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Medtech Project Manager Jobs in California (NOW HIRING)

LSP Recruitment

Project Manager

San Francisco, CA

Project Manager MedTech / Medical Devices / SF Bay Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies. They are currently ...

Karl Storz GmbH & Co. KG

Project Manager IV

Goleta, CA · Hybrid

As an independent, family-owned MedTech company, we ambitiously think in generations instead of quarters to improve patients' lives around the world. About the Role As the Project Manager IV , you ...

Karl Storz GmbH & Co. KG

Project Manager IV

Goleta, CA · On-site

As an independent, family-owned MedTech company, we ambitiously think in generations instead of quarters to improve patients' lives around the world. About the Role As the Project Manager IV , you ...

Brooksource

Project Manager - QMS

Santa Clara, CA · On-site

$70 - $85/hr

Technical Project Manager - QMS Transformation Santa Clara, CA | Hybrid (3 days/week) Long Term ... Medical device, MedTech, or regulated industry experience preferred * Knowledge of system ...

Johnson and Johnson

Manager R&D PMO

Irvine, CA · On-site

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Learn more at Purpose: The Project Manager is responsible for the end-to-end leadership and ...

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Medtech Project Manager information

What does a Medtech Project Manager do?

A Medtech Project Manager oversees the planning, execution, and delivery of projects related to medical technology, such as the development of medical devices or healthcare software. They coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with regulatory standards. Their role is crucial in bridging the gap between technical development, clinical requirements, and business goals to bring innovative medical solutions to market efficiently and safely.

What are the key skills and qualifications needed to thrive as a Medtech Project Manager, and why are they important?

To thrive as a Medtech Project Manager, you need a strong background in project management, biomedical engineering or life sciences, and a solid understanding of regulatory requirements, often supported by a relevant degree and PMP or similar certification. Familiarity with project management software like MS Project or Jira, as well as knowledge of FDA/CE regulations and quality management systems, is typically required. Exceptional leadership, communication, and problem-solving skills help drive cross-functional teams and manage stakeholder expectations. These abilities ensure timely product development, regulatory compliance, and successful project outcomes in the highly regulated Medtech industry.

How does a Medtech Project Manager typically collaborate with cross-functional teams during the product development lifecycle?

A Medtech Project Manager frequently works with cross-functional teams, including R&D, regulatory affairs, quality assurance, marketing, and manufacturing. They coordinate efforts by facilitating regular meetings, setting clear timelines, and ensuring all team members are aligned with project goals and compliance requirements. Strong communication skills are essential, as the Project Manager must translate technical updates between departments and resolve potential roadblocks promptly. This collaborative approach helps deliver innovative medical technologies efficiently while meeting regulatory standards.

What is the difference between Medtech Project Manager vs Medical Device Engineer?

AspectMedtech Project ManagerMedical Device Engineer
Required credentialsBachelor's in engineering, project management certification (PMP)Bachelor's or higher in biomedical, mechanical, or electrical engineering
Work environmentProject teams, cross-functional collaboration, client interactionsDesign, development, testing, and manufacturing of medical devices
Employer & industry usageMedical device companies, healthcare tech firmsMedical device manufacturing, R&D departments
Common search & comparison intentUnderstanding project management roles in medtechTechnical engineering roles in medical device development

The Medtech Project Manager focuses on overseeing medical device projects, coordinating teams, and ensuring timely delivery. In contrast, a Medical Device Engineer is primarily involved in designing, developing, and testing medical devices. Both roles require engineering backgrounds, but their daily tasks and responsibilities differ significantly, catering to different aspects of the medical device lifecycle.

What are popular job titles related to Medtech Project Manager jobs in California? For Medtech Project Manager jobs in California, the most frequently searched job titles are:
What job categories do people searching Medtech Project Manager jobs in California look for? The top searched job categories for Medtech Project Manager jobs in California are:
What cities in California are hiring for Medtech Project Manager jobs? Cities in California with the most Medtech Project Manager job openings:
Medtech Project Manager jobs near you
Infographic showing various Medtech Project Manager job openings in California as of July 2026, with employment types broken down into 100% Full Time. Highlights an 89% In-person, and 11% Remote job distribution.

Project Manager

LSP Recruitment

San Francisco, CA

Full-time

Posted 14 days ago

Job description

Project Manager

MedTech / Medical Devices / SF Bay

Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies.

They are currently seeking an experienced Project Manager to join their dynamic team. The successful candidate will have a robust background in the medical device industry, with specific experience in managing the development of medical devices from concept to completion.

Key responsibilities:

  • Overseeing projects from initiation to completion, ensuring they are completed on time, and within scope and budget.
  • Coordinating cross-functional teams, including engineering, production, quality, and regulatory affairs.
  • Establishing and maintaining processes for managing project scope throughout the lifecycle, setting performance standards, and assessing risks.
  • Ensuring compliance with all regulatory standards throughout the product lifecycle.
  • Communicating effectively with all stakeholders to ensure alignment and meet project objectives.

Qualifications:

  • Bachelor's degree in engineering, or related field.
  • 8+ years of industry experience in coordinating the development of medical devices.
  • Knowledge of FDA and ISO regulations for medical devices.

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