMP compliance in day-to-day work

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always upholding Novo Nordisk''s stringent quality standards and adhering to cGMP and regulatory requirements. Lead and manage aseptic manufacturing projects, specifically leveraging your expertise in areas like Formulation/Compounding, Filling, Washing & Sterilisation, Environmental Monitoring, or Clean Utilities. Developing and managing detailed project plans and timelines and communicating effectively with steering groups and key stakeholders. Monitoring progress and proactively securing necessary resources. Developing project risk grids and identifying mitigation strategies with both Novo Nordisk and our Contract Manufacturing Organisation (CMOs). Qualifications Bachelor’s or Master’s degree in engineering. Possess experience of 5-12Years of project management experience with a proven track record of successful project delivery in a highly regulated environment, especially internationally. Aseptic manufacturing experience is a must, and experience with Technology Transfer of biologics is a significant advantage. Professional experience balancing individual drive with effective stakeholder involvement. Proficiency in project management software (e.g., MS Project, Smartsheet, Jira, or equivalent). Demonstrated fluency in written and spoken English is essential. About the Department GCM DP RoW Projects is a dedicated team committed to providing life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department strives to make a meaningful impact on the quality of life for patients living with diabetes and obesity. Our projects are tailored to meet the unique requirements of each country, offering exciting growth opportunities. With a steadfast commitment to innovation and problem-solving, we work to overcome challenges and navigate complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Join us in making a difference.

Role & responsibilities Process Development: Conduct research and design experiments to develop and optimize synthetic routes for API molecules. Perform literature searches for identified API molecules to determine synthesis routes, polymorphs, and analytical methods. Conduct experimental trials to assess feasibility and optimize designed synthetic routes for API molecules. Documentation: Record all experiments in the laboratory notebook (LNB) and maintain corresponding analytical data in organized folders. Design synthetic routes for the synthesis and isolation of impurities and reference standards. Ensure all documentation meets Good Manufacturing Practices (GMP) and regulatory standards. Safety and Compliance: Adhere to all safety protocols and ensure a safe working environment in the laboratory. Develop non-infringing synthetic processes based on literature, raw material availability, and polymorph studies. Stay up-to-date with industry trends, regulatory guidelines, and advancements in chemical synthesis and analytical techniques.Team Collaboration: Plan daily activities for team members, focusing on feasibility studies, process optimization, and laboratory validation. Work closely with the Analytical Research and Development (ARD) team on method development, in-process testing, and reference standards qualification. Qualifications: Education: MSc/BSc in Organic Chemistry, Experience: Fresher or 1-2 years experience in process development and optimization in the pharmaceutical or bulk drug industry. Skills: Strong knowledge of synthetic organic chemistry and process chemistry. Proficiency in using and interpreting data from analytical instruments. Excellent problem-solving skills and attention to detail. Effective communication and teamwork skills. Ability to work independently and manage multiple projects simultaneously. Preferred candidate profile We are looking for a talented and driven junior R&D Associate to join our team. The successful candidate will be responsible for developing and optimizing chemical processes for synthesizing active pharmaceutical ingredients (APIs). This role requires a strong background in synthetic organic chemistry, process development, and scale-up techniques. The R&D Chemist will collaborate with cross-functional teams to ensure the smooth transition of processes from the lab to full-scale production. Perks and benefits

