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Director Engineering Medical Device Jobs in Utah

Ambition 24Hours Inc

Senior Manager ft

Salt Lake City, UT · On-site

$165K - $188K/yr

Lead and develop teams of scientists, engineers, and technical professionals * Drive materials ... Medical device industry experience * Leadership of teams (6-8 direct reports) * Minimum 3 years of ...

Varsity Tutors

Biomedical Engineering Tutor

Logan, UT · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Provo, UT · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

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All JobsEngineering Medical Device JobsDirector Engineering Medical Device JobsDirector Engineering Medical Device Jobs in Utah

Director Engineering Medical Device information

What is a director engineering medical device?

A Director of Engineering in the medical device industry leads the design, development, and testing of medical technologies while ensuring compliance with regulatory standards. They manage engineering teams, oversee project timelines, and collaborate with cross-functional departments, including R&D, quality assurance, and manufacturing. Their role involves strategic planning, resource allocation, and risk management to drive innovation and bring safe, effective medical devices to market.

What are the key skills and qualifications needed to thrive in the director engineering medical device position?

To excel as a Director Engineering Medical Device, you need extensive experience in engineering management, regulatory compliance (such as FDA and ISO standards), and a background in medical device design or related technical fields. Proficiency with product lifecycle management (PLM) tools, design control systems, and quality management certifications like Six Sigma or PMP are highly valuable. Outstanding leadership, strategic thinking, and the ability to communicate effectively across multidisciplinary teams help set top performers apart. These capabilities are crucial to successfully guide high-stakes projects, ensure regulatory compliance, and drive innovation in a highly regulated industry.

What are the typical challenges faced by a director of engineering in the medical device industry?

A Director of Engineering in the medical device field often navigates complex regulatory requirements while balancing innovation and speed-to-market. They frequently manage cross-functional teams, oversee rigorous testing and verification processes, and must ensure that all products meet strict quality and safety standards. Collaboration with regulatory, clinical, and marketing teams is essential to align technical development with business objectives. Additionally, adapting to evolving technology and changes in regulatory landscapes can present ongoing challenges, making strong leadership and adaptability key assets.

What are popular job titles related to Director Engineering Medical Device jobs in Utah?

For Director Engineering Medical Device jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Director Engineering Medical Device jobs in Utah look for?

The top searched job categories for Director Engineering Medical Device jobs in Utah are:

What cities in Utah are hiring for Director Engineering Medical Device jobs?

Cities in Utah with the most Director Engineering Medical Device job openings:

Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 18% Part Time, and 7% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Quality Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

$69K - $89K/yr

Contractor

Re-posted 9 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/