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Quality Technician II - 1st Shift

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: Boston Scientific Gruppe
Full Time position
Listed on 2026-05-09
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Data Analyst
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below

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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit
- High Performance

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 the role:

To provide quality support to product development and manufacturing. To develop, apply, monitor, measure, improve, and communicate quality methodologies from product development through product commercialization.

Work Mode

At Boston Scientific, we value collaboration and synergy. This role follows an onsite work model, requiring employees to be in our local office four days per week.

Relocation

Relocation assistance is not available for this position at this time.

VISA

Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time.

Your responsibilities will include:
  • Provide onsite support for quality-related issues on the manufacturing floor
  • Serve as a subject matter resource for quality processes, offering guidance and support to the business unit.
  • Identify, scope, and contain nonconforming products
  • Communicate quality concerns effectively to stakeholders through clear and timely email updates, ensuring critical information is disseminated appropriately.
  • Review Device History Records (DHR) and acceptance records to confirm all activities outlined in the Device Master Record (DMR) are completed and approved
  • Create and maintain Nonconforming Event and Prevention (NCEP) records, documenting quality issues with precise technical writing.
  • Support Corrective and Preventive Action (CAPA) activities
  • Identify opportunities for improvement and actively participate in continuous improvement initiatives.
  • Perform product and in-process testing, collect and analyze data, and report findings to ensure compliance with quality standards.
  • Assist during internal and external audit activities
  • Conduct product failure analysis to determine root causes and recommend corrective measures.
  • Develop and maintain data files, forms, and documentation systems, ensuring accuracy and accessibility.
  • Utilize documentation systems to research information and generate Change Requests in accordance with established procedures.
  • Train peers on quality processes, methods, and best practices
  • Initiate and assist in the investigation and disposition of nonconforming materials and systems
  • Update and manage databases and spreadsheets to track, monitor, and report departmental activities.
  • Use inventory and traceability management systems to transact and research material movements.
  • Perform basic statistical analysis and communicate results to cross-functional teams.
Required qualifications:
  • 2 years of experience with a high school diploma/degree/equivalent
Compensation

The anticipated annualized base amount or range for this full time position will be $ to $, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at  Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.

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