The candidate will utilize creative abilities and research methods to enhance existing products in accordance with industry trends and develop new products to cater to the company's target market. You will be responsible for identifying and reporting any technical product issues uncovered during evaluation, as well as overseeing product testing and trials to evaluate materials, process efficiency, and final product effectiveness. Responsibilities: - Leading key projects with R&D to align with business objectives. - Developing research programs incorporating the latest advancements to enhance existing products and explore the potential of new products. - Understanding customer expectations regarding forthcoming products. - Identifying and implementing improved technologies utilized by suppliers, competitors, and customers. - Establishing project goals and priorities through collaboration with Marketing and Operations. - Facilitating the transfer of new technologies, products, and manufacturing processes into and out of the company. - Conducting research, design, and evaluation of materials, assemblies, processes, and equipment. - Recommending training tools to improve employee performance and skill development. - Monitoring team metrics and objectives to ensure goal attainment. - Documenting all phases of research and development. - Managing customer relationships, conducting RFP reviews, customer visits, and product testing. - Establishing and maintaining testing procedures for assessing raw materials, in-process materials, and finished products. - Supervising complex research projects, analyzing results, and offering recommendations based on findings. - Evaluating the scope of research projects and ensuring adherence to timelines and budgets. - Supervising the quality assurance department and personnel, implementing and maintaining quality and reliability testing systems for the organization's products and development processes. - Ensuring compliance with federal, state, local, and organizational regulations, guidelines, and policies. - Identifying and analyzing issues, bugs, defects, and recurring problems across multiple products; recommending and facilitating solutions to address these challenges. Education: - A Bachelor's/Master's degree in the relevant field Experience: - Minimum 5 years of experience in Food Research & Development. - Preference will be given to candidates with certifications such as GHP & GMP, HACCP, ISO 9001, ISO 22000, HACCP, Auditing, etc. Required Skills: - Proficiency in MS Office especially Excel/Google Sheets. - Demonstrated experience in a related role. - Strong creative acumen for generating new product ideas and solving problems creatively. - Excellent problem-solving abilities. - Efficient multitasking skills and adept at time management. About Wellversed: Wellversed operates a range of nutrition brands to empower individuals to achieve their optimal state of wellness. Brands like Wellcore, YouWeFit, Ketofy, Zero Sugar, and Dynamite enable individuals to unlock their performance potential and lead healthier lives. These brands are accessible to customers through various channels including our eCommerce portal (www.wellversed.in). Location: Gurgaon, Haryana,

As an Assistant General Manager (AGM) in Formulation Development for Injectable products, you will be responsible for the development, scale-up, and validation of simple and complex Injectable dosage forms for various markets including US, EU, India, Canada, Brazil, and others. This role is based at the Matoda plant in Ahmedabad. Your key responsibilities will include: - Developing Injectable dosage forms for multiple markets - Scaling up and transferring technology for Injectable dosage forms - Designing formulation strategies and drug product development roadmaps - Reviewing trials processes, development records, and technology transfer documents - Analyzing stability data of products under development and validation batches - Handling regulatory queries and conducting studies as required - Organizing resources, facilitating communication, and coordinating timely drug product development with internal departments and external vendors - Troubleshooting product issues and actively participating in failure investigations - Providing technical guidance to subordinates and ensuring adherence to good laboratory practices and safety regulations - Following Good Documentation Practices and Data Integrity requirements during all GxP operations - Ensuring understanding and application of Data Integrity requirements and consequences for non-compliance - Reviewing GxP data in compliance with Data Integrity requirements specific to the job description You may also be required to perform any other activities designated by your supervisor to support the overall objectives of the organization.,

The Manager - Nasal Spray Formulation Development will lead the development of innovative nasal spray formulations, driving projects from concept to commercial scale-up. You will focus on the design, development, and optimization of nasal spray drug products, ensuring regulatory compliance and meeting quality standards. Leading a team of formulation scientists, you will collaborate with cross-functional teams to deliver high-quality, cost-effective nasal spray formulations for global markets. Key responsibilities include having relevant experience in developing and technology transferring Nasal Sprays, Dry Powder Inhalers, and Soft Mist Inhalers dosage forms for regulated markets like EU and US. You will be responsible for preparing and reviewing literature search reports for drug substances and products, proposing formulation strategies, guiding executives for development batches in the lab, providing expert input into formulation and process studies, and ensuring compliance with specifications. Additionally, you will evaluate vendors for packaging material, monitor stability studies, prepare Technology Transfer documents, coordinate with stakeholders, and adhere to GLP and GMP. Qualifications and Skills required for this role include an M.Pharm or Ph.D. in Pharmaceutics, Pharmaceutical Sciences, or related field with specialization in drug delivery systems or formulation science preferred. You should have 8-10 years of hands-on experience in formulation development, with at least 5 years focused on nasal spray or inhalation formulations. Technical expertise in nasal spray formulation techniques, drug-excipient interactions, device development, particle size distribution, viscosity, and droplet characteristics is essential. You should possess strong project management skills, experience in working with cross-functional teams, and knowledge of regulatory requirements for nasal spray formulations. Leadership qualities, excellent communication and presentation skills, problem-solving abilities, and a knack for innovation are crucial for this role. The work environment will primarily be based at the R&D center, with occasional travel to manufacturing sites, vendors, and regulatory meetings.,

