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 ...
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Lafayette, IN · On-site
$69K - $89K/yr
... medical device roles. I came across your profile and wanted to see if you are open to new ... Quality Engineer Location: Lafayette, IN Duration: 6-12 Month Contract Job Summary We are seeking a ...
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Lafayette, IN · On-site
$69K - $89K/yr
... medical device roles. I came across your profile and wanted to see if you are open to new ... Quality Engineer Location: Lafayette, IN Duration: 6-12 Month Contract Job Summary We are seeking a ...
Warsaw, IN · On-site
$69K - $89K/yr
CQE). * Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Travel Expectations Less than 20% overnight travel. EOE/M/F/Vet/Disability ...
Warsaw, IN · On-site
$69K - $89K/yr
CQE). * Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred Travel Expectations Less than 20% overnight travel. EOE/M/F/Vet/Disability ...
Warsaw, IN · On-site
$69K - $89K/yr
The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process.
Warsaw, IN · On-site
$69K - $89K/yr
The Post Market Quality Engineer is responsible for medical device complaint investigations and write-ups as part of the Complaint Handling, Medical Device Reporting and Vigilance Reporting process.
Summary The Quality Assurance Engineer will support the organization towards compliance of ... Ensure compliance with FDA, ISO 13485, and other relevant regulatory standards for medical device ...
Summary The Quality Assurance Engineer will support the organization towards compliance of ... Ensure compliance with FDA, ISO 13485, and other relevant regulatory standards for medical device ...
$87K - $120K/yr
Engineering services include process development, cell management, tool design, and CNC programming. Qualifications Familiarity with control procedures, such as the Engineering Change Notification ...
$87K - $120K/yr
Engineering services include process development, cell management, tool design, and CNC programming. Qualifications Familiarity with control procedures, such as the Engineering Change Notification ...
Plymouth, IN · On-site
$65K - $84K/yr
... CAPA's, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Plymouth, IN · On-site
$65K - $84K/yr
... CAPA's, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Warsaw, IN · On-site
$69K - $89K/yr
CQE). o Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred. o Bachelors degree in sciences, health care certificates, mechanical or biologic ...
Warsaw, IN · On-site
$69K - $89K/yr
CQE). o Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred. o Bachelors degree in sciences, health care certificates, mechanical or biologic ...
Plymouth, IN · On-site
$65K - $84K/yr
... CAPA's, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Plymouth, IN · On-site
$65K - $84K/yr
... CAPA's, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Westfield, IN · On-site
$61K - $122K/yr
Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Westfield, IN · On-site
$61K - $122K/yr
Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Westfield, IN · On-site
$50K - $101K/yr
Quality Engineer I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Westfield, IN · On-site
$50K - $101K/yr
Quality Engineer I Working at Abbott At Abbott, you can do work that matters, grow, and learn, care ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Westfield, IN · On-site
$61K - $122K/yr
Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Westfield, IN · On-site
$61K - $122K/yr
Quality Engineer II Working at Abbott At Abbott, you can do work that matters, grow, and learn ... Medical Device experience Apply Now Learn more about our health and wellness benefits, which ...
Plymouth, IN · On-site
$65K - $84K/yr
... CAPAs, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Quick apply
Plymouth, IN · On-site
$65K - $84K/yr
... CAPAs, Quality Alerts, Retraining and data collection as needed * Oversight of CMM programming ... Conform to ISO13485, 21 CFR Part 820, and medical device industry requirements * Other work-related ...
Participate in FDA-related activities and follow quality protocols. * Participate in grant writing ... Proven experience in embedded systems engineering, preferably in the medical device industry.
Participate in FDA-related activities and follow quality protocols. * Participate in grant writing ... Proven experience in embedded systems engineering, preferably in the medical device industry.
Participate in FDA-related activities and follow quality protocols. * Participate in grant writing ... Proven experience in embedded systems engineering, preferably in the medical device industry.
Quick apply
Participate in FDA-related activities and follow quality protocols. * Participate in grant writing ... Proven experience in embedded systems engineering, preferably in the medical device industry.
$68K - $88K/yr
Experience you'll need to have: * 6+ years of experience in manufacturing quality engineering in electronics, medical device, automotive, pharmaceutical, or precision manufacturing environments using ...
