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R&D Engineer (Packaging)

In United States

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R&D Engineer (Packaging)   

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JOB TITLE:

R&D Engineer (Packaging)

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

IRVINE United States

JOB DESCRIPTION:

Position Name: R&D Engineer (Packaging) Location: Irvine, CA Duration: Fulltime with client Rate: on W2   Job Description: Degree in Mechanical, Materials or Biomedical Engineering · The R&D Engineer with experience in catheters or equivalent higher-class devices. · · Prepare single use sterile package design verification testing (DVT) protocols and report against design requirement and risk assessment using external standards (Aging, Shipping, sterilization etc..,). · Expertise in ISO 11607-1 & -2 Packaging for terminally sterilized medical devices · Prepare technical product documentation including design history files, drawings, bills of materials, Design Verification protocols and reports, engineering change orders (ECO), etc. · Self-sustained capability to solve design-related challenges and timely support to cross-functional teams as a subject matter expert. · Design and develop test methods to support additional studies post-commercialization. Plan and execute on product development deliverables. · Leverage engineering knowledge in conducting complaint evaluations and CAPA investigations to understand potential device and systemic failures. · Hands on Solidworks Experience 2D / 2D. · R&D related Labeling Experience. · EU-MDR – documentation and process experience

Position Details

POSTED:

Dec 04, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16505712187531869

LOCATION:

United States

CITY:

IRVINE

Job Origin:

OORWIN_ORGANIC_FEED

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In Dallas Fort Worth
Aug 19, 2017 9am-6pm
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Position Name: R&D Engineer (Packaging) Location: Irvine, CA Duration: Fulltime with client Rate: on W2   Job Description: Degree in Mechanical, Materials or Biomedical Engineering · The R&D Engineer with experience in catheters or equivalent higher-class devices. · · Prepare single use sterile package design verification testing (DVT) protocols and report against design requirement and risk assessment using external standards (Aging, Shipping, sterilization etc..,). · Expertise in ISO 11607-1 & -2 Packaging for terminally sterilized medical devices · Prepare technical product documentation including design history files, drawings, bills of materials, Design Verification protocols and reports, engineering change orders (ECO), etc. · Self-sustained capability to solve design-related challenges and timely support to cross-functional teams as a subject matter expert. · Design and develop test methods to support additional studies post-commercialization. Plan and execute on product development deliverables. · Leverage engineering knowledge in conducting complaint evaluations and CAPA investigations to understand potential device and systemic failures. · Hands on Solidworks Experience 2D / 2D. · R&D related Labeling Experience. · EU-MDR – documentation and process experience


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