As a Formulation and Development Officer for our client based in Vatva, Gujarat, you will be responsible for various key tasks. Your primary duty will involve the development of formulations for all dosage forms such as tablets, capsules, ointments, creams, gels, oral liquids, injectables, and novel drug delivery systems for different markets including regulated, domestic, and ROW markets. This includes activities like document review, planning, and conducting stability studies of R&D batches. Additionally, you will be required to provide technical support for the scale-up and technology transfer to manufacturing processes. You will play a crucial role in troubleshooting formulation-related issues that may arise during production, ensuring a smooth manufacturing process. To qualify for this position, you should hold a Bachelors or Masters degree in Pharmacy. If you believe you possess the necessary qualifications and skills for this role, we encourage you to share your updated CV with us. We look forward to reviewing your application and will reach out to you promptly.,

Position Title: Team Member Formulation & Development – Tech Transfer ( Officer / Executive ) - OSD Department: Formulation & Development - Tech Transfer Location: Vadodara Reports To: Manager – Formulation & Development – Tech Transfer Job Overview: The Team Member will support the successful transfer of products from development to manufacturing by ensuring process accuracy, documentation integrity, and adherence to quality standards. This role involves close collaboration with cross-functional teams, participation in validation processes, and troubleshooting to optimize manufacturing efficiency. Key Responsibilities: Process & Documentation: Prepare Technology Transfer Dossiers (TTD) and ensure the accuracy and completeness of all transfer documents, including SOPs and batch records. Validation Support: Assist in process and equipment validation activities, ensuring alignment with manufacturing and regulatory requirements. Risk Management: Identify potential risks during technology transfer and collaborate with relevant teams to implement mitigation strategies. Collaboration: Work closely with cross-functional teams, including R&D, Quality Assurance, and Production, to ensure a seamless transfer process. Troubleshooting: Resolve issues encountered during the transfer process and manufacturing runs, and implement practical solutions. Training: Support and participate in training programs for team members to ensure understanding of processes and compliance requirements. Compliance: Ensure adherence to all regulatory and quality standards throughout the transfer process and during manufacturing. Reporting: Maintain accurate and comprehensive project documentation to support future references and regulatory inspections. Key Skills: Technical Skills: Knowledge of GMP, process validation, and regulatory standards. Familiarity with product development, manufacturing, and technology transfer processes. Soft Skills: Strong communication and collaboration abilities for effective teamwork. Analytical thinking and problem-solving skills to address challenges. Attention to detail to ensure accuracy and compliance. Qualifications & Experience: Education: B. Pharm or Master of Science (M. Sc). Experience: 4-7 years of experience in product development, manufacturing, and technology transfer. Skills: Hands-on expertise in GMP, validation processes, and adherence to regulatory guidelines.

We are looking for a skilled and enthusiastic UAV Pilots to join our team and to carry out drone operations across various locations. The role demands a combination of technical expertise and strong teamwork capabilities. This position plays a critical role in ensuring successful mission execution, compliance with regulations, and operational safety. Responsibilities: Demonstration of our products at client locations. Maintenance and record keeping of our UAV`s. Responsible for Pre-flight checks, Post flight Checks and live mission monitoring. Ensure crash-free operations with troubleshooting and emergency response. Adhere to safety and industry regulations. Responsible for all equipment and operational items at the flight location, ensuring proper setup, functionality, and secure handling before, during, and after missions Desired Skills: Hands on experience ground control stations like Mission Planner, QGround Control. Basic knowledge of electronics, aerodynamics and flight principles. They should have an understanding and knowledge of flight operations in different terrains. Experience Certifications: Prior experience in drone operations or aviation is compulsory. NCC Air Wing participation or equivalent aviation exposure will be preferable. Educational Background: Any Degree/Diploma holder in B.E And B.tech or a related field will be preferable Preferred: Bachelor in B.tech or specialized drone operation certifications. Qualification : Any Degree/Diploma holder in B.E And B.tech or a related field will be preferable Preferred: Bachelor in B.tech or specialized drone operation certifications

