Principal Scientist

2 months ago

Mumbai Maharashtra, India Kenvue Full time

Description

**Job Title**: Principal Scientist, Analytical - Lifecycle Management Projects

**Hiring Manager’s Title**: Associate Director, R&D

**Location**: [Choose a city]

**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 of 22,000 diverse and brilliant people, 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 the lives 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.

**What You Will Do**:
As a Principal Scientist in Analytical R&D - Lifecycle Management, you will work as the Analytical representative on cross-functional teams supporting the life cycle management of Over the Counter (OTC) self-care products. You will be responsible for technology transfer project deliverables such as method development, method validation, method transfer, and stability, ensuring that all analytical activities for currently marketed products comply with current and upcoming regulatory requirements.

**Key Responsibilities**:

- **Cross-Functional Team Support**: Serve as the Analytical representative on cross-functional teams for lifecycle management of OTC self-care products.
- **Technology Transfer**: Oversee and be accountable for technology transfer project deliverables, including method development, method validation, method transfer, and stability.
- **Regulatory Compliance**: Conduct periodic reviews and necessary analytical activities to ensure product specifications and methodologies meet current regulatory requirements.
- **Testing Strategy Optimization**: Collaborate with Quality Control laboratories to develop and implement optimized testing strategies to reduce product release testing cycle times.
- **Technical Expertise**: Utilize a broad base of knowledge in testing methodologies and specifications to work with Regulatory, Legal, and Toxicology teams to ensure compliance with compendia and ICH requirements.- **Leadership**: Act as a strong technical leader, providing guidance and mentorship to other scientists within the team.

Qualifications

**What We Are Looking For**:
**Required Qualifications**:

- Minimum of MSc, B Pharm, M. Pharm, Ph.D., or equivalent in a science stream with at least 10-12 years of relevant work experience.
- Applied experience with analytical techniques such as UPLC, HPLC, UV, GC, FTIR, and others.

**Desired Qualifications**:

- Experience in lifecycle management of OTC products.
- Strong technical leadership skills and experience in mentoring scientists.
- In-depth knowledge of regulatory requirements and compliance strategies.

**What’s In It For You**:

- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More
- Learning & Development Opportunities
- Employee Resource Groups

Kenvue is proud to be an 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.

Primary Location Asia Pacific-India-Maharashtra-Greater Mumbai

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