Quality Management Systems Specialist
Pearl, Inc.
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Benefits offered by this job
Job summary
Pearl is seeking a Quality Management Systems Specialist to maintain and improve our ISO 13485‑compliant QMS, drive CAPA and NCR closure, and own document control in Qualio. You will coordinate software release quality, audits, and regulatory readiness, while enabling cross‑functional teams in a remote‑first environment.
This hands‑on role focuses on QMS platform management, continuous improvement, and collaboration with Engineering, Regulatory, and Clinical Affairs to ensure compliant releases.
Qualifications
- 3–5 years of QMS experience in a regulated medical device or SaMD environment.
- Hands-on with ISO 13485, FDA 21 CFR Part 820, and MDSAP; EU MDR / Health Canada is a plus.
- Experience managing CAPAs, NCRs, and change events in a QMS platform (Qualio preferred).
- Software release quality coordination experience in a regulated setting.
- Strong written communication and collaborative work style.
Responsibilities
- Own CAPA/NCR lifecycle end-to-end, including root-cause and verification of effectiveness.
- Coordinate document control, change events, and regulatory traceability.
- Coordinate software release quality with engineering and regulatory teams.
- Support internal QMS audits and third-party certification readiness.
- Oversee complaint handling posture and related SOPs.
- Administer Qualio training and drive QMS tooling improvements.
Skills
Tools
Job description
We are looking for exceptional talent to join us in our mission to elevate the standard of care in dentistry and improve billions of lives worldwide.
Explore Opportunities
Operating Principles
We’re creating high-performance culture where highly talented people do the best work of their careers.
Deliver
We make bold, data-backed bets—and follow through with real results.
Step Up
Autonomy and accountability, not hierarchy and silos.
Speed
We use AI to move faster, think smarter, and build better.
Care
We encourage healthy, outcome-driven communication.
Benefits
Pearl goes the extra mile to take care of you.
Competitive salaries, meaningful equity, and a Fidelity 401k
Dental, health and vision insurance, plus a wellness stipend
Employer-backed continuing education opportunities
Paid time off whenever you need to recharge
Equip your office with the technology and supplies you need.
Work remotely, play together at off-sites, team dinners and happy hours.
Founded
2019
First FDA Clearance
2022
Team Members
200 and counting
Offices
Los Angeles
San Francisco
New York
Lehi, UT
London
Remote team worldwide
Success Stories
Teamwork and collaboration are the cornerstone of Pearl’s success.
View Jobs “It's rare to find a culture that blends high performance and creativity so perfectly. I’m continuously learning from my Pearl colleagues because they're so driven to innovate, both creatively and responsibly. That's true at every level and in every department – from sales and marketing to product and engineering.” Geraldine Moreno MARKETINGMANAGER Jobs
Join us and collaborate with the brightest – and kindest – minds in AI and dentistry.
United States - Remote
Full time
Remote
Compliance
Pearl is shaping the future of dentistry with a suite of AI solutions that raise the standard of care for patients worldwide. Since 2019, we've built FDA-cleared computer vision for 2D and 3D dental imagery, used by clinicians, practice owners, labs, and insurers to improve the efficiency, accuracy, and consistency of dental care globally. Our product suite spans Second Opinion, Practice Intelligence, Pearl Insurance, and Scribe, and we serve everyone from independent practices to the largest DSOs in the world.
At Pearl, we take the quality of that software as seriously as the science behind it. The QMS Specialist is the operational backbone of our Quality Management System: the person who keeps our ISO 13485-compliant QMS running day to day, drives CAPA and NCR closure, owns document control in Qualio, and makes sure Pearl can walk into any audit — MDSAP, third-party, or FDA — and walk out clean.
This is a hands-on, execution-heavy role. You'll own a live queue of CAPAs and NCRs at any given time, coordinate cross-functionally with Engineering, Clinical Affairs, and Regulatory, and serve as the Quality owner for software releases — ensuring every release ships with the right documentation and QMS coverage. You'll also play a significant role in QMS platform management and continuous improvement, including evaluating and onboarding next-generation QMS tooling.
