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Biomedical Project Manager Jobs in Riverside, CA

JenaValve

Associate, Project Manager

Irvine, CA · On-site

$120K - $130K/yr

Bachelor's degree in Engineering, Biomedical Sciences, or a related field. * Minimum 3 years' experience in project management/leading teams to implement product/manufacturing process improvements ...

Agiliti

Biomedical Technician

Anaheim, CA · On-site

$27.50 - $43.90/hr

We are a nationwide company of passionate medical equipment management experts who proudly serve ... Willingness to help with Field based biomedical accounts and support Inventory projects and ...

UHS

Director Biomedical Engineering

Corona, CA · On-site

$100K - $150K/yr

Biomedical Engineering Director - Corona Regional Medical Center located in Corona, Ca Manager ... Manages projects including device acquisition and installation and/or EOC committee assignments.

UHS

Director Biomedical Engineering

Corona, CA · On-site

Biomedical Engineering Director - Corona Regional Medical Center located in Corona, Ca Manager ... Manages projects including device acquisition and installation and/or EOC committee assignments.

PHS Bio-Medical Services

Area Manager

Chino, CA · On-site

$71K - $100K/yr

... coding, project management and more. We provide services to clinically excellent community ... Directs the Biomedical Department during regulatory inspections like The Joint Commission (TJC ...

Prime Healthcare

Area Manager

Chino, CA · On-site

$71K - $100K/yr

... coding, project management and more. We provide services to clinically excellent community ... Directs the Biomedical Department during regulatory inspections like The Joint Commission (TJC ...

PHS Bio-Medical Services

Area Manager

Chino, CA · On-site

... coding, project management and more. We provide services to clinically excellent community ... Directs the Biomedical Department during regulatory inspections like The Joint Commission (TJC ...

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

... management and cGxP best practices to drive your overall success. Projects range from design ... Mechanical, Biomedical, or related). * 2+ years of experience in a cGMP environment required.

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

... management and cGxP best practices to drive your overall success. Projects range from design ... Mechanical, Biomedical, or related). * 2+ years of experience in a cGMP environment required.

Concuir, Inc

Project Engineer II to III

Irvine, CA · On-site

$90K - $110K/yr

... management and cGxP best practices to drive your overall success. Projects range from design ... Mechanical, Biomedical, or related). * 2+ years of experience in a cGMP environment required.

Mentis Systems

Program Manager

Irvine, CA · On-site

The NPD (New Product Development) Program Manager in (APM) PMO Team will be responsible for ... Bachelor's Degree in (Mechanical, Biomedical, Systems, Electrical) Engineering or related field ...

Gentex Corp.

Project Engineer

Rancho Cucamonga, CA · On-site

$95K - $121K/yr

... Biomedical Engineering. * 4+ years of engineering experience in a product development team ... The Project Engineer works closely with Engineering, Program Management, Product Management and to ...

Gentex Corp

Project Engineer

Rancho Cucamonga, CA · On-site

$95K - $121K/yr

... Biomedical Engineering. * 4+ years of engineering experience in a product development team ... The Project Engineer works closely with Engineering, Program Management, Product Management and to ...

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All JobsBiomedical Project JobsBiomedical Project Manager JobsBiomedical Project Manager Jobs in Riverside, CA

Biomedical Project Manager information

See Riverside, CA salary details

$22

$48

$79

How much do biomedical project manager jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biomedical project manager in Riverside, CA is $48.24, according to ZipRecruiter salary data. Most workers in this role earn between $41.88 and $52.93 per hour, depending on experience, location, and employer.

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What is a biomedical project manager?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

How does a biomedical project manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What are the key skills and qualifications needed to thrive as a biomedical project manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.
What are popular job titles related to Biomedical Project Manager jobs in Riverside, CA? For Biomedical Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Biomedical Project Manager jobs in Riverside, CA look for? The top searched job categories for Biomedical Project Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Biomedical Project Manager jobs? Cities near Riverside, CA with the most Biomedical Project Manager job openings:
Biomedical Project Manager jobs near you
Infographic showing various Biomedical Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $100,346 per year, or $48.2 per hour.

Associate, Project Manager

JenaValve

Irvine, CA • On-site

$120K - $130K/yr

Full-time

Posted 11 days ago

Job description

Job Title: Associate, Project Manager
Supervisor/Manager Title: Senior Director, Program Management
Job Description Summary: Responsible for leading cross-functional teams through the development and launch of heart valves, delivery catheters, and related components, ensuring projects meet regulatory compliance, quality standards, and timelines while managing budgets, risks, and stakeholder expectations within the complex landscape of medical device development and commercialization. Projects may span globally across the organization to address the most critical business needs including Product Development, Operations, Quality and Regulatory.
Job Responsibilities:
  • Project Planning & Execution:
    • Develop comprehensive project plans, including scope definition, timelines, milestones, resource allocation, and budget management.
    • Lead cross-functional teams consisting of engineers, clinicians, regulatory specialists, quality assurance personnel, and marketing teams.
    • Manage project schedules, track progress against key performance indicators, and identify potential roadblocks to mitigate risks.
    • Ensure adherence to regulatory requirements (FDA, ISO, etc.) throughout the product development lifecycle.
  • Technical Expertise:
    • Understand medical device design principles, functionality, and technical specifications relevant to the project.
    • Collaborate with engineering teams to translate product requirements into technical design documents.
    • Stay updated on emerging technologies and industry trends in medical device development.
  • Stakeholder Management:
    • Facilitate communication and collaboration between different departments, including clinical research, manufacturing, sales, and marketing.
    • Present project updates and key decisions to senior management and stakeholders.
    • Manage stakeholder expectations and address concerns effectively.
  • Risk Management:
    • Identify and proactively mitigate potential risks associated with the project, including technical, regulatory, and clinical risks.
    • Develop contingency plans to address unforeseen challenges and ensure project continuity.
  • Quality Assurance:
    • Ensure compliance with quality management systems (QMS) and standard operating procedures (SOPs) throughout the project.
    • Monitor and address quality issues to maintain product safety and efficacy.

Education, Experience, and Certification:
  • Bachelor's degree in Engineering, Biomedical Sciences, or a related field.
  • Minimum 3 years' experience in project management/leading teams to implement product/manufacturing process improvements and/or develop complex line extensions or new products (within R&D, Manufacturing, Quality, Clinical or Regulatory).
  • Experience in FDA environment for PMA or NDA product development is highly desirable.
  • Project Management Professional (PMP) or equivalent project management training certification desired.
Required Skills and Qualifications:
  • Project Management Expertise: Proven experience in managing projects from concept to commercialization, ideally within the medical device industry.
  • Technical Knowledge: Understanding of medical device design principles, manufacturing processes, and regulatory requirements. Must take initiative and have the ability to create/edit/review documentation and timelines using standard MS Office tools.
  • Leadership Skills: Ability to lead cross-functional teams, motivate individuals, and foster collaboration.
  • Communication Skills: Excellent written and verbal communication skills to effectively convey complex technical information to diverse stakeholders.
  • Regulatory Compliance: Familiarity with FDA regulations and other relevant international standards for medical devices.
  • Problem-solving and Critical Thinking Skills: Ability to analyze complex situations, identify root causes, and develop effective solutions.
  • Flexibility:Ability to manage multiple projects/tasks with high attention to detail. Support global teams of varying size and focus across multiple time zones.

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