Boston Scientific Engineer III process 

Costa Rica, Cartago 

901598096

About the Role

· Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on multiple and moderately complex processes.

· Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.

· Executes the functional deliverables associated with the PDP/TDP, Project Management, and Quality Systems.

· Prepares and presents technical data and recommendations at technical reviews.

· Writes validation protocols and reports applicable to new processes.

· Ensures proper documentation is completed to meet quality systems requirements. (e.g., TMVs, OQ/PQ, MVPs, etc.)

· Plan development/execution builds associated with the project using special work requests.

· Develops qualified production lines and utilize lean essential tools to support ramp up and scalability.

· Provides Design for Manufacturability (DFM) input to the engineering print package.

· Contributes ideas to or generates Intellectual Property submissions.

· Trains and/or provides work direction to technicians and may train manufacturing personnel when required as part of a validation.

· May serve as core team member or extended team member on new product projects.

· May serve as a technical mentor or guide for new team members

· Basic project planning skills.

· Good communication skills oral and written

What We’re Looking For:

· Licenciature in Materials Engineering, Mechanical Engineering, Mecatronics Engineering, Electronic-Electrical Engineering, Industrial Engineering, Biomedical Engineering

· English Level required: B2+ (80% - 89%).

- At least 3 years of experience in similar positions

· Desired knowledge: Statistics, Problem Solving, Process Improvement, Project Management, Process Validation, Clinical Knowledge, mechanical design, test automation.