Manufacturing Engineer I: Med Device Process Innovator

Boston Scientific; Carlsbad (CA); On-site; USD 63,000 - 119,000; Full time

Job summary

Boston Scientific in Carlsbad, CA seeks a Manufacturing Engineer I to support catheter manufacturing operations, drive process improvement, and help ensure product quality. The role collaborates with Operations, Quality, R&D, and Regulatory Affairs to implement safe, efficient processes in a regulated environment.

The position emphasizes development of manufacturing processes, equipment qualification, and continuous improvement using Lean methods and process validation techniques. On-site role.

Qualifications

• Bachelor's degree in an engineering discipline.
• Zero to three years of manufacturing/regulated industry experience.
• Familiarity with statistical analysis and Lean Manufacturing.
• Experience with quality systems and design controls preferred.
• Proficiency with MS Office; knowledge of Minitab/SolidWorks a plus.

Responsibilities

• Provide day-to-day engineering support for catheter manufacturing operations.
• Investigate issues and support corrective actions to improve quality, yield and productivity.
• Support nonconforming material disposition and related quality issues.
• Assist with root cause investigations and PFMEA updates.
• Develop and improve manufacturing processes and validation activities.
• Create and revise manufacturing documentation and work instructions.
• Collaborate across Operations, Quality, R&D, Supply Chain and Regulatory.

Skills

Statistical analysis

Lean Manufacturing

Cross-functional collaboration

Problem solving

Analytical skills

Communication skills

Education

Bachelor's degree (Mechanical/Manufacturing/Biomedical/Industrial Engineering or related)

Tools

Minitab

SolidWorks

ERP/MES systems

Job description

Boston Scientific in Carlsbad, CA seeks a Manufacturing Engineer I to support catheter manufacturing operations, drive process improvement, and help ensure product quality. The role collaborates with Operations, Quality, R&D, and Regulatory Affairs to implement safe, efficient processes in a regulated environment.

The position emphasizes development of manufacturing processes, equipment qualification, and continuous improvement using Lean methods and process validation techniques. On-site role.