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Senior Quality & Regulatory Specialist

About Us:
VideaHealth is a cutting-edge AI-powered solution for dentistry, developed by a team of business operators, engineers, AI scientists, and clinicians spun out of MIT. Our vision is to be the first company to diagnose a billion people globally. Our product is already used by thousands of dental clinicians to improve the quality of care through faster diagnoses, lower operating costs, and improved patient understanding.

About this Position:
As the Senior QA/RA Specialist you will help shape the future of oral care by combining your own excellence in quality and regulatory processes with close collaboration with the technical Machine Learning (ML) and Operations teams. As a key member of the Quality & Regulatory Department, your expertise will aid the growth of the software as a medical device (SaMD) Quality Management System (QMS).  You will develop a roadmap and lead the implementation of QA/RA and security software modules.   You will drive cybersecurity management alongside the Information Security Officer and may be the deputy to the Management Representative and/or Information Security Officer.

You will lead premarket regulatory submissions for United States FDA clearances, European Union CE Mark, etc. and live out the Quality Management System (QMS) to deliver AI models with real world impact.  Your regulatory knowledge may lead institutional review board (IRB) activities and clinical investigation study oversight.

We are looking for an individual with a strong QA/RA background who is not shy to take proactive responsibilities in pursuit of operational excellence across the organization.  This is an impactful role that will grow your technical and leadership skills and ultimately improve the quality of dental care millions of people receive.  Your contributions will play a key role in building a great company from an early stage and we are excited to work with you to revolutionize dentistry!

This is a hybrid position in our Boston HQ.

Requirements:

  • Bachelor’s Degree in a relevant discipline.  Master’s Degree preferred.

  • 8+ years of experience in a quality & regulatory role

  • Experience, certification(s) or credential(s) for quality auditing, regulatory affairs, software quality assurance, or cybersecurity. 

  • Strong communication and collaboration mindset with external and internal stakeholders.

  • Build strong relationships by being a collaborative and dependable teammate across the software and machine learning teams as well as other key organizational stakeholders.

  • Strong technical or medical regulatory writing ability.

  • Experience with developing, implementing, and monitoring QMS processes such as document control, CAPA, complaint handling, and training.

  • Experience with internal and/or external QMS audits.  Lead internal auditor experience and/or experience in the front room as auditee is required.

  • Experience with cybersecurity and electronic protected health information (ePHI) processes.  This includes working knowledge of HITRUST, SOC2, HIPAA, and/or GDPR.

  • Experience with medical device premarket clearance submissions (USA FDA 510(K), EU MDR, others internationally) is required.

  • Experience managing or implementing internal business systems (eQMS, cybersecurity framework management software, etc.).

Bonus Points For:

  • Experience with SaMD testing processes is a plus.

  • Knowledge of or experience with statistical techniques.

  • RAPS certification

You'll thrive here if you have:

  • A strong sense of initiative alongside the ability to follow up and get things done.

  • Ownership and vision for QMS and regulatory processes to ensure they are value added.

  • Adaptable and creative approach to problem solving.

  • A sense of curiosity and interest in the Machine Learning and Dental industries.

What We Offer:

  • Fast paced and collaborative work culture in which you can gain experience, grow your technical skills and work on a wide variety of challenges over your time with us.

  • Competitive pay, equity and benefits.

  • Technical challenges on the leading edge of innovation where software, machine learning, and compliance meet.

  • Mentorship opportunities with the department lead; who has over 15 years of experience.

Don’t meet all the listed requirements? We still encourage you to apply! We are looking for the right teammate who is excited to contribute to our mission and are flexible on level of experience.

VideaHealth is committed to cultivating an equitable, inclusive, and supportive environment for all employees. We believe this environment creates a safe space for employees to share their experiences, brainstorm ideas, and grow their careers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

VideaHealth is supported by some of the best investors in the world, having raised over $67M in Venture Capital from Tier 1 investors such as Threshold ventures, Spark Capital (Twitter, SnapChat, SmileDirectClub), Zetta Venture (Kaggle), and Pillar VC (PillPack), as well as angel investors such as Frederic Kerrest (Co-founder of Okta). Our work has been featured in TechCrunch, Wall Street Journal, and many other outlets.

If you want to join a breakthrough healthtech company and help accelerate its impact and growth, we encourage you to apply for this exciting opportunity!

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CEO of VideaHealth
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Florian Hillen
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Average salary estimate

$115000 / YEARLY (est.)
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$100000K
$130000K

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What You Should Know About Senior Quality & Regulatory Specialist , VideaHealth

Are you ready to revolutionize the dental industry? VideaHealth, a leading AI-powered dentistry solution developed by a team of innovative minds from MIT, is looking for a Senior Quality & Regulatory Specialist in beautiful Boston. In this role, you will combine your extensive quality and regulatory expertise with collaborative efforts across our technical Machine Learning (ML) and Operations teams. Your leadership will help shape our software as a medical device (SaMD) Quality Management System (QMS), paving the way for faster diagnoses and improved patient care. As you implement QA/RA and security software modules, you'll ensure compliance with critical regulations, manage cybersecurity initiatives, and drive impactful premarket regulatory submissions for FDA and EU certifications. With your strong background in QA/RA, you'll actively pursue operational excellence, contributing to a mission that aims to improve the quality of dental care for millions. This role not only offers significant responsibilities and potential for growth but also the chance to develop technical and leadership skills in a vibrant, fast-paced environment. Join us at VideaHealth and make a difference in the future of oral care while enjoying the camaraderie of a passionate and supportive team. This hybrid position provides flexibility to balance your work and home life while being part of a company that's dedicated to innovation and improvement in healthcare.

