Sr Tech, Maint/mfg Support Eng - Provincia de Cartago, Costa Rica - Edwards Lifesciences

Edwards Lifesciences

Empresa verificada

Provincia de Cartago, Costa Rica

hace 1 semana

Publicado por:

Andrea Rodríguez

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Descripción

Sr Tech, Maint/Mfg Support Eng (automation technician / Controls technician) Turno A

Provide technical manufacturing support to Operations and Engineering.

Requerimientos especificos de la posicion:

Conocimientos intermedio-avanzados en programación y troubleshooting de equipos automatizados que tengan PLC (Controladores Lógicos Progamables) y HMI (Interfases Humano-Máquina) de las marcas Allen Bradley y Siemens principalmente.

Experiência en empresa médica (preferiblemente)
Conocimientos en solución de problemas en paneles eléctricos específicamente en el área de control.
Habilidad para crear documentos de validación de Software, IQs, etc (no indispensable).

Key Responsibilities:

Perform weekly preventive maintenance routines for equipment to avoid program down time
Check for failures in equipment and perform corrective actions to affected areas that have down time, including conducting and writing impact assessment reports of incidents
Execute experiments and tests (following protocols) to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results, make recommendations, and develop reports for Engineering review
Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment, including transferring information to appropriate locations, e.g., ECRs, SOPs, drawings, and tooling, for Engineering approval
Identify potential improvement opportunities and propose solutions to optimize equipment, e.g., redesign/design of basic equipment, tools, fixtures, for Engineering review
Troubleshoot basic manufacturing equipment
May lead small projects related to new equipment validation, equipment investigations, testing, objective evidence of product dispositions and rework
Utilize manufacturing software (e.g., JDE, QMS,PLM) to update documentation in systems
Provide coaching and guidance to technicians
Other incidental duties

Education and Experience:

Associate's Degree or equivalent in technical/certificate, 2 Years years experience previous experience in manufacturing and/or medical device experience Required or
4 Years years experience related experience Required

Additional Skills:

Good written and verbal communication, interpersonal, and relationship building skills
Problem solving methodology, root cause analysis, and GDP (Good Documentation Practices)
Good computer skills, including usage of MS Office Suite
Moderate knowledge of validation and improvement of automated equipment
Ability to troubleshoot manufacturing equipment
Basic knowledge of material compatibility in the proposed use environment
Moderate knowledge of routine preventive maintenance of production equipment
Moderate knowledge electrical, mechanical, electronic, pneumatic, and controls
Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment
Strict attention to detail
Must be able to work under limited supervision
Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control