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Manager Eu Mdr Jobs (NOW HIRING)

WilsonCTS

Project Manager - 587-1

Arlington, TN

$81/hr

We are seeking an experienced Project Manager to lead the implementation of European Union Medical Device Regulation (EU MDR) requirements at our Arlington manufacturing site. This role will be ...

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 ...

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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 Jul 13, 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, and why are they important?

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 in EU MDR compliance, 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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Manager Eu Mdr jobs near you

EU MDR Project Manager

DEV-X Consulting LLC

Exton, PA • Remote

$83K - $167K/yr

Contractor

Medical, Dental, Vision

Posted 18 days ago

Job description

We are looking for a team member who is highly organized, timely and has excellent communication skills

You will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. You will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members

This is a high visibility, tight-timeline project so we are looking for folks who are able to manage their own time as well as keep things on track for the teams

Must have experience within a highly regulated industry Medical Device or Pharmaceuticals

Must have a solid understanding of CERs within EU MDD MDR compliance 

Responsibilities

  • Set project timelines
  • Monitor project deliverables
  • Update relevant stakeholders or team members on the project progress
  • Coach and support project team members with tasks you assign them

Qualifications

  • Bachelor's Degree or equivalent experience
  • Strong business acumen in project planning and management
  • Strong verbal, written, and organizational skills
  • Understanding of Clinical Evaluations and EU MDR compliance