Engineering Technician
Irvine, CA - USA
Department:
Job Summary
Location: Irvine CA
Shift: 2nd Shift (Monday - Thursday 1:30pm - 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:
- Associates 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 (1630 lbs.)
Required Experience:
IC
About Company
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 d ... View more