Quality Engineer I

bostonscientificMaple Grove, MN
2d$58,200 - $110,500Onsite

About The Position

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About This Role: Provide Quality Engineering support to Maple Grove commercial manufacturing lines ensuring delivery of the highest quality product to the customer while supporting continuous improvement projects and quality initiatives. Partner with production and manufacturing engineers for operations support. This role will provide direct line support for our Watchman production lines. This role is in the Access and Delivery Solutions Assembly (ADSA) business unit. At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model requiring employees to be in our local office five days per week. Relocation assistance is not available for this position at this time. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

Requirements

  • Bachelor’s Degree
  • Good written and verbal communication skills.
  • Must be able to work independently under limited supervision
  • Knowledge of basic Quality Systems and good documentation practices

Nice To Haves

  • Bachelor of Science Degree in Engineering
  • Experience in medical device field in a manufacturing support role a plus
  • Experience in quality line support
  • Self-starter with the ability to identify improvement opportunities
  • Experience working in production support function
  • Experience leading cross-functional teams and driving projects to completion.
  • Demonstrated experience managing multiple projects covering diverse engineering (i.e. equipment qualification, process validation, test method validation) disciplines.
  • Prior interactions with the following disciplines: manufacturing engineering, CAPA, risk management, supplier quality, and process engineering
  • Knowledge of analytical techniques, problem solving and statistical analysis
  • Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook.
  • Familiarity with product/component documentation, inspection and testing, and Manufacturing Execution System (MES)

Responsibilities

  • Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements.
  • Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements.
  • Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices.
  • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
  • Assure in the development and execution of streamlined business systems which effectively identify and resolve quality issues.
  • Production floor support and line ownership.
  • Leading Corrective and Preventive Actions (CAPA) projects
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