Senior Scientist, Analytical R&D

Job description

Kenvue is currently recruiting for a: Senior Scientist, Analytical R&D What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.  We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: Manager - Analytical R&D Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What you will do Senior Scientist, R&D Analytical            Role reports to: Principal Scientist, R&D Analytical Location : Mumbai What you will do The Senior Scientist position will be a part of the team that is responsible for analytical deliverables of new product development projects, support changes to existing products and specific research-based activities, product investigations, etc. assigned as a part of Global operations. The delivery of the projects is expected to meet applicable compliance and quality requirements and established performance metrics. You will play a crucial role in ensuring the safety and quality of consumer health products through the use of advanced analytical instruments such as ICP-MS, LC-MS/MS, GC-MS/MS, focused on trace level impurities accurate quantification to support regulatory submissions and contribute to the scientific understanding of the impurities. Key Responsibilities • Develop, validate, and transfer LC-MS/MS, GC-MS/MS, ICP-MS, etc methods for accurately quantifying impurities (e.g., elemental impurities, residual solvents, extractables & leachable, nitrosamines, etc.) at trace levels (ppm to sub-ppb) with MS for their risk assessment and mitigation strategies. • Utilize mass spectrometry and other analytical instruments to solve complex structural and quantitative problems. • Strong skills in method development, optimization, verification/validation and deep understanding of chemistry principles and formulation design aspects for test methods. • Validate and transfer analytical methods to support product development and life cycle management projects. • Conduct chemical extraction studies on container closure systems and consumer products to identify potential E&L, elemental impurities, residual solvents. • Conduct method optimization, stability studies, and shelf-life assessments. • Perform testing using HPLC/UPLC, GC, IC, AAS, and other advanced instrumentation. • Manage method transfers to internal/external labs and manufacturing sites. • Coordinate outsourcing of analytical operations and research projects when required. • Author technical documents e.g., method development summary, method validation reports, method transfer, test methods, etc. • Well experienced in a wide range of analytical technologies and instrumentation. • Review and interpret analytical data against compliance to specifications and procedures and evaluate data trends. • Author technical documents e.g., method development summary, method validation reports, method transfer, test methods, etc. • Act as instrument owners for instrumentation and manage qualification and calibration activities and reports. • Represent as process owners or subject matter experts for assigned responsibilities, critical laboratory processes, and quality systems. • Participate in internal or regulatory audits as subject matter experts for assigned responsibilities. • Stay current with industry trends and technologies to drive innovation. • Independently manage analytical projects, including planning, execution, and stakeholder communication. • Represent analytical requirements on cross-functional project teams and global forums. • Participate in regional/global initiatives and share technical expertise. • Drive innovation in analytical science and risk mitigation strategies. • Collaborate across global teams to deliver high-quality outcomes. What we are looking for Required Qualifications • Education: Minimum MSc, B Pharm, M. Pharm, Ph.D. or equivalent science stream • Other Skills: MS office advanced • Work experience: Minimum 7 years to 12 years in Analytical development, Quality Control, or related functions in healthcare/pharma/FMCG/Food/Nutraceuticals sector with exposure to GMP and Quality environment preferred. • Strong hands-