Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Associate, Project Manager
Irvine, CA · On-site
$120K - $130K/yr
Job Title : Associate, Project Manager Supervisor/Manager Title: Senior Director, Program ... Understand medical device design principles, functionality, and technical specifications relevant ...
Associate, Project Manager
Irvine, CA · On-site
$120K - $130K/yr
Job Title : Associate, Project Manager Supervisor/Manager Title: Senior Director, Program ... Understand medical device design principles, functionality, and technical specifications relevant ...
Quality Engineer - Medical Device
Columbia, SC · On-site
$58K - $75K/yr
Quality Engineer - Medical Device Hybrid Role: 3-4 days a week onsite in Columbia, SC * Company ... Project Management Professional (PMP) certification * .Lean Six Sigma certification * .Experience ...
Quality Engineer - Medical Device
Columbia, SC · On-site
$58K - $75K/yr
Quality Engineer - Medical Device Hybrid Role: 3-4 days a week onsite in Columbia, SC * Company ... Project Management Professional (PMP) certification * .Lean Six Sigma certification * .Experience ...
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Manage project timelines, risks, and cross-functional coordination. * Support Design Verification ... Experience in Medical Device Component Development or Product Development. * Strong knowledge of:
Flexible Medical Device Project Manager information
See salary details
$38.5K - $49.7K
2% of jobs
$49.7K - $61K
6% of jobs
$61K - $72.2K
10% of jobs
$78.3K is the 25th percentile. Wages below this are outliers.
$72.2K - $83.4K
13% of jobs
$83.4K - $94.6K
14% of jobs
The median wage is $98.6K / yr.
$94.6K - $105.9K
15% of jobs
$105.9K - $117.1K
13% of jobs
$119.6K is the 75th percentile. Wages above this are outliers.
$117.1K - $128.3K
12% of jobs
$128.3K - $139.5K
7% of jobs
$139.5K - $150.8K
5% of jobs
$150.8K - $162K
3% of jobs
$38.5K
$102.7K
$162K
How much do flexible medical device project manager jobs pay per year?
As of Aug 21, 2026, the average yearly pay for flexible medical device project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Medical Device Project Manager jobs?
The most popular types of Medical Device Project Manager jobs are:
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.
- 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.
- Medical Device Product Development
- Supplier Quality & Component Qualification
- Risk Management & Regulatory Compliance
- Manufacturing Transfer & Validation
- Root Cause Analysis (CAPA, 8D)
- Stakeholder & Project Management