$68K - $88K/yr
Experience you'll need to have: * 6+ years of experience in manufacturing quality engineering in electronics, medical device, automotive, pharmaceutical, or precision manufacturing environments using ...
Indianapolis, IN · On-site
$68K - $88K/yr
Experience you'll need to have: * 6+ years of experience in manufacturing quality engineering in electronics, medical device, automotive, pharmaceutical, or precision manufacturing environments using ...
Indianapolis, IN · On-site
$68K - $88K/yr
Experience you'll need to have: * 6+ years of experience in manufacturing quality engineering in electronics, medical device, automotive, pharmaceutical, or precision manufacturing environments using ...
Westfield, IN · On-site
$17.25 - $21/hr
We are hiring a Medical Device Assembler with microscope experience to support the production of high-quality medical devices in a manufacturing environment. This role involves assembling, testing ...
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Westfield, IN · On-site
$17.25 - $21/hr
We are hiring a Medical Device Assembler with microscope experience to support the production of high-quality medical devices in a manufacturing environment. This role involves assembling, testing ...
Fishers, IN · On-site +1
$114K - $151K/yr
Senior Software Engineer We are a dynamic and innovative medical device startup developing a point ... Develop high-quality, efficient, and maintainable code. * Design intuitive and visually engaging ...
Fishers, IN · On-site +1
$114K - $151K/yr
Senior Software Engineer We are a dynamic and innovative medical device startup developing a point ... Develop high-quality, efficient, and maintainable code. * Design intuitive and visually engaging ...
$22.61 is the 25th percentile. Wages below this are outliers.
$20.36 - $24.62
47% of jobs
The median wage is $25.81 / hr.
$24.62 - $28.88
9% of jobs
$28.88 - $33.15
0% of jobs
$33.15 - $37.41
4% of jobs
$40.94 is the 75th percentile. Wages above this are outliers.
$37.41 - $41.67
17% of jobs
$41.67 - $45.94
8% of jobs
$45.94 - $50.20
7% of jobs
$50.20 - $54.46
4% of jobs
$54.46 - $58.72
0% of jobs
$58.72 - $62.99
0% of jobs
$62.99 - $67.25
2% of jobs
$20
$34
$67
| Aspect | Quality Engineer Medical Device | Quality Assurance Specialist Medical Device |
|---|---|---|
| Certifications | ISO 13485, Six Sigma, ASQ certifications | ISO 13485, Six Sigma, ASQ certifications |
| Work Environment | Design, development, manufacturing, and process improvement | Auditing, compliance, documentation, and process verification |
| Employer & Industry Usage | Medical device manufacturers, R&D labs | Medical device companies, regulatory agencies, consulting firms |
While both roles focus on quality in the medical device industry, a Quality Engineer Medical Device primarily works on product design, process development, and continuous improvement. In contrast, a Quality Assurance Specialist Medical Device emphasizes compliance, auditing, and ensuring adherence to regulatory standards. Both roles are essential for maintaining product safety and quality, but they differ in scope and daily responsibilities.
As a quality engineer for medical devices, you oversee the continual improvement of medical devices as well as the design and manufacturing of new devices. Your duties are to develop prototypes, assess the quality of manufacturing standards, and develop guidelines for technological improvement. You also work closely with medical device engineers to ensure sufficient documentation and standardization, which helps users and service technicians test and maintain the safety of devices. Your responsibilities as a medical device quality engineer relate to all aspects of the product life cycle, from prototyping to the supply chain to production.
$85K - $115K/yr
Full-time
Posted 4 days ago
TekWissen provides a unique portfolio of innovative capabilities that seamlessly combines clients insights, strategy, design, software engineering, and systems integration.
www.tekwissen.com
Responsible for gathering relevant, factual information and data in order to solve quality related problems. Resolve issues by identifying and applying solutions from acquired technical experience and guided precedents. Plan and lead projects by identifying and organizing activities into time dependent sequencing with realistic timelines. Work effectively/ productively with all departments by developing a team atmosphere. Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities.
B.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 of education and experience.
All your information will be kept confidential according to EEO guidelines.
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TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Recruiting and staffing services
501 - 1,000 Employees
Ann Arbor, MI, US
2009
