Demo

Regulatory & Quality Specialst

Carpe
Durham, NC Full Time
POSTED ON 12/15/2025 CLOSED ON 1/9/2026

What are the responsibilities and job description for the Regulatory & Quality Specialst position at Carpe?

To apply for this role, please email a non chatGPT paragrah of why you would be a good fit for this role, along with your resume to jess@mycarpe.com. Only emails will be considered for this role.


Regulatory & Quality Specialist

Location: Durham, NC (On-site)

Department: Product Development

Reports to: Head of Product Development

Employment Type: Full-Time


About Carpe

Carpe is the fastest-growing deodorant brand in the US. Our team is composed of ~25 insanely smart people working together in-person in downtown Durham, NC. Our office is rather open with many private niches, and our energy level is HIGH.


About the Role

We’re looking for a proactive, detail-driven, and organized teammate to join our Product Development group.


In this role, you’ll work across Regulatory, Quality, and Product Development to ensure every Carpe product meets our high standards from concept to launch. You’ll be hands-on in every step of the process: managing testing, documentation, and regulatory compliance submissions that keep each formula safe, effective, and ready for market.


If you love connecting details to big-picture outcomes and want to be part of every step of bringing innovative products to life, this role is for you.


What You’ll Do


Regulatory & Compliance

• Work directly with our external regulatory partners to identify regulatory requirements for every Carpe product

• Maintain regulatory submissions and renewals (MoCRA, NDC, WERCS, EPR)

• Ensure labels, ingredients, and packaging meet U.S., Canadian, and EU/UK cosmetic and OTC requirements

• Prepare and manage SDS, product technical files, and retailer documentation (Target, Amazon, CVS, etc.)

• Track and organize regulatory deliverables across consultants, legal, and internal teams

• Support claims, substantiation documentation, and filing


Quality Systems

• Conduct or coordinate onsite quality audits with contract manufacturers (CMs)

• Manage incoming lot inspections, supplier documentation, and CAPA follow-ups

• Support annual product reviews, deviation logs, and supplier quality programs

• Maintain audit readiness and document control for all quality and regulatory files

Product Development

• Support the regulatory and quality steps for each product launch from formula review through production

• Track product timelines, testing schedules, and sample status across multiple projects

• Maintain formulation, artwork, and testing documentation in shared systems

• Partner cross-functionally with Marketing, Operations, and Creative to ensure smooth, compliant launches


Partner Coordination

• Serve as the main contact for regulatory consultants and external testing partners

• Track deliverables and provide regular updates on project milestones to leadership

• Support internal knowledge and process documentation as Carpe builds internal capability at increasing scale 

• Approximately 10-15% travel for on-site visits to contract manufacturers or testing partners


Who You Are

• Bachelor’s degree in a STEM field (Cosmetic Science, Chemistry, Biology, or Toxicology preferred).

• 2–3 years of experience in Regulatory Affairs, Quality Assurance, or Research & Development in cosmetics, OTC, or personal care (or if you lack this experience, explain why you believe you have equivalent experience)

• Working knowledge of FDA regulations [e.g., The Food Drug and Cosmetic Act (FD&C Act), Modernization of Cosmetics Regulation Act (MOCRA)], global regulatory frameworks (including European Union, Canada and Asia markets), and OTC drug regulations/monographs

• Strong organizational and project management skills 

• Excellent attention to detail and accuracy 

• Clear communication and cross-functional collaboration skills 


Bonus If You Have

• Hands-on experience managing regulatory or quality documentation

• Exposure to global regulatory documentation, such as EU or Health Canada registrations

• Experience with quality audits 


What You’ll Get

• Competitive salary based on experience

• Health, vision, and dental benefits, with Carpe covering a portion

• Flexible PTO

• A front-row seat to the growth of one of the most disruptive brands in body care


Why You’ll Love It Here

• You’ll be part of every Carpe launch, seeing products through from idea to shelf.

• You’ll collaborate directly with leadership, consultants, and labs.

• You’ll help shape the systems and standards that build Carpe’s next stage of growth.

• You’ll work on products that genuinely improve people’s confidence and comfort.




To apply for this role, please email a non chatGPT paragrah of why you would be a good fit for this role, along with your resume to jess@mycarpe.com. Only emails will be considered for this role.

Salary.com Estimation for Regulatory & Quality Specialst in Durham, NC
$71,103 to $87,192
If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

What is the career path for a Regulatory & Quality Specialst?

Sign up to receive alerts about other jobs on the Regulatory & Quality Specialst career path by checking the boxes next to the positions that interest you.
Income Estimation: 
$78,244 - $97,353
Income Estimation: 
$99,704 - $121,947
Income Estimation: 
$77,272 - $101,684
Income Estimation: 
$95,800 - $126,196
Income Estimation: 
$97,803 - $128,184
Income Estimation: 
$95,508 - $129,349
This job has expired.
Employees: Get a Salary Increase
View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

Not the job you're looking for? Here are some other Regulatory & Quality Specialst jobs in the Durham, NC area that may be a better fit.

  • Inside Higher Ed Chapel Hill, NC
  • Department TraCS Institute-429801 Career Area Research Professionals Posting Open Date 04/07/2026 Application Deadline 04/20/2026 Open Until Filled No Posi... more
  • 10 Days Ago

  • ECU Health Greenville, NC
  • Position Summary Apply improvement methods to achieve successful outcomes: Use evidence-based structured improvement methods for all quality improvement pr... more
  • 3 Days Ago

AI Assistant is available now!

Feel free to start your new journey!