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Boston Scientific Designer HEREDIA 
Costa Rica, Heredia 
885546867

14.04.2025

Costa Rica-Heredia

Hybrid Roles:

About the role

Responsible for modeling/designing components for new and existing medical device products (e.g. assemblies/equipment/fixtures/programmers/leads/stents) into detail drawings and documentation using CAD and other tools.

Your responsibilities include:

  • Model product concepts using current tool, analysis techniques, and technologies through use of parametric CAD software and other mechanisms.
  • Perform Mechanical design/redesign of medical device products applying industry standards (e.g. ASME Y14.5M-1994) to detail drawings.
  • Create/modify/maintain documentation using CAD tools that are tied to a data management system.
  • Provide support for OEM device documentation and Bill of Material structure support.
  • Provide support for OEM device documentation. (VI)
  • Completes document packages by detailing parts and creating BOM and schematics following layouts, sketches and verbal instructions to ensure that all of the needed documentation is available for manufacturing process. (VI)
  • Reviews and verifies design work of peers to check for compliance with standards and corporate procedures.
  • May review engineering order (EO) package by reading information on EOs (e.g. document description) and supplemental information (e.g., preliminary sketch) in order to identify missing information.
  • May generate engineering change orders (ECOs). (CRM)
  • May provide illustrations, animation and web publishing solutions that allow communication of 2D/3D product information for interactive assembly, maintenance/ restoration of documentation, product presentations and Federal and International compliance.
  • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
  • For those individuals that supervise others, the following statements are applicable:
  • Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy.
  • Establishes and promotes a work environment that supports the Quality Policy and Quality System.

Required Qualifications:

  • Technical degree, 2+ Diplomado, 0+ Bachelor, 0+ An equivalent combination of education and work
  • Preferred Experience in the Medical Device Industry
  • Microsoft Office basic
  • Desirable competencies Customer Focus, Relationship Building, Quality Orientation, Communication, Execution, Follow up
  • Desire English Level B1 50-59%