Lead process scale-up from lab trials to pilot plant runs & full-scale manufacturing Design & execute pilot plant trials Translate lab processes into PFDs , P&IDs, and process documents for scaleup Support HAZOP, safety studies & compliance Required Candidate profile 14+years exp in process eng., preferably in specialty chemicals manufacturing Exp with batch & semi-batch processes including automation Understanding of regulatory & EHS compliance in chemical plants

Trending Job Description Key responsibilities. Responsible for working with Technology Transfer, Production, and the Client to generate, revise, and approve master production records (MPRs) and any other documents associated with the commercial products in the manufacturing, e.g., SOPs, material specifications, technical reports, etc. Preparing unplanned and planned deviations for responsible processes and forming the investigation team. Collaborates with Process Development (PD), Technology Transfer (TT), Operations, Quality Control (QC), and Quality Assurance (QA) in problem-solving activities, including deviation writing and CAPA closure. Work with project and engineering teams to replace existing/modify or buy equipments for continuous improvement or capacity enhancement Functions as the technical interface between PPS-Riverview and the Client, focusing on providing technical advice and support, engineering solutions, overseeing GMP runs in the plant equipment, analyzing production data to evaluate process performance, and writing production summaries. Will require solid understanding of manufacturing processes, GMP guidelines, site and corporate policies and procedures, hands-on experience, and complete understanding of production processes in the GMP environment as laid out at PPS-Riverview. Willingness to work flexible hours and shifts when there is a need. Responsible for providing independent production support during off-hours as needed. Ability to travel as needed. Ensures process data is being updated on a monthly basis and analysis manufacturing KPI performance for improvement and discussion with the client. Takes part in Operational Excellence activities for the plant. KEY INTERACTIONS. Production Technology Transfer External Clients Project Management Education/Experience. Bachelors Degree in Chemistry or Engineering or a similar discipline is required with at least 0-3 years of relevant experience. Additional Masters or Ph.D. is preferred in lieu of some experience. Demonstrated project management and technical leadership capabilities. Confident management of internal and external stakeholder relationships. Good written and oral communication skills. Demonstrated teamwork skill and professionalism in all interactions. Proven track record of successful technology transfer. Working knowledge of process and desktop computers. COMPLIANCE. Compliance with 21 CFR - Parts 210/211, EU Directives 91/356/EEC and ICH Q7. Compliance with SOPs, batch records, forms, logs of use and Quality Agreements. Recognizes common sources of failure and improves documentation to reduce deviations and errors. Works with Operations Personnel to improve compliance. Ensures work is in compliance with all state and federal regulations, including but not limited to OSHA, GMP, DEA, FDA, etc. Assists in the formulation of corrective procedures when needed. Uses appropriate PPE while inside a manufacturing area. Assumes responsibility for safety and knows appropriate emergency procedures in case of emergency. Knows the location of SDS binders and understand how the guidelines pertain to employees. JOB CONDITIONS The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. If any accommodations are needed, requests should be made to our Human Resources department. Physical Demands: Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected. Long periods of standing and walking can be expected in this position. This position may require long periods of sitting, typing, computer entry or looking at a computer. Work Environment: Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes. Potential limited exposure to hazardous chemicals. Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position. Job Info Job Identification 8173 Job Category Operations Posting Date 03/30/2025, 12:47 PM Job Schedule Full time Locations Ash Stevens LLC, Riverview, MI, 48193, US,

