Quality Technician I - 3rd Shift

Additional Location(s):  N/A

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.           

 

 

3rd Shift: 9:30pm - 5:30 am

 

About the role:

The Quality Technician I role in Core Tech Polymers (CTP) is the first point of contact for production personnel regarding quality issues.  The quality technician is responsible for documenting non-conforming events as well as identifying and segregating impacted material.  The position requires creative thinking and investigation skills to resolve problems that arise on extrusion production floor.  The quality technician will be responsible for supporting multiple production lines to keep material flowing and assuring quality requirements are maintained throughout the process.  Technical aptitude will be a key component as much of the technician role involves working with technology systems including MES, SAP, downtime tracking, and DataMetrics among others. 

 

Your responsibilities will include:

• Investigate and document non-conforming events in eCAPA system 
• Perform project and product testing 
• Assist engineers in failure analysis 
• Provide direct quality support for day to day production floor operations 
• Learn and create setups in Statistical Process Monitoring (SPC) program 
• Lead and participate in continuous improvement projects 
• Assist with quality issues and quality metrics related activities. 
• Document non-conforming events and quarantine impacted material 
• Perform testing, gather data, and analyze results of product testing and process monitoring. 
• Assist with CAPA activities 
• Use documentation systems to research information and generate Change Requests. 
• Assist in the investigation and disposition of nonconforming materials, designs and/or systems. 
• 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 
• Communicate with a wide variety of BSC personnel in and outside of the plant. 

 

Required qualifications:

• High school diploma/degree/equivalent work experience

 

Preferred qualifications: 

• 1-2+ years’ experience in a manufacturing environment 
• Proficient in Microsoft office (Excel, Word, PowerPoint, etc) 
• Strong verbal/written communication skills 
• AA degree or higher 
• 1-2 years in the medical device field 
• Experience in SAP/MES or equivalent MRP system 
• Lean manufacturing experience 
• Workstation error proofing experience 

 

 

Requisition ID: 615601 

Minimum Salary: $ 37544 

Maximum Salary: $ 63856 

 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

 

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus targe