About the role: :Works cross:functionally to lead process development of complex technologies on new products and ensures efficient and effective transfer of new product into production.
Youre Responsabilies Include:
:Assesses process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on platform or derivative projects.
: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.
:Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOMs, Routers, FMEAs, etc.)
:Develops qualified production lines.
:May supervise Technicians and Eng I in order to achieve projects goals.
:Additional Duties:
:Oversees development builds associated with the project using special work requests.
:Oversees development builds associated with the project using special work requests.
:Writes and reviews validation protocols and reports applicable to new processes.
:Plans, organizes, and conducts all aspects of technical reviews.
: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 engineers and may train manufacturing personnel when required as part of a validation.
:May serve as a core team member or extended team member on new product projects.
What Were Looking for:
:Licenciature in Industrial Engineering, Mechanical Engineering or related fields or equivalent experience.
:Experience: 5 years
:English: 80:89
:Problem Solving
:Process Improvement
:Lean manufacturing and Six Sigma knowledge
:PDP/TDP, Project Management, and Quality Systems.
:Process Validations deliverables: IQ, OQ,PQ, PPQ protocols and reports
Boston Scientific is an equal opportunity employer
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