One of India's fastest growing consumer health startups -- Clinikally -- is looking for a winning Growth Lead. You will work on further hacking growth for a first-of-its-kind digital health platform. Your role will be a vital step in building out a fun and inclusive team. The best fit Masters degree in Marketing, or equivalent Smart and knowledgeable in cosmeceutical products for skin, hair, and nutrition Good and indepth knowledge of various aspects of digital marketing, marketing, and branding Industry experience in this niche is highly preferred Fairly well-versed with Technology Transfer + R&D Significant knowledge of Google Analytics, Google Webmaster, and similar tools Good teamwork and leadership-related skills You Will Perform ROI analysis across different channels Perform A/B testing of various marketing and growth strategies for coming up with best outcomes Provide research-based data to our Marketing & Branding Team Make use of Data Science and Analytics for coming up with accurate and useful data Work on both short-term and long-term growth strategies Assist in creating product concepts based on common skin & hair concerns in dermatology Experiment with new channels or technologies to develop promising acquisition campaigns Chart the journey for our users to get a dermatologist consultation online What You Will Work On You will be working to optimise both the growth of our digital health platform across various channels preferred by our users, with both short-term and long-term perspectives. Moreover, your work will also be geared towards optimising for the post-launch strategy/narrative of our current and future proprietary solutions such as the Niacinamide serum for face, dark spot correcting cream & Vitamin C Serum.,

Job Title: AGM R&D Cosmetics Location: Mumbai Job Type: Full Time Job Requirements: Key Internal Interactions R&D / QC: Inputs to process selection & optimization. Planning for infrastructure & process development work in the pilot plant and analytical requirements. Sales & Marketing: Gather market information on new products/idea, screening of ideas, and Guidance on new product development in the pilot plant including product costing, job worker evaluation, process evaluation etc. Pilot plant: Overseeing of pilot plant operations; Planning, review & monitoring of product trials, Guidance, direction & inputs to pilot plant in charge. Manufacturing: Oversee planning & coordination for in-house plant trials, scale up of new products, Raw materials booking for job work process trials, performance analysis & review of in-house trials, for process improvement projects Purchase: Oversee Planning & Coordination for procurement of Raw materials/Equipments etc for process development work in pilot plant / Job work, for procurement of equipment for commercial plant, for techno-commercial evaluation & discussions with suppliers. Projects: Coordination for detail engineering package development, techno-commercial discussions with suppliers, CAPEX estimation & schedule workout for the project and project coordination. Key External Interactions Research Organizations/Educational Institutes: Liasoning for strengthening capabilities and projects Industry Forums: Interact and represent company in Industry forums, govt liasioning for R&D work Customer R&D and manufacturing heads: Understanding customer research and product improvement needs; analyze customer products and suggesting new/ improved products/ processes as per customer requirements Key Responsibilities:1. Planning and Strategizing Ensure that R&D Cosmetics projects are completed on time and within budget Formulate and execute the Research & Development strategy for the organization by understanding business needs and industry developments Plan and develop a product development strategy Develop new raw material vendors, Alternate vendors Oversee SAP BOM of Cosmetics for correctness 2. Policy and Process Design, Implementation and Review Documentation for FDA and Tech transfer Troubleshooting the operational and quality issues at mfg plants across the globe Suggest new process, improve existing process at plant to improve the quality of Cosmetics and productivity at Plant. Support implementation and design of processes to foster a continuous improvement environment Develop and govern process of generating new product basket, funneling, stage gate process, lab/pilot trials and commercialisation Oversee the design and implementation of all R&D &CI processes and policies -Cosmetics Champion new product development through sanctioning and approving proposals, obtaining patents and copyrights and reviewing product development team performance to ensure that customer expectations are met Review progress on continuous improvement projects and initiatives, such as suggestion schemes, continuous improvement teams, quality circles etc Review and approve product formulation as well as the change of production processes Review progress of R&D and CI projects -Cosmetics Interface with BU Heads, Function Heads, R&D business partners and customers/ clients to identify opportunities for product development Guide QC/QMS teams for system compliance to Cosmetics industry standards 3. Coordination, Interface, Imparting Training Technical support to Exim dept for correctness of HSN codes for Cosmetics category Technology transfer of New Cosmetics , syndets , Noodles at plant Participate in the routine oil purchase meetings and suggest oil combinations for cost-effective noodle preparations Provide scientific guidance and advice to the Cosmetics leadership team to enable them to decide on priorities and make cost-effective decisions Develop and maintain contacts with relevant organizations in the industry for exchange of ideas and information Interface with BU Heads, R&D business partners and customers/ clients to identify opportunities for product development Liasoning with Senior management for approvals/appraisals of the reporting team Participate in seminars and industry conferences to keep abreast with the latest development in the industry Influencing internal stakeholders to achieve targets on time Facilitating meetings with external suppliers for obtaining techno-commercial offers, workers for production trials etc. Review of SOPs for new product processing & facilitate training and skill development of team Customer approval for new products Coordination with the Supply chain for Expired raw materials management of Cosmeticss 4. Management of performance, capability and morale Suggest and initiate Cost saving projects in Cosmeticss Manage performance of the Cosmetics R&D team, support capability building and ensure that individual/ team morale and motivation is positive Mid-year and final appraisals completed on time for direct reports. 5. Infrastructure and Technology Investment and Management Develop and implement new processes and technology in Cosmeticss to improve business performance.Suggest new hardware and improve existing hardware of Cosmetics mfg at plants as and when reqired Development of Cosmeticss , syndet, noodles formulations for Global business requirement Ensure that new products in Cosmetics category are developed to improve business performance (New products includes variants of existing products) Encourage and sanction the use of up to date equipment and support team in learning about new technology Key Result Areas (KRAs)1. Technology Development Technology refinement for translucent noodles (min benchmark Jocil quality) Syndet Cosmetics throughput to be increased by dedicating line with support from cross cross-functional team 2. International Sites Technical support to International sites Technical support by demonstrating at the main plant at USA, Dubai, Poland & South Africa apart from India 3. Method Development Method development for active analysis at the factory instead of sending to 3P Lab Baddi First time right in commercial trials with quality documentation 4. OTIF Delivery OTIF delivery of NPD for both when we are developing formulations / supporting rollouts for CMB (timeliness of delivery & quality of roll out) Softsens products-Develop on the innovation requirements for Softens 5. People Development Improve service standard to internal stakeholders. Functional skill development Cross-functional training of R&D team in Cosmetics and Liquid technology., Analysis of products. Timesheet generation and monitoring Technical Skills & Knowledge Thorough understanding of the R&D environment, industry best practice and trends Thorough knowledge of compounds, processes, products, packaging etc relevant to the business Thorough understanding of manufacturing processes and standards Knowledge of the companys strategy, structure and practices Strong project management skills Job Types: Full-time, Permanent Schedule: Day shift Experience: total work: 10 years (Required) Cosmetics: 10 years (Required) Work Location: In person,

