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Medical Device Risk Management Jobs in Hemet, CA

MANSFIELD METAL SOLUTIONS LLC

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CNC Programmer / Machinist

Corona, CA · On-site

$95K - $105K/yr

  • PTO

Own CNC programming strategy for complex aerospace/medical device components from print review ... Define machining methodologies including sequencing, toolpaths, cutting strategies, and risk ...

MANSFIELD METAL SOLUTIONS LLC

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CNC Programmer / Machinist

Corona, CA · On-site

$95K - $105K/yr

  • PTO

Own CNC programming strategy for complex aerospace/medical device components from print review ... Define machining methodologies including sequencing, toolpaths, cutting strategies, and risk ...

Lubrizol Corporation

Senior Quality Engineer

Corona, CA

$91K - $123K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Coordinate and facilitate risk management activities in accordance with ISO 14971, including hazard ... medical device environment. * Experience with ISO 13485, FDA 21 CFR Part 820, ISO 14971, EU MDR ...

New

Jacobs Management Group

Tooling Supervisor

Corona, CA

  • Medical

  • Dental

  • Vision

  • Retirement

Tooling Supervisor Riverside County, CA · On-site A medical device manufacturer is hiring a ... Manage work assignments and coach the team on standard work and best practices * Troubleshoot ...

Jacobs Management Group

Tooling Supervisor

Corona, CA

  • Medical

  • Dental

  • Vision

  • Retirement

Tooling Supervisor Riverside County, CA · On-site A medical device manufacturer is hiring a ... Manage work assignments and coach the team on standard work and best practices * Troubleshoot ...

Abbott

Quality Manager

Temecula, CA

  • Medical

  • Retirement

... of medical device development, including: * Management and / or influence and development of ... Demonstrated and impactful experience in design control, test method validation, risk management ...

Abbott

Quality Manager

Temecula, CA · On-site

  • Medical

  • Retirement

... of medical device development, including: * Management and / or influence and development of ... Demonstrated and impactful experience in design control, test method validation, risk management ...

Abbott

Quality Manager

Temecula, CA

  • Medical

  • Retirement

... of medical device development, including: * Management and / or influence and development of ... Demonstrated and impactful experience in design control, test method validation, risk management ...

Techlink Systems

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Manufacturing Worker - 1st, 2nd, 3rd Shift (AO25)

Temecula, CA · On-site

$19 - $21/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Operator I / Medical Device Assembler Location: Temecula, CA (ONSITE) Contract Duration: 1-year ... We serve the contract staffing, direct hire, staff augmentation, recruitment, HR management, and ...

New

UHS

Lead Quality Risk Management - Grievance/Appeals

Riverside, CA · On-site

$32.89 - $47.69/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Our mission is to provide comprehensive multi-specialty medical services in the greater Riverside ... Any other responsibilities requested by Manager, Regional Director, and Medical Director . Benefit ...

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Showing results 21-40

All JobsMedical Device Risk Management JobsMedical Device Risk Management Jobs in Hemet, CA

Medical Device Risk Management information

See Hemet, CA salary details

$51.7K

$111.9K

$170.6K

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

As of Aug 15, 2026, the average yearly pay for medical device risk management in Hemet, CA is $111,939.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,300.00 and $129,400.00 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 job categories do people searching Medical Device Risk Management jobs in Hemet, CA look for?

The top searched job categories for Medical Device Risk Management jobs in Hemet, CA are:

What cities near Hemet, CA are hiring for Medical Device Risk Management jobs?

Cities near Hemet, CA with the most Medical Device Risk Management job openings:

Medical Device Risk Management jobs near you

CNC Programmer / Machinist

MANSFIELD METAL SOLUTIONS LLC

Corona, CA • On-site

$95K - $105K/yr

Full-time

PTO

Re-posted 24 days ago

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Job description

Role Overview

We are seeking a Principal CNC Programmer / Machinist to lead machining strategy, CNC programming, and complex process execution for aerospace and medical device components. This role is designed for a highly experienced professional who operates at the intersection of programming excellence, hands-on machining mastery, and shop-floor technical leadership.

This position is not a support role—it is a process owner role. The successful candidate will define how parts are machined, validate processes, resolve the most difficult manufacturing challenges, and serve as the highest level of machining and programming authority within the organization.

Core Responsibilities

CNC Programming & Process Ownership

  • Own CNC programming strategy for complex aerospace/medical device components from print review through production release

  • Develop, validate, and optimize CNC programs using CAM software and G-code

  • Define machining methodologies including sequencing, toolpaths, cutting strategies, and risk mitigation

  • Lead prove-outs, first-article runs, and process qualifications

  • Optimize cycle time, tool life, surface finish, and process capability

Machining & Setup Execution

  • Independently set up and run complex jobs on CNC mills and lathes, including:

    • Mills: Kitamura, Methods, Chevalier, Viper

    • Lathes: Takisawa, Hardinge, Yama Seiki

  • Design and implement advanced fixturing, workholding, and tooling solutions

  • Machine tight-tolerance, flight-critical components across a range of aerospace materials

  • Troubleshoot and resolve complex machining, tooling, and process issues

Technical Leadership & Standards

  • Serve as the primary subject matter expert for CNC programming and machining processes

  • Establish and maintain machining standards, setup documentation, and best practices

  • Provide technical guidance and mentorship to machinists and programmers

  • Support engineering, quality, and production teams with manufacturability input (DFM)

  • Participate in root cause analysis, corrective actions, and continuous improvement initiatives

Quality & Compliance

  • Ensure all machining processes meet AS9100, FAA, and customer requirements

  • Support first-article inspections, source inspections, and audit readiness

  • Apply advanced GD&T interpretation to real-world machining decisions

Required Qualifications

  • 10+ years of experience in aerospace or similarly regulated, high-precision manufacturing

  • Expert-level CNC programming capability combined with hands-on machining experience

  • Extensive experience with both CNC milling and CNC turning

  • Advanced knowledge of GD&T and aerospace drawing interpretation

  • Proven track record machining and programming tight-tolerance, high-complexity components

  • Deep understanding of aerospace materials including aluminum, stainless steel, titanium, and nickel-based alloys

  • Strong mechanical intuition and structured problem-solving skills

  • Ability to operate with full autonomy and technical accountability

Preferred Qualifications

  • Advanced 5-axis milling and/or multi-axis turning experience

  • High proficiency with CAM software (Mastercam, Fusion 360, NX, or similar)

  • Experience supporting prototype, first-article, and low-volume/high-mix aerospace work

  • Prior involvement in PFMEA, process qualification, or manufacturing risk assessments

  • Experience supporting AS9100 audits or customer source inspections

What This Role Offers

  • Authority over CNC programming and machining strategy

  • Ownership of the most complex and critical aerospace/medical device work

  • Direct influence on process standards, tooling strategy, and shop capability

  • A quality-driven, engineering-aligned manufacturing environment

  • Compensation aligned with principal-level technical expertise

Education

  • High school diploma or GED required

  • Technical degree, formal apprenticeship, or equivalent advanced training strongly preferred

Work Environment

  • Precision aerospace/medical device manufacturing facility

  • Hands-on role requiring regular machine interaction

  • Ability to lift up to 50 lbs

  • Exposure to industrial machinery, cutting fluids, and metal chips