... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
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... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
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... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
Quick apply
... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
Quick apply
... SOC‑MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability · Must pass City background check · Must comply with MDR/SOC security ...
Cybersecurity Analyst / SOC-MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability • Must pass City background check • Must comply with ...
Cybersecurity Analyst / SOC-MDR Specialist Location: City of Canton, Georgia Work Authorization: US Citizen Security Clearance / Suitability • Must pass City background check • Must comply with ...
Saint Paul, MN · On-site
Associated MDR/Vigilante Specialist Location: Mounds View, MN Duration: 12+ months (Possibility of extension) Roles and Responsibilities: * Participates in the company's medical device and/or drug ...
Saint Paul, MN · On-site
Associated MDR/Vigilante Specialist Location: Mounds View, MN Duration: 12+ months (Possibility of extension) Roles and Responsibilities: * Participates in the company's medical device and/or drug ...
Moundsview, MN · On-site
Associated MDR/Vigilance Specialist Location: Mounds View, MN Duration: 12+ months (Possibility of extension) ROLES & RESPONSIBILTIES Participates in the company's medical device and/or drug ...
Moundsview, MN · On-site
Associated MDR/Vigilance Specialist Location: Mounds View, MN Duration: 12+ months (Possibility of extension) ROLES & RESPONSIBILTIES Participates in the company's medical device and/or drug ...
... MDR Operations team ... This role combines hands-on leadership of our client-facing Cybersecurity Specialists with direct ...
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... MDR Operations team ... This role combines hands-on leadership of our client-facing Cybersecurity Specialists with direct ...
Exton, PA · Remote
$83K - $167K/yr
Must have Medical Device Experience within EU MDD and/or EU MDR 1. Coordinate the defined cadence of the EU MDR program work for claims with other copy review workstreams such as active CAPAs. When ...
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Exton, PA · Remote
$83K - $167K/yr
Must have Medical Device Experience within EU MDD and/or EU MDR 1. Coordinate the defined cadence of the EU MDR program work for claims with other copy review workstreams such as active CAPAs. When ...
Exton, PA · Remote
$83K - $167K/yr
Must have Medical Device Experience within EU MDD and/or EU MDR 1. Coordinate the defined cadence of the EU MDR program work for claims with other copy review workstreams such as active CAPAs. When ...
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Exton, PA · Remote
$83K - $167K/yr
Must have Medical Device Experience within EU MDD and/or EU MDR 1. Coordinate the defined cadence of the EU MDR program work for claims with other copy review workstreams such as active CAPAs. When ...
In this exciting role as an Associate MDR/Vigilance Specialist, you will have the responsibility and authority to document and evaluate product feedback and product analysis results for Medtronic ...
In this exciting role as an Associate MDR/Vigilance Specialist, you will have the responsibility and authority to document and evaluate product feedback and product analysis results for Medtronic ...
In this exciting role as an Associate MDR/Vigilance Specialist, you will have the responsibility and authority to document and evaluate product feedback and product analysis results for Medtronic ...
In this exciting role as an Associate MDR/Vigilance Specialist, you will have the responsibility and authority to document and evaluate product feedback and product analysis results for Medtronic ...
Moundsview, MN · On-site
Complete applicable Medical Device Reports (MDR) as required per internal policy & procedures and FDA regulations. Ensure complaint investigations are adequate, accurate, detailed and timely. Perform ...
Moundsview, MN · On-site
Complete applicable Medical Device Reports (MDR) as required per internal policy & procedures and FDA regulations. Ensure complaint investigations are adequate, accurate, detailed and timely. Perform ...
Moundsview, MN · On-site
$28 - $31/hr
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
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Moundsview, MN · On-site
$28 - $31/hr
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
Moundsview, MN · On-site
$25 - $30/hr
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
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Moundsview, MN · On-site
$25 - $30/hr
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
Medical Device Complaint Specialist Client : Medical Device Manufacturing Company Duration : 24 ... Support Medical Device Report (MDR) activities. * Review and process complaint records. * Manage ...
ProSidian Seeks a FOIA/MDR/Appeals Reviewer | Policy and Procedure Development, Appeals, Education, Outreach, and Appraisal Support [EHSS0009025] Engagement Team | Senior Advisor Labor Category - STD ...
