Supplier Quality Engineer

Katalyst HealthCares and Life Sciences

• $88K — $105K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering; Master's degree is a plus.
  • 3+ years of engineering experience, preferably in Manufacturing or Product Quality.
  • Expertise in process validation and verification, particularly in IQ, OQ, PQ.
  • SO, 13485 Lead Auditor certification is a plus.
  • Experience with plastic, metal, and electronics commodities.
  • Strong communication skills for effective interdepartmental collaboration.

Responsibilities

  • Achieve high-quality performance at Supplier partners using APQP and continuous monitoring.
  • Play a key role in the development and production flow of Philips IGTD's supply base.
  • Coordinate with Product Engineering, Supply Chain, and Suppliers to implement effective supply chain strategies.
  • Perform Process Validation and Verification for Spectrawave IGTD portfolios.
  • Collaborate with R&D and Quality Design Assurance on manufacturability and risk management.
  • Conduct thorough investigations of defects to identify supplier-caused issues and implement corrections.
  • Manage and troubleshoot supplier-related quality issues, monitoring trends and performance.

Benefits

  • Opportunity to work in a high-profile, cross-functional role.
  • Engagement with critical supply chain strategies in a leading company.
  • Involvement in continuous improvement projects based on industry standards and regulations.
  • Professional development opportunities in a dynamic engineering environment.
Full Job Description
Roles and Responsibilities:
  • Responsible for achieving a state of high-quality performance at our Supplier partners through the application and practice of Advanced Product Quality Planning 'APQP' , Supplier Qualification (Audit, Quality Agreement/Change Notice Agreement), and continuous monitoring the performance supplier to drive zero defect through Supplier Corrective Actions and notification.
  • You will fill a high-profile, cross functional position and play an integral role enabling development and production flow of Philips IGTD's critical supply base.
  • You will work in close coordination with Product Engineering, Supply Chain and Production and Suppliers to execute effective, creative and smart supply chain strategies to achieve production goals.
  • Perform Process Validation and Verification across Spectrawave IGTD portfolios for Consoles and Catheter parts.
  • Collaborate with R&D and Quality Design Assurance in Design for Manufacturability and Part Risk management per DFMAE and PFMEA.
  • Perform Process Validation , Verification, Test Method Validation, and assess CTS/CTQ criteria per APQP requirement for +700 parts.
  • Support Supplier Qualification including Audit, Quality Agreement and Change Notice Agreement.
  • Perform Problem solving in the case of FAI and APQP failure.
  • Deep dive Value Stream mapping across process.
  • Conducts thorough investigations of defects to determine if they are supplier-caused and implement corrections using the SCAR process.
  • Proactively manage, monitor, and troubleshoot supplier-related issues for quality of components, sub-assemblies, and assemblies includingmonitoring trends and managing Supplier Improvement and Supplier Quality Performance Monitoring.
  • Providing Quality oversight of product/process change requests from suppliers (SICRs: Supplier Initiated Chage Requests), ensuring appropriate regulatory review and adequate validation to support requested changes including following our APQP process and leading process validation, as necessary
  • Develop and oversee process validation plans, including equipment qualifications, with suppliers and lead continuous improvement projects based on process/product trends, customer complaints, industry standards, and government regulations.
Education and Experience:
  • Bachelor's degree engineering (Master Degree is plus).
  • 3+ years of engineering experience (Manufacturing Engineer and/or Product Quality is plus).
  • In-depth product manufacturing and quality experience in process validation and verification Subject Matter in IQ, OQ, PQ
  • SO, 13485 Lead Auditor certified is plus.
  • Experienced in plastic, metal, electronics commodities.
  • Strong written, oral and interpersonal skills to be able to effectively interface interdepartmentally and complete assignments with accuracy and a high attention to detail

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