Engineering Technician

Location: Irvine, CA

Shift: 2nd Shift (Monday - Thursday 1:00pm - 12:00am)
 

This is a 2nd shift position. During the initial training period, the selected candidate is expected to work 1st shift and will transition to 2nd shift upon completion of training.

As an Engineering Technician at ASP, this person provides technical support to maintain, troubleshoot, and sustain semi-automated and automated production equipment. Contributes to equipment reliability, quality compliance, and sustainable operation through effective maintenance and problem-solving.

Key Responsibilities:
- Troubleshoots, repairs, and maintains electro-mechanical and automated equipment to support safe, consistent, and compliant production.
- Performs preventive maintenance and documents activities according to GMP, ISO 13485, and sustainability expectations.
- Assists in equipment upgrades, retrofits, and component modifications as directed by engineering.
- Supports equipment commissioning, validations, verifications, and change order documentation.
- Maintains spare parts inventory and collaborates with procurement and suppliers to resolve equipment or component needs.
- Contributes to investigations and corrective/preventive actions and supports continuous improvement using Lean, Six Sigma, DFM, and SPC tools.
- Collaborates with cross-functional teams to resolve daily technical issues and support manufacturing operations.

Education and Experience:
- Associate's degree (preferred in Electrical or Mechanical Engineering).
- A minimum of 2 years’ experience in the Medical Device industry.
- Minimum of 2 years in a manufacturing environment.
- Preferred experience in semi-automated/fully automated equipment, robotics, and HMIs.

Role and Competencies Requirements:
- Ability to troubleshoot simple to complex manufacturing electro-mechanical process issues.
- Good verbal and written communication skills; ability to interface within cross-functional teams.
- Skilled with CAD modeling software (SolidWorks).
- Familiarity with ISO 13485, GMP, or FDA-regulated environment.
- Preferred certifications/licenses: Lean Six Sigma Green Belt.
- Preferred experience: Microsoft applications, SolidWorks, developing/writing/executing cGMP-based process and equipment validations, robotics.
- Travel: Domestic and International.
- On-call requirements.
- Lifting requirement: Medium (16–30 lbs.)

Fortive Corporation Overview

Fortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product design, and healthcare safety solutions.

We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in software-powered workflow solutions, data-driven intelligence, AI-powered automation, and other disruptive technologies. We’re a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to groundbreaking sustainability solutions.

We are a diverse team 18,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact. 

At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference. 

At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone. 

At Fortive, we believe in growth. We’re honest about what’s working and what isn’t, and we never stop improving and innovating.

Fortive: For you, for us, for growth.