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Quality Engineer II

Develop and implement process validation protocols for medical device manufacturing
Seattle
Mid-Level
$85,000 – 107,000 USD / year
yesterday
FUJIFILM

FUJIFILM

A multinational corporation known for its photography and imaging products, as well as its presence in healthcare and electronics.

Quality Engineer II

The Quality Engineer II is responsible for assisting in establishing, implementing, and maintaining systems and/or services to measure and improve product quality, cost, and customer service while ensuring full compliance to FDA and applicable ISO requirements. The Quality Engineer II will be responsible for driving activity around process validation, as well as participating in establishing and monitoring systems related to Inspection, Testing, Training, Supplier Qualification, New Product Introduction, Manufacturing, Complaints, Reporting and Corrective/Preventative Action.

At FUJIFILM Sonosite, we reinvent how healthcare is delivered with point-of-care ultrasound technology. As the leader in bedside ultrasound systems, our innovations save lives—from premature babies in NICUs to trauma patients in emergency rooms.

We're looking for purpose-driven team members ready to build technology that impacts real-world scenarios, including natural disasters and even war zones. By joining FUJIFILM Sonosite, you'll be part of a team that thrives on collaboration, out-of-the-box thinking, and a passion for life-saving innovations. Let's make a difference together.

Our headquarters in Bothell, Washington, blends riverside charm with urban amenities, quality schools, and an ever-evolving downtown—all part of the vibrant Seattle metro area.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles."

Essential Job Functions

  • Innovative thinker, knowledgeable and intensely committed to ensure that products we supply conform to the FDA Quality System Regulation and ISO 13485.
  • Understands and can implement standard approaches to problem solving and prevention.
  • Participate in Configuration Management initiatives.
  • Support new product development in ensuring compliance with Quality System requirements.
  • Review/approve engineering changes on behalf of QA.
  • Participate in Corrective and Preventative activities.
  • Partner with R&D and Operations in the development of verification and validation protocols for product designs and manufacturing processes.
  • Identify, plan, and participate in the implementation of process improvements.
  • Support Risk Management activities including Failure Mode and Effects Analysis.
  • Support the MRB process for discrepant material investigations and decisions.
  • Support Supplier Qualification and monitoring.
  • Review complex complaints and complaint trends and assist in failure investigations.
  • Support development and continuous improvement of quality system procedures.
  • Lead Quality related projects and Host Review Meetings.
  • Report to management on quality issues and trends.

Knowledge/Experience

  • BS or MS degree in Mechanical/Electrical/Industrial Engineering.
  • At least 2-4 years of experience working within the Quality organization of a Medical Device Manufacturer, Aerospace, Pharma, or other highly regulated industry.
  • Applications of Lean principles such as Value Stream Mapping, Standard Work, 5S, Kaizen.
  • Experience with domestic and overseas manufacturing and working directly with Contract Manufacturers and strategic vendors.
  • Experience with product lifecycle management (P/N creation, BoM creation, ECO generation and management, AVL management, etc.).
  • Quality engineering background and experience with AQLs, product inspections, vendor qualifications and audits.

Skills/Abilities

  • Ability to travel 10% domestically and internationally as needed.
  • Proficient in MS Office programs (Word, Excel, PowerPoint), Visio, MS Project; experience with document templates and scientific reference software is desirable.
  • Must be meticulous with strong written and oral communication skills.

Salary and Benefits

  • $85,000.00 - $107,000.00/yr depending on experience (Compensation will vary based on skills, experience and location; it is not typical to be hired at or above the top of the salary range).
  • Insurance: Medical, Dental & Vision; Life & Company paid Disability
  • Retirement Plan (401k): 4% automatic Company contribution; Fujifilm matches 50 cents for every dollar you contribute, up to 6% of your salary
  • Paid Time Off: You can accrue up to three (3) weeks of PTO in your first year of employment; PTO increases based on years of service
  • Employee Choice Holidays: Four (4) additional paid days off, based on date of hire in the calendar year
  • Paid Holidays: Eight (8) paid holidays per year

FUJIFILM Sonosite offers a fantastic compensation package, including benefits, and a 401k program. Visit us today to learn more about our exciting technologies and how you can make a difference.

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Quality Engineer II
Seattle
$85,000 – 107,000 USD / year
Engineering
About FUJIFILM
A multinational corporation known for its photography and imaging products, as well as its presence in healthcare and electronics.