Supplier Quality Engineer

Excelon solutions

  • Minneapolis, MN
  • 3 days ago

    Highlights

    Title: Supplier Quality Engineer with medical deviceLocation: Plymouth, MN - OnsiteLong-Term Contract RoleJD4+ years of experience in manufacturing engineering, preferably in the medical device industryExperience in Supplier Quality Engineering or Receiving Inspection, including working directly with suppliers and using quality toolsFamiliarity with SAP (supply chain or quality modules) or similar ERP systemsExperience with Windchill or other document control systems (change orders, BOM updates, etc.)Create and maintain inspection procedures, and develop or source inspection toolsSupport component specifications, testing, and approval for useCollaborate with Design Engineering on component selection, quality, and reliabilityAnalyze incoming material defects and communicate issues to suppliersReview designs for quality and manufacturabilityInvestigate supplier-related field failures and lead corrective actionsKnowledge of FDA, GMP, ISO 13485, and ISO 14971#J-18808-Ljbffr.

    Numbers & Facts

    LocationMinneapolis, MN

    Description

    Title: Supplier Quality Engineer with medical deviceLocation: Plymouth, MN - OnsiteLong-Term Contract RoleJD4+ years of experience in manufacturing engineering, preferably in the medical device industryExperience in Supplier Quality Engineering or Receiving Inspection, including working directly with suppliers and using quality toolsFamiliarity with SAP (supply chain or quality modules) or similar ERP systemsExperience with Windchill or other document control systems (change orders, BOM updates, etc.)Create and maintain inspection procedures, and develop or source inspection toolsSupport component specifications, testing, and approval for useCollaborate with Design Engineering on component selection, quality, and reliabilityAnalyze incoming material defects and communicate issues to suppliersReview designs for quality and manufacturabilityInvestigate supplier-related field failures and lead corrective actionsKnowledge of FDA, GMP, ISO 13485, and ISO 14971#J-18808-Ljbffr

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