Senior Manager, R&D Quality & Compliance

Kenvue is currently recruiting for a:

Senior Manager, R&D Quality & Compliance

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:

Reg Franchise Quality Ldr Skin Health

Location:

North America, United States, New Jersey, Summit

Work Location:

Hybrid

What you will do

The Senior Manager, R&D Quality & Compliance (Q&C) directs staff performing R&D Q&C activities at a site or function to ensure an integrated and comprehensive quality monitoring system for GMP, Analytical and Micro, and GLP activities is developed, implemented and maintained.  Quality monitoring activities include but are not limited to the quality reviews of key documents; review of metrics and support of CAPA activities for Non-conformances/Deviations, Audits, Change Control, and Health Authority inspection activities, and evaluation/implementation of corrective and preventative actions for effectiveness; review of activities to ensure ongoing inspection readiness.  Responsible for ensuring the timely and accurate completion of departmental R&D Quality & Compliance deliverables, management of CAPAs/NCs. 

Functions as an advisor concerning Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Good Documentation Practices (GDP), and provides appropriate compliance guidance to staff and R&D personnel. Contributes to management of processes and systems that lead to collection of data relevant to reporting quality metrics. 

Acts as the single-point of contact for assigned Site or Function/COE, and ensures appropriate escalation processes are implemented.  Leads efforts for maintaining R&D Quality & Compliance processes and guidelines and participates in process improvement projects, departmental decision-making, recruitment, resource assessments, budget management and end of year performance evaluations.  Assists Regional Head with interdepartmental and cross-functional strategic planning.  

Responsible for the development of all employees at a Site or Function/COE within the department by supporting the development of Human Resources Planning (HRP) programs including management development and training to meet current and future business needs.  Provide an environment which encourages the company's credo, commitment to equal employment opportunity and the value of a diverse work force. 

Key Responsibilities

• Provide management oversight of the R&D Quality & Compliance organization within the assigned site or function, maintaining quality monitoring and assessment programs to ensure the R&D organization is operating in compliance with company/division policies and procedures, as well as applicable regulatory requirements.  Ensure innovative compliance solutions are identified, when possible, to address project and process challenges. Ensure effective deployment of R&D Quality & Compliance resources to meet the current and future needs of the R&D organization.

• Provides ongoing mentoring, coaching and development of R&D Quality & Compliance staff.  Ensures staff are trained on procedures and systems associated with their assigned tasks.  Perform administrative tasks associated with performance reviews, salary administration, and other personnel issue.  Recruits/hires qualified staff for the department and ensures staff have the education, experience and tools to appropriately function as advisors of GMP, GLP and Good Documentation Practices.

• Participates on R&D compliance committees (e.g., CAPA reviews, Management Reviews, etc) in the regions and escalate issues appropriately.  Collaborate across regions and with Global Qua