Senior Manager, Ext Mfg. Quality

Senior Manager, Ext Mfg. Quality

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:

Director, External Mfg Quality Assurance

Location:

North America, United States, New Jersey, Summit

Work Location:

Hybrid

What you will do

The Senior Manager, External Manufacturing Quality (EMQA) is responsible for overseeing a defined portfolio of External Manufacturing (EM) sites and/or product categories within Skin Health/Essential Health. You will balance strategic priorities with hands-on operational oversight at EM sites, and provide tactical leadership, ensuring alignment with EMQA functional objectives.

Key Responsibilities

• Provide operational and tactical leadership of the EMQA team supporting assigned EM sites and/or product categories.

• Ensure manufacturing quality and compliance across assigned EM sites, acting as day-to-day quality leader.

• Serve as decision maker for high-impact compliance issues that do not require Director (D1) alignment.

• Lead strategy and execution for EM site remediation and continuous improvement initiatives.

• Review and approve Level 2 investigations (INVs), OTC NDA Annual Product Reviews (APRs), and additional quality documents as required.

• Collaborate cross-functionally within a matrix structure to resolve issues, drive efficient processes, and maintain compliance.

• Coach, mentor, and develop direct and indirect reports to strengthen functional capability and support succession planning.

• Monitor performance, drive accountability, and ensure EMQA activities align with overall Kenvue quality expectations.

What we are looking for

Required Qualifications

• A minimum of a bachelor’s degree is required. A focused degree in a science-related discipline is preferred.

• A minimum of 8 years of experience working in a regulated industry is required. Experience in over-the-counter drug and/or cosmetic manufacturing is highly desired. Experience with pharmaceutical and/or medical device manufacturing is a plus.

• Working knowledge of cGMP requirements, current FDA enforcement issues and current regulatory authority enforcement practices is required. Working knowledge of process validation, cleaning validation, manufacturing and packaging equipment train designs, microbiological controls, and assessing compliance to regulations is required.

• Experience in managing quality activities for large volume external manufacturing and supplier sites ensuring compliance with applicable regulations.

• Demonstrated ability to collaborate with internal and external partners to enhance relationships and interactions.

• Experience in the facilitation of internal and external audits and regulatory inspections.

• Demonstrated ability to build respectful and productive relationships with subordinates, peers, and leadership partners across multiple responsibility levels and within a high matrix structure is required.

• Strong communication (verbal, written, and presentation) and interpersonal skills, self-awareness and adaptability required.

• Demonstrated ability to lead as a key team member, developing strategy/plans and implementing successful outcomes is required.

• Demonstrated ability to address complex issues using deductive reasoning, critical analysis skills and systematic approaches is required.

• Demonstrated working knowledge of root cause analysis techniques including but not limited to: brainstorming, data collection and analysis tools, 5-whys, Fishbone (cause and effect), FMEA, and DMAIC is required.

• Results-oriented with strong track record of success in delivering on objectives.

• Ability to work in a fast-paced environment with multiple, concurrent priorities many needing immediate resolution.

Desired Qualifications

• Experience with QA or QC directly or indirectly is preferred.

• Professional Certification with Six Sigma Black or Green Belt is preferred.

What’s in it for you

$153,850.00 - $217,200.00

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.