Engineering Technician

Stealth mode (medical device); Chula Vista (CA); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Competitive salary and benefits

Job summary

Stealth startup is seeking an Engineering Technician to support assembly, testing, and production of medical devices in a regulated environment. The role requires hands-on experience with assembly processes, documentation, and quality systems, with a focus on lean improvements.

You will work closely with engineering, quality, and production teams to ensure on-time delivery, troubleshoot equipment, and maintain calibration and maintenance of devices and tooling.

Qualifications

• 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.

Responsibilities

• Perform complex assembly tasks for medical devices, ensuring compliance with blueprints, schematics, and work instructions.
• Inspect components and finished products for adherence to quality standards and regulatory requirements (GMP, ISO).
• Maintain accurate documentation for quality assurance and production records.
• Identify and implement process improvements to enhance efficiency and reduce waste; apply lean manufacturing principles.
• Troubleshoot assembly and equipment issues, collaborating with engineering and quality teams to resolve problems.

Skills

Attention to detail

GMP knowledge

GDP knowledge

Blueprint reading

Teamwork

Problem-solving

Multi-tasking under pressure

MS Office proficiency

Education

High School Diploma or equivalent

Technical certifications (preferred)

Tools

Microsoft Office

Job description

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.

Position Summary

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.

Key Responsibilities

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.

Qualifications

• 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.

Skills

• 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.

Why Join Us?

• 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.