Manufacturing Engineering Technician – On-Site, Growth & Equity

OrthAlign, Inc.

Irvine (CA)

On-site

USD 55,000 - 75,000

Full time

4 days ago
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Benefits offered by this job

Bonus and equity
Full benefits package
Career advancement
Top Place to Work in Orange County

Job summary

OrthAlign, Inc. is seeking an on-site Manufacturing Engineering Technician in Irvine, CA to support production, validation, and process improvements for medical devices.

You will work with cross-functional teams under Engineers and Managers, handling validation IQ/OQ/PQ, change orders, and documentation per SOPs. The role emphasizes hands-on assembly, testing, and documentation, with opportunities for growth within the manufacturing engineering team.

Qualifications

  • High school diploma or equivalent; associate or bachelor’s preferred.
  • Basic engineering technician skills in a medical device environment.
  • Proficiency with MS Office and clear written/verbal communication.
  • Attention to detail with the ability to work independently and in teams.
  • Knowledge of ISO 13485 regulations is a plus.

Responsibilities

  • Support and troubleshoot production issues, and help develop processes and fixtures.
  • Coordinate builds and related training for engineering and production.
  • Assist validation activities, IQ/OQ/PQ, and create validation reports.
  • Support design control documents and manufacturing procedures.
  • Plan process validation activities in collaboration with engineers.
  • Provide routine technical support for manufactured products.

Skills

Engineering basics
MS Office proficiency
Detail oriented
Team collaboration
Medical device knowledge
ISO 13485 knowledge
CAD SolidWorks
Independent with guidance
Domestic travel ability

Education

High school diploma or equivalent
Associate or Bachelor preferred

Tools

SolidWorks
Basic hand tools
MS Office

Job description

OrthAlign, Inc. is seeking an on-site Manufacturing Engineering Technician in Irvine, CA to support production, validation, and process improvements for medical devices.

You will work with cross-functional teams under Engineers and Managers, handling validation IQ/OQ/PQ, change orders, and documentation per SOPs. The role emphasizes hands-on assembly, testing, and documentation, with opportunities for growth within the manufacturing engineering team.

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