Scientist

我们做什么

在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。

我们是谁

我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.

Role reports to：

Principal Scientist - Analytical Chemistry

位置：

Asia Pacific, India, Maharashtra, Greater Mumbai

工作地点：

混合

你会做什么

Kenvue is currently recruiting for:

Scientist Analytical Chemistry

The job location is Mumbai.

Who We Are

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. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of 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.

What you will do

The objective of this position is to deliver analytical services to various Kenvue Consumer Health Global R&D sites for multiple product categories under various franchises such as Self Care (OTC drugs), Skin Health and Essential Health (Baby care, Oral Care, etc.)  The Scientist position will be a part of the team that is responsible for analytical deliverables of new product development projects, support changes to commercial products and specific research-based activities assigned as a part of Global operations. The key role is to deliver the analytical testing and related documentation activities with a compliance focus under the supervision of the team leader.

Key Responsibilities:

• ANALYTICAL DETERMINATIONS AND TECHNICAL ASSESSMENTS:

• Ensure qualifications on a wide range of analytical technologies and instrumentation for testing capabilities.
• Execute the assigned stability testing for shelf-life assessment of stability studies using various Analytical instrumentation such as HPLC, UPLC, GC, AAS, IC, UV, FTIR etc.
• Responsible for method development and subsequent method validation activities including technical documentation under the guidance of the team leader.
• Participate in method transfer process regarding testing activities.
• Work on specific research projects, if required.

• SUPPORT TO EQUIPMENT MANAGEMENT PROGRAM:

• Responsible for assigned qualification and calibration activities for lab instrumentation and technology.
• Deliver the instrument owner role for basic lab equipment and technology.

• TECHNICAL DOCUMENTATION:

• Partner with key responsible for providing data in technical documents e.g., stability reports, method transfer, method validation protocol and reports, etc.

• LAB PROCESS/QUALITY SYSTEMS MANAGEMENT:

• Support process owners or subject matter experts for assigned responsibilities, critical laboratory processes and quality systems.
• Provide oversight for basic lab processes and escalate wherever required.

• ENGAGEMENT ON REGIONAL/GLOBAL INITIATIVES:

• Participate and collaborate with regional and Global teams for assigned deliverables when nominated on such forums.

TECHNICAL COMPETENCIES

• Sound technical expertise related to chemistry, analytical techniques, and stability study assessment.
• Diligent execution of analytical projects with a right first-time approach.
• Adequate knowledge of current GMP, quality systems, site specific SOPs, regional/Global technical requirements
• Technical skills related to instrumentation principles and working, basic troubleshooting, good documentation practices, data integrity aspects, etc.
• Ability to work with digital tools and software applications.

LEADERSHIP COMPETENCIES

• Effective planning and execution of analytical projects independently
• Ability to grasp technical/compliance requirements and execute assigned work to meet the key performance indicators.
• Excellent oral and written communication and articulation skills
• Challenges the status quo and brings innovative ideas and suggestions.
• Displays technical curiosity and self-initiative to deliver beyond usual activities.

• Good interpersonal skills to partner across functions, sites, and regions
• Manage raw material, formula and packaging clearance projects, ensuring compliance with relevant regulatory requirements and Kenvue internal policies.
• Support monitoring and analysis of upcoming regulations affecting our portfolio and assess their implications.
• Oversee global change control processes and ensure timely execution.
• Collaborate with internal teams (e.g., Product R&D, Packaging R&D, Regional/ Local Regulatory Affairs, Tech ops, Quality assurance, Safety team, Materials team) and external partners to facilitate clear communication and alignment on compliance matters.
• Engage with Global stakeholders to ensure cohesive regulatory strategies and project execution.
• Work as part of a multidisciplinary team to drive compliance initiatives and promote a culture of regulatory excellence.
• Lead or Partner in Continuous improvements initiatives to bring agility to our work and team.

What We Are Looking For

Experience and Skills:

Required:

EDUCATION/WORK EXPERIENCE REQUIREMENTS:

• Education: Ph.D. (Pharmacy, Chemistry) from a reputed institute preferred. MSc, B Pharm, M. Pharm, or equivalent science stream.
• Other Skills: MS office advanced
• Work experience: Minimum 3 years and up to 6 years in Analytical development, Quality Control, or related functions in healthcare/pharma/FMCG sector with exposure to 21 CFR Guidelines, GMP and Quality environment must.

Kenvue is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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