Process Manufacturing Engineer I

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

Position Summary

Responsible to act as manufacturing liaison and coordinate all activities affecting the introduction of new products into the manufacturing cycle. Responsible for development and expense control of manufacturing capital equipment and tooling needed for new product manufacture. Participates in product design and overall project and manufacturing schedule development. Evaluates, selects and applies Manufacturing Engineering techniques to develop economical and efficient methods to produce piece parts and/or assemblies. Provides necessary input to develop cost, prepare manufacturing specifications for various operations/work stations. Recommends and implements design changes to improve reliability, manufacturability and cost.

Duties

• Review and help 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. Recommend rearrangement of plant facilities.
• 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, CONTINUOS IMPROVEMENT and TRAINING initiatives, which include but are not limited to: A3 Certification and projects, STOP Observations, Monthly Safety Audits, SQDC board maintenance, upgrade and administration of KPI for the area, propose and execute CIP (Cost Improvement Projects), maintenance of LSW sheet, upgrade and maintenance of initiatives using Dploy system.
• Maintain and improve the quality system in accordance with the requirements, as appropriate, of the following standards: ISO 9001, ISO 13485, MDSAP and FDA 21 CFR Part 820/211, EU MDR, NOM-241-SSA1, and other applicable standards.

Education Degree

Bachelor's Degree in Engineering General

Required Experience (1 Year)

• 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.

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.

STERIS strives to be an Equal Opportunity Employer.