Manages a few discrete projects with teams, operating within a defined PDP process delivering to ... Understanding of scientific principles and manufacturing processes used in medical device ...
Manages a few discrete projects with teams, operating within a defined PDP process delivering to ... Understanding of scientific principles and manufacturing processes used in medical device ...
To provide Medical Device expertise leadership and mentoring in areas of competence to Healthcare personnel. Key Responsibilities & Accountabilities * Plan and deliver Technical File Assessments ...
To provide Medical Device expertise leadership and mentoring in areas of competence to Healthcare personnel. Key Responsibilities & Accountabilities * Plan and deliver Technical File Assessments ...
NEW PRODUCT INTRODUCTION (NPI) MANAGER
Angola, IN · On-site
$157K - $162K/yr
The ideal candidate will have strong experience in medical device product development, manufacturing operations, project management, and cross-functional leadership within a regulated environment.
NEW PRODUCT INTRODUCTION (NPI) MANAGER
Angola, IN · On-site
$157K - $162K/yr
The ideal candidate will have strong experience in medical device product development, manufacturing operations, project management, and cross-functional leadership within a regulated environment.
NEW PRODUCT INTRODUCTION (NPI) MANAGER
Angola, IN · On-site
$157K - $162K/yr
The ideal candidate will have strong experience in medical device product development, manufacturing operations, project management, and cross-functional leadership within a regulated environment.
NEW PRODUCT INTRODUCTION (NPI) MANAGER
Angola, IN · On-site
$157K - $162K/yr
The ideal candidate will have strong experience in medical device product development, manufacturing operations, project management, and cross-functional leadership within a regulated environment.
Quality Engineer
Avon, IN · On-site
$70K - $90K/yr
... medical device industry. Position Summary The Quality Engineer will be responsible for supporting and maintaining Flotec's quality management system, manufacturing quality controls, regulatory ...
Quick apply
Quality Engineer
Avon, IN · On-site
$70K - $90K/yr
... medical device industry. Position Summary The Quality Engineer will be responsible for supporting and maintaining Flotec's quality management system, manufacturing quality controls, regulatory ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Business Development Manager
Shelbyville, IN · On-site
Medical Device, Automotive, & Advanced Manufacturing Reports To: Executive Director of Sales Who Should Apply: Experienced sales professionals with a proven track record in direct account management ...
Business Development Manager
Shelbyville, IN · On-site
Medical Device, Automotive, & Advanced Manufacturing Reports To: Executive Director of Sales Who Should Apply: Experienced sales professionals with a proven track record in direct account management ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Technical Project Manager
Indianapolis, IN · On-site
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Technical Project Manager
Indianapolis, IN · On-site
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Technical Project Manager
Indianapolis, IN · On-site
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Quick apply
Technical Project Manager
Indianapolis, IN · On-site
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Carmel, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Technical Project Manager
Indianapolis, IN · On-site
$85 - $115/hr
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Technical Project Manager
Indianapolis, IN · On-site
$85 - $115/hr
Stay current with ISO 13485, governmental regulations, medical device standards, and drug-device ... Track and manage project deliverables to ensure timely and quality completion * Adjust schedules ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Application Specialist
Indianapolis, IN · On-site
Own and implement the Medical Device Data Management System (MDMS), including scalable database and UI solutions that support web applications and data-driven workflows. * Leverage Python to automate ...
Medical Device Manager information
See Indiana salary details
$10.59 - $15.32
8% of jobs
$15.32 - $20.06
14% of jobs
$21.68 is the 25th percentile. Wages below this are outliers.
$20.06 - $24.79
8% of jobs
$24.79 - $29.52
8% of jobs
$29.52 - $34.25
6% of jobs
The median wage is $37.29 / hr.
$34.25 - $38.98
7% of jobs
$38.98 - $43.72
9% of jobs
$43.72 - $48.45
13% of jobs
$48.65 is the 75th percentile. Wages above this are outliers.
$48.45 - $53.18
6% of jobs
$53.18 - $57.91
16% of jobs
$57.91 - $62.65
3% of jobs
$10
$37
$62
How much do medical device manager jobs pay per hour?
What are the key skills and qualifications needed to thrive as a medical device manager?
What is a medical device manager?
What are some common challenges faced by medical device managers in ensuring regulatory compliance?
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.
- Medical Device Sales Associate Territory Account Manager
- Traveling International Medical Device Sales
- Locum Medical Device Design
- Part Time Medical Sales
- Remote International Medical Device Sales
- Pharmaceutical No Degree
- Registered Nurse Medical Device Sales Representative
- Per Diem Medical Device Sales
- Vice President Remote Medical Device Sales
- Associate Territory Manager

Full-time
Re-posted 27 days ago
Job description
Working at Freudenberg: We will wow your world!
Responsibilities:Lead development of accuratemanufacturing cost models, make-vs-buy decisions, work-center costs, and support quote generation and pricing strategy for new business or large sustaining initiatives.
Establish, track, and report key performance metrics for development, project progression, and launch; champion continuous-improvement and Lean/Six Sigma activities to boost quality, delivery, and cost.
Gather and translate user, customer, clinician, and/or market needs and inputs into clear product and business requirements; present data-driven recommendations to stakeholders.
Maintain project documentation in line with internal procedures and notified-body expectations, supporting audits and ensuring robust change-control and traceability. Prepare reports and project summaries to communicate the status of projects on a regular basis.
Provide technical and project-management leadership, set priorities, allocate tasks, mentor team members, and foster a culture of efficiency, innovation, and regulatory excellence across the organization.
Manages a few discrete projects with teams, operating within a defined PDP process delivering to achieve defined scope, schedule, and budget performance goals.
Familiarity with and managing efforts for compliance with ISO standards, country-specific (FDA, MDR, Health Canada, PMDA, etc.), GMP regulations, and customer requirements.
Input and review for design history files, device master records, risk analyses, and validation protocols/reports (IQ/OQ/PQ) to ensure designs, processes, equipment, and products meet client, regulatory, and business needs.
Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.
3+ years' experience in Medical Device or related industry
2+ years' experience in leading teams in a manufacturing or engineering environment, with demonstrated experience of managing work within a project plan framework, including managing a schedule, budget, scope, progress, and reporting.
Understanding of scientific principles and manufacturing processes used in medical device production, such as running equipment, injection molding, extrusion, catheter manufacturing, and assembly, including the materials used.
Demonstrated experience with formal problem-solving methodologies, critical thinking, and deductive skills.
Understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971, and 45001. Knowledge of GMP principles and their application in medical device manufacturing, including country-specific regulatory requirements (i.e., 21 CFR 820 in the United States, and EU MDR).
Demonstrated experience using Lean/Six Sigma tools as necessary for new and continuous improvement projects.
Demonstrated experience providing leadership and managing multiple projects of low to medium complexity.
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
Freudenberg Medical LLC