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Product Manager Medical Device Jobs in Raleigh, NC

Eisai

Mgr., Product Complaints (Hybrid)

Raleigh, NC · Hybrid

$104K - $137K/yr

The Manager, Product Complaints is responsible for the oversight, governance, and continuous ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

Eisai, Inc.

Mgr., Product Complaints (Hybrid)

Raleigh, NC · On-site

$104K - $137K/yr

The Manager, Product Complaints is responsible for the oversight, governance, and continuous ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

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 ...

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 ...

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 ...

Wolfspeed, Inc.

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 ...

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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 13, 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 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 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 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.

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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 83% Full Time, 2% Part Time, and 15% Contract. Highlights an 92% In-person, 2% Hybrid, and 6% Remote job distribution, with an average salary of $140,951 per year, or $67.8 per hour.

Senior Product Manager - Medication Process

Ll Oefentherapie

Raleigh, NC • On-site

$90 - $120/hr

Other

Re-posted 6 days ago

Job description

Oracle Health is seeking a Senior Product Manager to drive product management, regulatory and medical device documentation, cross‑functional delivery, and software development lifecycle across Oracle Health’s medication process portfolio. This role will help ensure that medication process products are designed, documented, delivered, and governed with the rigor required for patient safety, regulatory requirements, and medical device software. Our medication process portfolio plays a critical role in connecting ordering, verifying, dispensing, administration, drug content, and clinical workflow transformation across the healthcare ecosystem.

The ideal candidate combines strong product management judgment, product operations discipline, medical device submission or regulatory documentation experience, and technical program management skills. They will work across product management, engineering, clinical informatics, regulatory, legal, privacy, security, quality, UX, data science, release management, and executive stakeholders to strengthen how Oracle Health defines, tracks, documents, and delivers product work in a highly regulated healthcare environment.

This is a highly visible execution and operations role responsible for turning complex, ambiguous, cross‑functional initiatives into clear plans, accountable owners, high‑quality documentation, release‑ready deliverables, and repeatable operating practices that scale across the Pharmacy portfolio.

Required Qualifications
  • 5+ years of experience in product management, product operations, technical program management, regulatory program management, release management, delivery management, healthcare technology product delivery, or related roles.
  • Experience working in healthcare technology, regulated software, medical device software, clinical software, EHRs, pharmacy systems, or complex enterprise software environments.
  • Experience supporting or leading medical device documentation, regulatory documentation, technical documentation, conformity assessment readiness, clinical evaluation support, safety and performance documentation, or related compliance activities.
  • Experience with healthcare regulatory requirements, including FDA, EU MDR, HIPAA, NCPDP, clinical safety, privacy, security, and regulated healthcare delivery.
  • Experience partnering with product, engineering, design, QA, regulatory, legal, clinical, privacy, security, delivery, and business stakeholders.
  • Demonstrated ability to turn ambiguous requests into structured plans, owners, milestones, work items, risks, decisions, and executable follow‑through.
  • Strong organizational skills, attention to detail, and ability to manage multiple complex initiatives simultaneously.
  • Ability to communicate priorities, tradeoffs, risks, dependencies, and decisions clearly to technical, clinical, regulatory, business, and executive audiences.
  • Strong business judgment and ability to provide thoughtful recommendations when product, regulatory, technical, or customer priorities compete.
Preferred Qualifications
  • Experience with medical device submissions, medical device classification, software as a medical device, conformity assessment, notified body interactions, technical file preparation, clinical evaluation, safety and performance requirements, or post‑market documentation.
  • Experience defining or supporting product requirements, user stories, acceptance criteria, release plans, operational processes, governance routines, or SDLC documentation.
  • Strong understanding of software development lifecycle practices, release readiness, documentation governance, and cross‑functional delivery.
  • Experience supporting release governance, product readiness, regulatory readiness, documentation workflows, launch readiness, or customer‑facing release preparation.
  • Familiarity with Agile, Scrum, Kanban, scaled delivery models, or complex enterprise SDLC frameworks.
  • Experience building AI‑powered healthcare products, generative AI solutions, conversational AI, clinical decision support tools, or intelligent workflow automation.
  • Knowledge of AI/ML development lifecycles, model evaluation methodologies, and responsible AI practices.
  • Experience using Jira, Confluence, dashboards, trackers, operational scorecards, or similar systems of record.
  • Experience creating Jira dashboards, Confluence pages, release trackers, operational scorecards, decision logs, documentation matrices, or executive‑level status summaries.
  • Comfort operating across multiple teams without direct ownership of every product area or deliverable.
Success Profile

The successful candidate is a structured, pragmatic product manager who can operate across product management, product operations, regulatory readiness, and technical program management depending on what the initiative requires. They are able to both complete regulatory product documentation in addition to working across teams to ensure consistency in product and release processes. They understand that healthcare software operates under elevated expectations for quality, safety, documentation, traceability, release discipline, and customer trust.

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