Consumer Regulatory Affairs Specialist

  • Location
    Whippany, New Jersey
  • Job type
  • Category
    Medical & Science - Regulatory

Adecco is currently assisting a local client in their search to fill an exciting Consumer Regulatory Affairs Specialist role! Apply now if you meet the qualifications listed below!

POSITION: Consumer Regulatory Affairs Specialist
LOCATION: Whippany, NJ (Zip 07981)
DURATION: 8+ Months
PAY RATE: Negotiable
HOURS: 40 hrs per week

Questions about this role? Reach out to me now using our live chat!

**Must be eligible to work for any employer in the U.S. without sponsorship / no corp to corp or 3rd party contracting arrangement / Adecco W2 only.**

Seeking a team orientated Regulatory professional for contract position in the US Consumer Health Regulatory group. The position will be part of a 5 member team but reporting to Associate Director Regulatory Affairs, US Coppertone. The position is based in the Whippany, NJ site.

The ideal candidate will have a working knowledge of NDA/OTC monograph (topical) drugs, commodities & cosmetics. The position will require independent work with review of labeling for assigned OTC products as well as maintaining product databases for assigned products. The candidate must be able to accommodate changes and communicate them effectively.

Support regulatory activities associated with Coppertone sunscreens new and existing products such as preparing labeling documentation, coordinating & reviewing labeling. Attending project tracking meetings and keeping databases updated. Additionally, managing the folder systems to ensure projects are kept in order. Additional projects as needed.

In Summary;
• Manage Coppertone products with the oversight of Associate Director
o Prepare and approve labeling graphics.
o Review labeling in the Blue system.
o Attend project meetings to track labeling projects
• Update databases including Brain to reflect the most up-to-date information
• Prepare Drug (NDC) listings for assigned products
• Work on miscellaneous Coppertone projects as needed.
• 2nd reviewer for Nutritionals labeling in the blue system


Work experience
0-2 years’ experience in Pharmaceutical Regulatory Affairs. Consumer Regulatory Experience preferred working with OTC monographs.

Education Requirement(s):
• Bachelor’s degree with science background required
• Advanced degree- PharmD, MA, PhD preferred

Skill & Competency Requirements:
• Experience multi-tasking in a deadline controlled and highly regulated environment
• Ability to communicate effectively in English both verbally and in writing
• Proficiency in MS Office/ Excel
• Comfort with utilizing Systems/ Database
• Team and customer orientation
• Results driven
• Proofreading abilities
• Good organizational skills

• Advanced degree- PharmD

Questions about this role? Reach out to me now using our live chat!

IMPORTANT: This position is being recruited for by Adecco’s National Recruitment Center, not your local Adecco Branch Office. To be considered for this position, you must use the “apply now” button to submit your resume. If you have questions about the position, you may contact the recruiter recruiting for this position listed above. For other opportunities available at Adecco go to

If you have any questions surrounding the application process, please feel free to reach out to: Elena Jarvis at

The Adecco Group is a global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Group provides one of the most comprehensive benefits packages in the industry to contract workers to include Holiday, 401(k) and Insurance Benefit Plans.
Equal Opportunity Employer Minorities/Women/Veterans/Disabled

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Reference number US_EN_2_022862_402302