×
Register Here to Apply for Jobs or Post Jobs. X

Engr , Quality

Job in Salt Lake City, Salt Lake County, Utah, 84116, USA
Listing for: Kaygen Inc.
Full Time position
Listed on 2026-07-18
Job specializations:
  • Engineering
    Quality Engineering
Job Description & How to Apply Below
Position: Engr 3, Quality
KAYGEN is an emerging leader in providing top talent for technology-based staffing services. We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries. on site 4 days onsite and 5th day remote Duration: 5 months Project:
The projects currently in progress are a material change of an existing component, and revision of IFU's across a wide spectrum of products. However, the project load in general is dynamic and changes over time, being primarily sustaining related design control product changes (i.e. vendor driven changes mostly). Education Bachelor's or higher 5-6 years of experience Med Device required

Job Summary:

This position is accountable for supporting new product development and product maintenance through the application of Quality engineering skills for medical devices. This person will handle projects and tasks, from product inception through product launch and maintenance and play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements.

Job Responsibilities:

(Primary Duties, Roles, and/or Authorities):

- Consistent application of technical principles, theories, concepts, techniques and quality sciences / tools (e.g. Acceptance sampling theory and application, statistical process control methods and application, measurement systems / test method knowledge and analysis, quality planning, failure analysis and investigation, design of experiments, process mapping and value stream analysis, hypothesis testing, descriptive statistics, process capability analysis, basic quality tools: pareto, box plots, histograms, scatter diagrams etc.,

risk management, supplier quality management, auditing, design / development tools, process validation, software validation, etc.).

- Is a team member representing Quality on sustaining engineering projects.

- Writes, reviews, and approves protocols, reports, and data analysis.

- Ensures that all design control and production / process control projects meet applicable regulatory (local and international), Corporate, and Unit requirements.

- Reviews and has Quality Engineering approval authority for new and modified design / process specifications including product performance specifications, test methods, etc.

- Influences and/or directs others across organization and cross functionally.

Education and Experience:

Requires a minimum of a bachelor’s degree. A minimum of 5 years relevant experience or a combination of equivalent education and relevant experience. Candidates must have experience within the medical device or equivalent regulated industry. Preferred qualifications include:

- Candidates with a science, technology, engineering, or math degree. Applied knowledge of applicable quality, engineering, regulatory, Corporate and/or Unit requirements.

- Proven problem-solving skills.

- Working knowledge of statistical analysis and software use (Minitab preferred).

- Basic use of risk management tools.

- General application of design controls. Preferred skills:

- Oral and written communication.

- Ability to work in cross-functional teams.

- Process validation experience (IQ/OQ/PQ).

- Design change experience including:
Design Controls / Design verification / Design validation / Risk management - Corrective and Preventive action.

- Project management.

- Supervisory experience

Shift: ['21 CFR 820 / QMSR', 'Basic statistical analysis skills for interpreting test data.', 'Design Transfer', 'Experience in Design Control principles', 'Experience in Medical Device domain or related regulated industry', 'ISO 14971 Risk Management', 'Risk Management activities'] Start: ['Disposable medical device experience'] At KAYGEN, we are always looking for dynamic, talented and experienced individuals. We invite you to join our team of talented IT professionals, consulting at client locations across the globe.

Our culture is team-orientated; we strive to stand by our core values of respect, honesty and integrity. Our team of experienced staffing experts will work with you to find you the best opportunity. For more information, please visit us at  Benefits:
Free Healthcare Insurance Vision and Dental Insurance 401(k) Retirement Plan Free Life Insurance Sick Time Off Achieve your Kaizen by clicking here. A unique and exclusive talent community supported by Kaygen, that includes programs like:
Certifications Mentorship Program Referrals Family and Wellness benefits Continuous Growth and Career Development
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary