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We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections. There will be lot of engineering topics to also ...
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Be Seen First
We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections. There will be lot of engineering topics to also ...
Quick apply
Be Seen First
We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections. There will be lot of engineering topics to also ...
Warsaw, IN · On-site
$85K - $115K/yr
S. in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE) plus 3-5 years experience in a Quality Engineering role, or an equivalent combination ...
Warsaw, IN · On-site
$85K - $115K/yr
S. in engineering or an alternative Bachelor's degree program with certification as a quality engineer (e.g. CQE) plus 3-5 years experience in a Quality Engineering role, or an equivalent combination ...
Maple Grove, MN · On-site
Senior Design Assurance Engineer - Medical Device (Onsite - Arbor Lakes, MN) Contract Overview ... We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance ...
Maple Grove, MN · On-site
Senior Design Assurance Engineer - Medical Device (Onsite - Arbor Lakes, MN) Contract Overview ... We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance ...
Andover, MA · Hybrid
$89K - $121K/yr
... Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring endtoend design quality and compliance across the product ...
Andover, MA · Hybrid
$89K - $121K/yr
... Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring endtoend design quality and compliance across the product ...
Andover, MA · On-site
$89K - $121K/yr
... Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end-to-end design quality and compliance across the product ...
Andover, MA · On-site
$89K - $121K/yr
... Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end-to-end design quality and compliance across the product ...
Raynham, MA · On-site
$75K - $97K/yr
Collaborate with Operations, Engineering, Quality, Planning, and OpEx teams * Work with OEM ... Medical Device Experience * Root Cause Analysis * Technical Documentation * FDA Compliance
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Raynham, MA · On-site
$75K - $97K/yr
Collaborate with Operations, Engineering, Quality, Planning, and OpEx teams * Work with OEM ... Medical Device Experience * Root Cause Analysis * Technical Documentation * FDA Compliance
Software Engineer - Medical Device Product Development Location: Newark, DE (Hybrid) Experience: 7+ ... quality and regulatory requirements.The ideal candidate will have experience working in cross ...
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Software Engineer - Medical Device Product Development Location: Newark, DE (Hybrid) Experience: 7+ ... quality and regulatory requirements.The ideal candidate will have experience working in cross ...
Somerville, MA · On-site
$80K - $100K/yr
Somerville, MA Senior Mechanical Engineer - Medical Device Overview: Micro-Leads is a fast-paced ... Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and ...
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Somerville, MA · On-site
$80K - $100K/yr
Somerville, MA Senior Mechanical Engineer - Medical Device Overview: Micro-Leads is a fast-paced ... Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and ...
Somerville, MA · On-site
$80K - $100K/yr
Somerville, MA Senior Mechanical Engineer - Medical Device Overview: Micro-Leads is a fast-paced ... Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and ...
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Somerville, MA · On-site
$80K - $100K/yr
Somerville, MA Senior Mechanical Engineer - Medical Device Overview: Micro-Leads is a fast-paced ... Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and ...
Title: System Development Engineer- Medical Device Location: Zeeland, MI (Onsite) Duration: Long-Term Contract Key Requirements: * Bachelor's degree in Electrical Engineering, Computer Engineering ...
Title: System Development Engineer- Medical Device Location: Zeeland, MI (Onsite) Duration: Long-Term Contract Key Requirements: * Bachelor's degree in Electrical Engineering, Computer Engineering ...
Collaborate cross-functionally with Design, Quality, Regulatory, Manufacturing, and Project ... Experience in medical device development environments, particularly with Design History File (DHF ...
Collaborate cross-functionally with Design, Quality, Regulatory, Manufacturing, and Project ... Experience in medical device development environments, particularly with Design History File (DHF ...
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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 ...
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Be Seen First
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 ...
This role focuses on supporting Design History File (DHF) activities for medical device development projects, ensuring compliance with regulatory and quality system requirements. The engineer will be ...
This role focuses on supporting Design History File (DHF) activities for medical device development projects, ensuring compliance with regulatory and quality system requirements. The engineer will be ...
Raynham, MA · On-site
$74K - $96K/yr
Onsite Raynham MA We are seeking a Quality Engineer with strong Quality Systems (QMS) experience to support a leading medical device organization. This individual will play a key role in maintaining ...
