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:

Location:

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What you will do

Scientist R&D Materials

Roles and Responsibilities:

1.      To provide technical assessment of Raw materials/Products used at Internal and External Manufacturing sites to ensure alignment with current compendia, industry standards, product registrations, and internal procedures.

2.      To liaison between Global sites and Specification team by collaborating with business partners and stakeholders (Internal/External Manufacturing sites, Regulatory, Source Quality, Business Quality, Product team) to gather necessary information to process the spec request.

3.      To ensure compliance with upcoming versions of Pharmacopeia monographs and identifying affected changes to the impacted sites to ensure compliance, prior to its effective date.

4.      To have effective communication skills, for consistent, frequent collaborations with global sites, project team, and outsourced technical writers, via virtual meetings and mail correspondences.

5.      To follow team’s existing processes to ensure completeness, consistency, and accuracy, while finding opportunities and recommending solutions to improve timeliness of the Global Specification request.

6.      To have strategic and operations skills to prioritize and execute project based on business and compliance needs. Partnership and sense of urgency are required to meet the target dates of both global and regional initiatives.

7.      To become an expert in Standard Operating Procedure as well as provide feedback to necessary standard operating procedure owners to ensure procedure reflect business practices.

8.      Demonstrate clear engagement for action on priorities and get the projects targets demonstrating a great sense of urgency.

9.      Flexibility to lead with implementation changes according to new alignments or business need.

10.  Often participate of cross-functional project teams and communicative skills to discuss with different areas (business partners and off-shore technical writers)

11.  Approve specifications and change controls and drive to completion.

12.  Write and/or coordinate specifications and/or change control and guarantee written on time and right the first time.

13. To review the relevant documents / protocols / reports (including but not limited to Material Analytical Report - MAR)

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.