ZipRecruiter

Log In

1

Manager Eu Mdr Jobs (NOW HIRING)

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 ...

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 ...

Getinge

Senior Manager, Regulatory Affairs

Boston, MA · On-site

You just found it. Job Overview The Senior Manager, Regulatory Affairs, provides regulatory ... S. (FDA), EU MDR (2017/745), and applicable global regulations, enabling innovation and growth ...

CYNET SYSTEMS

Regulatory Affairs Associate

Sylmar, CA · On-site

$40 - $45/hr

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. Founded in 2010 and headquartered in ...

Getinge

Senior Manager, Regulatory Affairs

Boston, MA · On-site

You just found it. Job Overview The Senior Manager, Regulatory Affairs, provides regulatory ... S. (FDA), EU MDR (2017/745), and applicable global regulations, enabling innovation and growth ...

Getinge

Senior Manager, Regulatory Affairs

Wayne, NJ · On-site

You just found it. Job Overview The Senior Manager, Regulatory Affairs, provides regulatory ... S. (FDA), EU MDR (2017/745), and applicable global regulations, enabling innovation and growth ...

Getinge

Senior Manager, Regulatory Affairs

Nashua, NH · On-site

You just found it. Job Overview The Senior Manager, Regulatory Affairs, provides regulatory ... S. (FDA), EU MDR (2017/745), and applicable global regulations, enabling innovation and growth ...

Scarlet

Lead Auditor - Contractor role

Conduct remote audits of medical device manufacturers' Quality Management Systems under ISO 13485, EU MDR, and UK MDR. * Provide clear, structured audit documentation and evidence-based conclusions.

previous pagenext page

Showing results 21-40

All JobsEu Mdr JobsManager Eu Mdr Jobs

Manager Eu Mdr information

See salary details

$25.5K

$96.4K

$158K

How much do manager eu mdr jobs pay per year?

As of Aug 17, 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 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 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 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.

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.

More about Manager Eu Mdr jobs

What cities are hiring for Manager Eu Mdr jobs?

Cities with the most Manager 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 Manager Eu Mdr jobs?

States with the most job openings for Manager Eu Mdr jobs include:

What job categories do people searching Manager Eu Mdr jobs look for?

The top searched job categories for Manager Eu Mdr jobs are:

Manager Eu Mdr jobs near you
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.

Medical Device Project Manager

System One

Arlington, TN • On-site

$50 - $55/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago

Job description

Job Title: Medical Device Project Manager Location: Arlington, Tennessee Type: Contract Compensation: $50.00 - $55.00 per hour Work Model: Onsite Hours: M-F 8am to 5pm

Overview Join a collaborative, fast-paced medical technology manufacturing environment where you'll lead a high-impact regulatory compliance initiative with visibility across multiple functions. 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 impact on a critical business objective. Ideal candidates bring project management experience within the medical device industry or another highly regulated environment and thrive working independently while leading cross-functional teams.

Responsibilities

  • Lead a cross-functional team to implement the EU MDR requirements for the Arlington manufacturing site.
  • Develop and execute the project management plan, identifying risks and mitigation strategies.
  • Keep stakeholders updated on project progress.
  • Oversee plans and direct schedules as well as project budgets.
  • Monitor programs/projects from initiation through delivery, interfacing with internal customers or department personnel.
  • Organize project activities and interdepartmental meetings to ensure communication facilitates completion on schedule and within budget constraints.
  • Work independently with minimal supervision, applying professional expertise and judgment.

Requirements

  • Minimum of 4 or more years of applicable work experience in project management or related field.
  • Bachelor's Degree in Engineering or a similar field.
  • Experience within the Medical Device Industry (EU MDR) or a similar regulated environment.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific