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Manager Eu Mdr Jobs (NOW HIRING)

Heartflow

Director - Post Market Quality

Austin, TX · On-site

Your ability to convert post-market signal into credible, timely input for risk management, CAPA, and design teams - under 21 CFR Parts 820, 803, and 806, EU MDR, ISO 13485, and ISO 14971 - is ...

New

Abbott

$40 - $46/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Exposure to authoring and/or supporting PMA supplements and familiarity with EU MDR (2017/745 ... Typically reports to a manager or head of a unit/department. Consultants Eligible Benefits Upon ...

Revance

Regulatory Device Specialist

Johnson City, TN · On-site

  • Medical

  • Life

  • Retirement

  • PTO

Compile, submit, and manage international product registrations, license renewals, and registration amendments, including FDA 510(k)s, Health Canada Medical Device Licences, EU MDR Technical ...

New

Abbott

Regulatory Affairs Associate

Lake View Terrace, CA · On-site

$40 - $46/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Exposure to authoring and/or supporting PMA supplements and familiarity with EU MDR (2017/745 ... Typically reports to a manager or head of a unit/department. Consultants Eligible Benefits Upon ...

LivaNova

Manager, Medical Device Labeling and Operations

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Lead EU MDR labeling activities, including gap assessments, remediation plans, and implementation ... Manage labeling review, approval, and release processes, ensuring accuracy and compliance UDI ...

Revance

Regulatory Device Specialist

Johnson City, TN · On-site

  • Medical

  • Life

  • Retirement

  • PTO

Compile, submit, and manage international product registrations, license renewals, and registration amendments, including FDA 510(k)s, Health Canada Medical Device Licences, EU MDR Technical ...

New

Morgan Stanley

Director, Regulatory Affairs

Littleton, CO · On-site

$177 - $266/hr

  • Medical

  • Retirement

  • PTO

Manage external partners, consultants, and regulatory service providers as needed ... Strong knowledge of FDA and EU MDR regulatory frameworks; familiarity with additional markets (e.g ...

SharkNinja

Compliance Engineer

Needham, MA · On-site

... EU MDR 2017/745. Assist in preparing regulatory filings including FDA 510(k) submissions and ... Execute risk management activities in accordance with ISO 14971, including hazard identification ...

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Manager Eu Mdr information

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$25.5K

$96.4K

$158K

How much do manager eu mdr jobs pay per year?

As of Aug 16, 2026, the average yearly pay for manager eu mdr in the United States is $96,382.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $118,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Manager EU MDR?

To thrive as a Manager EU MDR, you need in-depth knowledge of European Medical Device Regulation (MDR), regulatory affairs experience, and a relevant degree in science, engineering, or a related field. Expertise in using regulatory submission systems, quality management tools (like ISO 13485), and familiarity with notified body processes are typically required. Exceptional organizational, leadership, and communication skills help manage cross-functional teams and complex documentation. These skills ensure compliance, product approval, and successful navigation of the evolving EU medical device regulatory landscape.

What is the difference between Manager Eu Mdr vs Regulatory Affairs Specialist?

AspectManager Eu MdrRegulatory Affairs Specialist
CredentialsTypically requires advanced degrees and experience in medical devices and EU regulationsUsually holds a degree in life sciences or regulatory affairs, with certifications in regulatory processes
Work EnvironmentLeads teams, manages compliance projects, and interacts with multiple departmentsFocuses on preparing documentation, ensuring regulatory submissions, and supporting compliance tasks
Industry UsageCommonly used in medical device companies within the EUFound across medical device, pharmaceutical, and biotech industries
Search & Comparison IntentOften compared for roles with managerial responsibilities in EU MDR complianceCompared for specialized regulatory roles supporting EU MDR adherence

The Manager Eu Mdr oversees compliance teams and strategic implementation of EU MDR regulations, while the Regulatory Affairs Specialist handles documentation and submission tasks. Both roles require regulatory knowledge, but the manager has broader leadership responsibilities.

What does a Manager EU MDR do?

A Manager EU MDR oversees an organization’s compliance with the European Union Medical Device Regulation (EU MDR). They are responsible for developing, implementing, and maintaining processes to ensure that medical devices meet all regulatory requirements for sale in the European market. This role includes coordinating regulatory submissions, managing documentation, and liaising with notified bodies and regulatory authorities. The manager also stays updated on regulatory changes and ensures that the company’s products and processes are continuously compliant. They often provide guidance and training to internal teams on EU MDR requirements.

