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

What you will do

The Specialist, R&D Quality & Compliance (R&D Q&C) is responsible for administering integrated and comprehensive quality systems and controls to ensure R&D functions operate in compliance with sound scientific practices, cGMP requirements, and company procedures. Responsibilities include documentation review and approval, audits, inspections, archival activities, internal assessments, support of R&D study releases, and regulatory guidance. 

Key Responsibilities

• Review and approve GMP documentation and batch records, including laboratory batches with process controls. 
• Conduct quality inspections of supplies for R&D studies.  
• Serve as Quality representative on R&D project teams.  
• Provide GMP regulatory guidance and training.  
• Maintain GMP documentation, storage and archival processes.  
• Participate in GMP/Q&C procedure development, revision, and implementation, and support related process improvements. 
• Perform internal assessments and support inspection readiness. 
• Collect, compile, and report North America R&D Quality metrics across Kenvue sites (monthly & semiannual). 
• Support internal and GRC audit preparation and execution; including coordinating and gathering documentation for pre-audit requests.
• Manage non-marketed product quality complaints in accordance with applicable procedures.
• Assist in compiling documentation for R&D study release and inspection readiness activities. 
• Provide additional training and procedural guidance to R&D personnel on Quality processes & GMP documentation.
• Identify and escalate quality and compliance gaps with assigned areas of responsibility. 

What we are looking for

Required Qualifications

• Bachelor's degree in a relevant field or equivalent experience.
• Requires 2-4 Years in pharmaceutical, cosmetics, consumer products, or FDA-regulated environment.
• Experience with working effectively in a team-based environment. 
• Strong Organizational Skills
• Strong Communication/Interpersonal and Facilitation Skills (verbal, written and presentation)
• Expertise in Handling Multiple Priorities
• Strong experience using the Microsoft Office suite of applications (Word, Excel, PowerPoint)

Desired Qualifications

• Developing Product development process experience; knowledge of cGMP/cGLP requirements for cosmetic, OTC, and medical device products.  

What’s in it for you

This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit 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.