Location: Maple Grove, [[state]], United States (US)
Additional Locations: (n/a)
Purpose and Passion Comprehensive Benefits Life-Work Integration Community Career Growth
At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purposeimproving lives through your life's work.
QUALITY TECHNICIAN I
About This Role
This Quality Technician I is in direct support of medical device manufacturing. You will be responsible for driving continuous improvement in product quality and compliance, owning and reporting non-conformances, and will be a key partner to the Production and Manufacturing teams in achieving metrics and objectives.
To provide quality support to manufacturing in the coating, stent delivery system and packaging factory. This role will be required to support the weekend 1st shift (Saturday and Sunday 6am - 6pm) plus additional shifts within the M-F work week (e.g., Friday 6am 2pm) to meet minimum 40 hour requirement. Flexibility available M-F.
Function or Divisional Overview
At Boston Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions including heart, digestive, pulmonary, vascular, urological, pelvic health, and chronic pain conditions. We are a leading innovator of medical solutions that improve the health of patients around the world. We continue to innovate in key areas and are extending our innovations into new geographies and high-growth adjacency markets.
Your responsibilities will Include:
Provide technical and quality support to the production floor as needed
Identify areas of improvement and participate in continuous improvement projects
Create and maintain data files and forms
Use documentation systems to research information and generate Change Requests
Initiate and assist in the investigation and disposition of nonconforming materials, designs and/or systems
Communicate with a wide variety of BSC personnel in and outside of the plant.
Review device history records (DHR) and acceptance records to ensure all activities in the Device Master Record (DMR) have been performed and approved.
Update databases and spreadsheets used to track, monitor, and report department activities.
Use the inventory and traceability management systems to transact and research material.
What we're looking for:
High School diploma and 1-2 years of experience in a manufacturing environment
Good oral and written communication abilities
Demonstrates good documentation practices and ability to maintain deadlines
Previous application of Microsoft Excel and Word
2-3 years of experience in a manufacturing environment
Independent organization and prioritization of multiple tasks
Must work effectively in a dynamic work environment
Able to communicate technical information to engineers and collaborate to identify root cause of issues
Must be able to work independently under limited supervision as well as in a team environment
Good interpersonal skills and organizational skills
As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you're looking to truly make a difference to people both around the world and around the corner, there's no better place to make it happen.
Boston Scientific is an Equal Opportunity Employer
Requisition ID: 435450