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Quality Director Medical Device Jobs (NOW HIRING)

Quasent

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Medical Device Technician

Carlsbad, CA · On-site

$1K/wk

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You ... Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols. * Ability ...

Quasent

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Medical Device Technician

Vista, CA · On-site

$1K/wk

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You ... Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols. * Ability ...

Quasent

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Medical Device Technician

Vista, CA · On-site

$1K/wk

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You ... Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols. * Ability ...

Quasent

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Medical Device Technician

Carlsbad, CA · On-site

$1K/wk

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You ... Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols. * Ability ...

Lancesoft INC

Assembler (Medical device)

Durham, NC · On-site

$18 - $18.20/hr

Conduct quality inspections on production lines to ensure compliance with standards * Follow SOPs ... Medical device or manufacturing assembly experience * Experience using measuring tools or ...

Marquee Staffing - OC

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1st Shift - Medical Device Assembler

Irvine, CA · On-site

$21 - $25/hr

... play a direct role in assembling high-quality medical devices in accordance with approved ... Experience with medical device manufacturing (preferred) * Experience or certification as a trainer ...

Quasent

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Medical Device Technician

Carlsbad, CA · On-site

$1K/wk

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You ... Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols. * Ability ...

SlingShot Connections

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Medical Device Assembler

San Clemente, CA · On-site

$20.25 - $22.27/hr

... direct oversight * Other duties as assigned to support production, engineering, clinical, and QA ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

Spherion Staffing Corporation

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Medical Device Assembler

Milpitas, CA · On-site

$25 - $27/hr

We are seeking a Medical Device Assembler to support the build and integration of capital medical ... Strictly follow cGMP and quality-driven procedures; knowledge of ESD is a plus. ● Communication:

Kellton Tech

Medical Device Quality Engineer

Madison, WI · On-site

$40 - $45/hr

Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 Schedule: Onsite, Monday-Friday (standard business hours) Summary The Senior Quality Analyst/Engineer is responsible ...

Belcan

Assembler - Medical Device

Pittsburgh, PA

$18/hr

Job Title: Assembler - Medical Device Location: Pittsburgh, PA ZIP Code: 15238 Start Date: Right ... Perform visual inspections and quality checks * Use testing and inspection equipment to verify ...

IT MINDS L.L.C.

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a remediation project here on site in Delaware. What is the project the contractor will be working on? • ...

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Quality Director Medical Device information

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$31K

$125.6K

$213.5K

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

As of Jun 14, 2026, the average yearly pay for quality director medical device in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What are some common challenges a Quality Director faces in the medical device industry, and how can they be addressed?

A Quality Director in the medical device industry often encounters challenges such as navigating complex regulatory requirements, maintaining compliance across global markets, and ensuring consistent product quality during rapid growth or innovation. Proactive communication with cross-functional teams, continuous training on evolving standards like ISO 13485 and FDA regulations, and implementing robust quality management systems are key strategies to address these challenges. Building a culture of quality and fostering close collaboration between departments like R&D, manufacturing, and regulatory affairs are also essential for success in this role.

What are the key skills and qualifications needed to thrive as a Quality Director in the Medical Device industry, and why are they important?

To thrive as a Quality Director in the Medical Device industry, you need deep expertise in quality management systems (such as ISO 13485), regulatory compliance (FDA, EU MDR), and a background in engineering or life sciences. Familiarity with risk management tools, CAPA systems, and regulatory submission processes, along with certifications like ASQ CQE or Six Sigma, is highly valued. Strong leadership, problem-solving, and communication skills are essential for managing teams and fostering a culture of quality. These skills and qualifications are crucial to ensuring product safety, regulatory approval, and continuous improvement within highly regulated environments.

What does a Quality Director do in the medical device industry?

A Quality Director in the medical device industry is responsible for overseeing the development, implementation, and maintenance of quality management systems to ensure products meet regulatory and industry standards. They lead quality assurance teams, manage compliance with FDA and international regulations, and drive continuous improvement initiatives. Their work helps guarantee that medical devices are safe, effective, and reliable for patients and healthcare providers.
More about Quality Director Medical Device jobs
What cities are hiring for Quality Director Medical Device jobs? Cities with the most Quality Director Medical Device job openings:
What are the most commonly searched types of Quality Medical Device jobs? The most popular types of Quality Medical Device jobs are:
What states have the most Quality Director Medical Device jobs? States with the most job openings for Quality Director Medical Device jobs include:
What job categories do people searching Quality Director Medical Device jobs look for? The top searched job categories for Quality Director Medical Device jobs are:
Quality Director Medical Device jobs near you
Infographic showing various Quality Director Medical Device job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.
Medical Device Technician

Medical Device Technician

Quasent

Carlsbad, CA • On-site

$1K/wk

Contractor

PTO

Posted 4 days ago

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Job description

We are seeking 10 Mechanical Assemblers to manufacture intricate medical device components. You will use precise measurement tools to build products that directly impact professional and college athletes.

Responsibilities:

  • Construct medical devices, subassemblies and components following exact engineering drawings and Standard Operating Procedures (SOPs).
  • Conduct visual inspections and use precision measuring instruments (calipers, micrometers, microscopes) to verify parts meet strict tolerances.
  • Practice good documentation practices (GDP) by accurately filling out Device History Records (DHRs), work orders, and production logs.
  • Utilize a variety of hand/power tools, soldering equipment, bonding materials, and epoxy delivery systems.

Basic Requirements:

  • High School, GED or equivalent.
  • 2+ years of mechanical, electro-mechanical or medical device assembly experience.
  • Exceptional manual dexterity and fine motor skills to handle microscopic or intricate components under a microscope.
  • Basic understanding of GMP guidelines, ISO 13485 quality standards and safety protocols.
  • Ability to sit or stand for extended periods, wear required safety equipment and lift up to 30 pounds.