Pilot Medical Device Specialist II

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.

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.

• Work independently with limited direction.
• Must have the ability to write as well as verbally communicate inputs/outputs.
• Work directly with project leads, engineering leads, technicians as well as outside vendors.
• Attend project team/build meetings.
• Adjust their schedule based on project needs.
• Adjust their schedule based on space and machine availability.
• Keep a detailed Artemis tracking project time/times (some work on multiple projects).
• Understand, adhere to and promote safety policies and practices.
• Responsible for quality and adhere to manufacturing process requirements, the Boston Scientific Corporation Quality Policy and the Strategic Quality Process (SQP). Proactively identify and communicate quality issues and concerns; actively pursue resolution of issues by utilizing all resources.
• Build product by following all processes in which certified (in their most current revision), and completing other assigned work, while meeting manufacturing goals and metrics. Act as a role model to others while demonstrating optimum proficiency.
• Demonstrate, promote and suggest ideas for Lean Manufacturing and related principles. Take an active leadership role in implementing and driving Lean activities.
• Champion the flex strategy, rotate as necessary and work well with all group members, both within the team and cross-functionally.
• Demonstrate proficiency in all communication, including written and spoken, as well as strong math skills.
• Maintain accurate records, including training files and shop floor paperwork (SFP). Consistently ensures the team is maintaining records accurately.
• Required to participate in Shared Responsibility. Identify opportunities for continuous improvement and assist in their implementation.
• Understand, follow and promote all BSC and site-specific policies and procedures.
• Responsible for attending and passing all required core BSC and site-specific training (i.e. QS Basics, RTK, Lean Training).
• Understand the functions of SAP, including running reports. Responsible for conducting basic and routine trouble‑shooting if applicable to the area.
• Willing to become a Certified Back‑Up Trainer (CBT) as determined by the supervisor. If acting as a CBT, responsible for training others and maintaining.

• High School Diploma or equivalent
• Minimum of 2 years of work experience in manufacturing is required
• Previous experience in manufacturing, performing inspections, operating equipment
• Experience with Lean Manufacturing and related principles
• Experience with maintaining accurate records including training files and shop floor paperwork
• Experience with SAP or other manufacturing execution software programs
• Experience training others

• 5 years of work experience in manufacturing is preferred
• Previous medical device experience preferred, but not required

This position requires proficiency in communication and understanding of English, including reading work instructions to consistently build defect‑free medical products.

Minneapolis

This role is deemed safety‑sensitive and candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with applicable law.

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