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Endologix
Santa Rosa, CA | Full Time
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Endologix
Santa Rosa, CA | Full Time
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Manufacturing Engineer
Endologix Santa Rosa, CA
$112k-133k (estimate)
Full Time | Medical Technology 1 Week Ago
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Endologix is Hiring a Manufacturing Engineer Near Santa Rosa, CA

OverviewDesign and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality, Support new product transfers to manufacturing.
Responsibilities
  • Design and develop manufacturing processes for new products, product changes and enhancements, and related tooling and fixtures which are consistent with a zero defect level as well as low product cost.
  • Investigate benefits and features of capital equipment and generate capital appropriation justifications.
  • Create and maintain accurate documentation of concepts, designs concepts, tool drawings and shop orders in coordination with the Quality Assurance and R&D functions.
  • Perform Installation Qualification (IQ) equipment protocols and reports.
  • Provide engineering support to production department in troubleshooting and resolving technical problems.
  • Coordinate work with outside vendors, assigned technicians and tool room personnel.
  • Plan and schedule projects in a manner consistent with corporate objective.
  • Contribute to the intellectual property position of the company via invention and patent applications.
  • Maintain accurate documentation of concepts, designs, and processes.
  • Maintain current knowledge of medical, technical, and biomedical developments as related to company products.
  • Support prototype and pilot production of new products, product changes, and enhancements in coordination with the Manufacturing and Quality Control functions.
  • Provide engineering support to production department in troubleshooting and resolving technical problems.
  • Work with new product development staff to ensure that new manufacturing processes are designed for manufacturability, help resolve issues.
  • Maintain GMP compliance in coordination with the Document Control, R&D, and Quality Assurance functions
  • Complete accurate and timely manufacturing documentation including manufacturing procedures, materials records, etc.
  • Support company goals and objectives, policies and procedures, Good Manufacturing Practices, and FDA regulations.
  • Ensure that all regulatory and internal policies are followed.
  • Identifies hazards and mitigates risk associated with identified hazards in Process FMEA.
  • Perform other duties as assigned by supervisor
Qualifications
  • Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors.
  • Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
  • May determine methods and procedures on new assignments and may provide guidance to other lower-level personnel.
  • Utilizes Solid Works drafting skills when appropriate
Education
  • Requires a Bachelor degree or equivalent in engineering or related discipline.
  • Masters preferred
Experience
  • Requires a minimum of 2-3 years related experience.
Compensation: $63,000 to 106,000 depending on experience. This position is eligible for a discretionary bonus and equity.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Medical Technology

SALARY

$112k-133k (estimate)

POST DATE

05/30/2024

EXPIRATION DATE

06/27/2024

WEBSITE

endologix.com

HEADQUARTERS

PITTSBURGH, PA

SIZE

200 - 500

FOUNDED

1992

TYPE

Private

REVENUE

$50M - $200M

INDUSTRY

Medical Technology

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About Endologix

Endologix manufactures and commercializes minimally invasive spine surgery system for the treatment of aortic disorders.

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