The regulatory function is vital in making safe and effective healthcare products available worldwide. Individuals who ensure regulatory compliance and prepare submissions, as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals.
One of our most valuable contributions to the profession is the Regulatory Code of Ethics. The Code of Ethics provides regulatory professionals with core values that hold them to the highest standards of professional conduct.
Like all professions, regulatory is based on a shared set of competencies. The Regulatory Competency Framework describes the essential elements of what is required of regulatory professionals at four major career and professional levels.
Join the brightest minds in regulatory at the annual Regulatory Convergence. See the global regulatory community in action. Intensive workshops. Topical sessions. Meet ups with regulators. This is where it all comes together.
Biotechnology, Medical Device, Quality/Risk Management
4 Year Degree
This position is a key member of the Aziyo Biologics team and as such is involved in setting the Company’s long-term vision and short- term goals and objectives.
The Regulatory Affairs Manager works directly with the Food and Drug Administration (FDA), and other domestic and international regulatory agencies, and internal personnel to obtain and maintain product approvals and maintain regulatory compliance.
This position reports to EVP, Regulatory & Scientific Affairs
Essential Duties & Responsibilities
• Contribute to and develop regulatory strategies for product approval by both domestic and foreign agencies. • Prepare timely and compliant submissions to domestic and international regulatory agencies (510(k), IDE, PMA, HDE, IND, BLA, CE dossiers, supplements, responses, state licensure/certifications, export certifications, product registrations, etc.). • Identify, collect, review and evaluate information critical to submission packages. • Interpret regulations and related information for Research & Development, Operations, Quality Assurance, and Marketing. • Evaluate and recommend changes to labeling, marketing literature, and clinical protocols for regulatory compliance to recognized laws or regulations. • Contact FDA and other government agencies as needed and assist in facility inspections from local, state, federal, and international agencies. • Responsible for the identification of issues and initiation of actions to prevent the occurrence of any nonconformity relating to products, processes, and the quality system as applicable to the responsibilities outlined with this job description.
Experience and Skills
Work Experience Required: • Minimum of 5 years’ experience in medical device Regulatory Affairs
Aziyo Biologics is a fully integrated, commercially oriented regenerative medicine company. Since its founding in 2015 the company has expanded through acquisitions and strategic partnerships, creating a high growth commercial entity. Its proprietary products are used in orthopedic, cardiovascular, and other medical specialties.