Associate Scientist, Analytical Chemistry

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.

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Role reports to:

Manager - Analytical R&D

Location:

Asia Pacific, India, Maharashtra, Greater Mumbai

Work Location:

Fully Onsite

What you will do

Associate Scientist - Analytical Development & Testing

R&D Operations | Consumer Health

About the Role

At Kenvue, we believe science is at the heart of exceptional consumer healthcare. We are seeking a highly motivated Associate 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.

This 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.

As 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.

Key Responsibilities

Analytical Testing, Method Development & Technical Excellence

• Perform analytical testing to support product development, stability programs, and commercial product lifecycle initiatives.
• Execute stability studies and shelf-life assessments utilizing analytical instrumentation, including:
  • HPLC/UHPLC
  • Gas Chromatography (GC)
  • Ion Chromatography (IC)
  • Atomic Absorption Spectroscopy (AAS)
  • UV-Visible Spectroscopy
  • ICP-MS
  • Dissolution
  • Additional modern analytical platforms as required
• Develop, optimize, validate, and document analytical methods for OTC drugs, cosmetic products, and consumer healthcare formulations.
• Support analytical method transfers and ensure successful implementation across laboratories.
• Perform scientific investigations and technical assessments to solve analytical challenges and drive project outcomes.
• Contribute to research-focused initiatives and innovation projects as assigned.

Advanced Instrumentation & Laboratory Technology

• Maintain proficiency across a broad range of analytical technologies and laboratory systems.
• Serve as an equipment owner for designated laboratory instruments and technologies.
• Support instrument qualification, calibration, maintenance, and performance monitoring programs.
• Drive continuous improvement in analytical capabilities through adoption of modern technologies and digital tools.

Technical Documentation & Compliance

• Author and review scientific and technical documentation, including:
  • Stability protocols and reports
  • Method development reports
  • Method validation protocols and reports
  • Method transfer documentation
  • Investigation reports and technical assessments
• Ensure compliance with Good Documentation Practices (GDP), data integrity requirements, and internal quality standards.

Quality Systems & Operational Excellence

• Support laboratory quality systems and critical analytical processes.
• Ensure adherence to cGMP, regulatory requirements, and global quality standards.
• Participate in root cause investigations, CAPA activities, and continuous improvement initiatives.
• Promote a culture of quality, compliance, and "right-first-time" execution.

Global Collaboration & Scientific Partnership

• Collaborate with regional and global R&D, Quality, Regulatory, and Operations teams.
• Contribute to cross-functional projects and global initiatives.
• Share scientific insights and technical expertise to support successful project delivery across multiple markets.

Technical Competencies

• Strong foundation in analytical chemistry and pharmaceutical sciences.
• Experience with analytical method development, validation, troubleshooting, and data interpretation.
• Hands-on expertise with modern analytical instrumentation and laboratory technologies.
• Understanding of stability study design and product shelf-life assessment.
• Working knowledge of cGMP, data integrity principles, and quality management systems.
• Familiarity with regulatory expectations and audited environments.
• Proficiency in digital laboratory systems and scientific software applications.
• Strong technical writing and documentation skills.

Leadership & Professional Competencies

• Demonstrates ownership, accountability, and a commitment to high-quality execution.
• Applies scientific curiosity and critical thinking to solve complex analytical challenges.
• Embraces innovation and continuously seeks opportunities to improve processes and capabilities.
• Communicates effectively with diverse stakeholders across functions, sites, and geographies.
• Builds collaborative partnerships and fosters a culture of teamwork and inclusion.
• Delivers results with agility while maintaining the highest standards of quality and compliance.

Qualifications & Experience

Education

• M.Sc., B.Pharm., M.Pharm., Ph.D., or equivalent qualification in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related scientific discipline.

Professional Experience

• 1 to 5 years of relevant experience in:
  • Analytical Development
  • Quality Control
  • Pharmaceutical or Consumer Health R&D
  • Healthcare, Pharmaceutical, Medical Device, or FMCG industries

Preferred Experience

• Exposure to analytical method development and validation.
• Experience working within GMP-regulated laboratories.
• Knowledge of 21 CFR Part 11 and data integrity requirements.
• Experience supporting regulatory inspections and quality audits.
• Familiarity with global quality and compliance standards.

Digital Skills

• Advanced proficiency in Microsoft Office Suite.
• Experience with laboratory informatics systems, chromatography data systems, and electronic documentation platforms is desirable.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.