ZipRecruiter

Log In

1

Product Manager Medical Device Jobs in Raleigh, NC

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 - ... products highly desired * Knowledge and experience with document management systems (EDMS, eTMF ...

NCBiotech

Associate Director, Device Lead

Zebulon, NC · On-site

$143 - $238/hr

Perform risk management activities (e.g. risk file review/approval) when working with product and ... DHF, MDR, FDA Medical Device guidance. Preferred Qualifications * Knowledge of pharmaceutical ...

New

Zoetis

Global Hatchery Product Manager

Durham, NC · On-site

A key responsibility will be establishing metrics to monitor and report device and parts issues to ... Experience with medical and/or automation equipment. * Headquarters and/or cross-functional ...

New

Abaxis

Global Hatchery Product Manager

Durham, NC

Support device strategy development and execution with local markets. * Support GPM in the ... Experience with medical and/or automation equipment. * Headquarters and/or cross-functional ...

New

Cree

Product Manager - Materials BU

Durham, NC · On-site

Wolfspeed is looking for a Materials Product Manager, who will be primarily responsible for product ... Understanding of basic semiconductor device technology Note: This position requires the lawful ...

GlaxoSmithKline

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 ...

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 ...

Cree

Product Manager - NPI

Durham, NC · On-site

Wolfspeed is looking for a Product Manager who will be responsible for product management and ... Understanding of basic semiconductor device technology and assembly We are an equal opportunity ...

next page

Showing results 1-20

All JobsProduct Medical Device JobsProduct Manager Medical Device JobsProduct Manager Medical Device Jobs in Raleigh, NC

Product Manager Medical Device information

See Raleigh, NC salary details

$60

$67

$74

How much do product manager medical device jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for product manager medical device in Raleigh, NC is $67.76, according to ZipRecruiter salary data. Most workers in this role earn between $64.28 and $71.25 per hour, depending on experience, location, and employer.

What does a product manager do in the medical device industry?

The job duties of a medical device product manager may include managing the technical aspects of product design and development, and defining the target market that the product serves. Your responsibilities in this role may consist of planning the process that the company uses to develop a medical device. This process may include obtaining relevant documentation and approval from medical regulatory bodies. Some medical device product managers focus on marketing products by developing a marketing strategy, defining a target market, and coming up with a pricing strategy.

What are the key skills and qualifications needed to thrive as a product manager in medical devices, and why are they important?

To thrive as a Product Manager in Medical Devices, you need a background in engineering, life sciences, or business, combined with knowledge of product development and regulatory requirements. Familiarity with tools like project management software, CRM systems, and understanding of FDA or CE Mark processes is typically required. Strong communication, problem-solving, and stakeholder management skills set outstanding candidates apart in this field. These skills ensure safe, compliant, and market-driven product launches that meet both user needs and regulatory standards.

What are some common challenges faced by product managers in the medical device industry, and how can they be addressed?

Product Managers in the medical device field often navigate strict regulatory requirements, complex cross-functional collaboration, and the need to balance innovation with patient safety. Staying current with evolving FDA and international regulations is essential, as is fostering clear communication between engineering, clinical, and marketing teams. Building strong relationships with stakeholders and having a structured process for gathering user feedback can help address these challenges and ensure the product meets clinical needs and compliance standards.

What is the difference between Product Manager Medical Device vs Regulatory Affairs Specialist in the medical device industry?

AspectProduct Manager Medical DeviceRegulatory Affairs Specialist
Required CredentialsBachelor's degree, experience in product management, knowledge of medical devicesBachelor's degree, certification in regulatory affairs, knowledge of FDA regulations
Work EnvironmentCross-functional teams, product development, marketingRegulatory compliance, documentation, liaising with authorities
Employer & Industry UsageMedical device companies, healthcare firmsMedical device manufacturers, regulatory agencies
Common Search & Comparison IntentUnderstanding roles in product developmentUnderstanding regulatory responsibilities

The Product Manager Medical Device focuses on developing, launching, and managing medical device products, ensuring market success. In contrast, the Regulatory Affairs Specialist ensures products meet regulatory standards and obtain necessary approvals. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

More about Product Manager Medical Device jobs

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

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

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

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

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

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

Product Manager Medical Device jobs near you
Infographic showing various Product Manager Medical Device job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $140,951 per year, or $67.8 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 16 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