Associate Scientist, Analytical Chemistry

Kenvue; Mumbai; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Kenvueは現在、アナリティカル開発・試験のAssociate Scientistを募集しています。インド・ムンバイのオンサイト勤務で、OTC・スキンケア・ベビーケア・オーラルケア製品の分析法開発・バリデーションを担当します。

グローバルR&D分析部門と連携し、品質・規制要件を遵守しつつ、新製品開発・改善プロジェクトを推進します。科学的厳密さとデータ完全性を重視するポジションです。

Qualifications

• 分析化学と薬学系の学位を有すること。
• 分析法の開発・バリデーション経験が求められる。
• GxP/データ完全性の理解と規制対応があること。

Responsibilities

• 製品開発・安定性プログラムをサポートする分析試験の実施。
• OTC・化粧品・消費者向けヘルス製品の分析法開発・バリデーションを担当。
• 分析機器の適格性評価・保守・性能監視を実施。
• 文書作成・報告書作成・GDP・データ完全性の遵守。
• グローバルチームと協力して品質・規制対応を推進。

Skills

Analytical chemistry

Method development

Data integrity

Regulatory compliance

Education

M.Sc./M.Pharm./Ph.D. in Chemistry or Pharmaceutical Sciences

Tools

HPLC/UHPLC

GC

AAS

ICP-MS

UV-Vis

Dissolution

Job description

Kenvueは現在、以下求人を募集しております。

Associate Scientist, Analytical Chemistry

私たちがしていること

私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。

Who We Are

私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。

Role reports to:

Manager - Analytical R&D

場所:

Asia Pacific, India, Maharashtra, Greater Mumbai

勤務地:

フルオンサイト

あなたがすること

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.

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