Frequently Asked Questions (FAQs) for Senior Quality & Regulatory Specialist Role at VideaHealth
What qualifications are needed for the Senior Quality & Regulatory Specialist at VideaHealth?

To excel as the Senior Quality & Regulatory Specialist at VideaHealth, candidates should hold a Bachelor’s Degree in a relevant field, with a Master’s Degree preferred. Additionally, a minimum of 8 years of experience in quality and regulatory roles, coupled with necessary certifications in areas such as quality auditing, regulatory affairs, and software quality assurance, is essential.

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What are the primary responsibilities of the Senior Quality & Regulatory Specialist at VideaHealth?

As a Senior Quality & Regulatory Specialist at VideaHealth, your main responsibilities include developing and implementing QMS processes, leading regulatory submissions for FDA and CE Mark clearances, overseeing cybersecurity management, and collaborating with both internal teams and external stakeholders to ensure compliance and operational excellence.

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What skills are essential for the Senior Quality & Regulatory Specialist position at VideaHealth?

Essential skills for the Senior Quality & Regulatory Specialist at VideaHealth include strong communication and collaboration abilities, technical regulatory writing proficiency, experience with QMS processes, cybersecurity knowledge, and the capacity to build robust relationships across teams within the organization.

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Is experience with medical device regulatory submissions required for the Senior Quality & Regulatory Specialist at VideaHealth?

Yes, experience with medical device premarket clearance submissions, such as USA FDA 510(K) and EU MDR, is a key requirement for the Senior Quality & Regulatory Specialist position at VideaHealth. Your expertise will directly impact the approval of our cutting-edge dental solutions.

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What work culture can the Senior Quality & Regulatory Specialist expect at VideaHealth?

The Senior Quality & Regulatory Specialist at VideaHealth can expect a fast-paced, collaborative work culture that fosters innovation and professional growth. The role offers technical challenges at the intersection of software, machine learning, and compliance, all while being part of a supportive team dedicated to advancing healthcare.

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Common Interview Questions for Senior Quality & Regulatory Specialist
Can you describe your experience with quality management systems and their implementation?

In answering this question, highlight specific QMS projects you've led, detailing your role in developing, implementing, and monitoring processes. Discuss the various elements of QMS you've worked on, such as document control, CAPA, and training, to showcase your hands-on experience.

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What strategies do you use to ensure compliance with regulatory requirements?

Effective responses should detail your proactive approach to monitoring regulatory changes, implementing training for teams, and conducting audits. Discuss examples where your strategies led to successful regulatory submissions or compliance achievements.

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How do you handle conflicts or miscommunications with team members regarding regulatory issues?

Discuss your approach to conflict resolution, emphasizing communication and collaboration. Provide an example of a conflict you resolved, highlighting your ability to listen, understand differing perspectives, and work towards a common solution.

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What experience do you have with premarket regulatory submissions?

Outline your specific experiences with regulatory submissions, portraying your understanding of processes such as FDA 510(K) and EU MDR. Detail a challenging submission you managed, focusing on how you navigated obstacles to achieve success.

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Can you explain your experience with cybersecurity in regulatory contexts?

When answering, emphasize your knowledge of electronic protected health information (ePHI) regulations and how you incorporate cybersecurity protocols into QA/RA processes. Discuss any specific frameworks such as HITRUST or HIPAA you've worked with.

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Describe a successful QA/RA project you spearheaded in the past.

Share a narrative of a project that highlights your leadership skills and technical knowledge. Discuss the objectives, challenges, and results demonstrating your ability to manage regulatory aspects successfully and impact an organization positively.

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In what ways do you keep current with evolving regulations in the health tech industry?

Discuss strategies such as attending industry conferences, subscribing to regulatory newsletters, and engaging in professional networks. Highlight any relevant certifications or courses you have taken that reflect your commitment to staying informed.

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How do you build effective relationships with cross-functional teams?

Emphasize the importance of clear communication and mutual respect. Share specific strategies you use to foster collaboration, such as regular meetings, shared goals, and recognizing contributions from all team members.

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What are your thoughts on the role of AI in regulatory processes?

Discuss the potential of AI to streamline regulatory processes, enhance quality control, and improve compliance monitoring. Share any experience you have with AI tools in a regulatory context to illustrate your insight and practical understanding.

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What motivates you in a Senior Quality & Regulatory Specialist role?

Reflect on your passion for enhancing patient outcomes and contributing to innovative healthcare solutions. Share how the role's responsibilities align with your aspirations and reinforce your drive to make a positive impact in dental care.

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Full-time, hybrid
DATE POSTED
March 27, 2025

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