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Medical Device Manager Jobs in Raleigh, NC (NOW HIRING)

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · On-site

$40 - $42/hr

Medical Device Vigilance Professionals Location: Raleigh, NC Pay Rate: $40-42/HR on W2 Full time - ... Strong organizational and project management skills. * Strong verbal and written communication ...

GSK

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... medical devices within combination products. Responsibilities include risk management ... Monitor and trend site KPIs for device processes, identify risks, and support development of ...

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Medical Device Manager information

See Raleigh, NC salary details

$10

$38

$64

How much do medical device manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for medical device manager in Raleigh, NC is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $22.31 and $51.81 per hour, depending on experience, location, and employer.

What is a medical device manager?

Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.

What are the key skills and qualifications needed to thrive as a medical device manager?

To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.

What are some common challenges faced by medical device managers in ensuring regulatory compliance?

Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.

What is the difference between Medical Device Manager vs Medical Equipment Coordinator?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging equipment inventory, maintenance, and distribution

The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.

What are the most commonly searched types of Medical Device jobs in Raleigh, NC?

The most popular types of Medical Device jobs in Raleigh, NC are:

What are popular job titles related to Medical Device Manager jobs in Raleigh, NC?

For Medical Device Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Medical Device Manager jobs in Raleigh, NC look for?

The top searched job categories for Medical Device Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Medical Device Manager jobs?

Cities near Raleigh, NC with the most Medical Device Manager job openings:

Medical Device Manager jobs near you
Infographic showing various Medical Device Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $80,489 per year, or $38.7 per hour.

Medical Device Vigilance professionals

Raleigh, NC • On-site

AA2IT
IT Services • 11 - 50 employees
Learn more about AA2ITexternal

$40 - $42/hr

Other

Posted 29 days ago

Job description

Medical Device Vigilance Professionals

Location: Raleigh, NC

Pay Rate: $40-42/HR on W2

Full time - fully Onsite - 3 days a week in office requirement (flexible days) for 6 months, WFH 2 days a week.

Responsible for all tasks related to the collection, processing, follow up and regulatory reporting of adverse events (AEs), serious AEs from clinical trials (SAEs), adverse events of interest (AEIs) and pregnancy reports for all of Merz Aesthetics marketed and investigational products.

This position will routinely process all types of reports for all categories of products (medical device, cosmetic and OTC products).

Major Duties Description:

  • Post Marketing Adverse Event Processing
  • Clinical Study SAE Processing
  • On Time Submission of AE Reports
  • Evaluation of Individual AE Reports and Safety Data
  • Literature Reviews
  • Safety Database Proficiency
  • Review and Update of Departmental Documents
  • Provides Training Regarding AE Reporting
  • Audit Support
  • Supports Regional Safety/Vigilance
  • Collaborate with Other Global Functions

Technical & Functional Skills:

  • Thorough knowledge and experience in all aspects of safety reporting for clinical trials and marketed products – both drugs and medical devices.
  • Strong knowledge and experience with validated safety databases (Argus, ARISg, SIAB, etc.). This also includes MedDRA, WHODrug, and IMDRF coding.
  • Must work effectively/collaboratively in a fast-paced yet efficient team environment with individuals at all levels within an organization.
  • Strong knowledge of FDA and EU regulations governing clinical safety and vigilance.
  • Strong organizational and project management skills.
  • Strong verbal and written communication skills.

Minimum Qualifications:

  • Bachelor's degree in a science or health care-related field or RN/PharmD
  • 5+ years of experience in drug safety or medical device vigilance (preferred) in an industry setting or equivalent

Preferred Qualifications:

  • Direct health care experience with injectable products highly desired
  • Knowledge and experience with document management systems (EDMS, eTMF, etc.)
  • Experience in vendor management
  • Demonstrates relationship building and problem-solving skills

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