Engineering Technician

ADP, Inc.; Westminster (CO); On-site; USD 34,000 - 40,000; Full time

Job summary

TriSalus Life Sciences in Westminster, CO is seeking a hands-on engineer-in-training to support the development and manufacturing of catheter-based medical devices. You will assist the engineering team with lab work, prototype assembly, and testing under FDA and ISO 13485 guidelines.

Candidates should have 1–3 years in a lab or medical device setting, strong mechanical aptitude, ability to read drawings, and familiarity with SolidWorks.

Qualifications

• High school diploma or GED required.
• 1–3 years of experience in a lab or medical device manufacturing environment.
• Mechanical aptitude.
• Experience with physical and mechanical testing; ISO/ASTM testing preferred.
• Ability to read and interpret engineering drawings.
• Basic knowledge of SolidWorks preferred.

Responsibilities

• Support the engineering team in development of catheter-based medical devices and improvement of manufacturing processes.
• Assist with day-to-day lab and manufacturing activities.
• Assemble medical device prototypes for evaluation and testing.
• Perform testing using standard lab and inspection equipment.
• Build tools and fixtures for testing and manufacturing.
• Support installation, troubleshooting, and maintenance of R&D equipment.
• Ensure activities comply with 21 CFR 820 and ISO 13485 requirements.
• Maintain safety and effective communication with supervisors and team members.

Skills

Mechanical aptitude

Physical & mechanical testing

Read engineering drawings

Independent work

Education

High school diploma or GED

Tools

SolidWorks

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Full Time TriSalus Life Sciences, Westminster, CO, US

Salary Range: $25.00 To $29.00 Hourly

Duties and Responsibilities: Support the engineering team in development of new catheter-based medical devices and improvement of manufacturing processes in accordance with FDA and international regulations.

• Support day-to-day engineering activities including hands on laboratory and manufacturing support.
• Assemble medical device prototypes for product evaluation and testing.
• Perform testing using standard laboratory and inspection equipment (e.g. force testers, calipers, flow models, gauges, etc.)
• Build tools and fixtures utilizing experience with common shop tools.
• Support installation, troubleshooting, and maintenance of R&D equipment.
• Execute work according to approved procedures and provide feedback to update or generate new procedures as needed.
• Ensure that product development and manufacturing activities are performed in accordance with U.S. Quality System Regulations (21 CFR 820) and ISO 13485 requirements.
• Assure individual and group safety when conducting all activities.
• Maintain clear and effective communication with supervisors and cross-functional team members.

Education & Certifications:

• High school diploma or GED required

Work Experience:

• 1-3 years experience working in a lab or medical device manufacturing environment.

Knowledge, Skills & Abilities:

• Mechanical aptitude
• Experience with physical and mechanical testing. ISO and ASTM testing experience preferred.
• Ability to read and interpret engineering drawings.
• Basic knowledge/capability of SolidWorks is preferred.
• Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices

Physical Requirements:

• Able to use a microscope and operate machinery.
• Must be able to lift and carry up to 40 lbs.