Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
Vendor Management: Communicates effectively with system vendors to maintain working relationships ... program.pdf and signing the agreement to the DRP. Need help finding the right job? We can recommend ...
... management, and the VA system. What You Will Be Doing · Develop and execute a comprehensive ... CME programs. · Build long-term customer loyalty by aligning Alpha-Stim with clinical goals ...
Quick apply
... management, and the VA system. What You Will Be Doing · Develop and execute a comprehensive ... CME programs. · Build long-term customer loyalty by aligning Alpha-Stim with clinical goals ...
FDA Quality Management System Regulation (QMSR) / 21 CFR Part 820, as applicable * ISO 13485, as applicable * Medical Device Single Audit Program (MDSAP), where applicable * European Union Medical ...
New
FDA Quality Management System Regulation (QMSR) / 21 CFR Part 820, as applicable * ISO 13485, as applicable * Medical Device Single Audit Program (MDSAP), where applicable * European Union Medical ...
New
FDA Quality Management System Regulation (QMSR) / 21 CFR Part 820, as applicable * ISO 13485, as applicable * Medical Device Single Audit Program (MDSAP), where applicable * European Union Medical ...
New
FDA Quality Management System Regulation (QMSR) / 21 CFR Part 820, as applicable * ISO 13485, as applicable * Medical Device Single Audit Program (MDSAP), where applicable * European Union Medical ...
New
As a Medical Device & Pharmaceutical Indirect Sales Manager, you will lead strategic business development initiatives across Northern Europe, helping expand the adoption of innovative healthcare ...
As a Medical Device & Pharmaceutical Indirect Sales Manager, you will lead strategic business development initiatives across Northern Europe, helping expand the adoption of innovative healthcare ...
... medical device regulatory guidelines and pathways highly preferred Management experience preferred Ability to communicate effectively, multi-task and manage several projects at once Legally ...
... medical device regulatory guidelines and pathways highly preferred Management experience preferred Ability to communicate effectively, multi-task and manage several projects at once Legally ...
... programs. * Assist in the identification of investigators and sites for company-sponsored clinical trials. * Maintain a thorough and detailed working knowledge of the organization and its products ...
... programs. * Assist in the identification of investigators and sites for company-sponsored clinical trials. * Maintain a thorough and detailed working knowledge of the organization and its products ...
... for medical devices highly preferred • Familiarity with FDA medical device regulatory guidelines and pathways highly preferred • Management experience preferred • Ability to communicate ...
... for medical devices highly preferred • Familiarity with FDA medical device regulatory guidelines and pathways highly preferred • Management experience preferred • Ability to communicate ...
Familiarity with FDA medical device regulatory guidelines and pathways highly preferred *Management experience preferred *Ability to communicate effectively, multi-task and manage several projects at ...
Familiarity with FDA medical device regulatory guidelines and pathways highly preferred *Management experience preferred *Ability to communicate effectively, multi-task and manage several projects at ...
Program Manager
Lees Summit, MO · On-site
Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K, and ... Program Manager Responsibilities Include: * This position requires extensive analytical ability to ...
Program Manager
Lees Summit, MO · On-site
Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K, and ... Program Manager Responsibilities Include: * This position requires extensive analytical ability to ...
Systems/Controls Engineer II
Saint Louis, MO · On-site
$81K - $105K/yr
The candidate will serve as a software-focused Systems Engineer supporting a medical device program ... The role requires strong organizational skills, the ability to manage multiple concurrent ...
Systems/Controls Engineer II
Saint Louis, MO · On-site
$81K - $105K/yr
The candidate will serve as a software-focused Systems Engineer supporting a medical device program ... The role requires strong organizational skills, the ability to manage multiple concurrent ...
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Program Manager
Saint Louis, MO · On-site
$60K/yr
Ensures the scheduling and assistance of clients in all medical appointments and procedures ... Join us as a Program Manager where you can make a significant impact on our team's success while ...
New
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Program Manager
Saint Louis, MO · On-site
$60K/yr
Ensures the scheduling and assistance of clients in all medical appointments and procedures ... Join us as a Program Manager where you can make a significant impact on our team's success while ...