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Raynham, MA · On-site
$74K - $96K/yr
Onsite Raynham MA We are seeking a Quality Engineer with strong Quality Systems (QMS) experience to support a leading medical device organization. This individual will play a key role in maintaining ...
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 ...
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 ...
... quality production processes. Working closely with R&D, QARA, and Production, the X-Ray Engineer ... medical device industry environment. Experience: * High-Voltage testing & process transition ...
... quality production processes. Working closely with R&D, QARA, and Production, the X-Ray Engineer ... medical device industry environment. Experience: * High-Voltage testing & process transition ...
Brooklyn Park, MN · On-site
$100K - $151K/yr
Quality Engineer Sr Position Summary The Quality Engineer Sr will support the Cretex Medical New ... Support and comply with the company Quality System, ISO, and medical device requirements * Read ...
Brooklyn Park, MN · On-site
$100K - $151K/yr
Quality Engineer Sr Position Summary The Quality Engineer Sr will support the Cretex Medical New ... Support and comply with the company Quality System, ISO, and medical device requirements * Read ...
Eden Prairie, MN · On-site
$105K - $125K/yr
Working alongside Engineering, Quality, Regulatory, Clinical, Marketing, and Operations, you'll ... Familiarity with medical device standards such as IEC 60601, IEC 62366, ISO 10993, or similar. Why ...
Eden Prairie, MN · On-site
$105K - $125K/yr
Working alongside Engineering, Quality, Regulatory, Clinical, Marketing, and Operations, you'll ... Familiarity with medical device standards such as IEC 60601, IEC 62366, ISO 10993, or similar. Why ...
Brooklyn Park, MN · On-site
$100K - $151K/yr
Quality Engineer Sr Position Summary The Quality Engineer Sr will support the Cretex Medical New ... Support and comply with the company Quality System, ISO, and medical device requirements * Read ...
Brooklyn Park, MN · On-site
$100K - $151K/yr
Quality Engineer Sr Position Summary The Quality Engineer Sr will support the Cretex Medical New ... Support and comply with the company Quality System, ISO, and medical device requirements * Read ...
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 ...
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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 ...
$23.76 is the 25th percentile. Wages below this are outliers.
$21.39 - $25.87
47% of jobs
The median wage is $27.12 / hr.
$25.87 - $30.35
9% of jobs
$30.35 - $34.83
0% of jobs
$34.83 - $39.31
4% of jobs
$43.02 is the 75th percentile. Wages above this are outliers.
$39.31 - $43.79
17% of jobs
$43.79 - $48.27
8% of jobs
$48.27 - $52.75
7% of jobs
$52.75 - $57.23
4% of jobs
$57.23 - $61.71
0% of jobs
$61.71 - $66.19
0% of jobs
$66.19 - $70.67
2% of jobs
$21
$36
$70
| Aspect | Freelance Quality Engineer Medical Device | Freelance Quality Assurance Specialist Medical Device |
|---|---|---|
| Certifications | ISO 13485, FDA regulations, GMP knowledge | ISO 13485, FDA regulations, GMP knowledge |
| Work Environment | Design, development, testing, and validation of medical devices | Auditing, compliance checks, documentation, and process validation |
| Employer & Industry Usage | Medical device manufacturers, R&D labs, consulting firms | Medical device companies, regulatory agencies, consulting firms |
Both roles require similar certifications and industry knowledge, but the Quality Engineer focuses on product development and testing, while the Quality Assurance Specialist emphasizes compliance, audits, and documentation. Freelance professionals in both roles serve the medical device industry but with different core responsibilities.
Contractor
Medical, Dental, PTO
Posted 18 days ago
We need good Freelance Quality Inspector or even a good Quality engineer (either junior or retired) who is oriented towards carrying out inspections.
There will be lot of engineering topics to also inspect as a part of ONSOURCE INSPECTION.
on source inspector Stamping part supplier
Position: Source Inspector (Stamping Parts Supplier
Job Summary:
Perform source inspections at metal stamping suppliers to ensure parts comply with engineering drawings, quality standards, and purchase order requirements before shipment. Verify product conformity, documentation, and supplier process compliance to support on-time delivery of defect-free components.
Key Responsibilities:
Zobility is RGBSI's workforce management and staffing division. RGBSI is a multi-national corporation headquartered in Troy, MI with branches throughout the USA, Canada, Germany, and India.
Sourced by ZipRecruiter
Recruiting and staffing services
1,001 - 5,000 Employees
Troy, MI, US