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Quality Manager Medical Device Jobs in Riverside, CA

Prismatik

Project Manager - Medical Device

Irvine, CA · On-site +1

$81K - $115K/yr

This is a hands-on role at the center of engineering, R&D, quality, and manufacturing, where you'll ... Minimum three (3) years of experience in project management; medical device industry experience, a ...

Prismatik

Project Manager - Medical Device

Irvine, CA · On-site

$81K - $115K/yr

This is a hands-on role at the center of engineering, R&D, quality, and manufacturing, where you'll ... Minimum three (3) years of experience in project management; medical device industry experience, a ...

Aerotek

Medical Device Assembler

Irvine, CA

$19.50 - $21/hr

Identify and report defects, quality concerns, or process issues * Package finished products ... Previous medical device assembly experience is a plus! * High School Diploma or GED * Ability to ...

Aerotek

Medical Device Assembler

Irvine, CA

$19 - $23.25/hr

You will work with microscopes and small components to produce high-quality products that support ... Minimum of 2 years of medical device assembly experience, preferably in a clean room environment.

Aerotek

Medical Device Solderer

Irvine, CA

$22 - $25/hr

Inspect finished products to verify they meet all quality standards and specifications. * Package medical devices and related components according to defined procedures. * Use computer-based tools ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.67/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... QC Management. Responsibilities * Inspecting and disposition of raw materials and labels ... High School diploma or equivalent education require * 1 year of experience in a medical device or ...

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... QC Management. Responsibilities * Inspecting and disposition of raw materials and labels ... High School diploma or equivalent education require * 1 year of experience in a medical device or ...

Techlink Systems

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Medical Device Assembler - KS2026

Irvine, CA · On-site

$19/hr

... related medical device assemblies. * Performs routine assignments according to specified and ... Support all Divisional initiatives as identified by divisional management and in support of Quality ...

Marquee Staffing - OC

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Medical Device Assembly-2nd Shift

Irvine, CA · On-site

$19 - $21/hr

... producing high-quality work. * 2nd Shift: Mon-Thurs, 3:30 PM-2:00 AM | $19-$21/hr differential ... Medical device experience preferred * Ability to work in a cleanroom and use a microscope * Strong ...

VOLT

Medical Device Assembler - 2nd Shift

Irvine, CA · On-site

$9/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

VOLT

Medical Device Assembler - 2nd Shift

Irvine, CA · On-site

$18 - $19.75/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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Showing results 1-20

All JobsQuality Medical Device JobsQuality Manager Medical Device JobsQuality Manager Medical Device Jobs in Riverside, CA

Quality Manager Medical Device information

See Riverside, CA salary details

$25K

$89.9K

$164.8K

How much do quality manager medical device jobs pay per year?

As of Aug 19, 2026, the average yearly pay for quality manager medical device in Riverside, CA is $89,887.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,900.00 and $141,900.00 per year, depending on experience, location, and employer.

What does a quality manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.

What are some common challenges quality managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

What is the difference between Quality Manager Medical Device vs Quality Engineer Medical Device?

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What are popular job titles related to Quality Manager Medical Device jobs in Riverside, CA?

For Quality Manager Medical Device jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Quality Manager Medical Device jobs in Riverside, CA look for?

The top searched job categories for Quality Manager Medical Device jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Quality Manager Medical Device jobs?

Cities near Riverside, CA with the most Quality Manager Medical Device job openings:

Quality Manager Medical Device jobs near you
Infographic showing various Quality Manager Medical Device job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $89,887 per year, or $43.2 per hour.

Project Manager - Medical Device

Prismatik

Irvine, CA • On-site, Remote

$81K - $115K/yr

Full-time

Re-posted 3 days ago

Job description

We're looking for a Project Manager to lead the development of new medical devices from concept through launch.

This is a hands-on role at the center of engineering, R&D, quality, and manufacturing, where you'll drive projects through Design Control, manage timelines and resources, and keep teams aligned from early development through final testing. You'll tackle technical and project challenges, manage risk, and make sure products move forward with the quality and rigor required in a regulated environment.

Essential Functions:
  • Leads the project team through all phases of Design Control to achieve project goals within established scope, time, and quality constraints.
  • Creates or directs preparation of all documents including, but not limited to protocols, reports, traceability matrices, SDS documents and labeling required for the Design History Files of medical devices.
  • Determines and tracks resources such as time, capital, labor, and equipment required to complete projects.
  • May assist executive management in the preparation of project proposals including scope, schedule, budget, and deliverables.
  • Manages progress of projects to ensure alignment with business strategy, sound application of engineering principles, and adherence to Prismatik's Quality Manual and applicable industry standards.
  • Manages and implements appropriate action with respect to timelines, milestones, planning, and resource allocations.
  • Identifies elements impacting project, such as personnel issues and project gaps, bottlenecks, and risks. Develops solutions and/or implements corrective actions to ease issues, eliminate delays, and mitigate risks using appropriate knowledge, skills, and techniques.
  • Evaluates and analyzes final testing results. Provides manufacturing guidance.
  • Communicates with project stakeholders, various departments, and applicable vendors to achieve design intent.
  • Updates management regarding project strategy, progress, and alignment with executive direction.
  • Creates and produces reports regarding projects for management and team members.
  • Performs other related duties and projects as business needs require at direction of management.
Minimum Qualifications:
  • Bachelor's degree in Engineering or scientific related discipline, preferred.
  • Minimum five (5) years of experience in R&D performing higher value-added roles and functions.
  • Minimum three (3) years of experience in project management; medical device industry experience, a plus.
  • Demonstrated knowledge of International Organization for Standardization (ISO) and Food and Drug Administration (FDA) standards and requirements for medical devices.
  • Certification in Project Management, a plus.
Pay range: $81,000-115,000/yr
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time

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