New
Be Seen First
Program Manager
Saint Louis, MO · On-site
$60K/yr
Ensures the scheduling and assistance of clients in all medical appointments and procedures ... Join us as a Program Manager where you can make a significant impact on our team's success while ...
New
Quick apply
Be Seen First
Program Manager
Saint Louis, MO · On-site
$60K/yr
Ensures the scheduling and assistance of clients in all medical appointments and procedures ... Join us as a Program Manager where you can make a significant impact on our team's success while ...
New
Program Manager
Maryland Heights, MO · On-site
We are seeking a strong IT Program Manager to support a high-visibility fraud portfolio within a ... We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and ...
Program Manager
Maryland Heights, MO · On-site
We are seeking a strong IT Program Manager to support a high-visibility fraud portfolio within a ... We offer comprehensive benefits including medical/dental/vision insurance, HSA, FSA, 401(k), and ...
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Program Manager
Kansas City, MO · On-site
$60K/yr
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Program Manager
Kansas City, MO · On-site
$60K/yr
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Program Manager
Kansas City, MO · On-site
$60K/yr
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Program Manager
Kansas City, MO · On-site
$60K/yr
Program Managers play a critical leadership role in ensuring daily operations run safely ... Medical, Dental & Vision insurance through BCBS (6 plan options) * 401(k), HSA, and Flexible ...
Senior Device Engineer
$101K - $138K/yr
... Medical Device Directives * Understanding of production and production systems in a GMP regulated environment * Strong technical project management, critical thinking, and problem-solving skills.
Senior Device Engineer
$101K - $138K/yr
... Medical Device Directives * Understanding of production and production systems in a GMP regulated environment * Strong technical project management, critical thinking, and problem-solving skills.
Medical Device Program Manager information
See Missouri salary details
$36.1K - $46.2K
5% of jobs
$46.2K - $56.3K
6% of jobs
$56.3K - $66.4K
9% of jobs
$72.7K is the 25th percentile. Wages below this are outliers.
$66.4K - $76.5K
6% of jobs
$76.5K - $86.6K
5% of jobs
$86.6K - $96.7K
6% of jobs
$96.7K - $106.8K
5% of jobs
The median wage is $108.8K / yr.
$106.8K - $117K
31% of jobs
$117.3K is the 75th percentile. Wages above this are outliers.
$117K - $127.1K
7% of jobs
$127.1K - $137.2K
15% of jobs
$137.2K - $147.3K
3% of jobs
$36.1K
$100.8K
$147.3K
How much do medical device program manager jobs pay per year?
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 the key skills and qualifications needed to thrive as a Medical Device Program Manager, and why are they important?
What is a Medical Device Program Manager?
How does a Medical Device Program Manager typically collaborate with cross-functional teams during product development?

Full-time
Re-posted 23 days ago
University Of Kansas Health System rating
7.5
Based on 174 frontline employees who took The Breakroom Quiz
232nd of 884 rated healthcare providers
Job description
Responsibilities and Essential Job Functions
Serves as a Tier-II support resource, engaging other team resources as necessary and as defined by support processes.
Functions as a coordination point for issues related to systems between all IT teams. Act as an escalation point for issues with assigned systems that cannot be resolved in TRC.
Inventory Medical and IoT Devices: Maintains an inventory of medical and IoT devices and maintains up to date information regarding location, status, security posture, life-cycle phase, ongoing maintenance, etc.
Data Flow Mapping: Performs data flow mapping activities to document the flow of data both into and out of medical and IoT devices. This task utilizes both written and visual tools to appropriately represent the flow of data and the data types being processed.
Implementation/Connectivity: Performs implementation, integration, and connectivity tasks in concert with vendor resources and other internal teams such as Biomed, Networking, Systems Administration, clinical staff, etc.
Vendor Management: Communicates effectively with system vendors to maintain working relationships and proper systems support. Verifies vendor actions meet the expectations of the hospital.
Medical Device and IoT Security: Evaluates the security posture of medical devices and IoT and identifies potential risks. Works with Information Security and Networking to effectively mitigate risks through network segmentation or other mitigating factors.