What are some common challenges faced by a Manager EU MDR, and how can they be effectively addressed?

A Manager overseeing EU MDR (Medical Device Regulation) compliance often encounters challenges such as keeping up with evolving regulatory requirements, coordinating cross-functional teams, and managing documentation for audits. Staying informed through continuous professional development and industry updates is key to staying compliant. Effective communication and collaboration with regulatory, quality, and R&D teams can help streamline processes and ensure timely submissions. Leveraging regulatory management software and establishing clear SOPs can also improve efficiency and reduce errors.
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Infographic showing various Manager Eu Mdr job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $96,382 per year, or $46.3 per hour.

Director - Post Market Quality

Heartflow

Austin, TX • On-site

Full-time

Posted 3 days ago

New

HeartFlow rating

7.8

Company rating: 7.8 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

136th of 244 rated software companies

Job description

Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFRCT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare.
Heartflow is a publicly traded company (HTFL) that has received international recognition for exceptional strides in healthcare innovation, is supported by medical societies around the world, cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 500,000 patients worldwide.
As the Director of Post-Market Quality, you own the systems that tell Heartflow how its products perform in the field, and the regulatory obligations that follow from what those systems reveal. You will lead the Designated Complaint Handling Unit, Product Investigations team, global adverse event reporting (FDA MDR, EU Vigilance), field actions, and the post-market surveillance processes required under EU MDR. This role requires deep, working expertise in post-market requirements applied to AI Software as a Medical Device (SaMD), where failure modes may be more algorithmic rather than mechanical. This role is highly visible with direct interaction and collaboration with leadership and executive management throughout Heartflow.
You will lead a high-performing team of complaint specialists, product investigators, and engineers working on investigations. You will lead the championing a Quality-first, patient-centric culture and driving data-driven decisions, while modernizing a proactive approach to obtaining feedback data as it relates to product quality and performance. Your ability to convert post-market signal into credible, timely input for risk management, CAPA, and design teams - under 21 CFR Parts 820, 803, and 806, EU MDR, ISO 13485, and ISO 14971 - is essential to our success.
Job Responsibilities:
Complaint Handling
  • Working through the Manager of Complaint Handling, direct the designated complaint handling unit, ensuring intake, triage, documentation, investigation, and closure satisfy ISO 13485:2016, the FDA Quality Management System Regulation (21 CFR Part 820, as amended), and EU MDR requirements.
  • Own complaint handling processes, procedures, and decision criteria, ensuring every complaint carries a robust documented reportability decision and a defensible closure rationale in the record.
  • Approve closure of high-severity complaint files, including event coding to IMDRF adverse event terminology, and ensure coding is applied consistently enough to support credible and robust trending.
  • Manage complaint cycle time against defined service levels, escalating aged, high-severity, or patient-impacting cases to the Executive Leadership Team.
  • Ensure customer-facing investigation responses are technically accurate, consistent with the underlying investigation record, and insightful to the customers.
  • Utilize emerging AI tools to incorporate improved quality, consistency, and efficiency within the complaint handling process and incorporate proactive monitoring of SaMD algorithm performance in the field.

Product Investigations
  • Lead the Product Investigations (PI) function through the Manager of PI, ensuring root cause analysis is evidence-based, proportionate to risk, and traceable from the reported symptom through to disposition for robust trend analysis.
  • Route confirmed product issues into CAPA, risk management file updates, and other non-conformance and corrective action subsystems.
  • Enhance the investigation process to ensure a tiering system for product investigations, while partnering with R&D, Clinical, and Product Management on investigations requiring algorithm review and/or design enhancements.

Adverse Event Reporting
  • Own reportability decision-making and timely submission of FDA Medical Device Reports under 21 CFR Part 803, including 30-day, 5-day, and supplemental reports.
  • Own international reporting, including EU vigilance obligations under EU MDR and coordinate with the Heartflow Japan team to ensure proper and timely reporting to PMDA, including serious incident reporting and Field Safety Corrective Actions to Competent Authorities and the Notified Body within prescribed timelines.
  • Maintain and defend the reportability decision trees, rationale documentation, and non-reportable justifications that underpin every complaint file.
  • Govern reporting timeliness as a standing, executive-visible quality metric, with root cause and corrective action in case of any missed or late submission.

Field Actions, Recalls and Health Hazard Evaluation
  • Own the Health Hazard Evaluation process in relation to the post-market processes.
  • Ensure complaint files align with documented, risk-based assessment of severity, probability of occurrence, and population at risk.
  • Direct corrections and removals under 21 CFR Part 806, including the written report to FDA within ten working days, engagement with the Recall Coordinator, and records for non-reportable actions.

