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Risk Management Quality Engineer Jobs in Utah (NOW HIRING)

TekCommands Inc

Quality Engineer

Draper, UT · On-site

$67K - $86K/yr

... risk management files, review and revise pFMEAs in conjunction with BU PMS team where applicable ... Other: CQE (Certified Quality Engineer), if applicable Preferred * Good documentation ...

Quality Electrical Systems

Quality Engineer

West Jordan, UT · On-site

$67K - $86K/yr

Overview The Quality Engineer is responsible for developing, maintaining, and improving Quality ... Manage corrective actions and verify the effectiveness of implemented solutions. Conduct internal ...

Spectrum Plastics Group

Senior Quality Engineer

Sandy, UT · On-site

$118 - $128/hr

Position Sr. Quality Engineer Location 8760 South Sandy Parkway, Suite 200, Sandy, UT 84070 Job ... Maintain Risk Management Files, dFMEAs, pFMEAs, and Control Plans. Support customer calls and be ...

SPECTRUM PLASTICS MASTER

Senior Quality Engineer

Sandy, UT · On-site

$118K - $128K/yr

POSITION: Sr. Quality Engineer LOCATION: 8760 South Sandy Parkway, Suite 200, Sandy, UT 84070 JOB ... Maintain Risk Management Files, dFMEAs, pFMEAs, and Control Plans. Support customer calls and be ...

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Risk Management Quality Engineer information

What is the difference between Risk Management Quality Engineer vs Quality Engineer?

AspectRisk Management Quality EngineerQuality Engineer
CertificationsISO 9001, Six Sigma, Risk Management certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentManufacturing, aerospace, automotive, industries with risk assessment focusManufacturing, software, healthcare, quality assurance roles
Primary FocusIdentifying and mitigating risks to ensure product safety and complianceEnsuring product quality, process improvements, defect reduction

The Risk Management Quality Engineer focuses on identifying and mitigating risks to ensure safety and compliance, often working in industries like aerospace and automotive. In contrast, a Quality Engineer concentrates on improving product quality and reducing defects across various sectors. While both roles require similar certifications and work environments, their core responsibilities differ in scope and focus.

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Risk Management Quality Engineer jobs near you

Quality Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

$69K - $89K/yr

Contractor

Re-posted 26 days ago

Job description

Hi,

My name is Sravani Dasari, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Quality Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows.

Job Title: Quality Engineer
Location: West Valley City, UT
Duration: Long Term

Position Overview

We are seeking an experienced Quality Engineer to support new product development, design quality, and remediation initiatives within a medical device environment. The ideal candidate will possess strong technical expertise in traceability matrix verification (TMV), risk management, verification and validation (V&V), and design integration activities. This role requires hands-on experience developing and executing quality engineering activities while ensuring compliance with applicable regulatory requirements.

Key Responsibilities

• Support new product development and design quality activities throughout the product lifecycle.
• Develop and execute traceability matrix verification (TMV), risk management, and verification & validation (V&V) activities.
• Participate in design integration and design remediation initiatives to ensure product quality and regulatory compliance.
• Support Design History File (DHF) remediation and documentation updates.
• Implement Design for Manufacturing (DFM) principles and support risk management architecture.
• Collaborate with cross-functional teams including R&D, Manufacturing, Regulatory Affairs, and Quality Assurance.
• Ensure compliance with FDA Quality System Regulations and internal quality procedures.
• Contribute to continuous improvement initiatives and quality system enhancements.

Required Qualifications

• Bachelor's Degree in Engineering or a related technical discipline.
• 4+ years of Quality Engineering experience within the medical device industry.
• Experience in New Product Development (NPD) and Design Quality activities.
• Strong knowledge of FDA 21 CFR Part 820 and medical device quality system requirements.
• Hands-on experience developing and executing TMV, Risk Management, and Verification & Validation (V&V) activities.
• Experience with Design Integration, Design Remediation, and Design History File (DHF) remediation.
• Knowledge of Design for Manufacturing (DFM) principles and risk management methodologies.
• Experience with vascular medical devices such as catheters, stents, guidewires, or related products is highly preferred.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/