Cluster Commercial Quality Head (m/f/d) - Central Europe-2407022085W
Description
Kenvue is currently recruiting for:
Cluster Commercial Quality Head (m/f/d) - Central Europe
This position reports into Director Commercial Quality EMEA and is based at Neuss, Germany.
Who we are
At, 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 by 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.
What you will do
The Central Europe Cluster Commercial Quality Head is a management representative with the responsibility and authority of ensuring that the appropriate Quality Standards and Systems are implemented and maintained for Kenvue operations in the Central Europe Cluster.
As the Leader, you will also be responsible for managing a group of professionals and ensuring compliance with good distribution and good manufacturing practices and applicable regulations.
Key Responsibilities
·Responsible for the oversight of the Quality Management System of the Local Operating Companies (LOCs) at the corresponding geographical area and responsible for optimization of quality systems and processes in alignment with the company's Principles and Quality Policy, the relevant procedures and the applicable local regulations
·Responsible for obtaining and maintaining relevant compliance certificates, licenses, and required quality agreements
·Responsible for the inspection readiness across the Local Operating Companies in the corresponding geographical area
·Identifying opportunities to continuously improve quality; leading and supporting improvement opportunities and problem solutions; maintaining understanding and awareness of current and emerging regulations and the impact to quality and distribution practice
·Responsible in defining and implementing departmental strategies and services
·Participating in the preparation and execution of the Cluster Quality Management Review process
·Be the point of contact for quality issues within the Affiliates for:
·The Managing Director and their team in the relevant geographical area
·The local partners from Regulatory Affairs
·All employees of the LOCs involved in regulated activities
·Health authorities: influence, alert and/or analyze the current or emerging regulations that impact quality systems, implement appropriate changes as necessary
·External stakeholders such as suppliers and distribution centers.
·Ensure active leadership and presence of Kenvue in external associations dealing with compliance and quality topics (unions and professional organizations). This involves providing valuable contribution to new legislation, regular exchange of experiences, ideas and viewpoints with different representatives
·Optimize and harmonize processes and create synergies in the Cluster
Qualifications
What we are looking for
Required Qualifications
·Minimum of 8-10 years of related experience in quality assurance, with a proven track record of success in managing quality programs and teams.
·Bachelor's degree or equivalent Pharmaceutics, Chemistry, Engineering or Life Sciences subject, with a strong understanding of quality management principles and practices.
·Strong understanding of regulatory requirements and industry standards.
·Experiences as Auditor and Responsible Person will be preferred
·Ability to collaborate effectively with cross-functional teams.
·Team and people management experience.
·Being able to work independently and result oriented.
·Advanced level of English.
Desired Qualifications
·Experience in the pharmaceutical or medical device industry
·In-depth knowledge of quality management systems and regulatory requirements, including EU GDP
·Strong analytical and problem-solving skills.
·Excellent communication and interpersonal skills, with the ability to build strong relationships with internal and external stakeholders
·Proven track record of driving continuous improvement and achieving results
·Strong leadership and management skills, with the ability to motivate and inspire a team
What’s in it for you
·Annual base salary for new hires in this position ranges takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors.
·Competitive Benefit Package*
·Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
·Learning & Development Opportunities
·Employee Resource Groups
·This list could vary based on location/region
*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.