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:
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.
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.
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 Manager information
See Ohio salary details
$10.33 - $14.94
8% of jobs
$14.94 - $19.56
14% of jobs
$21.14 is the 25th percentile. Wages below this are outliers.
$19.56 - $24.17
8% of jobs
$24.17 - $28.79
8% of jobs
$28.79 - $33.40
6% of jobs
The median wage is $36.37 / hr.
$33.40 - $38.02
7% of jobs
$38.02 - $42.63
9% of jobs
$42.63 - $47.24
13% of jobs
$47.44 is the 75th percentile. Wages above this are outliers.
$47.24 - $51.86
6% of jobs
$51.86 - $56.47
16% of jobs
$56.47 - $61.09
3% of jobs
$10
$36
$61
How much do medical device manager jobs pay per hour?
As of Sep 5, 2026, the average hourly pay for medical device manager in Ohio is $36.60, according to ZipRecruiter salary data. Most workers in this role earn between $21.09 and $49.00 per hour, depending on experience, location, and employer.
What is a medical device manager?
Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.
What are the key skills and qualifications needed to thrive as a medical device manager?
To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.
What are some common challenges faced by medical device managers in ensuring regulatory compliance?
Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.
What is the difference between Medical Device Manager vs Medical Equipment Coordinator?
| Aspect | Medical Device Manager | Medical Equipment Coordinator |
|---|---|---|
| Certifications | Regulatory and management certifications, such as RAC or PMP | Basic healthcare or equipment management certifications |
| Work Environment | Healthcare facilities, manufacturing companies, regulatory agencies | Hospitals, clinics, equipment suppliers |
| Employer & Industry | Medical device companies, hospitals, biotech firms | Hospitals, clinics, medical equipment vendors |
| Primary Focus | Overseeing device development, compliance, and lifecycle management | Managing equipment inventory, maintenance, and distribution |
The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.
What are the most commonly searched types of Medical Device jobs in Ohio?
The most popular types of Medical Device jobs in Ohio are:
What are popular job titles related to Medical Device Manager jobs in Ohio?
For Medical Device Manager jobs in Ohio, the most frequently searched job titles are:
- Contract Medical Device Auditor
- Medical Device Quality Assurance
- Medical Device Sales Training
- Medical Device Quality Control
- Associate Medical Device Sales Representative
- Medical Device Sales Representative
- Medical Device Sales Distributor
- Medical Device Sales Enablement
- Medical Device Auditor
- Medical Device Rep
What job categories do people searching Medical Device Manager jobs in Ohio look for?
The top searched job categories for Medical Device Manager jobs in Ohio are:
What cities in Ohio are hiring for Medical Device Manager jobs?
Cities in Ohio with the most Medical Device Manager job openings:
Full-time
This job post has expired 1 day ago. 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