Boston Scientific Engineer II Mfg Turno B 

Costa Rica, El Amparo 

587889001

Hybrid Roles:

You're Responsibilities include:

• Demonstrate knowledge and responsibility for GMP's/QSR and ISO requirements.
• Evaluate and trouble-shoot manufacturing processes in an outsourced environment.
• Analyze, design and develop processes, tools, equipment necessary to produce products in a lean manufacturing environment.
• Support the successful completion of all manufacturing project activities, defining, developing, verifying and validating products for successful commercialization.
• Create practical solutions to technical challenges and provide technical support across functions; and establish equipment specifications and requirements in the development of new equipment or improvements to existing equipment as appropriate.
• Analyzes and assesses designs and plans layout for activities including machining, metal forming, plastics processing, welding and brazing, assembly, and materials handling.
• Develop, implement and qualify production tooling for components, assemblies and packaging.
• Develop and execute test methods and reports to assure appropriate design and process validation.
• Develop process controls leveraging statistical process control and data analysis.
• Provides design input to R&D engineering including appropriate Design for Manufacture (DFM) and Assembly (DFA) analyses.
• Provides operations engineering input to develop risk analyses and abatement plans and actions.
• Performs tool qualifications and validations including IQ, OQ, and PQ’s.
• Utilizes advanced problem solving techniques and skills to rapidly resolve and implement technical solutions in alignment with project and organizational objectives.
• Other duties may be assigned.

What We’re Looking For:

• Bachelor's degree in: Electromechanical Engineering, Materials Engineering or Mechanical Engineering.
• English Level desired: Advanced
• Experience:2+ years’ experience in Medical Device Manufacturing (ISO13485), Problem Solving, Equipment Qualifications, Process Validations, Lab Studies, Process Characterization, Tolerance Stack up Analysis, Good Documentations Practices, Knowledge in Statistics,
• Desired knowledge: GD&T,CAD experience preferably Solidworks, DFM.
• Schedule: 2nd Shift