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Medtech Project Manager Jobs in Riverside, CA (NOW HIRING)

Manager Preclinical Research

Irvine, CA · On-site

$49K - $50K/yr

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Serving as a preclinical research representative for new product development projects. The main ...

Manager Preclinical Research

Irvine, CA · On-site

$49K - $50K/yr

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Serving as a preclinical research representative for new product development projects. The main ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... projects. * Manages team of clinical research professionals to manage clinical trials; * Is ...

New

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Strong project management skills to balance multiple projects * Excellent interpersonal skills ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... manage project timelines, and oversee process improvements to improve the functioning of the ...

Showing results 21-40

Medtech Project Manager information

See Riverside, CA salary details

$40.2K

$107.1K

$169K

How much do medtech project manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medtech project manager in Riverside, CA is $107,125.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,900.00 and $128,300.00 per year, depending on experience, location, and employer.

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?

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 Riverside, CA? For Medtech Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Medtech Project Manager jobs in Riverside, CA look for? The top searched job categories for Medtech Project Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Medtech Project Manager jobs? Cities near Riverside, CA with the most Medtech Project Manager job openings:
Infographic showing various Medtech Project Manager job openings in Riverside, CA as of June 2026, with employment types broken down into 98% Full Time, 1% Temporary, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $107,125 per year, or $51.5 per hour.

NPI & LCM Senior Engineering Manager

Johnson & Johnson

Irvine, CA • On-site

Full-time

Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Johnson & Johnson rating

8.2

Company rating: 8.2 out of 10

Based on 111 frontline employees who took The Breakroom Quiz

32nd of 86 rated pharmaceutical


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Process Improvement

Job Category:

People Leader

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

We are searching for the best talent for a NPI & LCM Senior Engineering Manager based out of Irvine, CA.

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Purpose:

TheNPI&LCMSr.Engineering Managerwill direct and coordinate activities of one or more engineering programs withinSupply Chainin support of new product development,externaltransfersand Lifecycle ManagementofAccess and Accessoriesdevices supporting Electrophysiology catheters. These programs will include Manufacturing/Process Engineering,ElectricalEngineering, Systems Engineering, Process Transfers, Technology Development, Tooling (Design, Fabrication, Assembly, Procurement and Calibration).

Responsibilities:

  • Manages and works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.

  • Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

  • Directs and coordinates engineeringactivitiesthrough subordinate engineers and technicians to attainbusinessgoals consistent with cost, high quality, reliability and delivery requirements and Designfor Manufacturability.

  • Leads New Product IntroductionandLifecycle Engineering teamsto improve existing processes for newand existingproducts.

  • Determines direction and adequacy of processes/designs and test results andrecommendschanges.

  • Directs, coordinates, and exercises project management principles, methods, tools and techniques for the effective planning, scheduling, organization, control, integration, and completion of project(s) of limited scope and duration by performing the following duties personally or through subordinates.

  • Individualwill have demonstrated creativity, foresight and mature technical judgment in anticipating and solving problems, determining technical program objectives/requirements, organizing/leading projects and developing standards & guides for technical activities.

  • Provides effective management of subordinates to achieve desired results. Possesses excellent communication, motivation, team building, employee involvement, diplomacy, delegating skills, as well as confidence and enthusiasm.

  • Coordinates cross functional teams to drive business and organizational results. Sets business metrics for the team and provides performance feedback to employees.

  • Plans, schedules, conducts, and manages various engineering projects, ensuring all projects adhere to acceptable engineering practices and compliance regulations, are appropriately staffed, and are run within budget. Assists with troubleshooting problems, discrepancies, and investigations of nonconformance.

  • Developsstandard operating procedures. Provides engineering expertise and maintains a high level of competency and business development acumen.

  • Has full technical and administrative responsibility for interpreting, organizing, executing and coordinating assignments into manufacturing.

  • Establishes operational goals and objectives to meet corporate goals and strategies. Prepares project schedules and coordinates engineering activities to ensure output meets specifications as well as corporate goals and objectives.

  • Plans anddevelopsprojects (engineering, process development, maintenance systems,external manufacturingtransfers).

  • Maintains liaison with individuals and project leaders within or outside his/her organization, with responsibility for acting independently on technical or business matters pertaining to his/her field.

  • Implements systems and procedures goals to ensure that machines and equipment meet operational performance and utilization requirements. Reviews equipment and machine requirements based on productionneeds. Determines and oversees implementation of capital requirements forprocessimprovements.

  • Reviews and approves process specifications and designrequirements.Reviews and approves changes to documentation.

  • Practices company safety and quality policies and procedures; actively requires conformance.

  • Carries out supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

  • Practices company safety and quality policies and procedures. Actively requires conformance.

  • Responsible for performing design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.

  • Responsible for communicating business related issues or opportunities to next management level.

  • Responsible for followingand ensuring that subordinatesfollowall Company guidelines related to Health, Safety and Environmental practices.

  • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

Qualifications:

  • BSEngineeringdegree in relevant discipline.

  • 10+years of related engineering experience.

  • MSdegree preferredin a related engineering discipline.

  • Has significant complex level engineering experience.

  • Experience in Manufacturing Engineering environment

  • Financial background experience in the field ofSupply Chainwould be beneficial.

  • Experience in the medical device industry would be an asset.

  • Must possess a clear mastery of theoretical and practical fundamentals and experimental engineering techniques.

  • Strong English communication skills, written and oral.

  • Ability to present presentations to upper management a plus.

  • Knowledge of drafting software systems such asAutoCadand Solidworks is required.

  • Knowledge of statistical software packages such as Minitab a plus.

  • Project Management skills a plus.

  • Process Excellence tools such as Lean and Six Sigma certification a plus.

  • Business/financial acumen

  • A demonstrated ability to work in team environment with focus on internal and external relationship development is required.

  • Good interpersonal skills with ability to present complex informationisrequired.

  • Able to prioritize requests and propose effective alternatives when necessary is required.

  • Knowledge in project management tools and processes andableto use these in broad range of business settings is required

#LI-AM

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against based on disability.

For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :

$122,000.00 - $212,750.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation -120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year
Holiday pay, including Floating Holidays -13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave - 80 hours in a 52-week rolling period10 days
Volunteer Leave - 32 hours per calendar year
Military Spouse Time-Off - 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

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