Regulatory Affairs Analyst Jobs in North Carolina
Regulatory Affairs Analyst jobs in North Carolina are concentrated in the Research Triangle and Charlotte metro, with steady demand from the state's dense pharmaceutical, biotechnology, and medical device sectors. Employers such as Novo Nordisk, Becton Dickinson, and Merck maintain significant North Carolina operations and regularly hire analysts at associate through senior levels. Specialties in FDA submission management, clinical trial documentation, and combination product compliance see the most consistent openings across the state. Scan the live roles below and apply to whichever ones fit.
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See related jobsMarket 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
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 Analyst Jobs in North Carolina
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Find JobsRegulatory Affairs Analyst Jobs by City in North Carolina
Where North Carolina roles are concentrated, by current openings.
Regulatory Affairs Analyst 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 analyst jobs across North Carolina.
- Bachelor's degree in life sciences, pharmacy, engineering, or a closely related field
- Experience preparing and submitting regulatory filings to the FDA or equivalent agencies
- Familiarity with FDA regulations including 21 CFR Parts 11, 820, or 210 and 211
- Proficiency with regulatory information management systems such as Veeva Vault
- Strong technical writing skills for preparing submissions, SOPs, and compliance documents
- Experience in pharmaceutical, biotechnology, or medical device environments preferred
Regulatory Affairs Analyst Jobs in North Carolina: Frequently Asked Questions
How do you become a regulatory affairs analyst in North Carolina?
Most regulatory affairs analyst roles in North Carolina require a bachelor's degree in a life science, engineering, or pharmacy-related field, with many employers in the Research Triangle also accepting degrees in chemistry or biomedical engineering. There is no state-issued license specific to the role, but the Regulatory Affairs Professionals Society credential is widely recognized by North Carolina employers and signals demonstrated competency. Entry-level candidates often begin in quality assurance or clinical operations before moving into dedicated regulatory roles.
Which companies hire regulatory affairs analysts in North Carolina?
North Carolina regulatory affairs analyst roles are posted by BASF, SCN BestCo, and Market America and others right now, based on current listings on Migrate Mate as of September 2026. The Research Triangle Park corridor anchors much of this hiring, drawing pharmaceutical and medical device companies that maintain global regulatory operations from their North Carolina headquarters or R&D campuses.
Which North Carolina cities have the most regulatory affairs analyst jobs?
Raleigh, Nashville, and Greensboro account for the most regulatory affairs analyst openings in North Carolina. The Research Triangle anchors the bulk of demand because of the concentration of pharmaceutical and biotech headquarters and R&D centers in that corridor, while Charlotte adds openings tied to medical device companies and healthcare system compliance teams operating from its corporate offices.
Are there remote regulatory affairs analyst jobs in North Carolina?
Yes, and more than most fields. About 50% of regulatory affairs analyst openings tied to North Carolina are remote or hybrid as of September 2026, reflecting the desk-based, document-driven nature of the work. Submission preparation, regulatory strategy, and labeling review are the functions most frequently offered on a fully remote basis by North Carolina employers.
How can I get hired as a regulatory affairs analyst in North Carolina with little or no experience?
The most realistic entry path is moving laterally from a quality assurance associate or clinical data coordinator role at a Research Triangle Park employer, where you gain direct exposure to FDA documentation workflows. Large North Carolina employers such as Biogen and Syneos Health run rotational or associate programs that place candidates without dedicated regulatory experience into entry-level analyst tracks. Earning the Regulatory Affairs Professionals Society Foundation credential before applying strengthens a candidate's profile significantly.
Where can I find and apply to regulatory affairs analyst jobs in North Carolina?
You can find and apply to regulatory affairs analyst jobs in North Carolina on Migrate Mate, which lists current North Carolina openings. Search the available roles, identify the ones that match your background and location preference, and apply directly to whichever positions fit.
See All 5 Regulatory Affairs Analyst Jobs in North Carolina
Find roles in North Carolina that match your experience and apply in just a few clicks.
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