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Quality Systems Manager Medical Device Jobs (NOW HIRING)

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 ...

Senior Manager, Quality Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a ...

Manager, Quality Systems

Warrendale, PA · On-site

$115K - $130K/yr

... medical device production unit in Warrendale, PA. The position is responsible for reporting on the health of regulatory compliance and partnering with functional managers to develop and maintain ...

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... Medical Device company. The perfect candidate will perform the following activities: Key ... Complete the bulk download of documents and records from a Quality Management System. Required ...

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

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Ensure work is completed in compliance with company quality system and medical device regulations. Essential Functions * Assemble, test, and repair work per established work instructions, policies ...

Job Title: Medical Device Project Manager Location: Arlington, Tennessee Type: Contract ... quality. System One not only serves as a valued partner for our clients, but we offer eligible ...

Job Title: Medical Device Project Manager Location: Arlington, Tennessee Type: Contract ... quality. System One not only serves as a valued partner for our clients, but we offer eligible ...

WI · On-site

Leads the ongoing vision and implementation of the Quality Management System (QMS) -- spanning consumer, research, and medical device (SaMD) quality, including AI/ML-enabled and generative AI ...

Senior Specialist, Quality Systems

Carlsbad, NM · On-site

$69K - $95K/yr

Prior experience successfully implementing Quality Management Systems and electronic Quality System tools in regulated medical device and/or diagnostic companies * Expert knowledge of U.S. FDA ...

Quality Engineer

Longview, TX · On-site

$64K - $82K/yr

... management system meets the company's medical device expectations and goals. § Formulate and maintain accurate documentation to meet all quality system and medical device expectations. § Lead and ...

Showing results 21-40

Quality Systems Manager Medical Device information

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$54K

$98.6K

$154K

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

As of Sep 10, 2026, the average yearly pay for quality systems manager medical device in the United States is $98,613.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $122,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Quality Systems Manager Medical Device jobs?

For Quality Systems Manager Medical Device jobs, the most frequently searched job titles are:

Infographic showing various Quality Systems Manager Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $98,613 per year, or $47.4 per hour.

Project Manager - Medical Device

Irvine, CA • On-site, Remote

$81K - $115K/yr

Full-time

Re-posted 25 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