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Temp Quality Engineer Medical Device Jobs (NOW HIRING)

Talentry, LLC

Be Seen First

Sr. Mechanical Engineer - Medical Device

San Diego, CA · On-site

$130K - $180K/yr

Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a ... You'll work closely with systems, electrical, quality, regulatory, operations, and lab teams to ...

Saxon Global

QA ENGINEER

Saint Augustine, FL · On-site

Medical Device Quality Engineer Position Type :Contract Projected Start Date :08-09-2017 Zip Code :33716 City :St. Petersburg State :FL Required Skills : ISO 9000 Not looking for a Design or testing ...

Mizuho OSI

Systems Engineer, Medical Device

Union City, CA · On-site

$82K - $150K/yr

... Systems Engineer you will be part of a small, agile team; responsible for medical device ... Understand, follow and support Mizuho OSI's internal Quality System policies, procedures and work ...

Stark Pharma Solutions Inc

Quality Engineer

Cambridge, MA · On-site

$78K - $101K/yr

Medical Device / Pharmaceutical Job Summary We are seeking a highly motivated and detail-oriented Quality Engineer to support quality assurance and compliance activities within a GMP-regulated ...

Mizuho OSI

Systems Engineer, Medical Device

Union City, CA · On-site

$82K - $150K/yr

... Systems Engineer you will be part of a small, agile team; responsible for medical device ... Understand, follow and support Mizuho OSI's internal Quality System policies, procedures and work ...

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Temp Quality Engineer Medical Device information

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$45K

$84K

$119K

How much do temp quality engineer medical device jobs pay per year?

As of Aug 17, 2026, the average yearly pay for temp quality engineer medical device in the United States is $84,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $93,000.00 per year, depending on experience, location, and employer.

What is the difference between Temp Quality Engineer Medical Device vs Temp Quality Technician Medical Device?

AspectTemp Quality Engineer Medical DeviceTemp Quality Technician Medical Device
CredentialsBachelor's in Engineering, Quality or related field; certifications like CQE often preferredHigh school diploma or associate degree; technical certifications beneficial
Work EnvironmentDesign, develop, and improve quality systems; collaborate with engineering teamsPerform inspections, testing, and documentation; support quality assurance processes
Employer & Industry UsageUsed in medical device manufacturing companies for process developmentCommonly employed in quality control labs and manufacturing lines

The Temp Quality Engineer Medical Device focuses on developing and improving quality systems, requiring more technical expertise and engineering knowledge. In contrast, the Temp Quality Technician Medical Device primarily handles testing, inspections, and documentation tasks. Both roles are essential in ensuring product quality but differ in responsibilities and required qualifications.

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Temp Quality Engineer Medical Device jobs near you
Infographic showing various Temp Quality Engineer Medical Device job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.

Manufacturing Engineer - Medical Device

Volto USA

Raynham, MA • On-site

$75K - $97K/yr

Contractor

Re-posted 29 days ago

Job description

About the Role

We are seeking a Manufacturing Engineer with experience in medical device or regulated manufacturing environments to support manufacturing process development, validation, and production readiness activities. The ideal candidate will have hands-on experience with validation protocols, process engineering, equipment commissioning, and cross-functional collaboration in a highly regulated environment.

This role requires strong technical writing skills, process validation expertise, and the ability to support manufacturing operations, quality initiatives, and continuous process improvements.

Key Responsibilities
  • Author and execute validation protocols and reports including IQ, OQ, and PQ
  • Develop and implement manufacturing processes and production procedures
  • Support process studies, investigations, root cause analysis, and corrective actions
  • Update manufacturing specifications, routes, travelers, and procedures within PLM systems
  • Coordinate new asset commissioning and manufacturing readiness activities
  • Collaborate with Operations, Engineering, Quality, Planning, and OpEx teams
  • Work with OEM equipment manufacturers to define user requirements
  • Ensure compliance with FDA regulations and quality system requirements
  • Prepare technical reports, presentations, and manufacturing documentation
  • Support continuous improvement and process optimization initiatives
Required Skills
  • Manufacturing Engineering
  • Process Validation
  • IQ/OQ/PQ Protocols
  • Medical Device Experience
  • Root Cause Analysis
  • Technical Documentation
  • FDA Compliance
  • Process Engineering
  • PLM Systems
  • Microsoft Office
Preferred Qualifications
  • Experience with machining or metal finishing processes
  • Laser processing or automation experience
  • Knowledge of Minitab and statistical analysis tools
  • Understanding of GD&T principles
  • Experience working in regulated manufacturing environments
  • Ability to support global projects and travel as required
Qualifications
  • 2–4 years of manufacturing or process engineering experience
  • Bachelor’s degree in Engineering or related discipline preferred
  • Strong communication and interpersonal skills
  • Ability to work effectively with cross-functional teams
Preferred Industry Experience
  • Medical Devices
  • Regulated Manufacturing
  • Production Automation
  • Manufacturing Operations