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Medical Device Manager Jobs in Kansas (NOW HIRING)

Senior Mechanical Engineer

Olathe, KS · On-site

$101K - $133K/yr

... for the medical device * Design, develop, and implement highly robust mechanical parts and ... Manage a limited number of concurrent projects primarily of a mechanical scope in a team consisting ...

Our teams help biopharma, medical device and diagnostic companies get their therapies to the people ... Demonstrated ability to manage and develop an assigned territory via inside sales #LI CES IQVIA is ...

... management and implantable cardiac devices . The role blends self-paced learning, classroom ... Comprehensive benefits for medical, prescription drug, dental, vision, behavioral health and ...

QA Technician

Lenexa, KS · On-site

$20 - $23/hr

Background in Medical device, cGMP, or ISO certified environment. * Data entry skills and familiarity with inventory management systems such as SAP. * Proven ability to work effectively as a member ...

Medical Device / Pharma company experience * Strong organizational and project management skills, capable of handling multiple tasks simultaneously, meeting deadlines, and managing unexpected ...

Showing results 41-60

Medical Device Manager information

See Kansas salary details

$9

$35

$59

How much do medical device manager jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for medical device manager in Kansas is $35.35, according to ZipRecruiter salary data. Most workers in this role earn between $20.38 and $47.33 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?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging 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 Kansas?

The most popular types of Medical Device jobs in Kansas are:

What are popular job titles related to Medical Device Manager jobs in Kansas?

For Medical Device Manager jobs in Kansas, the most frequently searched job titles are:

What cities in Kansas are hiring for Medical Device Manager jobs?

Cities in Kansas with the most Medical Device Manager job openings:

Infographic showing various Medical Device Manager job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $73,526 per year, or $35.3 per hour.

Senior Mechanical Engineer

Vantage MedTech

Olathe, KS • On-site

$101K - $133K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago


Job description

Job Title: Mechanical Engineer (Senior)
Location: Olathe, KS
Department: Hardware, Technical Services
Reports to: Engineering Manager, Mechanical / Director, Hardware
Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. We develop and manufacture new products for the treatment of heart failure, cancer, stroke, Gene Therapy, COPD, TBI, Atrial Fibrillation, Blood Clots, Brain Surgery, and many more! We are searching for top-tier talent to apply their gifts to making life better for hundreds of thousands of patients worldwide.If this is something you aspire to, we would like to talk with you!
Vantage MedTech is seeking a Senior Mechanical Engineer to join our team. This position will be responsible for designing, fabricating, and testing mechanical components for state-of-the-art medical devices in an environment where safety, efficacy, and innovation are compulsory. The ideal candidate is a self-starter with experience developing electro-mechanical devices, and a passion for being part of a team developing medical technologies that improve people's lives.
**This is not a remote opportunity. This position is based in Olathe, KS. Local candidates only. We do not offer relocation assistance.
Key Responsibilities:
  • Quickly understand novel technologies and engage with moving them forward towards a product.
  • Apply critical thinking and analytical skills to determine mechanical specifications for the medical device
  • Design, develop, and implement highly robust mechanical parts and assemblies, starting with building a proof-of-concept prototype followed by the design and implementation of a final production quality medical device.
  • Participate in technical design and design review meetings to discuss challenges related to the medical device.
  • Work closely with electrical and firmware engineers to solve cross-functional design challenges.
  • Create and maintain documentation packages suitable for manufacturing transfer and regulatory submission.
  • Support sustaining engineering activities for released and legacy products, including root cause investigation, design updates, documentation changes, and field issue resolution.
  • Drive continuous improvement and cost optimization (VAVE) initiatives to enhance product performance, manufacturability, and cost efficiency
  • Support design changes and engineering change orders (ECOs), ensuring proper documentation, traceability, and compliance with design control processes
  • Interface with Business Development to transfer new activities into the company.
  • Manage a limited number of concurrent projects primarily of a mechanical scope in a team consisting of 4 - 6 engineers from multiple disciplines.
  • Prepare project reports and other programs or technical documentation.
  • Provide senior technical leadership and mentoring to the Mechanical Team members.
Education and Experience:
  • Bachelor's Degree in Mechanical Engineering. Master's Degree in Mechanical Engineering (preferable)
  • 10+ years of industry experience in design, development and testing of mechanical systems.
  • Ability to generate mechanical architecture and componentry concepts for complex mechanical systems
  • Intermediate to advanced proficiency in CAD modelling SW.
    • Proficiency with advanced part modelling, surface modelling and parametric feature modelling is preferred.
  • Utilize and maintain SolidWorks PDM for version control, design release, and documentation traceability (experience preferred).
  • Ability to generate, dimension, and tolerance engineering drawing packages for assemblies of moderate to high complexity.
    • Understands GD&T and tolerance stack-ups.
  • Ability to lead mechanical hazard analysis, product, and hardware FMEA processes.
  • Ability to generate design input requirements for complex mechanical systems and components.
  • Ability to interpret and design for compliance with medical / mechanical safety standards (IEC 60601-1).
  • Ability to conduct biocompatibility analyses and design for compliance with ISO 10993-1 preferred.
  • Ability to select appropriate sterilization processes and analyze material effects preferred.
  • Experience with 3D printing and / or model making for usability testing.
  • Machine shop experience to support rapid prototyping, fixture design, and hands-on debugging of mechanical systems
  • Experience with design for manufacturing, assembly, and cost; manufacturing methods and production processes.
  • Experience with static structural finite element analysis (FEA or FEM).
    • Experience with CFD for simple fluidic systems is preferred.
    • Experience with heat transfer and fluid flow analysis is preferred.
  • Experience working in a safety-related quality process is preferred.
Additional Qualifications:
  • Ability to interact effectively with clients.
  • Excellent critical thinking and analytical skills.
  • High level of initiative with ability to self-manage.
  • Strong written and verbal communication skills as well as reporting and presentational skills.
  • Investigate clinical requirements.
  • Regulatory agency experience including UL, CE and FDA approval processes preferred.
Top Benefits/Perks:
As a team member at Vantage MedTech, you'll enjoy:
  • Comprehensive benefits package, including health, vision, and dental insurance.
  • Generous Paid Time Off.
  • Company retirement plan with matching.

Vantage MedTech values a diverse team and is an Equal Opportunity Employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. All applicants must be authorized for full-time employment in the United States. For more information, visit www.vantagemedtech.com
No third-party candidates please.