Senior Associate Regulatory Specialist

Senior Associate Regulatory Specialist

Join to apply for the Senior Associate Regulatory Specialist role at Kenvue.

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.

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!

Director RA Dietary Supplements

North America, United States, New Jersey, Summit

Hybrid

The Senior Associate Regulatory Specialist is responsible for ensuring compliance with regulatory agency regulations, preparing responses to regulatory agencies’ questions, gathering necessary information for submissions, and providing solutions to problems of moderate scope and complexity.

• Lead regulatory submissions for new product approvals and post-approval changes.
• Develop and maintain regulatory strategies to ensure compliance with global regulations.
• Provide regulatory guidance to cross‑functional teams on product development and lifecycle management.
• Conduct regulatory intelligence to stay abreast of changes in regulations and guidelines.
• Collaborate with regulatory agencies to address inquiries and resolve issues.
• Lead and manage regulatory activities for a diverse portfolio of products.
• Collaborate with cross‑functional teams to develop and implement regulatory strategies.
• Review and approve promotional materials to ensure compliance with regulatory guidelines.
• Provide guidance and support on regulatory processes such as Drug Listing and Periodic Safety Reporting.
• Develop and maintain reporting schedules for regulatory submissions.
• Present status updates on regulatory activities to key stakeholders.
• Participate in joint company/trade association initiatives and regulatory agency meetings.
• Drive continuous improvement in Regulatory Affairs processes and best practices.
• Ensure quality and compliance in all regulatory actions.

• Bachelor’s degree in a scientific discipline or related field.
• 4-6 years of experience in regulatory affairs within the pharmaceutical industry.
• Strong knowledge of global regulatory requirements and guidelines.
• Proficiency in Word, Excel, PowerPoint, Email, and Internet applications.
• Strong attention to detail and problem‑solving skills.

• Experience with regulatory processes such as IDMP and safety reporting.
• Excellent communication and interpersonal skills.
• Collaborative approach and ability to work effectively in a fast‑paced and dynamic environment.
• Ability to multitask and deliver high‑quality work under pressure.
• Effective communication and stakeholder management skills.

Annual base salary for new hires in this position ranges: $ - $.

• Competitive Benefit Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Kenvuer Impact Networks
• 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.

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. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

• Seniority level:
  Mid‑Senior level
• Employment type:
  
  Full‑time
• Job function:
  Legal
• Industries:
  Personal Care Product Manufacturing