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Medical Device Risk Management Jobs in Wyoming, MN

Medtronic

Sr. Software Systems Engineer

Fridley, MN · On-site

... risk management, verification and validation, and regulatory expectations for medical device development. Key Responsibilities * Provide design quality support for software and software-enabled ...

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All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Wyoming, MN

Medical Device Risk Management information

See Wyoming, MN salary details

$51.2K

$110.8K

$168.9K

How much do medical device risk management jobs pay per year?

As of Aug 12, 2026, the average yearly pay for medical device risk management in Wyoming, MN is $110,831.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,400.00 and $128,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device risk management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a medical device risk management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.
What cities near Wyoming, MN are hiring for Medical Device Risk Management jobs? Cities near Wyoming, MN with the most Medical Device Risk Management job openings:
Medical Device Risk Management jobs near you

Senior Project Manager - Medical Device (Hybrid - Arden Hills, MN) Possible Temp-to-Hire

Pharmavise

Saint Paul, MN • On-site

Contractor

Re-posted 15 days ago

Job description


Our F500 Medical Device client has an exciting opportunity for a Senior Project Manager.
Job Summary:
This role manages the development and implementation of cross functional projects that support medical device Quality organization, with a focus on cardiology products once they are out on the market. Operating across global sites (US MN, Ireland, Costa Rica), this position ensures high quality execution of project initiatives tied to medical device post market surveillance, medical device risk management, and medical device manufacturing quality operations.
As the first dedicated project manager that serves a team with ~50 key leaders, the individual will independently establish project management structure and play a key role in incorporating project management methodologies into the organization. The role requires strong collaboration, proactive communication, and the ability to understand complex interdependencies across multiple projects to drive prioritization, execution, and patient centric outcomes. This role does not require technical knowledge of the functional work performed by the Quality organization but will need to obtain working knowledge of the processes in place to best serve the cross-functional teams.
Key Responsibilities:
Project Planning & Execution
• Estimate project level of effort and resource needs using standard project management techniques and tools.
• Prepare and maintain project plans, schedules, and budgets using Microsoft Project and related project management tools.
• Direct project execution by assigning tasks, tracking progress, identifying risks, and implementing contingency plans.
• Resolve project related issues in collaboration with team members and stakeholders.
Cross Functional Leadership & Stakeholder Engagement
• Work across key Quality functions to identify organizational priorities, project needs, and stakeholder expectations.
• Conduct regular check ins with project leaders to understand their goals, ensure alignment to business needs, and monitor progress.
• Hold team members accountable to timelines and escalate risks when necessary.
• Proactively engage stakeholders to understand requirements and maintain strong relationships.
• Monitor resource allocation across the organization.
Metrics, Reporting & Communication
• Define, obtain, and monitor key organizational performance metrics.
• Partner with data analysts to generate and visualize project performance dashboards.
• Deliver clear, concise communication to leadership through status updates, monthly and quarterly reviews, and management level storytelling.
Quality & Compliance
• Maintain compliance with the Quality Policy and all documented procedures, demonstrating commitment to patient safety and product quality.
• For supervisory scenarios: ensure adequate resources and foster a work environment supporting Quality System compliance.
Project Management Expertise & Continuous Improvement
• Apply standard methodologies to assure project quality and drive consistent execution.
• Mentor project leaders and share project management knowledge across internal teams.
• Understand project interdependencies and provide recommendations on prioritization to support business needs.
Qualifications:
5+ Years with BA; 3+ Years with MBA
• Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort.
• Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to complete project.
• Directs project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.
• Assures project quality by using standard development methodologies to develop and execute project quality plans.
• Communicates project status by preparing standard status reports, and by participating in departmental and customer project status update meetings.
• Resolves project issues by working with team members, project customers, and others as appropriate.
• Consults with internal project groups by sharing project management knowledge and assisting or mentoring more junior project leaders in project management processes and techniques.
• Participates in external project management organizations, conferences and seminars to keep current with industry best practices in project management by joining professional associations and implementing a professional development plan with focus on project management.
Excellent communication, leadership, problem-solving, and interpersonal skills
Preferred:
PM Certificate
Medical device experience
Other Details:
Schedule: 08:00:AM - 04:30:PM
Work Setup: Hybrid in Arden Hills, MN
Contract Length: 9 Months (2/16/2026 - 11/15/2026)

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