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Quality Assurance Associate Medical Devices Jobs

NY · On-site

Responsibilities Role Summary Quality Assurance Associate independently performs tasks with minimal ... A thorough knowledge of cGMP regulations as they apply to Drugs and Medical Devices is required.

The Quality Assurance Associate must demonstrate a high level of individual responsibility and ... medical condition, family care status, marital status, domestic partner status, sexual orientation ...

The Quality Assurance Associate must demonstrate a high level of individual responsibility and ... medical condition, family care status, marital status, domestic partner status, sexual orientation ...

Quality Assurance Associate

Redwood City, CA · On-site

$41.47 - $62.21/hr

The Quality Assurance Associate must demonstrate a high level of individual responsibility and ... medical condition, family care status, marital status, domestic partner status, sexual orientation ...

... medical industry. Our commitment to the highest standards is absolute, from the time the client ... The Quality Assurance Associate will ensure each center process adheres to all federal, local, and ...

ECOM is a company focused on subsurface data and insights, and they are seeking a QA Associate to ensure quality assurance and testing for their software applications. The role involves web testing ...

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Quality Assurance Associate Medical Devices information

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$12

$29

$62

How much do quality assurance associate medical devices jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for quality assurance associate medical devices in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What are popular job titles related to Quality Assurance Associate Medical Devices jobs?

For Quality Assurance Associate Medical Devices jobs, the most frequently searched job titles are:

Infographic showing various Quality Assurance Associate Medical Devices job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

QUALITY ASSURANCE ASSOCIATE/ Medical Device

Philadelphia, PA • On-site

Full-time

Re-posted 28 days ago


Job description

Company Description

Our client is a medical device company dedicated to offering innovative solutions for treatment of chronic heart failure. The Company's developments are based on its proprietary technology for administrating Cardiac Contractility Modulation therapy.


Job Description
  • Write and review of SOPs and other quality assiuance related technical data forms and quality documents
  • proper maintenance of control documents in Quality Assurance
  • Control documents to differents departments
  • Review validation protocols for GMP compliance
  • Assist in carrying out internal quality audits on company systems and documentations
  • perform investigations on non-conformances and customer complaint close out and corrective actions
  • Audit on-going vendors, systems and documents to assure quality assurance compliance with regard to all internal procedures as well as regulatory guidelines
  • Provide GCP/ QA support and avdvice to internal and external clients
  • Ensure the timely and effective follow up  to all identified or assigned quality issues
  • Maintains and demonstrates understanding of global standards, regulation and regulatory bodies to include but not limited to ISO13485, 21FR; part 820 AIMD
  • Assist in the maintenance ogf Quality Management System under direction of Director, Quality Assurance
  • Participate in Mock inspections for FDA inspection preparation


Qualifications

Ability to work independently with little or no supervision

Exeptional oral and written communication capabilities

Advance computer knowledge in MS Office programs

Bachelors's Dregree in related field

4-6 years  related experience

Experience working in regulated environment with medical devices

Experience with FDA inspections and /or Notified Bodies Audits desirable

Additional Information

All your information will be kept confidential according to EEO guidelines.