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Medical Device Manager Jobs in California (NOW HIRING)

Mizuho OSI

Systems Engineer, Medical Device

Union City, CA · On-site

$82K - $150K/yr

... medical device development projects starting from technology exploration, product definition, to ... Develop, manage and maintain design history files and related deliverables. * Develop, maintain and ...

Maxonic

Be Seen First

Preventive Maintenance Technician (Medical Device)

Sunnyvale, CA · On-site

$33/hr

Job Title: Preventive Maintenance Technician (Medical Device) Job Type: Contract Job Location ... Escalates any safety issues with supervisor or manager. * Report any safety device on equipment ...

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Medical Device Manager information

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$11

$39

$65

How much do medical device manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for medical device manager in California is $39.20, according to ZipRecruiter salary data. Most workers in this role earn between $22.60 and $52.49 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 California?

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

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

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

What job categories do people searching Medical Device Manager jobs in California look for?

The top searched job categories for Medical Device Manager jobs in California are:

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

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

Medical Device Manager jobs near you
Infographic showing various Medical Device Manager job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $81,542 per year, or $39.2 per hour.

Project Manager -- Medical Device (Hybrid -- Irvine, CA ) Contract

Pharmavise Corporation

Irvine, CA • On-site

$120 - $170/hr

Other

Posted 8 days ago

Job description

Project Manager — Medical Device (Hybrid — Irvine, CA ) Contract

Irvine, United States | Posted on 05/07/2026

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Job Description

Our F500 Medical Device client has an exciting opportunity for a Project Manager.

Summary:

We are looking for a talented business leader to join our Urology Project Management Organization (PMO). We have an exciting opportunity for a Senior Project Manager that will lead the Software Integration as part of various Product Integration workstreams associated with our recent Axonics Acquisition. In this role, you will lead cross-functional teams to execute the integration projects required to integrate the Axonics Product Portfolio into Client’s Systems. We are seeking an experienced candidate who has demonstrated software project management and effective cross-functional leadership experience. Prior experience managing software projects within the Medical Device field and experience with quality system and risk management process are preferred.

Responsibilities and Job Requirements
  • Provide Project Management leadership of a cross-functional Teams as part of the Axonics Integration, leveraging agile methodologies and common divisional processes and tools.
  • Influence stakeholders and team members to drive alignment, develop plans and deliver results. Build team ownership and commitment to project plans.
  • Partner and collaborate with a variety of functions to achieve project objectives. This includes identifying resources required for project activities, timeline development, and project prioritization.
  • Communicate progress and status to Integration Lead.
  • Prioritize, delegate, and manage tasks among projects and team members, as appropriate, to drive execution of project deliverables and minimize risk.
  • Support development, implementation, and revision of detailed project plans, including deliverable lists, risk management, communication plans, etc.
  • Ensure Client policies and practices are followed.
Minimum Qualifications
  • Bachelor’s Degree in Science, Engineering or Business and 5+ years of work experience in software, product development or related field AND
  • 5+ years Project Management experience in the Medical Device industry
  • Demonstrated project management experience leading cross functional teams and managing project scope, schedule, and budget
  • Excellent organizational, interpersonal, and communication skills (verbal written, and presentation)
  • Results-oriented, positive attitude focused on delivering timely, accurate and best in class execution
  • Ability to draw conclusions and make business recommendations based on cross-functional team input
  • Proficiency in MS Office applications including MS Project
  • Proficiency in MS SharePoint
  • Ability to travel intermittently (up to 20%) to support effective team performance and collaboration
Preferred Qualifications
  • Experience with utilizing agile project management
  • 5+ years Project Management experience managing software projects within the Medical Device field, knowledge and application of applicable software ISO and IEC standards in the project scope
Other Details
  • Location: Hybrid –Irvine, CA or Arden Hills, MN

Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.

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