Scientist, R&D Analytical

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

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 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

• 5 to 10 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.