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:
Senior Medical Device Engineer
Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.
New
Senior Medical Device Engineer
Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.
New
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:
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:
Medical Device Program Manager information
See Ohio salary details
$36.6K - $46.8K
5% of jobs
$46.8K - $57.1K
6% of jobs
$57.1K - $67.3K
9% of jobs
$73.7K is the 25th percentile. Wages below this are outliers.
$67.3K - $77.6K
6% of jobs
$77.6K - $87.8K
5% of jobs
$87.8K - $98.1K
6% of jobs
$98.1K - $108.3K
5% of jobs
The median wage is $110.2K / yr.
$108.3K - $118.5K
31% of jobs
$118.9K is the 75th percentile. Wages above this are outliers.
$118.5K - $128.8K
7% of jobs
$128.8K - $139K
15% of jobs
$139K - $149.3K
3% of jobs
$36.6K
$102.2K
$149.3K
How much do medical device program manager jobs pay per year?
As of Sep 3, 2026, the average yearly pay for medical device program manager in Ohio is $102,162.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $126,000.00 per year, depending on experience, location, and employer.
What is a medical device program manager?
A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.
How does a medical device program manager typically collaborate with cross-functional teams during product development?
A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.
What are the key skills and qualifications needed to thrive as a medical device program manager, and why are they important?
To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.
What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?
| Aspect | Medical Device Program Manager | Medical Device Quality Engineer |
|---|---|---|
| Credentials | Project management certifications, engineering degree | Quality assurance certifications (e.g., CQE), engineering degree |
| Work Environment | Cross-functional teams, project planning, product development | Quality systems, compliance, testing, and validation |
| Employer & Industry Usage | Medical device companies, manufacturing, R&D | Regulatory agencies, manufacturing, quality departments |
| Search & Comparison Intent | Managing projects, product launches, timelines | Ensuring quality, compliance, risk management |
The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.
What are popular job titles related to Medical Device Program Manager jobs in Ohio?
For Medical Device Program Manager jobs in Ohio, the most frequently searched job titles are:
- Trainee Medical Sales Rep
- Orthopedic Sales Representative
- Oncology Medical Sales
- Vice President Medical Sales Representative
- Remote Per Diem Medical Sales Representative
- Medical Sales Rn
- Junior Medical Sales Representative
- Virtual Medical Sales Representative
- Aesthetic Clinic
- Remote National Healthcareer Association Nha
What job categories do people searching Medical Device Program Manager jobs in Ohio look for?
The top searched job categories for Medical Device Program Manager jobs in Ohio are:
What cities in Ohio are hiring for Medical Device Program Manager jobs?
Cities in Ohio with the most Medical Device Program Manager job openings:
Full-time
Posted 21 days ago
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