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Weekend Medical Device Quality Assurance Jobs (NOW HIRING)

Medical Device Quality Inspector Location: Madison, WI Pay Rate: $30/hr. Position Summary: The ... within the QA unit. * Conduct quality reviews for quarantine releases on non-reportable, non ...

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... of Quality Assurance experience in a cGMP-regulated environment (medical device experience ... Primarily onsite Monday-Friday, with occasional extended hours, weekends, or holidays to support ...

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $25-30/hr. on W2 **Opportunity to earn overtime pay** The Medical Device Quality Inspection group is responsible for assuring ...

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Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $30/hr. on W2 Job Summary The Medical Device Quality Inspector is responsible for ensuring that materials, processes, and ...

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QA/RA Consultant

Boston, MA · On-site

$130K - $150K/yr

You've built or significantly improved quality systems at medical device companies, consulting firms, or high-growth startups, and you're excited to combine your regulatory expertise with AI-powered ...

... medical device standards. ● Develop, implement, and maintain quality system processes, including procedures for design control, production, process validation, and post-market activities. ● Lead ...

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Weekend Medical Device Quality Assurance information

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$12

$29

$62

How much do weekend medical device quality assurance jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for weekend medical device quality assurance 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 is the difference between Weekend Medical Device Quality Assurance vs Medical Device Quality Control Technician?

AspectWeekend Medical Device Quality AssuranceMedical Device Quality Control Technician
CertificationsISO 13485, Six Sigma, GMP trainingISO 13485, GMP, inspection certifications
Work EnvironmentPart-time, weekend shifts, office/lab settingFull-time, day shifts, manufacturing/inspection setting
Primary FocusEnsuring quality processes and complianceInspecting and testing devices for defects
Industry UsageUsed in regulated medical device companiesUsed in manufacturing and quality labs

Weekend Medical Device Quality Assurance roles focus on maintaining quality standards and compliance during weekend shifts, often involving process audits and documentation. Medical Device Quality Control Technicians primarily perform inspections and testing of devices to identify defects during manufacturing. While both roles require knowledge of industry standards, QA roles emphasize process oversight, whereas QC roles focus on product testing.

More about Weekend Medical Device Quality Assurance jobs
What cities are hiring for Weekend Medical Device Quality Assurance jobs? Cities with the most Weekend Medical Device Quality Assurance job openings:
What are the most commonly searched types of Medical Device Quality Assurance jobs? The most popular types of Medical Device Quality Assurance jobs are:
What states have the most Weekend Medical Device Quality Assurance jobs? States with the most job openings for Weekend Medical Device Quality Assurance jobs include:
What job categories do people searching Weekend Medical Device Quality Assurance jobs look for? The top searched job categories for Weekend Medical Device Quality Assurance jobs are:
Infographic showing various Weekend Medical Device Quality Assurance job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.
Sr. Manager, Medical Device Quality Assurance

Sr. Manager, Medical Device Quality Assurance

Regeneron Pharmaceuticals

Valley, AL

$126K - $206K/yr

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

13th of 73 rated pharmaceutical


Job description

Build our future together:

Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will lead a team engineer and quality specialists.

When & where:

  • Monday-Friday, 8am-4:30pm
  • Location: East Greenbush, New York, United States

What you'll do:

  • Manage, mentor, and develop quality engineering and compliance teams
  • Standardize, streamline, and improve processes across sustaining and compliance
  • Implement digital, data-driven tools for accurate, consistent, and timely reporting
  • Lead teams through complex, ambiguous challenges in a pharmaceutical/medical device environment
  • Sustaining Engineering Support:
    • Support sustaining engineering programs through risk assessment, design change management, and maintenance of the Design History File and Risk Management File
    • Advice and actively participate in Design Reviews associated with combination products
    • Provide QA and technical support to quality engineers and project teams during ongoing maintenance of the combination product
    • Interact with partners and contract organizations to ensure accurate completion of project milestones, including post-commercialization activities
  • Combination Product Support:
    • Act as Management Representative for the combination products QMS; own policies and procedures
    • Support regulatory inspections and partner audits for combination products
    • Keep the QMS current and inspection-ready via monitoring, gap assessments, and updates

This role requires:

  • B.S in Engineering and 8+ years of experience; including combination product or medical device experience; or equivalent combination of education & experience
  • Previous supervisory/ people leadership experience
  • Knowledge of the combination device development and lifecycle process

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$126,300.00 - $206,100.00

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