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 mangement 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.

• Beneficios de acuerdo a la LFT
• seguro de vida
• bonos anuales
• caja de ahorro
• comedor
• fondo de ahorro
• transporte
• uniforme
• seguro de gastos médicos
• utilidades garantizadas
• servicios médicos en planta
• Seguro de gastos funerarios
• Seguro dental
• Acciones de la compañía
• Becas educativas
• Nutriológo
• Clases de Yoga