Roles & Responsibilities

- Lead initiatives focused on yield improvement, material cost reduction, capacity enhancement, and outsourcing of assemblies.
- Evaluate and challenge mechanism designs for process reliability, serviceability and manufacturability. Provide suggested change proposals.
- Creating budget estimates for tooling, test equipment, prototype designs, and first article activities.
- Ensure the processes meet the specified requirements for operation including adherence to parameters, specifications avoiding variations in the manufacturing process.
- Provides technical support analyzing and/or performing failure analysis for discrepant production components, assemblies and field returns.
- Qualify, document and introduce production processes.
- Take responsibility for developing and maintaining compliance with the quality system.
- Evaluate and select suppliers for mechanical parts. Help resolve supplier quality issues.
- Must possess strong communication skills to interface with suppliers, product development, planning, purchasing, regulatory, inspection, customer support and clinical marketing organizations.
- Performs other duties as required.
- Travel: Position may require 5-10% travel, primarily within U.S.
- Drive our Culture Strategy by fostering our mission, founding principles,



individual and leadership expectation

Skills, Experience, Education, & Training

Required

- Candidate must be of high character and energy with regard for detail.
- Demonstrated Mechanical and/or Process Engineering ability.
- Demonstrated ability in failure analysis and continuous improvement.
- BS degree in Mechanical Engineering or equivalent.
- Minimum 3 years manufacturing engineering management experience with mid/high volume complex manufacturing processes.

Preferred

- MS degree in an Engineering discipline.
- 3 to 5 years of experience as design or manufacturing engineer supporting product with significant mechanical/process content.
- Prior experience with various mechanical and or electronics applications and technologies, including reliability and performance assessment.
- Prior experience working in FDA 21 CFR820/ISO 13485 medical device manufacturing environment.
- Demonstrate ability to design/execute experiments.
- Prior responsibility for process or product validation/verification.
- Experience with ASME Y14.5 Geometric Dimensioning and Tolerance.
- Experience in Just-In-Time, Demand Flow Technology, and Lean Manufacturing techniques.

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📌 Manufacturing Engineering Manager (Mexicali)
🏢 Intuitive Surgical, S. De R. L De C. V.
📍 Mexicali