Pilot Plant Responsibilities: Managing manpower based on shift activities in Pilot Plant. Demo batch monitoring for new NPDs or development of existing products in R&D. Equipment mapping for the new projects to be performed in Pilot Plant. Identifying requirements and involving in facility modifications as per process CCPs and HACCPs with the maintenance team. Facilitating the requirements of raw materials (RMs), chemicals, solvents, and packing materials (PMs) for pilot batches. Preparation and review of master BMR. Involving and monitoring CCPs with the R&D team during batch execution. Compilation and preparation of scale-up reports. Following project stage cycle after scale-up until commercial production. Preparing capacity calculations and costing for scale-up completed projects by coordinating with Production and Finance teams. Reviewing physical monthly stock in Pilot Plant as per SAP. Coordinating with cross-functional teams in reviewing and approving TTD. Involving in preparation of validation documents for commercial batches. Monitoring validation batches at commercial scale. Ensuring online documentation of Pilot Plant as per SOP. Involving in trial batches performed at 3P sites. Involving in new equipment trials and compiling reports. Ensuring adherence to environmental health and safety rules and procedures. Preferred candidate profile Diploma in chemical Engineering/ B.Tech In Chemical Engineering Kilo Lab/Pilot Plant - Extraction process experience would be added advantage Male candidates preferred Should be willing to travel SAP Knowledge Reach out to saheed.s@omniactives.com to share cv or refer the suitable candidates.

