Magnolia Medical Technologies
Magnolia Medical Technologies

Manufacturing Engineering Manager

$140,000 – $160,000 per year

TLDR

Lead transfers and process improvements for sterile disposable medical devices with global contract manufacturers under FDA and ISO 13485 requirements.

Manufacturing Engineering Manager

Position Summary 

The Manufacturing Engineering Manager is responsible for providing technical leadership and engineering support for commercialized products and outsourced manufacturing partners. This role ensures product quality, manufacturing excellence, regulatory compliance, and continuous improvement throughout the product lifecycle.
This role reports to our downtown Seattle Corporate Office, onsite, with the ability to travel (up to 20% as needed.)

Primary Responsibilities

Contract Manufacturing Management 

  • Primary technical liaison with contract manufacturers 
  • Support supplier sourcing, negotiation, qualification, audits, process reviews and issue resolution 
  • Lead manufacturing transfers, change management, and capacity expansion activities 
  • Cross functional program and project leadership 

Sustaining Engineering 

  • Experienced project management and design control / stage gate development processes 
  • Provides specification analysis, component
    selection and product structure organization 
  • Utilize Solidworks and other software tools to execute design changes as necessary, updates, Drawings, BOM’s and ensure DHF and DMR are updated 
  • Lead root cause investigations and CAPA activities 
  • Analyze quality and field performance data 
  • Drive yield improvement and scrap reduction initiatives 

Manufacturing Engineering 

  • Support IQ/OQ/PQ validations 
  • Develop and optimize manufacturing processes 
  • Identify and Implement DFM/DFA improvements 
  • Actively manages intercompany resources and outside vendors in support of prototype fabrication, assembly, and validation testing 

Quality & Compliance 

  • Ensure compliance with FDA and ISO 13485 requirements 
  • Maintain manufacturing documentation and work instructions 

Required Qualifications 

  • Bachelor's degree in Engineering or related technical field
  • 8-10 years of manufacturing, sustaining, or product engineering experience
  • Experience in sterile, disposable medical devices and global contract manufacturing

Competencies 

  • Familiarity with a variety of prototyping processes
  • Experience identifying and working with suppliers for a wide variety of medical device components. 
  • Working understanding of FDA Quality Systems Regulations and product development within the regulated environment
  • Knowledgeable of statistical methods
  • Strong problem solving, technical leadership, communication, project management and cross-functional collaboration skills
  • Ability to analyze and provide simple solutions to challenging situations
  • Expertise in materials such as silicone, PVC, MABS, polypropylene, polycarbonate, TPEs highly desired 
  • Ability to work onsite in our downtown Seattle office; some minimal travel (up to 20%) may be required occasionally
  • Ability to work in an office and laboratory setting, using computers, fine motor skills and excellent hand dexterity with the ability to lift up to 25 lbs. occasionally

Magnolia Medical Technologies is focused on improving the precision of sepsis testing through its innovative Steripath® device, which significantly reduces blood culture contamination. This solution is aimed at healthcare providers, setting a new benchmark for blood culture integrity with extensive clinical validation and an expanding intellectual property portfolio.

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