ZipRecruiter

Log In

1

Medical Device Training Manager Jobs in Raleigh, NC

AA2IT

Medical Device Vigilance professionals

Raleigh, NC · On-site

$40 - $42/hr

Provides Training Regarding AE Reporting * Audit Support * Supports Regional Safety/Vigilance ... Strong organizational and project management skills. * Strong verbal and written communication ...

Danaher

Sales Representative Medical Device

Raleigh, NC · On-site

$90K - $100K/yr

This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

Danaher

Sales Representative Medical Device

Raleigh, NC · On-site +1

$90K - $100K/yr

This position reports to the Regional Sales Manager and is part of the Blood Gas Sales Team and ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

Eisai, Inc.

Mgr., Product Complaints (Hybrid)

Raleigh, NC · On-site

$104K - $137K/yr

This role ensures that medical device complaints are consistently captured, appropriately triaged ... Manage complaint sample handling (shipping, tracking) to external sites for investigation. * Review ...

Eisai

Mgr., Product Complaints (Hybrid)

Raleigh, NC · Hybrid

$104K - $137K/yr

This role ensures that medical device complaints are consistently captured, appropriately triaged ... Manage complaint sample handling (shipping, tracking) to external sites for investigation. * Review ...

GlaxoSmithKline

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... medical devices within combination products. Responsibilities include risk management ... We provide training, mentorship, and opportunities to grow your technical and leadership skills. We ...

GSK

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... medical devices within combination products. Responsibilities include risk management ... We provide training, mentorship, and opportunities to grow your technical and leadership skills. We ...

GSK

Device Engineer

Zebulon, NC · On-site

Experience with design controls, risk management and quality processes used in medical device development. Preferred Qualifications: If you have the following characteristics, it would be a plus:

GSK

Device Engineer

Zebulon, NC · On-site

Experience with design controls, risk management and quality processes used in medical device development. Preferred Qualifications: If you have the following characteristics, it would be a plus:

GlaxoSmithKline

Device Engineer

Zebulon, NC

Experience with design controls, risk management and quality processes used in medical device development. Preferred Qualifications: If you have the following characteristics, it would be a plus:

next page

Showing results 1-20

All JobsMedical Device Training JobsMedical Device Training Manager JobsMedical Device Training Manager Jobs in Raleigh, NC

Medical Device Training Manager information

See Raleigh, NC salary details

$24.3K

$49K

$93.3K

How much do medical device training manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for medical device training manager in Raleigh, NC is $48,990.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,500.00 and $55,900.00 per year, depending on experience, location, and employer.

What does a medical device training manager do?

A Medical Device Training Manager is responsible for developing, coordinating, and delivering training programs for medical device users, such as healthcare professionals and internal staff. They ensure that users are knowledgeable about the safe and effective operation of medical devices, including compliance with regulatory standards. Their role often involves creating training materials, conducting workshops, and assessing the effectiveness of training sessions to support product adoption and patient safety.

What are the key skills and qualifications needed to thrive as a medical device training manager, and why are they important?

To thrive as a Medical Device Training Manager, you need expertise in medical device technology, training program development, and a background in healthcare or biomedical sciences, often supported by a relevant degree. Familiarity with learning management systems (LMS), instructional design software, and industry-specific certifications (such as AAMI or device-specific credentials) is typically required. Outstanding communication, leadership, and organizational skills are essential for effectively delivering training to diverse audiences and managing multiple projects. These competencies ensure that clinical staff are properly educated, devices are used safely and effectively, and regulatory compliance is maintained.

How does a medical device training manager typically collaborate with clinical teams and sales representatives?

A Medical Device Training Manager often works closely with both clinical teams and sales representatives to ensure that end users fully understand the proper use of medical devices. This involves organizing and leading hands-on training sessions, developing instructional materials tailored to different audiences, and providing ongoing support to address product updates or new regulatory requirements. Regular communication and feedback loops with these teams help the Training Manager identify knowledge gaps and adapt training strategies, ensuring both clinical efficacy and sales success. Effective collaboration fosters strong relationships and enhances overall device adoption and patient safety.

What is the difference between Medical Device Training Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Training ManagerMedical Device Quality Assurance Specialist
Required CredentialsRelevant certifications (e.g., CPT, CQA), industry experienceISO certifications, QA training, industry standards knowledge
Work EnvironmentTraining departments, clinical settings, manufacturing facilitiesQuality assurance labs, manufacturing plants, regulatory offices
Employer & Industry UsageMedical device companies, hospitals, training providersManufacturers, regulatory agencies, compliance firms
Common Search & Comparison IntentUnderstanding training roles, certifications, responsibilitiesQuality standards, compliance processes, certification requirements

The Medical Device Training Manager focuses on developing and delivering training programs for medical device staff, ensuring compliance and effective product use. In contrast, the Medical Device Quality Assurance Specialist concentrates on maintaining product quality, regulatory compliance, and conducting audits. Both roles require industry-specific certifications and work within the medical device industry, but their core responsibilities differ significantly.

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

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

Medical Device Training Manager jobs near you

Medical Device Vigilance professionals

AA2IT

Raleigh, NC • On-site

$40 - $42/hr

Other

Posted 7 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

Apply