{"id":3458511,"url":"https://alion.io/job/kenvue-scientist-rd-analytical","title":"Scientist, R&D Analytical","company":{"id":7095,"name":"Kenvue","domain":"kenvue.com","url":"https://alion.io/company/kenvue","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":92,"open_postings":29,"ghost_share":0,"stale_share":0.517,"repost_share":0.034,"time_to_fill_p50_days":13,"computed_at":"2026-10-31T05:58:55Z"}},"role":"Science & Research","role_family":"Science & Research","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Mumbai, India"],"countries":["IN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":15500,"max_usd":35000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":1296},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Chromatography","optional":false},{"name":"GMP","optional":false},{"name":"HPLC","optional":false},{"name":"21 CFR Part 11","optional":true},{"name":"Microsoft Office","optional":true}],"status":"live","first_seen_at":"2026-10-29T13:01:12Z","employer_posted_date":"2026-10-29","last_verified_at":"2026-10-31T05:56:53Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Kenvue is currently recruiting for a:\nScientist, R&D AnalyticalWhat we do\nAt 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.\nWho We Are\nOur 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.\nRole reports to:\nManager - Analytical R&DLocation:\nAsia Pacific, India, Maharashtra, Greater MumbaiWork Location:\nFully OnsiteWhat you will do\nScientist - Analytical Development & Testing\nR&D Operations | Consumer Health\nAbout the Role\nAt Kenvue, we believe science is at the heart of exceptional consumer healthcare. We are seeking a highly motivated Scientist - Analytical Development & Testing to join our Global R&D Analytical Operations team and contribute to the development and lifecycle management of some of the world's most trusted consumer health brands.\nThis role offers an exciting opportunity to work across a diverse portfolio of Self Care (OTC), Skin Health, Baby Care, and Oral Care products while leveraging state-of-the-art analytical technologies in a world-class laboratory environment.\nAs a key member of the Global Analytical Sciences organization, you will support new product development, commercial product enhancements, analytical method development and validation, stability assessment, and research initiatives. The position requires a strong commitment to scientific rigor, quality, compliance, data integrity, and operational excellence.\nKey Responsibilities\nAnalytical Testing, Method Development & Technical Excellence\nPerform analytical testing to support product development, stability programs, and commercial product lifecycle initiatives.\nExecute stability studies and shelf-life assessments utilizing analytical instrumentation, including:HPLC/UHPLC\nGas Chromatography (GC)\nIon Chromatography (IC)\nAtomic Absorption Spectroscopy (AAS)\nUV-Visible Spectroscopy\nICP-MS\nDissolution\nAdditional modern analytical platforms as required\n\nDevelop, optimize, validate, and document analytical methods for OTC drugs, cosmetic products, and consumer healthcare formulations.\nSupport analytical method transfers and ensure successful implementation across laboratories.\nPerform scientific investigations and technical assessments to solve analytical challenges and drive project outcomes.\nContribute to research-focused initiatives and innovation projects as assigned.\nAdvanced Instrumentation & Laboratory Technology\nMaintain proficiency across a broad range of analytical technologies and laboratory systems.\nServe as an equipment owner for designated laboratory instruments and technologies.\nSupport instrument qualification, calibration, maintenance, and performance monitoring programs.\nDrive continuous improvement in analytical capabilities through adoption of modern technologies and digital tools.\nTechnical Documentation & Compliance\nAuthor and review scientific and technical documentation, including:Stability protocols and reports\nMethod development reports\nMethod validation protocols and reports\nMethod transfer documentation\nInvestigation reports and technical assessments\n\nEnsure compliance with Good Documentation Practices (GDP), data integrity requirements, and internal quality standards.\nQuality Systems & Operational Excellence\nSupport laboratory quality systems and critical analytical processes.\nEnsure adherence to cGMP, regulatory requirements, and global quality standards.\nParticipate in root cause investigations, CAPA activities, and continuous improvement initiatives.\nPromote a culture of quality, compliance, and \"right-first-time\" execution.\nGlobal Collaboration & Scientific Partnership\nCollaborate with regional and global R&D, Quality, Regulatory, and Operations teams.\nContribute to cross-functional projects and global initiatives.\nShare scientific insights and technical expertise to support successful project delivery across multiple markets.\nTechnical Competencies\nStrong foundation in analytical chemistry and pharmaceutical sciences.\nExperience with analytical method development, validation, troubleshooting, and data interpretation.\nHands-on expertise with modern analytical instrumentation and laboratory technologies.\nUnderstanding of stability study design and product shelf-life assessment.\nWorking knowledge of cGMP, data integrity principles, and quality management systems.\nFamiliarity with regulatory expectations and audited environments.\nProficiency in digital laboratory systems and scientific software applications.\nStrong technical writing and documentation skills.\nLeadership & Professional Competencies\nDemonstrates ownership, accountability, and a commitment to high-quality execution.\nApplies scientific curiosity and critical thinking to solve complex analytical challenges.\nEmbraces innovation and continuously seeks opportunities to improve processes and capabilities.\nCommunicates effectively with diverse stakeholders across functions, sites, and geographies.\nBuilds collaborative partnerships and fosters a culture of teamwork and inclusion.\nDelivers results with agility while maintaining the highest standards of quality and compliance.\nQualifications & Experience\nEducation\nM.Sc., B.Pharm., M.Pharm., Ph.D., or equivalent qualification in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related scientific discipline.\nProfessional Experience\n5 to 10 years of relevant experience in:Analytical Development\nQuality Control\nPharmaceutical or Consumer Health R&D\nHealthcare, Pharmaceutical, Medical Device, or FMCG industries\n\nPreferred Experience\nExposure to analytical method development and validation.\nExperience working within GMP-regulated laboratories.\nKnowledge of 21 CFR Part 11 and data integrity requirements.\nExperience supporting regulatory inspections and quality audits.\nFamiliarity with global quality and compliance standards.\nDigital Skills\nAdvanced proficiency in Microsoft Office Suite.\nExperience with laboratory informatics systems, chromatography data systems, and electronic documentation platforms is desirable.\nIf you are an individual with a disability, please check our Disability Assistance page for information on how to request an 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