CAPA & NCR Management
Own end-to-end lifecycle for corrective and preventive actions and nonconformance reports in Qualio: initiation, root cause investigation, action plan development, implementation tracking, and verification of effectiveness
Run the CAPA/NCR queue as a standing agenda item in weekly team meetings; keep the team current on status, risks, and blockers
Partner with Engineering and other departments on remediation actions, ensuring task timeliness and documentation meets QMS requirements
Document Control & Change Management
Manage the full document control lifecycle in Qualio: authoring, review routing, approval, release, and periodic review
Own change events from initiation through closure, coordinating cross-functional input and ensuring regulatory traceability
Draft, update, and maintain SOPs, work instructions, and policies in alignment with ISO 13485, FDA 21 CFR Part 820, and MDSAP requirements
Software Release Quality Coordination
Serve as the Quality representative in the software release process, participating in release go/no-go reviews and ensuring QMS requirements are satisfied before sign-off
Own and maintain the release documentation package: ensure change events, risk register updates, usability file updates, design history file entries, and any required regulatory notifications are complete and linked prior to each release
Coordinate with Engineering, Regulatory, and Clinical Affairs to identify quality-relevant changes in each release and confirm appropriate documentation coverage
Maintain and improve the release sign-off workflow in Qualio, ensuring traceability between software changes and QMS records
Internal Audits & Regulatory Readiness
Coordinate and support internal QMS audits; track findings and ensure follow-through on corrective actions
Serve as the primary QMS point of contact for third-party and certification body audits (MDSAP, ISO/MDR); prepare documentation packages and respond to findings
Monitor the regulatory landscape for changes affecting QMS compliance requirements
Complaint Handling Oversight
Own Pearl's complaint handling compliance posture: ensure the complaint handling SOP and associated work instructions are current, understood, and consistently followed across the organization
Monitor complaint handling activity for policy adherence — escalating trends, documentation gaps, or systemic issues — without owning individual complaint investigations
Serve as the policy authority for complaint classification questions (complaint vs. feedback, native integration edge cases, etc.), providing guidance to complaint handlers and driving decisions to closure
Coordinate periodic complaint data reviews to surface quality signals for CAPA consideration and post-market surveillance reporting
Training & QMS Administration
Administer the Qualio training module; track completion rates across the organization and follow up on outstanding assignments to maintain compliance targets
Drive companywide QMS training campaigns; create Loom walkthroughs and guidance materials to support staff in a remote-first environment
Evaluate and support onboarding of new QMS platform capabilities (e.g., SBOM management, vulnerability tracking, dependency management)
3–5 years of QMS experience in a regulated medical device or SaMD environment
Hands‑on familiarity with ISO 13485, FDA 21 CFR Part 820, and MDSAP; experience with EU MDR and/or Health Canada regulatory requirements is a plus
Direct experience managing CAPAs, NCRs, and change events in a QMS platform (Qualio experience strongly preferred)
Experience participating in software release processes in a Quality capacity — able to connect software changes to QMS documentation requirements
Comfortable owning a live, multi‑item compliance queue and maintaining visibility for leadership in weekly reviews
Strong written communication skills — you can draft a clear SOP, a root cause analysis, and a company-wide training announcement, and they all land differently in the right way
Organized, detail‑oriented, and able to manage multiple in‑flight items without dropping the ball on deadlines or documentation
Collaborative and low‑ego — this role touches almost every team at Pearl, and success depends on relationships as much as process knowledge
Nice to Have
Experience supporting MDSAP renewal audits and responding to certification body findings
Familiarity with SaMD‑specific quality considerations (e.g., software validation, algorithm change protocols, IEC 62304)
Experience evaluating or implementing next‑generation QMS platforms beyond legacy document management systems
Background in post‑market surveillance and complaint trend analysis for AI‑powered medical devices
What We Offer
Competitive benefit and compensation offerings
Ongoing training and development opportunities
Unaccrued, flexible PTO
Remote work
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