Coordination with Biomed: Assists Biomed as needed on preventative maintenance (PM), installs, and end-of-life planning.
System Support: Maintains usable systems for end-users with the ability to work with vendors or other outside resources as well as internal hospital teams to resolve system issues within service level agreements.
Decommissioning: Documents and performs end-of-life tasks to decommission medical and IoT devices in a safe, eco-friendly, and HIPAA complaint way. Coordinates these tasks with appropriate teams such as Biomed, Desktop Support, and Asset Management.
Vendor Remote Access: Configures and manages vendor remote access to medical and IoT devices through enterprise approved methods.
Enterprise Imaging: Configures DICOM connectivity for imaging modalities in coordination with Systems Administration, Radiology IT, and Biomed. Documents these connection points through data flow mapping.
Training: Performs training tasks for fellow team members and technical staff. Training content is primarily limited to connectivity and data flow and should not include clinical interpretation or proper use during patient care.
Medical and IoT Device Documentation: Maintains documentation on the medical and IoT devices technical configuration, contacts and functionality. Contributes and maintains common troubleshooting tips in the designated knowledge base. Keeps current vendor and system data owner's contact information in the designated location. Maintains relevant training materials.
System Updates: Responsibilities include planning and scheduling medical and IoT device upgrades and updates. This also includes coordination with other HITS teams, vendors, users, interfaces, and other systems that feed or accept information from these devices. Follows department change request processes.
System Integrity/Retention: Requires verification of application logs and other monitoring tools to resolve issues that could cause data integrity issues. Ensure retention periods for medical device and IoT data follow hospital and regulatory requirements.
Data Backup/Recovery: Verifies that devices are completing a normally scheduled and approved backup methodology. Verifies that data can be restored in the event of a failure or disaster.
Troubleshooting: Basic problem-solving skills and capabilities to resolve medical device and IoT issues under stressful conditions. Uses appropriate methods of escalation to both internal and external resources.
Technical Foundation: Understands technical concepts including, but not limited to, databases, networking, hardware, software, interfaces, medical devices, IoT devices, desktop support, operating systems, and others as necessary.
Must be able to perform the professional, clinical and or technical competencies of the assigned unit or department.
These statements are intended to describe the essential functions of the job and are not intended to be an exhaustive list of all responsibilities. Skills and duties may vary dependent upon your department or unit. Other duties may be assigned as required.
Required Education and Experience
Associates Degree Information Systems or related field or 2:1 equivalent experience.
3 or more years experience in a related Information Systems field
Preferred Education and Experience
Bachelors Degree Information Systems or related field
1 or more years experience in a healthcare setting
Preferred Licensure and Certification
Technical certifications related to ITIL, Windows Administration, Linux Administration, or other IT or system related field of study.
The health system is an equal employment opportunity employer. Qualified applicants are considered for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, ancestry, age, disability, veteran status, genetic information, or any other legally-protected status. See also Diversity, Equity & Inclusion.
The health system provides reasonable accommodations to qualified individuals with disabilities. If you need to request reasonable accommodations for your disability as you navigate the recruitment process, please let our recruiters know by requesting an Accommodation Request form using this link asktalentacquisition@kumc.edu.
Employment with the health system is contingent upon, among other things, agreeing to the health-system-dispute-resolution-program.pdf and signing the agreement to the DRP.
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About University of Kansas Health System
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Operating within the healthcare industry, The University of Kansas Health System is a renowned medical institution located in Kansas City, KS, United States. Established in 1905, this not-for-profit health system has evolved to offer an extensive range of products and services, which spans across a variety of specialist areas such as cancer care, neurology, cardiology, and organ transplants, among others. The core mission of The University of Kansas Health System is to enhance the health and wellness of individuals and communities by providing world-class healthcare services, quality education and conducting advanced research. They are also known for their unwavering commitment to academic medicine, which sets them apart from their peers.
Industry
Health care and social assistance
Company size
5,001 - 10,000 Employees
Headquarters location
Kansas City, KS, US