EU MDR Post-Market Surveillance
  • Own the Post-Market Surveillance (PMS) system under EU MDR including the PMS plan, the PMS Report, and the Periodic Safety Update Reports, as applicable to device classification.
  • Direct Post-Market Clinical Follow-up planning and evaluation with Clinical and Regulatory Affairs, ensuring PMCF output feeds the Clinical Evaluation Report on a defined cycle.
  • Establish proactive trending and signal detection across complaints, service data, and published literature, with statistically justified thresholds and a documented route from signal to risk management, including trend reporting.
  • Establish real-world performance monitoring for AI/ML-enabled device functions, with predetermined thresholds for accuracy and subgroup performance, and a defined escalation path when drift or performance disparity is detected.
  • Ensure post-market output is demonstrably fed back into the risk file, Clinical Evaluation Report, labelling, and design controls.

Strategic Leadership, Governance and Team Development
  • Lead, mentor, and scale a team of complaint specialists and product investigators, owning hiring, onboarding, performance management, and succession for a function that runs to regulatory clocks.
  • Serve as the primary subject matter expert for post-market topics during FDA inspections, Notified Body audits, and MDSAP assessments.
  • Own post-market inputs to Management Review.
  • Champion a "Quality-first", patient-centric mindset, using impactful KPIs, robust training, reportability timeliness, investigation cycle time, complaint closure rate, and signal escalation - to drive accountability and data-driven decisions.
  • Collaborate with leaders and partners in Regulatory Affairs, Clinical, R&D, Customer Support, and Commercial to integrate post-market processes seamlessly, balancing compliance with business objectives.
  • Manage departmental resources, including headcount planning, budget, and long-term strategic planning for a fast-growing business.

Skills Needed:
  • Effective, clear, and concise communication skills, bringing clarity to complex decisions across the leadership spectrum.
  • Sound regulatory judgement under time pressure, with the confidence to make and defend a reportability decision on incomplete information within a regulatory clock.
  • Operating with high integrity and patient-centric decision-making
  • Ability to coach, mentor, and drive a collaborative quality culture through influence.
  • Deep understanding of complaint handling, MDR and vigilance reporting, post-market surveillance, and field action management for regulated medical devices.
  • Experience interacting with auditors, including Notified Body auditors and FDA Investigators.
  • Understanding of Software as Medical Device products, ideally AI based SaMD.

Educational Requirements & Work Experience:
  • Bachelor's degree in engineering or scientific discipline, or equivalent.
  • 13+ years of progressive experience in Quality within the medical device industry, with at least 7+ years in a leadership/management role.
  • Expert-level knowledge of relevant regulations and standards, including 21 CFR Parts 803 and 806, the FDA Quality Management System Regulation, EU MDR, ISO 13485, and ISO 14971.
  • Demonstrated ownership of MDR and vigilance reporting decisions.
  • Proven track record of successfully leading or playing a key SME role in regulatory inspections (FDA, Notified Body).

Preferred:
  • Direct experience with AI/ML-driven SaMD and cloud-based medical device platforms.
  • Experience defining and monitoring real-world performance thresholds for an AI/ML-enabled device, including drift and subgroup performance.
  • Experience authoring and defending Periodic Safety Update Reports and Post-Market Surveillance Reports at Notified Body audit.
  • Experience running complaint handling using modern tools to incorporate quality, compliance, and efficiency.
  • Experience implementing and scaling post-market processes in a fast-paced and growing environment.

A reasonable estimate of the base salary compensation range for the San Francisco Bay Area is $180,000 to $225,000 per year, cash bonus, and equity. #LI-Hybrid
Heartflow is an Equal Opportunity Employer. We are committed to a work environment that supports, inspires, and respects all individuals and do not discriminate against any employee or applicant because of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. This policy applies to every aspect of employment at Heartflow, including recruitment, hiring, training, relocation, promotion, and termination.
Positions posted for Heartflow are not intended for or open to third party recruiters / agencies. Submission of any unsolicited resumes for these positions will be considered to be free referrals.
Heartflow has become aware of a fraud where unknown entities are posing as Heartflow recruiters in an attempt to obtain personal information from individuals as part of our application or job offer process. Before providing any personal information to outside parties, please verify the following: A) all legitimate Heartflow recruiter email addresses end with "@heartflow.com" and B) the position described is found on our careers site at www.heartflow.com/about/careers/.

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