Regulatory Affairs Associate/Senior Associate

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. For more information, visit Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Brief Team/Department Description As part of the Regulatory Affairs team at Azurity, the Regulatory Affairs Associate/Senior Associate will assist in preparing, reviewing, and submitting regulatory filings to the FDA and other global health agencies. The person will play a crucial role in managing the 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 Operations, Quality Assurance, Clinical Development, and Medical Affairs. Principal 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 on 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. Qualifications and Education Requirements Minimum of a Bachelor of Science or a 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 year 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 a changing environment and circumstances requiring flexibility, tolerance, and a great sense of urgency while ensuring that all cGMP and regulatory requirements are met. Ability to successfully communicate, negotiate, and influence regulatory strategy with key stakeholders. Physical & Mental Requirements 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 (401(k)) 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. #J-18808-Ljbffr Azurity Pharmaceuticals