Regulatory Affairs Jobs in North Carolina
Regulatory affairs jobs in North Carolina are in steady demand, concentrated in the pharmaceutical, biotechnology, medical device, and consumer goods sectors that anchor the state's Research Triangle region, with openings at every level from entry-level specialist through senior director. The greatest volume of hiring falls in Raleigh, Durham, and Morrisville, where companies like Novo Nordisk, Syneos Health, and Labcorp maintain large operations. The most in-demand specialties are drug regulatory submissions, FDA compliance, and combination product oversight. Find a role that fits below and apply directly.
Find Regulatory Affairs JobsOverview
Showing 5 of 5+ Regulatory Affairs jobs








Looking for more regulatory affairs jobs?
Explore related role searches to find more openings that fit.
See related jobs
Market America a Global Product Brokerage and Internet Marketing company that specializes in One-to-One Marketing, is seeking a Director of Quality Control & Regulatory Affairs.
The Director of Quality Control will manage the overall operations of the Quality and Regulatory Department to ensure that goals are met in a timely and effective manner. Directs and supervises any lead and managerial staff.
Essential Function and Responsibilities:
Serves as Senior Staff member of the Quality Assurance and Regulatory Affairs team to support, educate, motivate and direct the team. To ensure a clear understanding of duties, provide accountability for performance and help maximize high pay off activities that will increase their productivity and profitability of product lines. Responsible for the systems and processes implemented to ensure compliance to Good Manufacturing Practices; compliance with State, Federal and International regulatory standards; and the quality standards of our vendors.
Essential Duties and Responsibilities:
- Maintains accountability to the direction provided by the Executive Vice President and Vice President of Product Management.
- Anticipates, evaluates and controls risks associated with complying with industry and government regulations
- Ensures timely completion of projects assigned to the team.
- Predicts, detects, estimates, and measures product defects
- Oversees labeling changes in compliance with government regulations, including allergen labeling, ingredient, warnings and nutrient content labeling
- Develops, implements, and trains on departmental policies and procedures that impact job performance. Determines areas for improvement and quality.
- Collaborates with other departments to ensure all parties have the required information for success in their roles.
- Manages the Quality Control Department in order provide any needed information such as label review, vendor issues, and manufacturing changes.
- Ensures that all products drugs, dietary supplements, cosmetics, skin care) are manufactured, tested, stored, and distributed according to Good Manufacturing Practices (cGMP) and other applicable regulations and specifications
- Complies with Company policies and procedures
- Performs other duties as assigned.
Education and Experience
- PHD in Chemistry, or related field preferred
- 10+ years of experience in Quality Control, Pharmaceutical, Science Operations, and staff supervision.
Market America offers competitive salary and generous benefits, including health, dental, vision, life, short and long-term disability insurance, a 401(k) retirement plan with company match.
Qualified candidates should apply online. This position will work on site based in our Greensboro NC offices. Sorry, we are NOT able to sponsor for this position.
Market America is proud to be an equal opportunity employer.
Market America is changing the way people shop and changing the economic paradigm so anyone can become financially independent by creating their own economy and converting their spending into earning with the Shopping Annuity®.
ABOUT MARKET AMERICA, INC.
Market America Worldwide is a global e-commerce and digital marketing company that specializes in one-to-one marketing and is the creator of the Shopping Annuity Its mission is to provide a robust business system for entrepreneurs, while providing consumers a better way to shop. Headquartered in Greensboro, North Carolina, and with eight sites around the globe, including the U.S., Market America Worldwide was founded in 1992 by Founder, Chairman & CEO JR Ridinger.
For more information about Market America Worldwide: MarketAmerica.com
See All 5 Regulatory Affairs Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Regulatory Affairs JobsRegulatory Affairs Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Regulatory Affairs Job Market in North Carolina
A snapshot from current North Carolina openings, updated as new roles post.
Who's Hiring



What North Carolina Employers Look For
The qualifications that appear most often in regulatory affairs jobs across North Carolina.
- Bachelor's degree in life sciences, chemistry, pharmacy, or a closely related field
- Working knowledge of FDA regulations including 21 CFR Parts 210, 211, and 820
- Experience preparing and submitting regulatory dossiers such as INDs, NDAs, or 510(k)s
- Familiarity with ICH guidelines and global regulatory frameworks for pharmaceutical or device products
- Strong technical writing skills for authoring SOPs, protocols, and regulatory submissions
- RAC certification from the Regulatory Affairs Professionals Society preferred for senior positions
Regulatory Affairs Jobs in North Carolina: Frequently Asked Questions
How do you become a regulatory affairs specialist in North Carolina?
The most direct path is earning a bachelor's degree in a life science, pharmacy, or engineering field, then applying to entry-level regulatory affairs or quality assurance roles at pharmaceutical or medical device companies. North Carolina does not require a state-issued license specific to regulatory affairs, but the Regulatory Affairs Certification (RAC) credential from the Regulatory Affairs Professionals Society is widely recognized by Research Triangle employers and strengthens candidacy for both junior and mid-level positions.
How much do regulatory affairses make in North Carolina?
Regulatory affairses in North Carolina earn a median of about $78,500 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $45,690 for the lowest 10% to over $131,180 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire regulatory affairs specialists in North Carolina?
Employers hiring regulatory affairs specialists in North Carolina right now include BASF, SCN BestCo, and Market America, based on current listings on Migrate Mate as of September 2026. North Carolina's Research Triangle Park concentration of pharmaceutical, biotech, and contract research organizations makes it one of the more active regulatory affairs hiring markets on the East Coast.
Which North Carolina cities have the most regulatory affairs jobs?
The cities with the most regulatory affairs openings in North Carolina are Raleigh, Nashville, and Greensboro. The Research Triangle anchors most of the volume because Raleigh, Durham, and their suburbs host a dense cluster of global pharmaceutical headquarters, biotech startups, and contract research organizations, while Charlotte adds openings tied to medical device and consumer health companies based there.
Are there remote regulatory affairs jobs in North Carolina?
Yes, and more than most fields. Regulatory affairs work is largely document-driven and does not require a physical lab or production floor presence, making it well suited to remote arrangements. About 50% of regulatory affairs openings tied to North Carolina are remote or hybrid as of September 2026, reflecting broad industry acceptance of distributed work. Submission writing, labeling review, and regulatory intelligence roles tend to be the most consistently remote.
How can I get hired as a regulatory affairs specialist in North Carolina with little or no experience?
The most realistic entry path is through a quality assurance associate or clinical data coordinator role at a Research Triangle contract research organization or pharmaceutical manufacturer, where internal transfers into regulatory affairs are common. Companies like Syneos Health and ICON Plc run structured associate programs that accept candidates from adjacent fields. Completing an RAC prep course or a graduate certificate in regulatory science from a North Carolina university strengthens an application considerably, as does any hands-on experience with FDA submission tools or document management systems.
Where can I find and apply to regulatory affairs jobs in North Carolina?
You can find and apply to regulatory affairs jobs in North Carolina on Migrate Mate, which lists current North Carolina openings updated regularly. Search the listings, find roles that match your background and location preference, and apply directly to the ones that fit.
See All 5 Regulatory Affairs Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
Find Regulatory Affairs Jobs