Kenvue is currently recruiting for-

Principal Scientist Global RD Self Care Stability

This position reports into Manager RD and is based at Greater Mumbai, India.

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 .

The position is responsible for-

• The Principal Scientist – Global RD Self-Care Stability is responsible for providing guidance and support for the global developmental stability programs for technical transfers, newly developed products, and changes to commercialized/marketed products in EMEA markets.

• With guidance from RD Global Self-Care Stability Management, the incumbent will be expected to work independently, to ensure regional stability requirements are met.

• Partner with cross functional peer groups and manage the planning and execution of stability project tasks within established timelines.

• Develop stability strategies based on global regulatory requirements, internal procedures, technical information, and historical stability data.

• Facilitate execution of the established stability strategy across functional areas and across internal and external sites, including stability study initiation, stability sample management, stability storage, and stability testing.

• Document stability assessments, technical justifications, stability protocols, stability reports, and perform statistical analysis of stability data.

• Present and discuss stability strategies and report stability results to project teams, management, and governance boards.

• Participate in and lead initiatives to improve cross-functional collaboration, process efficiency, cycle times, and productivity.

• Maintain training proficiency on SOP’s, work instructions, and data analysis.

• 6+ years of experience with BS or equivalent

• 4+ years of experience with MS

• 2+ years of experience with PhD

Experience must be in the area(s) of stability, quality, and/or laboratory within a drug, device, or biologics environment. At a minimum, a bachelor’s degree is required. A focused degree in Science or Engineering is preferred.

• Experience preparing/reviewing stability protocols/reports, including performing statistical analysis of stability data, is highly

• preferred. Previous experience managing or mentoring others is preferred.

• Knowledge and understanding of GMPs, ICH, CFR, stability guidance documents, latest regulatory trends, and global Health

• Authority regulations is preferred. Excellent oral and written communication skills is preferred. Strong project management,

• coordination, and multi-tasking skills is preferred. A demonstrated ability to effectively influence people, work with cross [1] functional teams, manage multiple projects, and complete tasks of various levels of complexity is preferred.

• 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 identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.