Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at raps@raps.org if you need assistance.
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.
Learn More About RegulatoryOne 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.
Follow the CodeYour membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
Get StartedLike 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.
LEARN MOREJoin 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.
LEARN MOREFor 20 years, our flagship publication, Fundamentals of US Regulatory Affairs, has been giving regulatory professionals the insights and answers they need, right at their fingertips.
BUY NOWThere are hundreds of RAC testing centers available worldwide. Either RAC exam (Devices and Drugs) may be taken at any location. Find an upcoming exam at a location near you.
VIEW SCHEDULE POSITION SUMMARY: The Director of Donor Quality Assurance position is responsible for the management of the Donor Quality Assurance department, its employees and the donor record review and medical release process. This individual is responsible for ensuring the timely review and release of all RTI tissue donor records in compliance with RTI policies and procedures and regulatory requirements. Approaching this role with a focus on process improvement will be vital to ensuring the department’s ability to improve and succeed in its abilities and outcomes. This position must effectively interact on a regular basis with senior members of the recovery partners' management team as well as the RTI Medical Directors. Working collaboratively with VP and Director of Donor Services, the Director DQA works closely with recovery partners to manage metrics/KPI’s relating to the record release process and outcomes associated. Additionally, the Director must implement processes with a focus on engaging the recovery partners to ensure a positive customer experience and improved/continued client satisfaction. The Director will join cross-functional internal teams to assist in ensuring the timely and successful release of donor records needed by the operations division. This position will be critical to the success of the company in helping RTI Donor Services maximize the number of patients served while maintaining a high level of quality and patient safety. RESPONSIBILITIES
CORE COMPETENCIES:
|
EDUCATION/EXPERIENCE REQUIRED AND/OR PREFERRED:
|
Program Director, Master of Science in Regulatory Affairs | Claremont, California |
Keck Graduate Institute | Today |
Director of Quality Assurance and Regulatory Affairs | Littleton, New Hampshire |
Adventure Ready Brands | Yesterday |
Head of Regulatory Affairs | Atlanta, Georgia |
Alimera Sciences | 4 Days Ago |