Vivos Therapeutics, Inc
Company Employees
Cindy Sullivan
Operations Manager @Grow United LLC
Verified
Cindy Sullivan is a seasoned professional with extensive experience in operations management. She currently serves as the Operations Manager at Grow United LLC, an ag focused blockchain technology company. Cindy has a proven track record of managing operational processes, implementing strategic plans, and promoting company growth. She is known for her strong leadership skills, ability to streamline operations, and a consistent focus on improving and automation, all while serving as the voice of the customer. Cindy is a seasoned professional and has continuously updated her skills with relevant professional courses. She is a dedicated team player who is always eager to drive efficiency and productivity within any business setting. Cindy is a HighLevel super fan, an automations and AI geek, and an unabashed teller of bad (dad) jokes.More...
Kimberley Griffith
Director of Compliance and Quality Assurance @Vivos Therapeutics, Inc
Verified
Kimberley Griffith serves as the Director of Compliance and Quality Assurance at Vivos Therapeutics, Inc., where she spearheads initiatives to ensure regulatory adherence and uphold the highest standards of product quality. With over 15 years of experience in the legal support and compliance industry, Kimberley has successfully led cross-functional teams to achieve FDA and ISO certification and streamline compliance processes. Her strategic vision and commitment to excellence have been instrumental in enhancing operational efficiency and fostering a culture of continuous improvement.More...
KS
Kerrigan Samuelson
Compliance Specialist @Vivos Therapeutics, Inc
Verified
I’m Kerrigan Samuelson, a Quality Assurance and Compliance Specialist in the medical device field. I didn’t originally set out to work in quality assurance—but after stepping into the role, I unexpectedly discovered how much I enjoy it. There’s something really rewarding about creating structure, solving problems, and ensuring that products meet the highest standards for safety and performance. In my current role, I manage Device Master Records, review and maintain controlled documentation, and support complaint investigations and rework evaluations. I also lead trend analysis reporting, assist with CAPAs, and develop SOPs and work instructions that align with FDA, ISO 13485, and MDSAP requirements. I’m detail-oriented, systems-driven, and committed to continuous improvement. I enjoy collaborating across teams and helping create processes that are not only compliant but practical and effective.More...