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Vp Medical Device Product Development Jobs (NOW HIRING)

PB consulting

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ...

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Vp Medical Device Product Development information

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$42.5K

$127K

$144.5K

How much do vp medical device product development jobs pay per year?

As of Aug 17, 2026, the average yearly pay for vp medical device product development in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What does a VP of Medical Device Product Development do?

A VP of Medical Device Product Development leads the strategy, design, and execution of new medical device products from concept to market launch. They oversee cross-functional teams, manage budgets and timelines, and ensure products meet regulatory standards. This role also involves collaborating with R&D, engineering, quality assurance, and marketing to drive innovation and address market needs. The VP plays a critical part in setting the vision and ensuring the company's medical devices are safe, effective, and commercially successful.

What are the key skills and qualifications needed to thrive as a VP of Medical Device Product Development?

To excel as a VP of Medical Device Product Development, you need deep expertise in biomedical engineering, regulatory compliance, and product lifecycle management, often backed by an advanced degree and extensive industry experience. Familiarity with design control systems, FDA and ISO 13485 standards, and project management tools is essential. Strong leadership, cross-functional collaboration, and strategic vision are critical soft skills for guiding diverse teams and driving innovation. These skills ensure safe, effective products are developed efficiently while meeting regulatory requirements and market needs.

What are some common challenges faced by a VP of Medical Device Product Development when bringing new devices to market?

A VP of Medical Device Product Development often faces challenges such as navigating complex regulatory requirements, ensuring cross-functional team alignment, and managing timelines and budgets amid shifting priorities. Balancing innovation with compliance is critical, as is fostering collaboration between engineering, clinical, marketing, and quality teams. Additionally, staying ahead of technological advancements and competitor activity is essential to ensure the product's success in a highly regulated and competitive market.

What is the difference between Vp Medical Device Product Development vs Medical Device Project Manager?

AspectVp Medical Device Product DevelopmentMedical Device Project Manager
CredentialsAdvanced degrees (e.g., MBA, engineering), industry certificationsRelevant project management certifications (PMP), bachelor's degree in related field
Work EnvironmentExecutive leadership, cross-functional teams, strategic planningProject execution teams, timelines, resource management
Employer & Industry UsageMedical device companies, R&D divisionsManufacturers, clinical settings, regulatory agencies
Search & Comparison IntentHigh-level strategic roles, leadership in product developmentProject execution, timelines, team coordination

The Vp Medical Device Product Development focuses on strategic leadership, overseeing the entire product lifecycle, and guiding R&D efforts. In contrast, the Medical Device Project Manager handles day-to-day project execution, managing timelines and resources. Both roles are essential but differ in scope, responsibilities, and seniority within the organization.

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Vp Medical Device Product Development jobs near you
Infographic showing various Vp Medical Device Product Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.

Medical Device Component Development Engineer

PB consulting

Bromley, KY • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking a Medical Device Component Development Engineer to support component development, product lifecycle management, and engineering change activities for regulated medical devices. The ideal candidate will have expertise in design controls, verification & validation, supplier quality, process validation, and regulatory compliance.

Roles and Responsibilities
  • Lead component development and engineering change projects from concept to implementation.
  • Manage project timelines, risks, and cross-functional coordination.
  • Support Design Verification & Validation (V&V), test protocols, and technical documentation.
  • Partner with suppliers on component qualification, DFM reviews, tooling, and process capability.
  • Support manufacturing transfer, IQ/OQ/PQ, pilot builds, and production readiness.
  • Apply Design Controls, PLM, ECO/ECN/ECR, Risk Management, and Quality System requirements.
  • Review engineering drawings, GD&T, specifications, and acceptance criteria.
  • Drive root cause analysis using CAPA, 8D, 5 Whys, and Fishbone methodologies.
  • Communicate project status, risks, and technical recommendations to stakeholders.
Required Qualifications
  • Experience in Medical Device Component Development or Product Development.
  • Strong knowledge of:
    • Product Lifecycle Management (PLM)
    • Design Controls & Engineering Change Management (ECO/ECN/ECR)
    • Design Verification & Validation (V&V)
    • ISO 14971, DFMEA, PFMEA
    • ISO 13485 & FDA 21 CFR Part 820/QMSR
    • Supplier Quality Engineering & Design for Manufacturability (DFM)
    • Process Validation (IQ/OQ/PQ)
    • GD&T and engineering drawings
  • Strong project management, communication, and problem-solving skills.
  • Experience working with cross-functional teams in a regulated medical device environment.
Preferred Skills
  • Medical Device Product Development
  • Supplier Quality & Component Qualification
  • Risk Management & Regulatory Compliance
  • Manufacturing Transfer & Validation
  • Root Cause Analysis (CAPA, 8D)
  • Stakeholder & Project Management

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