1

Medical Device Project Manager Jobs in California

Mfg. Engrs - Project Manager COMPANY OVERVIEW Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...

Mfg. Engrs - Project Manager COMPANY OVERVIEW Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...

Mfg. Engrs - Project Manager COMPANY OVERVIEW Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest ...

We are a medical device company that is focused on improving the lives of patients with sacroiliac pelvic conditions. We are looking for people who are passionate about our mission and who are ...

Engineering Project Manager

Santa Clara, CA · On-site

$110K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Minimum 2 years of experience in project / program management of medical device development. * Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality ...

Enterprise software product development Medical device, pharma, or life science research domains ... Specific Project Management training and/or certification. Experience: * Minimum (required): 6 ...

Engineering Project Manager

Santa Clara, CA · On-site

$110K - $125K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Minimum 2 years of experience in project / program management of medical device development. * Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality ...

It would be great if you have experience at a medical device company * You have more than 4 years related engineering experience * You have Project Manager experience with software methodologies ...

Showing results 41-60

Medical Device Project Manager information

What is a medical device project manager?

A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.

What are the day-to-day responsibilities of a medical device project manager?

As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.

What are the key skills and qualifications needed to thrive in a medical device project manager position, and why are they important?

To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.

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

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

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

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

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

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

Infographic showing various Medical Device Project Manager job openings in California as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 3% Part Time, 3% Temporary, and 15% Contract. Highlights an 95% In-person, 2% Hybrid, and 3% Remote job distribution.

Mfg. engrs - Project Manager

medplast

Fremont, CA • On-site

Full-time

Posted 5 days ago


Job description

Mfg. Engrs - Project Manager

COMPANY OVERVIEW

Viant Medical is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.

POSITION SUMMARY

The R&D Project Manager leads from the front, applying hands-on technical expertise to drive projects through all medical device product lifecycle stages. This role ensures customer needs are met, facilitates regular communication, and maintains budget control. The PM fosters seamless collaboration between internal teams and customers to deliver best-in-class design and quality.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Leverage technical expertise to lead projects from discovery to design transfer, taking ownership of key milestones and deliverables.
  • Manage consistent information flow among team members, management, and clients.
  • Identify and communicate project risks such as changes to scope, timeline and budget.
  • Organize, delegate and track tasks across internal teams and external partners (vendors, clients) to ensure projects stay on schedule and within budget.
  • Analyze and track current project deliverables and ensure alignment with internal and external stakeholders.
  • Develop project plans outlining phases, tasks, dependencies, timelines, resource allocation, and costs.
  • Establish and track weekly, monthly goals, budgets and schedules for projects and team members.
  • Lead design reviews and risk management documentation.
  • Ensuring the planning, coordination, execution, tracking and reporting using software tools like MS Project, Smartsheet, JIRA etc.
  • Working Proficiency with MS Office.
  • Maintain detailed project documentation throughout all phases of research and development.
  • Employ excellent communication, negotiation and interpersonal skills with all levels of personnel and management.   

REPORTING STRUCTURE

  • N/A

REQUIRED EDUCATION, EXPERIENCE, SKILLS AND KNOWLEDGE

  • Bachelor’s degree in Mechanical, Electrical or Biomedical Engineering is desired, Masters preferred
  • 1-3 years of medical device product design and development experience
  • Familiarity with FDA and ISO 13485 medical device regulations and standards
  • Working knowledge in one or more areas is desired:
    • Technical areas (example: CAD modeling of housings; design of experiments, PCBA development etc.
    • Product areas (example: interventional/diagnostic medical devices; intravascular devices; bioelectronics devices)
    • Risk Management, Manufacturing Quality and Operations
    • Financial Budgetary Tracking and Reporting
  • Strong communication are critical to the position
    • Concise, timely and professional communications (verbal, written) are a must
    • Express ideas, recommendations and solutions clearly, logically and concisely
  • Management of resources
    • Well organized and uses time efficiently. Familiar with all reference materials and can locate needed information as necessary. 
    • Takes initiative for self-development. Prioritizes tasks effectively. Demonstrates initiative and creativity in the use of available resources.
  • Ability to work in a fast-paced, fast-growth R&D/business environment
  • Flexibility, persistence, passion, resourcefulness, a drive to succeed, and an entrepreneurial spirit are highly desired
  • PMP Certification desired.

CORE COMPETENCIES

Communication Skill

All verbal and written communications are concise, technically accurate, timely, and professional.  Demonstrates strong verbal presentation and negotiation skills. Represents in a positive and professional manner.  Expresses ideas, recommendations and solutions clearly, logically and concisely in both written and verbal communications. Demonstrates tact and diplomacy in communications. Demonstrates active listening skills and ability to resolve discrepancies with customers

Management of Resources

Well organized and uses time efficiently. Familiar with all reference materials and can locate needed information as necessary.  Takes initiative for self-development. Prioritizes tasks effectively. Demonstrates initiative and creativity in the use of available resources.

Customer Focus

Provide professional, reliable and prompt service to internal and external customers Work in partnership with others to meet and exceed customer expectations. Interpret customer needs and take appropriate action. Follow through on customer inquiries in a professional and timely manner.

WORKING CONDITIONS / PHYSICAL DEMANDS

Must be able to move throughout office and laboratory space, using a complete variety of office equipment and laboratory machinery, and tools.  May lift up to 30 pounds and stand for extended periods of time. Must tolerate exposure to chemicals found in the VIant Medical Inc environment

The above statements are intended to describe the general nature and level of work being performed by people assigned to do this job. The above is not intended to be an exhaustive list of all responsibilities and duties required.

External and internal applicants, as well as position incumbents who become disabled as defined under the Americans with Disabilities Act must be able to perform the essential job functions (as listed) either unaided or with the assistance of a reasonable accommodation to be determined by management on a case-by-case basis.