Engineering Technician

We are an innovative stealth startup dedicated to transforming the treatment of Peripheral Artery Disease (PAD) and Coronary Artery Disease (CAD) through a novel catheter-based technology. We’re seeking a motivated and energetic team member to help us bring life-changing solutions to market.

The Engineering Technician will play a key role in supporting engineering and production activities in the development, assembly, and testing of medical devices. This position requires advanced technical skills and a strong understanding of manufacturing processes, quality standards, and lean principles. The ideal candidate will have extensive experience in assembly operations, troubleshooting, and process improvement within regulated environments.

Assembly & Production Support:

• Perform complex assembly tasks for medical devices, ensuring compliance with blueprints, schematics, and work instructions.

Quality Assurance & Compliance:

• Inspect components and finished products for adherence to quality standards and regulatory requirements (GMP, ISO).
• Maintain accurate documentation for quality assurance and production records.

Process Improvement:

• Identify and implement process improvements to enhance efficiency and reduce waste.
• Apply lean manufacturing principles and support continuous improvement initiatives.

Technical Expertise:

• Troubleshoot assembly and equipment issues, collaborating with engineering and quality teams to resolve problems.
• Assist in equipment calibration and maintenance to ensure optimal performance.

Cross-Functional Collaboration:

• Coordinate with engineering, quality control, and logistics teams to meet production schedules and project deadlines.
• Provide feedback to management on production issues.

• High School Diploma or equivalent; technical certifications preferred.
• 2-5+ years of experience in medical device manufacturing or related industry.
• Strong knowledge of assembly processes, tools, and quality systems regulations.
• Ability to read and interpret technical documents, blueprints, and schematics.
• Basic knowledge of mechanical, electrical, or computer systems.

• Attention to detail and problem-solving ability.
• Proficiency in Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Ability to follow technical instructions, procedures, and test methods with attention to detail.
• Working knowledge of Microsoft Office Applications (Word, Excel, PowerPoint).
• Excellent work ethic with strong attention to detail.
• Ability to work as a team member and ability to be very flexible, adaptable, and to work under pressure.
• Honesty, integrity, the ability to work with minimal supervision, a conscientious approach to meeting goals and

objectives, and the ability to handle pressure with grace and humor are equally important.

• Must be able to multi-task, remain calm, and adapt to the ever-changing requirements of a dynamic company.

• Be a key contributor to the development of life-saving medical technologies.
• Collaborate with a talented, multidisciplinary team in a highly innovative and regulated environment.
• Work with an experienced team with experience in small start-ups and large medical device companies.
• Competitive salary and benefits package, with opportunities for professional growth and development.