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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INTRODUCTION
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
ROLE AND RESPONSIBILITIES
Brief team/department description: As part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Associate/Senior Associate will assist in preparing, review and submission regulatory filings to the FDA and other global health agencies. The person will play crucial role in managing lifecycle of IND, NDA, ANDA, etc. The Regulatory Affairs Associate/Senior Associate will report to the Associate Director, Regulatory Affairs and will work cross-functionally with other Azurity teams including but not limited to Technical Operation, Quality Assurance, Clinical Development, Medical Affairs.
Principle Responsibilities:
- Provide regulatory assistance with due diligence requests to support new business development activities.
- Support interaction with FDA and other regulatory agencies for assigned commercial products.
- Assist in compiling and authoring regulatory filings (IND, NDA, ANDA, etc.) and post marketing supplements for assigned products.
- Manage the timelines associated with regulatory submissions such as post-marketing periodic reports.
- Manage archival of regulatory submissions, regulatory correspondence and associated logs and tracking mechanisms.
- Provide regulatory guidance on requirements for post-approval changes, as required, for assigned products.
- Review and provide regulatory assessments for change control documentation.
- Provide regulatory support to regulatory leadership meetings and presentations.
- Keep abreast of current regulations and regulatory guidance, assessing impact to assigned products and internal processes.
- Participate in various activities of setting goals, tracking deliverables and process improvements within the regulatory department.
- Other duties as assigned.
BASIC QUALIFICATIONS
- Minimum of Bachelor of Science or preferred advanced health care discipline degree (PharmD, PhD, Master of Science, etc.) or equivalent qualification.
- Minimum of 3 years in the pharmaceutical industry with at least 1 of those years in regulatory affairs.
- Combination of education and applicable job experience may be considered.
- Excellent organizational, interpersonal, verbal, and written communication skills, strong grammar, and proofreading/editing skills, and MS Office skills are required.
- Ability to work independently with minimal supervision in a fast-paced deadline driven environment.
- Keen attention to detail.
- Ability to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance and great sense of urgency while ensuring that all cGMP and regulatory requirements are met.
- Ability to successfully communicate, negotiate and influence regulatory strategy to key stakeholders.
PHYSICAL & MENTAL REQUIREMENTS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Must be able to sit for long periods of time.
- While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear.
- May occasionally climb stairs and/or ride elevators.
- The employee must occasionally lift and/or move up to 25 pounds.
- Employee must be able to manipulate keyboard, operate a telephone and hand-held devices.
- Other miscellaneous job duties as required.
BENEFITS WE OFFER
- Unlock Your Earning Potential: Join our team and be rewarded with a competitive compensation package, including an annual bonus based on company performance, that recognizes your exceptional talent.
- Sales - In lieu of annual bonuses, we offer an Incentive compensation program that allows you to earn more - even over plan.
- Fuel Your Success: Sales Only - We understand the value of your hard work and provide a car reimbursement program and gas card for both business and personal use as part of our commitment to supporting you.
- Comprehensive Health Coverage: We value your well-being and offer excellent medical, dental, vision, and prescription coverage to ensure you and your family are always taken care of.
- Flexibility for Your Lifestyle: Achieve work-life balance with our hybrid work model, allowing you to work two days from home and three days in the office. Excludes Sales, Manufacturing, and some Operations positions.
- Invest in Your Future: Our Retirement Savings Plan (401K) is designed to help you secure a comfortable retirement by matching dollar for dollar up to 5%.
- Time Off That Counts: Take advantage of our generous time off policy, which offers up to 15 vacation days annually + rollover (up to 40 hours) as well as five sick/wellness days. For new employees, vacation accrual will be prorated based on your start date.
- Meaningful Time with Your Loved Ones: We close between Christmas and New Year’s to give you an extra week off to spend quality time with your family and recharge.
- Enjoy the Holidays: Over the course of the year, Azurity recognizes 13 holidays.
- Invest in Your Education: We support your professional growth with tuition reimbursement for undergraduate and graduate level courses or certifications.
- Recognize and Be Recognized: Our Azurity High Five peer recognition platform allows you to celebrate your colleagues' accomplishments and receive recognition for your own outstanding work.
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See All 18 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



Top Industries Hiring
- Medical Devices
- Biotechnology & Pharmaceuticals
- Manufacturing
- Science & Research
- Healthcare & Medical Services
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 Dentsply Sirona, Azurity Pharmaceuticals, and Grifols and others right now, based on current listings on Migrate Mate as of July 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?
Durham, Raleigh, and Charlotte 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 75% of regulatory affairs analyst openings tied to North Carolina are remote or hybrid as of July 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 18 Regulatory Affairs Analyst Jobs in North Carolina
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