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Intern Medical Device Engineer Jobs in Utah (NOW HIRING)

ELITechGroup Inc.

Bioengineering Intern

Logan, UT · On-site

$13 - $17.25/hr

Summary Applies knowledge of engineering, biology, and biomechanical principles to support the ... Currently pursuing a Bachelor's degree or equivalent in medical technology, medical device, biology ...

Epoch BioSciences

Bioengineering Intern

Logan, UT · On-site

$13 - $17.25/hr

Summary Applies knowledge of engineering, biology, and biomechanical principles to support the ... Currently pursuing a Bachelor's degree or equivalent in medical technology, medical device, biology ...

ELITechGroup Inc.

Bioengineering Intern

Logan, UT · On-site

$13 - $17.25/hr

SummaryApplies knowledge of engineering, biology, and biomechanical principles to support the ... medical device, biology, bioengineering, chemistry, or a related field from a four-year college or ...

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Showing results 21-40

All JobsIntern Medical Device Engineer JobsIntern Medical Device Engineer Jobs in Utah

Intern Medical Device Engineer information

What does an intern medical device engineer do?

An Intern Medical Device Engineer assists in the design, development, and testing of medical devices under the supervision of experienced engineers. Their responsibilities may include conducting research, creating prototypes, analyzing data, and ensuring products meet regulatory standards. Interns often collaborate with cross-functional teams and gain hands-on experience in the medical device industry. This role provides valuable exposure to engineering processes and helps interns build skills required for a future career in biomedical engineering.

What types of projects and responsibilities can an intern medical device engineer expect during their internship?

As an Intern Medical Device Engineer, you can expect to participate in hands-on projects such as assisting in prototype development, performing laboratory testing, and collecting and analyzing data for product improvement. You'll often work closely with senior engineers, quality assurance teams, and regulatory specialists to ensure devices meet safety and compliance standards. Interns may also help prepare technical documentation and contribute to brainstorming sessions for new product features, providing a well-rounded exposure to the medical device development process. This collaborative environment offers valuable experience and networking opportunities for future career growth.

What are the key skills and qualifications needed to thrive as an intern medical device engineer?

To thrive as an Intern Medical Device Engineer, you need a solid background in biomedical engineering or a related field, along with foundational knowledge of device design and regulatory standards. Familiarity with CAD software, prototyping tools, and basic laboratory testing equipment is typically required, and coursework or certification in medical device regulations can be advantageous. Strong problem-solving, teamwork, and communication skills help interns contribute effectively to multidisciplinary projects and adapt to feedback. These competencies are crucial for ensuring safe, innovative device development and successful collaboration in a regulated industry.

What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?

AspectIntern Medical Device EngineerJunior Medical Device Engineer
CredentialsTypically pursuing or recently completed a relevant degreeBachelor's or Master's in biomedical, mechanical, or related engineering
Work EnvironmentInternship setting, supervised, learning-focusedEntry-level professional role, more independent tasks
Employer & Industry UsageMedical device companies, research labs, internshipsMedical device companies, manufacturing, R&D teams

Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.

What are the most commonly searched types of Medical Device Engineer jobs in Utah?

The most popular types of Medical Device Engineer jobs in Utah are:

Intern Medical Device Engineer jobs near you

CQV Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

Contractor

Re-posted 19 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a CQV Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: CQV Engineer
Location: West Valley City, Utah
Duration: Long Term

Position Overview

We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities within a pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on ensuring that manufacturing equipment, utilities, facilities, and cleanroom systems are commissioned, qualified, and validated in compliance with GMP and regulatory requirements. The ideal candidate will have strong expertise in validation protocols, equipment qualification, regulatory compliance, and cross-functional collaboration to ensure reliable and compliant manufacturing operations.

Key Responsibilities

• Execute Commissioning, Qualification, and Validation (CQV) activities for manufacturing equipment, utilities, facilities, and cleanroom systems.

• Develop, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.

• Support commissioning and qualification of process equipment, HVAC systems, clean utilities, and facility infrastructure.

• Ensure compliance with GMP, FDA, ISPE, ASTM, and company quality standards throughout validation activities.

• Prepare validation documentation, technical reports, summary reports, and protocol deviations.

• Collaborate with Engineering, Manufacturing, Quality Assurance, Validation, and Maintenance teams to support project execution.

• Assist with investigations, deviations, CAPA, change control, and risk assessments related to validation activities.

• Participate in equipment startup, factory acceptance testing (FAT), site acceptance testing (SAT), and commissioning activities.

• Maintain validation documentation and ensure all records comply with regulatory and quality system requirements.

• Support continuous improvement initiatives to enhance validation processes, compliance, and operational efficiency.

Required Qualifications

• Bachelor's Degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, Biomedical Engineering, or a related engineering discipline.

• 3+ years of experience in Commissioning, Qualification, and Validation (CQV), Validation Engineering, or Equipment Qualification within pharmaceutical, biotechnology, or medical device manufacturing environments.

• Hands-on experience developing and executing IQ, OQ, and PQ protocols for manufacturing equipment, utilities, cleanrooms, and facility systems.

• Strong knowledge of GMP, FDA, ISPE, ASTM, validation lifecycle, and regulatory compliance requirements.

• Experience with equipment commissioning, facility qualification, utility validation, and cleanroom validation.

• Familiarity with validation documentation, protocol execution, deviation management, CAPA, change control, and risk assessment processes.

• Experience supporting FAT, SAT, equipment startup, and engineering project activities.

• Strong technical documentation, analytical, troubleshooting, and problem-solving skills.

• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated manufacturing environment.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Knowledge of computerized systems validation (CSV), process validation, Lean Manufacturing, or Six Sigma methodologies is an added advantage.

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/