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Project Engineer Medical Device Jobs in California

Project Manager - Medical Device

Irvine, CA · On-site +1

$81K - $115K/yr

This is a hands-on role at the center of engineering, R&D, quality, and manufacturing, where you'll ... Minimum three (3) years of experience in project management; medical device industry experience, a ...

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Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

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Project Engineer Medical Device information

What does a project engineer do in the medical device industry?

A Project Engineer in the medical device industry is responsible for planning, coordinating, and managing projects related to the development and manufacturing of medical devices. They oversee project timelines, budgets, and resources, ensuring that all technical and regulatory requirements are met. Their work involves collaborating with cross-functional teams, such as design, quality assurance, and regulatory affairs, to bring safe and effective medical devices to market. Project Engineers also help resolve technical challenges and ensure products comply with industry standards and government regulations.

What are the key skills and qualifications needed to thrive as a project engineer in the medical device industry?

To excel as a Project Engineer in medical devices, you need a solid background in engineering (typically a degree in biomedical, mechanical, or electrical engineering), experience with product development, and knowledge of regulatory standards like FDA and ISO 13485. Familiarity with CAD software, project management tools, and validation protocols is highly valuable, along with certifications such as PMP or Six Sigma. Strong problem-solving abilities, collaboration, and effective communication are essential soft skills for leading cross-functional teams and resolving technical challenges. These skills and qualifications ensure safe, compliant, and innovative device development that meets patient and market needs.

How does a project engineer in the medical device industry typically collaborate with cross-functional teams during product development?

As a Project Engineer in the medical device field, you’ll work closely with cross-functional teams such as R&D, quality assurance, regulatory affairs, and manufacturing. Collaboration involves coordinating project timelines, ensuring design requirements are met, and facilitating communication between departments to address technical challenges and regulatory compliance. Regular meetings and clear documentation are essential to keep all stakeholders aligned, and you may often serve as a bridge between engineering and non-engineering teams. This collaborative environment fosters innovation and helps ensure the successful and timely launch of safe, effective medical devices.

What is the difference between Project Engineer Medical Device vs Quality Engineer Medical Device?

AspectProject Engineer Medical DeviceQuality Engineer Medical Device
Required CredentialsBachelor's in Engineering, certifications like PMP beneficialBachelor's in Engineering or Science, certifications like CQE preferred
Work EnvironmentDesign, development, and project management teams in manufacturing or R&DQuality assurance, compliance, and inspection teams in manufacturing
Employer & Industry UsageMedical device companies focusing on product development and project executionMedical device companies ensuring product quality and regulatory compliance
Common Search & Comparison IntentUnderstanding project management roles in medical device industryUnderstanding quality assurance roles in medical device industry

The Project Engineer Medical Device focuses on managing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Quality Engineer Medical Device concentrates on maintaining product quality, compliance with regulations, and conducting inspections. Both roles are essential in medical device companies but serve different functions within the product lifecycle.

Infographic showing various Project Engineer Medical Device job openings in California as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution.

Clinical Engineering Medical Device Security Engineer II

Commonspirit Health

San Luis Obispo, CA • On-site

Other

Re-posted 21 hours ago


CommonSpirit Health rating

7.0

Company rating: 7.0 out of 10

Based on 533 frontline employees who took The Breakroom Quiz

414th of 887 rated healthcare providers


Job description

Where You'll Work
Inspired by faith. Driven by innovation. Powered by humankindness. CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation's largest nonprofit Catholic healthcare organizations, CommonSpirit Health delivers more than 20 million patient encounters annually through more than 2,300 clinics, care sites and 137 hospital-based locations, in addition to its home-based services and virtual care offerings. CommonSpirit has more than 157,000 employees, 45,000 nurses and 25,000 physicians and advanced practice providers across 24 states and contributes more than $4.2 billion annually in charity care, community benefits and unreimbursed government programs. Together with our patients, physicians, partners, and communities, we are creating a more just, equitable, and innovative healthcare delivery system.
Job Summary and Responsibilities
This position will serve the state of California region (specifically South of Bakersfield, CA) and would require travel up to 75% of the time with non-traveling work being from a home office. We are looking for a candidate with residence in this region.
As our Clinical Engineering Medical Device Security Engineer II, you will be a key architect of CommonSpirit Health's robust medical device cybersecurity framework, providing advanced expertise to safeguard patient safety and device integrity across the system. This senior role involves not only mitigating vulnerabilities but also proactively designing and implementing cutting-edge security solutions and evaluating the effectiveness of controls. You will be instrumental in developing and delivering critical security tool and process training, ensuring our teams are equipped to handle the evolving cyber threat landscape.
Every day you will lead collaborations with cross-functional teams to architect innovative security solutions that harden technical controls for network-connected medical devices, all while meticulously preserving device functionality and patient safety. This includes expertise in areas like network architecture, Active Directory, group policies, Windows images, and endpoint security tools. You will continuously leverage advanced technology and analytical insights to evaluate the efficacy of existing security controls, recommending strategic adjustments and enhancements to bolster our defenses. Furthermore, you will provide system-wide medical device security training, troubleshoot complex issues, and expertly lead recovery efforts for devices impacted by upgrades, patching, or security incidents, embodying all the responsibilities of the Medical Device Security Engineer I role.
To be successful in this pivotal role, you will possess significant experience in medical device security engineering, cybersecurity architecture, and system-level vulnerability management. Your expertise in incident response, forensics, and the development of secure medical device environments will be crucial. We are seeking a highly skilled and strategic professional with a proven track record in developing and implementing advanced security solutions without compromising operational integrity. Strong communication and training capabilities are essential, along with a deep understanding of relevant cybersecurity regulations and the ability to conduct comprehensive risk assessments and remediation strategies.
  • Architect and implement robust security solutions for networked medical devices
  • Continuously evaluate and enhance existing security controls against evolving threats
  • Provide system-wide medical device security training
  • Lead troubleshooting and recovery efforts for affected medical devices
  • Mitigate vulnerabilities and lead incident response for medical device security
  • Conduct comprehensive security assessments and ensure regulatory compliance

The job summary and responsibilities listed above are designed to indicate the general nature of the work performed within this job. They are not designed to contain or be interpreted as a comprehensive inventory of all job responsibilities required of employees assigned to this job. Employees may be required to perform other duties as assigned.
Job Requirements
Required:
  • Bachelors degree in HTM, Computer Science, Technology or Business Discipline upon hire or equivalent professional experience required.
  • 4-7 years of experience working in healthcare/IT Security, System Administration, Software Development or related field.
  • 2-5 years experience working in a healthcare/medical environment.
  • Experience working with specialized medical equipment in a healthcare setting.
  • Experience with Cybersecurity and Infrastructure Security Agency (CISA) HIPAA/HITECH compliance standards.
  • Valid Driver's License

Preferred:
  • Experience working with the software development life cycle or project management methodologies preferred
  • Certified Biomedical Equipment Technician (CBET)
  • Certified Radiology Equipment Specialists (CRES)
  • Certified Healthcare Tech Manager (CHTM)
  • CompTIA A+ Certification (A-PLUS)
  • CompTIA Network A+ (NTWK-PLUS)

This position requires participation in a rotational on-call schedule, including nights, weekends, and holidays. Candidates must be available to respond to urgent service needs outside of regular business hours and may be required to return to the facility on short notice.

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