ZipRecruiter

Log In

1

Eu Mdr Jobs (NOW HIRING)

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

Getinge

Senior Manager, Regulatory Affairs

Boston, MA · On-site

S. (FDA), EU MDR (2017/745), and applicable global regulations, enabling innovation and growth while maintaining regulatory integrity throughout the product lifecycle. This leader collaborates with ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$70 - $79/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

System One

Medical Device Project Manager

Arlington, TN · On-site

$50 - $55/hr

This onsite Project Manager contract role offers the opportunity to drive EU MDR implementation efforts, manage project timelines, budgets, and stakeholder communications, and make a measurable ...

next page

Showing results 1-20

All JobsEu Mdr Jobs

Eu Mdr information

See salary details

$45K

$84K

$119K

How much do eu mdr jobs pay per year?

As of Jul 13, 2026, the average yearly pay for eu mdr in the United States is $84,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $93,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Eu Mdr position, and why are they important?

To excel as an EU MDR (European Union Medical Device Regulation) Specialist, you need expertise in regulatory compliance, medical device standards, and a relevant degree such as in engineering, life sciences, or a related field. Familiarity with regulatory submission software, ISO 13485 quality management systems, and certification as a Regulatory Affairs Professional (RAPS) is highly beneficial. Strong analytical thinking, attention to detail, and effective cross-functional communication skills help you stand out in this role. These abilities are crucial for ensuring that medical devices meet the strict EU MDR requirements, maintaining patient safety, and achieving ongoing market access for products.

What is a EU MDR job?

A EU MDR job involves ensuring compliance with the European Union Medical Device Regulation (EU MDR), which governs the safety and performance of medical devices in the EU market. Professionals in this role work on regulatory submissions, post-market surveillance, risk management, and quality assurance. They help medical device companies navigate regulatory requirements to achieve and maintain product certification. This role often requires knowledge of regulatory standards, clinical evaluation processes, and technical documentation.

What are some of the main responsibilities and challenges faced by an EU MDR Specialist on a daily basis?

As an EU MDR Specialist, your primary responsibilities include interpreting and implementing the evolving regulatory requirements of the EU MDR for medical devices, preparing comprehensive technical documentation, and facilitating regulatory submissions. You may regularly coordinate with product development, quality assurance, and clinical teams to ensure compliance throughout the device lifecycle. One of the main challenges in this role is staying current with complex, frequently updated regulations while meeting tight deadlines. Effective collaboration and adaptability are essential, as the work often involves cross-disciplinary teamwork and responding quickly to regulatory changes or audits.

More about Eu Mdr jobs
What cities are hiring for Eu Mdr jobs? Cities with the most Eu Mdr job openings:
What are the most commonly searched types of Eu Mdr jobs? The most popular types of Eu Mdr jobs are:
What states have the most Eu Mdr jobs? States with the most job openings for Eu Mdr jobs include:
What job categories do people searching Eu Mdr jobs look for? The top searched job categories for Eu Mdr jobs are:
Eu Mdr jobs near you
Infographic showing various Eu Mdr job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, 11% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.
Regulatory Affairs Associate

Regulatory Affairs Associate

Abbott

Lake View Terrace, CA • On-site

$40 - $46/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 18 days ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

156th of 527 rated manufacturers

Job description

Title: Regulatory Affairs Associate
Location: Sylmar, CA
Duration: 7 Months
100% Onsite
Summary:
Responsible for filing necessary regulatory applications and supporting interactions with U.S. and international regulatory authorities for products requiring governmental approval. Authoring and submitting U.S. PMA supplements (30-day Notices, Real-Time Reviews, 180-Day Supplements, Annual Reports), as well as supporting EU MDR Technical Documentation updates, change assessments, and Notified Body submissions.
Review/approval of engineering study protocols/reports and validation study protocols/reports. Review and approval of manufacturing and design changes for Class III implantable medical devices, including assessment of regulatory impact under both FDA and EU MDR requirements.
Requires a bachelor's degree in a scientific or related discipline and at least 1+ years of direct regulatory experience in the medical device field.
Recent experience with Class III implantable medical devices preferred.
Exposure to authoring and/or supporting PMA supplements and familiarity with EU MDR (2017/745) requirements are desirable.
Working knowledge of FDA PMA guidance documents, 21 CFR regulations, and EU regulatory frameworks.
Relies on experience and judgment to plan and accomplish assigned goals. Performs a variety of tasks with guidance as needed. Demonstrates accountability for deliverables and ability to follow through on submissions and regulatory activities. A moderate degree of creativity and latitude is expected. Typically reports to a manager or head of a unit/department.
Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High-Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
  • Published on 26 Jun 2026, 9:50 PM

What Abbott employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply