Senior Manager Regulatory Affairs (m/f/d) UK & Ireland

Job Description - Senior Manager Regulatory Affairs (m/f/d) UK & Ireland (2407026947W)

Kenvue is currently recruiting for a:

Senior Manager Regulatory Affairs (m/f/d)

Location: UK & Ireland

This position reports to Director Regulatory Affairs and is based at High Wycombe.

Who we are

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 Brand Adhesive Bandages that you already know and love. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers.

What you will do

The Senior Manager of Regulatory Affairs (Market) is a country expert with an in-depth understanding of the regulatory environment within their geographical area of responsibility as well as requirements and strategies for regulatory submissions, approval pathways and compliance activities.

Key Responsibilities:

1. Leads the Regulatory Affairs team, ensuring the success of new product registrations, line extensions and new indications and claims in alignment with the business plan.
2. Create an environment of operational excellence through regulatory expertise by managing and developing direct reports and collaborating with cross-functional teams.
3. Manages the coordination, compilation, submission of new drug applications, cosmetics, medical devices, food supplements or any similar product to the regulatory agencies.
4. Facilitates and cultivates external relationships, representing Kenvue with relevant regulatory agencies and industry associations.
5. Represents the Regulatory Affairs function in Cluster functional and business Leadership teams.

What we are looking for

Required Qualifications:

1. Relevant Bachelor's Degree or higher.
2. 8+ years related regulatory experience.
3. Excellent communication skills, able to articulate complex regulatory or technical issues clearly.
4. Strong interpersonal skills; able to build effective personal networks.
5. Highly collaborative with a strong sense of ownership.
6. Strong organizational and time management skills.
7. Demonstrable commercial focus and business acumen.
8. In-depth knowledge of the Regulatory Affairs function and cross-functional business partners.
9. Able to work effectively in a multi-cultural, highly matrixed organization.
10. Experience in cultivating and leveraging strategic networks and partnerships.
11. Proficiency in English.

Desired Qualifications:

1. Membership in a Pharmacist association.
2. Designation as QP by the Health Authorities.
3. Knowledge of GMP and European legislation for pharmaceutical products.
4. Knowledge of production, Quality Assurance, Quality Control, validation.
5. At least 2 years of experience as QP deputy.

What’s in it for you:

1. Competitive Total Rewards Package.
2. Paid Company Holidays, Paid Vacation, Volunteer Time & More!
3. Learning & Development Opportunities.
4. Employee Resource Groups.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic.