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Full Time Eu Mdr Jobs (NOW HIRING)

Synectics Inc

Program Engineer

North Chicago, IL

$55.26 - $69.07/hr

... 13485, and EU MDR preferred. * Expertise in Systems Engineering principles including user and ... Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time ...

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Philips

Senior Regulatory Affairs Specialist

Bothell, WA · On-site

$105K - $168K/yr

... EU MDR Technical Documentation authoring experience required. Experience with SaMD or SiMD ... Onsite roles require full-time presence in the company's facilities. Field roles are most ...

Elucent Medical

Director of Quality

Eden Prairie, MN · On-site

$155K - $170K/yr

... EU MDR as appropriate. * Serves as Quality Management Representative, maintains inspection ... Fulltime Employees are provided: 401(k) 401(k) matching (4%) Dental insurance Health insurance ...

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How much do full time eu mdr jobs pay per year?

As of Aug 10, 2026, the average yearly pay for full time 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 is the difference between Full Time Eu Mdr vs Medical Device Quality Assurance Specialist?

AspectFull Time Eu MdrMedical Device Quality Assurance Specialist
CertificationsEU MDR compliance knowledge, regulatory certificationsISO 13485, GMP, regulatory certifications
Work EnvironmentRegulatory compliance teams, medical device companiesQuality assurance departments, manufacturing sites
Industry UsageRegulatory affairs, compliance roles in medical devicesQuality management, validation, audits

Full Time Eu Mdr professionals focus on ensuring medical devices meet EU MDR regulations, often working within regulatory or compliance teams. Medical Device Quality Assurance Specialists concentrate on maintaining quality standards, conducting audits, and ensuring products meet ISO and GMP requirements. While both roles require regulatory knowledge, Full Time Eu Mdr roles are more compliance and documentation-oriented, whereas Quality Assurance Specialists focus on product quality and process validation.

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What are the most commonly searched types of Eu Mdr jobs? The most popular types of Eu Mdr jobs are:
What job categories do people searching Full Time Eu Mdr jobs look for? The top searched job categories for Full Time Eu Mdr jobs are:
Full Time Eu Mdr jobs near you

Quality Engineer I - Compliance

Paragon 28, Inc.

Englewood, CO • On-site

$60K - $80K/yr

Full-time

Re-posted 10 days ago

Job description

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.


What You Can Expect

Ready to build your career in orthopedic innovation? Paragon 28-a Zimmer Biomet company specializing in foot and ankle solutions-is looking for a Quality Engineer I - Compliance to join our team in Englewood, Colorado.

In this impactful role, you'll help uphold and strengthen our Quality Management System, with a focus on Corrective and Preventive Actions (CAPA) and Supplier CAPA processes. You'll play a key part in ensuring product quality and regulatory compliance by investigating medical device complaints, supporting product evaluations, and analyzing system performance.

This is an excellent opportunity for someone who thrives on problem-solving, values precision, and wants to contribute to the continuous improvement of life-changing medical technologies.

This is an onsite position with some remote work flexibility.

How You'll Create Impact
  • Manage CAPA and SCAR systems; Execution, monitoring and managing tasks, and balance multiple priorities while meeting deadlines and quality objectives.
  • Perform CAPA investigations as assigned.
  • Conduct product evaluations in a timely manner to support complaint investigations; Verification of product intended use, product related risk, probable root cause.
  • Maintain and analyze department data; perform statistical analysis and identify the need for escalation and/or opportunities for improvement.
  • Prepare accurate department reports and present as required.
  • Carry out effective resolution when tasked with difficult or unexpected situations in the workplace, as well as complex business challenges.
  • Assist in establishing efficient and streamlined processes across the department.
  • Accurately represent Paragon processes to internal and external customers. Ensure compliance with requirements per the QMS, ISO 13485, FDA QSR, EU MDR and any other applicable regulations or standards.
  • Provide support to Quality Department as requested and complete assigned tasks accurately and on time.
  • Other duties as assigned.
Your Background
  • Bachelor's degree and at least 1 year of related experience.
  • Familiarity with 21 CFR 820/ISO13485 and other government/ISO standards preferred.
  • Experience in regulated industries.
  • Medical device experience preferred.
  • Strong computer skills (MS Office Suite and Adobe).

Work Environment

  • This job operates in an office and warehouse environment. This role routinely uses standard office equipment such as computers, phones and copy machines.

Physical Demands

  • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
  • While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee is required to have close visual acuity to perform activities such as inspecting small parts, viewing computer terminal and reviewing reports. The employee frequently is required to move about the facility. The employee may be required to lift up-to 15 lbs. by themselves.

Position Type/Expected Hours of Work

  • This is a full-time position with typical business hours. It may reasonably require additional hours during the week and weekend; specific requirements will be determined with Manager.
Travel Expectations

Less than 10% overnight travel.

Compensation Data

Salary Range: $60,000 - $80,000 USD annually based on skills and experience. Eligible for annual bonus.


EOE

Employment Type: OTHER

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