Associate Technician, Engineering - Clean Room Environment

Comrise; Salt Lake City (UT); On-site; USD 26,000 - 37,000; Full time

Benefits offered by this job

Training provided

On-site role

Clean room environment

Job summary

Comrise is seeking an Associate Technician, Engineering to support engineering and product development in a clean room environment. This hands-on role involves building prototypes, testing, documenting results, and aiding development of processes and equipment.

Training will be provided. Full-time onsite work with various early-morning schedules, including a 30-minute lunch break. The candidate will join cross-functional teams to ensure GLP/QS compliance and high-quality outputs.

Qualifications

• Two-year technical degree or equivalent practical experience.
• Hands-on experience with mechanical assembly, prototyping, tooling, fixturing, or similar technical work.
• Strong analytical, troubleshooting, and problem-solving skills.
• Good written and verbal communication skills.
• Strong attention to detail and commitment to quality.
• Ability to manage multiple assignments and work effectively with engineers and cross-functional teams.
• Experience coordinating with external vendors is preferred.
• Previous experience in medical device development, engineering, or a regulated manufacturing environment is a plus.

Responsibilities

• Assemble prototypes and products according to engineering designs, plans, and specifications.
• Perform prototype testing by following established engineering instructions and procedures.
• Accurately document test results and maintain required technical records.
• Assist engineering teams with obtaining necessary materials, supplies, tooling, and external services.
• Communicate project progress, assignment status, and potential issues to project engineers.
• Assist with the development and implementation of new product processes and procedures, including training others as needed.
• Support bench fixturing, tooling, and other hands-on prototyping activities.
• Ensure all work meets established quality standards and applicable Good Laboratory Practice (GLP) and Quality System (QS) requirements.
• Verify that products are tested using current, validated methods, processes, and specifications.
• Maintain a clean, organized, and compliant work environment while following applicable safety and quality procedures.

Skills

Mechanical assembly

Prototyping

Troubleshooting

Documentation

Communication

Quality consciousness

Education

Two-year technical degree

Job description

Location: Onsite

Pay Rate: $23/hour

Schedule: 6:00 AM–2:30 PM, 7:00 AM–3:30 PM, or 8:00 AM–4:30 PM

Position Overview

We are seeking an Associate Technician, Engineering to support engineering and product development activities in a clean room environment. In this hands‑on role, you will work alongside engineers, scientists, and cross‑functional teams to build prototypes, conduct testing, document results, and support the development of products, materials, processes, and equipment.

This is an excellent opportunity for a technically minded individual who enjoys hands‑on work, troubleshooting, and learning new processes. Training will be provided to help the selected candidate succeed in the role.

Key Responsibilities

• Assemble prototypes and products according to engineering designs, plans, and specifications.
• Perform prototype testing by following established engineering instructions and procedures.
• Accurately document test results and maintain required technical records.
• Assist engineering teams with obtaining necessary materials, supplies, tooling, and external services.
• Communicate project progress, assignment status, and potential issues to project engineers.
• Assist with the development and implementation of new product processes and procedures, including training others as needed.
• Support bench fixturing, tooling, and other hands‑on prototyping activities.
• Ensure all work meets established quality standards and applicable Good Laboratory Practice (GLP) and Quality System (QS) requirements.
• Verify that products are tested using current, validated methods, processes, and specifications.
• Maintain a clean, organized, and compliant work environment while following applicable safety and quality procedures.

Qualifications

• Two-year technical degree, associate degree, technical certificate, or equivalent practical experience.
• Hands‑on experience with mechanical assembly, prototyping, tooling, fixturing, or similar technical work.
• Strong analytical, troubleshooting, and problem‑solving skills.
• Good written and verbal communication skills.
• Strong attention to detail and commitment to quality.
• Ability to manage multiple assignments and work effectively with engineers and cross‑functional teams.
• Experience coordinating with external vendors is preferred.
• Previous experience in medical device development, engineering, or a regulated manufacturing environment is a plus.

Preferred Experience

• Two or more years of technical work experience, preferably in medical device development.
• Experience building prototypes, working with tools, assembling components, or conducting technical tests.
• Familiarity with technical documentation, test procedures, and quality requirements.

Work Environment and Schedule

• Full-time onsite position in a clean room environment.
• Available work schedules include 6:00 AM–2:30 PM, 7:00 AM–3:30 PM, or 8:0 AM–4:30 PM.
• A 30-minute lunch break is provided.
• Training will be provided for selected candidates.