Endologix

Manufacturing Associate III

Job ID
2025-3044
Location
US-CA-Irvine
Category
Operations

Overview

Join our exciting team as a Manufacturing Associate III! 

 

Endologix, LLC. is a California-based, global medical device company dedicated to improving patients’ lives by providing innovative therapies for the interventional treatment of vascular disease. 
 
We have a therapeutic portfolio designed to treat diseases which currently have clinically relevant unmet needs. Our existing products can treat a wide spectrum of vascular disease through abdominal aortic aneurysms to lower limb peripheral vascular disease. We obtain excellent clinical outcomes through meticulous attention to product design, manufacturing, and training, all backed by industry-leading clinical evidence. 

 

Job Summary:

The Manufacturing Associate III is responsible for assembling high quality medical devices in accordance with approved manufacturing process instructions and Standard Operating Procedures, assisting in the evaluation and resolution of line issues, and suggesting possible method / process improvements. Other job duties will be assigned as needed.

Responsibilities

  • Comply with Endologix’s policies, procedures, and quality standards as well as stretching exercises, safety and environmental regulations.
  • Assemble product as required utilizing small hand tools, calibrated instruments, measurement equipment, microscopes, and test fixtures.
  • Identify and communicate any safety, quality, process issues or concerns as needed.
  • Maintain controlled environment integrity by using proper attire and adherence to controlled environment practices and procedures.
  • Perform in-process quality checks as required while giving timely feedback as issues arise.
  • Recognize and report any unacceptable materials and/or sub-assemblies to engineering and/or supervisor.
  • Responsible for 100% compliance to Endologix Quality and Regulatory policies and adhere to Endologix Core Values.
  • Responsible for quality of work and adhering to manufacturing methods and quality records.
  • Understand and comply with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
  • Work with supervisors, engineers and technicians to resolve line issues and suggest improvements.
  • Be familiar with terminology used in the production area.
  • Participate in lean activities and 5S improvement efforts.
  • Understand and demonstrate Lean manufacturing techniques and principles.
  • Actively pursue resolution of issues by collaborating with and utilizing all resources.
  • Aware of common defects within manufacturing departments and the results caused by variations during the manufacturing processes.
  • Capable of moving from one station to another without continuous mistakes.
  • Be certified as a trainer and train other production employees on manufacturing processes.
  • Coach and provide guidance to others on manufacturing processes and standard operating procedures.
  • Capability to read and interpret engineering drawings, specs and method sheets.
  • Electronic systems entry.
  • Support supervisor, as required.

Qualifications

Education:

  • High School Diploma or equivalent.
  • Demonstrates basic English reading, writing and spoken skills.

Experience:

  • Minimum of 3 years of Manufacturing Experience (Medical Device Preferred).
  • Work with small components, adhesives, and microscopes.
  • Experience working within a clean room environment.
  • Lean & 5S experience desired.

Join us, and bring your point of view, talents, and contributions so we can all grow together!

 

Endologix, LLC. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 

 

 

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