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Quality Manager Medical Device Jobs in Riverside, CA

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Medical Device Assembler, 4/10 Schedule 1st or 2nd Shift

Irvine, CA · On-site

$19 - $21.50/hr

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... quality results while using a microscope in a cleanroom environment. Essential Duties and ...

BioTalent

Verification Manager

Irvine, CA · On-site

Verification Manager - Medical Device Location: Irvine, CA (hybrid, 3 days onsite) with some ... S., partnering with Quality and Regulatory Affairs on MDR, CAPA, and vigilance documentation * Hire ...

Applied Medical

Quality Inspector

Lake Forest, CA

$18 - $23/hr

Applied Medical is a new generation medical device company with a proven business model and ... Demonstrate excellent time management and organizational skills. Preferred The following skills and ...

Applied Medical

Quality Inspector

Lake Forest, CA · On-site

$18/hr

Applied Medical is a new generation medical device company with a proven business model and ... Demonstrate excellent time management and organizational skills. Preferred The following skills and ...

Applied Medical

Quality Inspector

Lake Forest, CA

$18 - $23/hr

Applied Medical is a new generation medical device company with a proven business model and ... Demonstrate excellent time management and organizational skills. Preferred The following skills and ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

This role requires strong leadership, project management, and working knowledge of medical device quality system regulations and standards. Essential Functions and Main Duties * Manage Nihon Kohden ...

Nihon Kohden USA

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

This role requires strong leadership, project management, and working knowledge of medical device quality system regulations and standards. Essential Functions and Main Duties * Manage Nihon Kohden ...

Balda C Brewer

Quality Manager

Ontario, CA · On-site

$140K - $180K/yr

Responsible to manage, promote, and continuously maintain a compliant quality management system by ... At least 5 years of leading and implementing quality systems in a pharmaceutical or medical device ...

Aerotek

Assembler

Irvine, CA · On-site

$21 - $22.50/hr

What You'll Do As a Medical Device Assembler, you'll use precision tools and microscopes to assemble and inspect critical medical components that meet the highest quality standards. Key ...

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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.

P/T Quality Systems Complaints Specialist

OrthAlign Inc.

Irvine, CA • On-site

$30/hr

Part-time

Posted 11 days ago

Job description

OrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for a Quality Systems Complaints Specialist. The Quality Systems Complaints Specialist determines the legitimacy of complaint feedback and processes complaint files. This role works with cross-functional teams to communicate with customers and coordinate complaint product return. This role also reviews complaint device history records, supports complaint investigation, and contributes to the ongoing improvement of the quality system.


NOTE: Only local candidates will be considered for the position. Out of state candidates are not eligible.

You will:

  • Perform initial assessment of customer feedback to determine if the information represents a complaint.
  • Support the investigation of returned complaint product and complaints where product was not returned.
  • Perform reviews of the complaint device history records.
  • Collaborate with Customer Service, Engineering and Operations teams to process complaints in a compliant and timely manner.
  • Communicate with customers as applicable, including issuance of closeout letters.
  • Develop and maintain product knowledge of existing and new products. Identify, propose, and drive opportunities for improvement, including review and revision of procedures and associated documents.

You need:

  • At least 1 year of experience in medical device quality or operations environment
  • Strong proficiency using MS Office Suite (e.g., Word, Excel, Outlook)
  • Familiarity with medical device regulations ISO 13485, 21CFR820 and complaints
  • Strong verbal and written communication skills are essential
  • Experience with problem solving and root cause analysis
  • Strong interpersonal skills including negotiating and relationship management
  • Keen attention to detail and strong organizational skills
  • Experience using an electronic quality management system (e.g. - QCBD, EtQ, etc.) and an electronic document management system/PLM (e.g. - Oracle's Agile, Documentum, etc.)


NOTE: We are unable to provide any type of sponsorship at this time.

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