Manufacturing Process Engineer I — Medical Devices

STERIS; Guadalupe; Presencial; MXN 600.000 - 900.000; Jornada completa

Descripción de la vacante

STERIS is seeking a Manufacturing Engineer to coordinate introduction of new products into the manufacturing cycle. You will develop and control capital equipment and tooling costs for new product manufacture, participate in design and project planning, and apply manufacturing engineering techniques to create economical, efficient processes.

You will review drawings, reduce manufacturing costs through value analysis, develop schedules and plans for prototype to production, and establish clear

Formación

• Bachelor's Degree in Engineering General.
• Experience in manufacturing engineering disciplines, with progressively more responsibility.
• Must be technically knowledgeable to Good Manufacturing Practices relating to machines, metal forming, metal joining, assembly.
• Experience working in engineering and/or manufacturing of medical equipment.

Responsabilidades

• Review and generate product documentation pertaining to engineering drawings including initial release and subsequent revisions.
• Review products for the purpose of reducing cost of manufacturing through value analysis, material substitution, process changes, make/buy decisions.
• Helps to develop manufacturing schedules and generates manufacturing plans for prototype, pre-production and production.
• Develop clear and concise manufacturing specifications/instructions to maintain quality and to assure smooth work flow through the factory.
• Provide floor support during the manufacturing cycle, verify standards, and update manufacturing specifications.
• Develop workmanship standards to accommodate manufacturing/inspection and assure conformance to specifications.
• Develop standard cost estimates and establishes standard cost.
• Assure manufacturing facilities, tooling and test equipment are available to meet production requirements.
• Perform manufacturing studies leading to recommendations for new and improved methods, procedures and equipment utilization.
• Review and evaluate plant capacity and capabilities; recommend action to optimize burden absorption.
• Perform related Human Resources functions associated with supervision, including but not limited to hiring, performance evaluation, training, employee development, corrective action, and employment separation.
• Active participation of the SAFETY, CONTIUOS IMPROVEMENT and TRAINING initiatives, including A3 Certification etc., CIP, KPI maintenance.
• Maintain and improve the quality system in accordance with ISO 9001, ISO 13485, MDSAP and FDA 21 CFR Part 820/211, EU MDR, NOM-241-SSA1, and other applicable standards.

Conocimientos

Manufacturing Engineering

Cost reduction

Quality systems

Project coordination

Process improvement

Educación

Bachelor's Degree in Engineering General

Herramientas

ISO 13485

MDSAP

FDA 21 CFR Part 820/211

Descripción del empleo

STERIS is seeking a Manufacturing Engineer to coordinate introduction of new products into the manufacturing cycle. You will develop and control capital equipment and tooling costs for new product manufacture, participate in design and project planning, and apply manufacturing engineering techniques to create economical, efficient processes.

You will review drawings, reduce manufacturing costs through value analysis, develop schedules and plans for prototype to production, and establish clear