Quality Engineering Fall Co-Op

Hiring Manager: [[hiringManagerName]]
Recruiter: Kayleigh Elise Flanigan

 

About Role: Quality Engineering Fall Co-Op 

 

 We will consider qualified applicants of all ages who are starting (or restarting) their careers

 

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

 

Relocation and housing assistance may be available to those who meet the eligibility criteria.

 

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

 

 

 

Our Purpose: 

Our mission is to serve more patients with improved product experiences through 4 key objectives creating the best culture, best agility, best performance and best compliance. Develops, establishes, and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support within new product development, operational, or system/services support. 

  

Your Opportunity: 

As a co-op at Boston Scientific, you will… 

• Lead in the implementation of assurances, design and process controls, and CAPA systems designed to meet or exceed internal and external requirements. 
• Act 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. 

 

Your Impact 

Examples of meaningful work: 

• Support the execution of design changes for commercialized products and documentation of associated design verification activities.
• Evaluate and analyze post market complaint data to identify and escalate signals related to product performance, support complaint investigation efforts, and identify corrective/preventive activities for continuous improvement.
• Update and maintain risk management files.

Required Qualifications: 

• Currently pursuing a BS in Mechanical or Biomedical Engineering.