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Senior Supplier Quality Engineer

Job in Sunnyvale, Santa Clara County, California, 94086, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer, Manufacturing Engineer
Job Description & How to Apply Below

Job Title

Roles and Responsibilities

  • Support Value Engineering and Quality Improvement Part Qualification efforts
  • Lead Core Product Teams in defining appropriate Part Qualification requirements
  • This includes defining testing and inspection requirements prior to system integration to maximize ISI factory efficiency
  • Support transfer of parts between suppliers
  • Complete Production Part Qualification Process deliverables:
    Supplier pFMEA, Special Process Validations, FAI, and Process Capability Analysis
  • Perform product/process risk analysis and ensure mitigations are implemented and effective prior to product introduction
  • Establish sustainable process capability at supplier and critical sub-tier suppliers
  • Support Manufacturing Line Escalations from manufacturing teams
  • Drive corrective actions through use of various Root Cause tools (8D, 5 Why, etc), determining true root cause, implementing effective and lasting corrective and preventive actions

Manufacturing Process Selection and Development

  • Lead manufacturing process selection
  • Identify the correct process for manufacturing the part, considering process quality, long term capacity and total lifecycle cost.
  • Identify where DFM is appropriate to achieve higher quality, lower costs or better supply chain capacity
  • Educate internal customers and suppliers regarding supplier quality, process and operational capabilities, best value manufacturing methods and tooling for key supplier processes

Manage Change

  • Drive improvements to ISI requirements as necessary by proposing and managing changes to specifications and drawings through the ECO process
  • Manage the planning and implementation of supplier change management projects using the Supplier Change Request process (SCR) post Design V&V
  • Provide status of the readiness (quality, capacity, delivery) of the supply chain for major production process changes
  • Work cross-functionally to improve supplier engineering processes

Supplier Selection and Evaluation

  • Support Supplier Selection
  • Work with Product Design, Commodity Managers and other stake holders to identify high capability suppliers necessary for New Products based on assessment of business need and supplier capability.
  • Evaluate new supplies through informal assessments and formal assessment by supporting lead auditors in QMS evaluations

Foster Supplier Relationships

  • Support audit team in addressing findings to develop suppliers' quality and business systems in order to meet ISI's requirements
  • Manage supplier relationships to effectively partner with ISI suppliers

Skill/Job Requirements

  • BS degree in Engineering field
  • 10 years related experience in Manufacturing, Supplier Process Engineering, Design, or related field
  • Excellent written and verbal communication skills
  • Experience creating and aggregating DFM feedback
  • Demonstrable knowledge in evaluating and challenging supplier technical, quality, and business capabilities
  • Experience with a wide range of manufacturing processes including understanding of key input variables for quality, cost and capacity
  • Desired product experience in the following categories:
  • Machining, including 4 & 5-axis holdings, FMS and bar-fed lathes
  • Metal Fabrication, Welding and/or other bonding processes
  • Plastic Injection Molding or other plastic forming processes
  • Die casting or Thixomolding
  • Mechanical Motion Products (Bearings, Gears and Screws)
  • Mechanical Motion Control Products (Motors, Brakes)
  • Motion Control Sensors (Encoders, Inertial Sensors, Resolvers)
  • Medical Gas Line Processing
  • Proven ability to motivate suppliers and lead teams to solve difficult technical and process problems
  • Knowledge of pFMEA, process validation, inspection and test techniques
  • Familiarity with 21 CFR part 820 and ISO 13485
  • Experience in auditing suppliers to these standards is preferred
  • At a minimum, candidate should understand GDP and QMS methods
  • Significant computer experience using Windows, Word, Excel, Access and ERP Information Systems, preferably SAP
  • Ability to read and interpret detailed specifications and schematics and communicate technical information
  • Experience in a medical device company is a preferred
  • Experience with low-volume high-mix production environments is a preferred
  • Ability to travel to suppliers on an as needed basis – domestic and international
Position Requirements
10+ Years work experience
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