ProSidian Seeks a FOIA/MDR/Appeals Reviewer | Policy and Procedure Development, Appeals, Education, Outreach, and Appraisal Support [EHSS0009025] Engagement Team | Senior Advisor Labor Category - STD ...
Anasco, PR · On-site
$35/hr
Indotronix is looking to hire a Project Validation Specialist in Anasco, PR for a contract role ... The position is to support the European Union Medical Device Regulation (EU MDR) program at Añasco ...
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Anasco, PR · On-site
$35/hr
Indotronix is looking to hire a Project Validation Specialist in Anasco, PR for a contract role ... The position is to support the European Union Medical Device Regulation (EU MDR) program at Añasco ...
Moundsview, MN · On-site
$25 - $27/hr
Job Title: Medical Device Complaint Specialist Client: Medical Device Manufacturing Company ... Prepare and submit MDR, Vigilance Reports (VR), and Adverse Drug Experience (ADE) reports.
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Moundsview, MN · On-site
$25 - $27/hr
Job Title: Medical Device Complaint Specialist Client: Medical Device Manufacturing Company ... Prepare and submit MDR, Vigilance Reports (VR), and Adverse Drug Experience (ADE) reports.
Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional ...
Responsible for preparation and timely submissions of MDR/Vigilance reports to FDA/Competent Authorities and other regulatory agencies. Where necessary, seek and document relevant additional ...
Moundsview, MN · On-site
$24 - $27/hr
Job Title: Medical Device Complaint Specialist Client: Medical Device Manufacturing Company ... Medical Device Reporting (MDR) * Adverse event processing * Regulatory compliance support * Safety ...
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Moundsview, MN · On-site
$24 - $27/hr
Job Title: Medical Device Complaint Specialist Client: Medical Device Manufacturing Company ... Medical Device Reporting (MDR) * Adverse event processing * Regulatory compliance support * Safety ...
$32.5K - $38.8K
4% of jobs
$38.8K - $45K
3% of jobs
$45K - $51.3K
4% of jobs
$51.3K - $57.6K
8% of jobs
$61.3K is the 25th percentile. Wages below this are outliers.
$57.6K - $63.9K
9% of jobs
$63.9K - $70.1K
10% of jobs
The median wage is $74K / yr.
$70.1K - $76.4K
18% of jobs
$76.4K - $82.7K
18% of jobs
$83K is the 75th percentile. Wages above this are outliers.
$82.7K - $89K
18% of jobs
$89K - $95.2K
5% of jobs
$95.2K - $101.5K
3% of jobs
$32.5K
$73.4K
$101.5K
An MDR (Medical Device Reporting) Specialist ensures compliance with regulatory requirements by monitoring, investigating, and reporting adverse events related to medical devices. They analyze incidents, assess potential risks, and submit reports to regulatory authorities such as the FDA or EU MDR. Their role is critical in maintaining patient safety and ensuring that medical devices meet strict industry standards. MDR Specialists often collaborate with quality, regulatory, and clinical teams to address reporting obligations and improve device safety.
MDR Specialists are responsible for preparing and maintaining regulatory documentation, ensuring compliance with medical device regulations, and coordinating submissions for product approvals. On a daily basis, they often interact with cross-functional teams including quality assurance, engineering, and clinical affairs to gather the necessary technical data and respond to regulatory authorities. Additionally, they monitor changes in international regulations and update internal processes accordingly to maintain compliance. This role requires a proactive approach to problem-solving and clear communication to keep all departments aligned and informed.
To thrive as an MDR Specialist, you need a strong understanding of medical device regulations, quality assurance practices, and compliance processes, often supported by a degree in life sciences or engineering. Familiarity with regulatory databases, document control systems, and relevant certifications such as RAC (Regulatory Affairs Certification) or ISO 13485 is beneficial. Exceptional attention to detail, communication skills, and the ability to collaborate cross-functionally help MDR Specialists stand out. These skills are crucial for ensuring regulatory submissions are accurate, timely, and aligned with evolving industry requirements.
Cities with the most Mdr Specialist job openings:
States with the most job openings for Mdr Specialist jobs include:
The top searched job categories for Mdr Specialist jobs are:

Full-time
Posted 27 days ago
Sourced by ZipRecruiter
Software development
11 - 50 Employees
Herndon, VA, US
2003