Position: Research Scientist - Cosmetic Products- Formulation Development - Regulated market Experience : 5 to 10 Years Qualification : B. Tech/M.Tech in Cosmetics or M. Pharm Description : 1) Hands on experience on formulation development of Cosmetic products like Sun screen lotions & creams, Face wash, Moisturizers, Shampoos, Conditioners etc.. 2) Product development design and planning. 3) Preparation of various study protocols for development studies. 4) Handling Technology transfer activities. 5) Timely escalation to senior management and take guidance of process. Please share your updated CV along with CTC details at jobs.hr@ipca.com

Alembic Group is looking for Junior Executive - Formulation Development to join our dynamic team and embark on a rewarding career journey They work under the guidance of senior executives and managers to support the organizations goals and objectives Must have excellent written and verbal communication skillsMust be able to analyze complex problems and develop effective solutions Managing internal and external communication, including preparing reports, presentations, and other materials

Alembic Group is looking for Executive - Formulation Development 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.

Role & responsibilities • Responsible for specific developmental projects assigned by HOD or seniors • Carrying out experiments, analysis etc. to establish the product quality and process, as guided by HOD or seniors. • Maintaining the progress of new products development in the form of monthly / daily report, as the case may be. • Responsibility to work together with PBL / pilot plant for new developed product. • Arrangement of lab developed sample for customer validation, as suggested by HOD or seniors. • To take care of all analytical equipment and reagents available in the lab. • Preparation and standardization of reagent solution required for analysis. Preferred candidate profile

RM and PM receiving and documentation of the same. Proper arrangement of the Received COA of RM and PM. Sampling of Received RM and PM, sending the samples to ADL for analysis. Preparation of indent for trial activity and ensure the availability in defined time. Taking of daily trial batches, discussion of issue with immediate supervisor. Entry of trial batch data in lab notebook and preparation of BMR for stability batches. Maintaining the files of individual products like RM and PM COA, Trial COA and Stability Reports after updating in Excel Sheet. Ensure GMP practice in Laboratory routinely. Documentation of stability batches. Calibration of instruments in the laboratory. Literature search and review for the newly identified products for EU/UK/Raw market. SOP preparation and submission to DQA. Ensure utility in good condition in laboratory during all development batches. Adhere Good Manufacturing Practice and Good Laboratory Practice throughout lifecycle of the product. Technically sound in development of Injectable/ Oral solid products and semisolid and liquid dosage forms. If additional knowledge of regulatory documents preparation is essential

As the leading international supplier of active pharmaceutical ingredients (APIs), we at TAPI take pride in our extensive portfolio of over 350 API products and our reputation as a trusted partner for 80% of the top 50 global pharmaceutical companies. With a history dating back over 80 years, we have established ourselves as industry leaders through our experience, expertise, technologies, and exceptional customer service. Our success is driven by our dedicated team of over 4,000 professionals spread across 14 sites worldwide, with state-of-the-art production facilities in multiple countries. We are committed to continuous innovation and investment in research and development to ensure a steady flow of high-quality APIs and the timely introduction of new products to the market. In this role, you will be responsible for various aspects of product transfer, scale-up, proposals, Capex evaluations, and process engineering calculations. Your key tasks will include improving the yield, efficiency, and cost effectiveness of developed APIs by introducing new technologies, troubleshooting plant-related problems, and contributing novel ideas during technical discussions. Additionally, you will be involved in cycle time reduction, capacity enhancement, and coaching and developing a team of engineers to drive performance and engagement. The ideal candidate will have a solid background in API manufacturing, with a deep understanding of scale-up processes and experience in handling CDMO products. You should possess expertise in chemical process unit operations, Quality by Design, process safety, technology transfer, and commercial production. Strong communication, project management, and supervisory skills are essential for collaborating effectively with internal teams and external stakeholders. To qualify for this role, you should hold a B.Tech/M.Tech in Chemical Engineering from a reputable institute and have 14-16 years of experience in the field, including at least 5 years in people management. Your ability to handle multiple projects simultaneously, troubleshoot issues, and use process modelling tools will be critical for success in this position. If you are a proactive, detail-oriented professional with a can-do attitude and a passion for driving excellence in API manufacturing, we invite you to join our team at TAPI and play a key role in our mission to deliver high-quality pharmaceutical ingredients to the global market. This position reports to the Associate Director, MS&T.,