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Remote Medical Device Project Manager Jobs in Riverside, CA

M&A Finance Manager

Irvine, CA · On-site +1

$133K - $222K/yr

Remote or Hybrid or Onsite ***If you reside within a commutable distance to Irvine, this role will ... Experience in manufacturing or medical device industries preferred. * Knowledge of US GAAP and SOX ...

Remote work options may be considered on a case-by-case basis and if approved by the Company. This ... Vision (JJV) medical device portfolio. This includes identifying key strategy and goals ...

Remote work options may be considered on a case-by-case basis and if approved by the Company. This ... Vision (JJV) medical device portfolio. This includes identifying key strategy and goals ...

Senior Manager, Clinical Compliance

Irvine, CA · On-site +1

$160K - $170K/yr

Remote - Home Office Summary: Reporting to the Vice President, Clinical Affairs, the Senior Manager ... medical device experience strongly preferred. * Minimum 3 years dedicated GCP audit or clinical ...

Specialist, Clinical Compliance

Irvine, CA · On-site +1

$80K - $90K/yr

Senior Manager, Clinical Compliance Job Location & Environment: Remote - Home Office Summary ... Working knowledge of ICH E6 GCP guidelines and FDA regulations applicable to medical device ...

Contribute to safety management plans for assigned protocols and support safety review meetings ... Bachelor's degree in life science or related field * 2-4 years of experience in medical device ...

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Showing results 1-20

Remote Medical Device Project Manager information

See Riverside, CA salary details

$40.2K

$107.1K

$169K

How much do remote medical device project manager jobs pay per year?

As of Jun 23, 2026, the average yearly pay for remote medical device 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 are the key skills and qualifications needed to thrive as a Remote Medical Device Project Manager, and why are they important?

To thrive as a Remote Medical Device Project Manager, you need strong project management skills, a background in engineering or life sciences, and knowledge of medical device regulations, often supported by a PMP certification or similar credential. Familiarity with project management tools like Microsoft Project, collaboration platforms, and regulatory submission systems (such as FDA eCTD) is commonly required. Exceptional communication, leadership, and problem-solving abilities help in leading cross-functional remote teams and managing stakeholders. These skills are crucial for ensuring regulatory compliance, timely product development, and effective coordination in a dispersed work environment.

What are some common challenges faced by Remote Medical Device Project Managers, and how can they be addressed?

Remote Medical Device Project Managers often face challenges such as coordinating cross-functional teams across different time zones, maintaining clear communication with stakeholders, and ensuring regulatory compliance from a distance. These challenges can be addressed by establishing regular virtual meetings, using project management tools to track progress, and implementing standardized documentation practices. Building strong relationships with team members and fostering an open communication culture are also key to overcoming these hurdles and ensuring project success.

What does a Remote Medical Device Project Manager do?

A Remote Medical Device Project Manager oversees the planning, execution, and completion of projects related to medical devices, all while working remotely. They coordinate cross-functional teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders to keep projects on track. Their role is crucial for ensuring that new medical devices are developed efficiently and safely, meeting both company goals and industry standards.

What is the difference between Remote Medical Device Project Manager vs Remote Medical Device Quality Assurance Specialist?

AspectRemote Medical Device Project ManagerRemote Medical Device Quality Assurance Specialist
CertificationsPMP, CAPM, or equivalent project management certificationsISO 13485 Lead Auditor, CQE, or similar quality assurance certifications
Work EnvironmentOversees project timelines, teams, and deliverables remotely within medical device companiesEnsures compliance, audits, and quality processes remotely in medical device manufacturing or development
Employer & Industry UsageUsed by medical device firms managing product development projects remotelyCommon in companies focusing on quality standards and regulatory compliance remotely

The Remote Medical Device Project Manager focuses on managing project timelines, teams, and deliverables remotely, ensuring successful product development. In contrast, the Remote Medical Device Quality Assurance Specialist concentrates on maintaining quality standards, conducting audits, and ensuring regulatory compliance remotely. Both roles require specialized certifications and are vital in the medical device industry, often working in similar remote environments but with distinct responsibilities.

What are popular job titles related to Remote Medical Device Project Manager jobs in Riverside, CA? For Remote Medical Device Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Remote Medical Device Project Manager jobs in Riverside, CA look for? The top searched job categories for Remote Medical Device Project Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Remote Medical Device Project Manager jobs? Cities near Riverside, CA with the most Remote Medical Device Project Manager job openings:
Associate Director, Clinical Affairs

Associate Director, Clinical Affairs

Becton, Dickinson and Company

Irvine, CA • On-site, Remote

Full-time

Posted 10 days ago


BD rating

7.2

Company rating: 7.2 out of 10

Based on 136 frontline employees who took The Breakroom Quiz

268th of 418 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

About the role:

This is a senior leadership role responsible for endtoend oversight of complex clinical studies and registries within a highly regulated environment. The role leads managers and teams across multiple largescale initiatives, partners closely with investigators, hospitals, CROs, and internal stakeholders, and ensures regulatory compliance, data integrity, and study execution from initiation through completion. Ideal candidates bring deep clinical operations experience, strong people leadership capability, and a proven ability to manage risk and deliver results across highimpact, crossfunctional programs.

Key responsibilities include:

  • Manage senior managers, managers, and professionals to oversee the work of multiple projects and/or initiatives and may have financial budget responsibilities.
  • Develop a robust talent development plan in alignment with functional growth strategies of the department.
  • Identify risk, develop and lead in the implementation of broad and more complex projects, initiatives and/or strategies which may include negotiations with internal and external parties.
  • Develop mitigation strategies, alternative solutions, resolve issues, etc. in collaboration with cross functional and/or matrix teams
  • Plan and direct complex activities with large scale or significant business impact with the accountability for successful completion of all deliverables including but not limited to:
  • Oversee the relationship management of physicians/investigators, other medical professionals, Research Organizations (CRO's), hospitals, research institutions and/or vendors
  • Ensure compliance to applicable regulatory requirements including safety reporting and device related complications through appropriate oversight
  • Oversee clinical studies/registries from initiation to completion, while ensuring study compliance and data completeness
  • Serve as a point of escalation for complex project issues (e.g., sponsor site interaction for IRBs, contract, and training)
  • Oversee the Clinical Affairs Trial Management Team during clinical trial cases with physicians, hospital staff and coordinators
  • Oversee the accuracy/effectiveness of device accountability

Required education and experience

  • Bachelor's Degree (preferably in life sciences)
  • At least 10 years of professional clinical research, clinical operations, or trial management in a regulated environment (Device, Pharma, or Clinical Research Operations).
  • Endtoend leadership experience of clinical studies/registries
  • At least 5 years of people management experience or leading sizeable cross functional teams
  • Experience overseeing complex, high-impact programs in regulated environment (medical device research required) industry sponsored researchpreferred
  • Demonstrated experience leading managers and senior managers across multiple concurrent projects or initiatives.
  • Strong risk assessment, mitigation planning, and issueresolution skills within complex, crossfunctional environments.
  • Experience overseeing clinical studies/registries from initiation through completion, ensuring compliance and data integrity.
  • Solid understanding of regulatory requirements, including safety reporting and devicerelated event oversight

Preferred qualifications:

  • Experience serving as an escalation point for IRB interactions, contracts, training, and complex study issues. (Institutional Review Board)
  • Background supporting clinical trial teams during live case support with physicians and hospital staff.
  • Familiarity with device accountability processes and oversight procedures.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work LocationUSA CA - Irvine Laguna CanyonAdditional LocationsWork Shift

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$175,800.00 - $281,300.00 USD Annual

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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