Production Supervisor - Mexicali, México - Intuitive
Descripción
Company Description:
Descripción de la empresa
En Intuitive, estamos unidos detrás de nuestra misión: creemos que la atención mínimamente invasiva es la atención que mejora la vida.
Como pioneros y líderes del mercado en cirugía robótica, nos esforzamos por fomentar un equipo inclusivo y diverso, comprometido con marcar la diferencia.
Durante más de 25 años, hemos trabajado con hospitales y equipos de atención de todo el mundo para ayudar a resolver algunos de los desafíos más difíciles de la atención médica y avanzar en lo que es posible.
Intuitive se ha construido gracias a los esfuerzos de grandes personas de diversos orígenes.Creemos que las grandes ideas pueden provenir de cualquier lugar:
nos esforzamos por fomentar una cultura inclusiva basada en la diversidad de pensamientos y en el respeto mutuo.
Lideramos con inclusión y capacitamos a los miembros de nuestro equipo para que trabajen de la mejor manera y manifiesten su auténtica personalidad.
Las personas apasionadas que quieren marcar la diferencia impulsan nuestra cultura: los miembros de nuestro equipo se basan en la integridad, tienen una sólida capacidad para aprender, la energía para hacer las cosas, y aportan experiências diversas del mundo real para ayudarnos a pensar de nuevas maneras.
Invertimos activamente en los miembros de nuestro equipo para apoyar su crecimiento a largo plazo y así poder continuar avanzando en nuestra misión y alcanzar su máximo potencial.
Únase a un equipo comprometido a dar grandes pasos hacia delante para una comunidad global de profesionales de atención médica y sus pacientes.
- Hire, train, develop, and motivate production personnel to follow procedures, meet high quality standards, production schedules, productivity requirements and Recognition.
- Update and revise Manufacturing Process Instructions to ensure that MPIs are accurate and complete
- Address line support issues as they arise, including technicalrelated issues
- Work closely with All Support departments to resolve production issues and actively participant in quality improvement initiatives.
- Document, report and escalate any variances, problems, issues, or concerns.
- Provide production personnel with expectations and performance feedback quarterly and on stan ups.
- Write and conduct formal annual performance reviews for production personnel and execute Monthly One on One Feedback
- Plan, supervise, drive improvement, and report production performance including output, yields, root cause failures, efficiencies, and trends
- Understand, train personnel, and enforce strict adherence to the applicable DOPs and SOPs of the Quality System, as well as the Manufacturing Guidelines
- Assist in setting and attaining quarterly and annual production goals, Business unit strategy, VSM, HK Gool deployment
- Learn and enforce company safety policies and practices and develop safety project initiatives, line risk assessment, 8d plan, Turn over line plan, Layer Audits.
- Lead or support various Lean Manufacturing initiatives that involve a Mfg. based team thru Corporate Projects, Project Management, Kaizen, Green Belts or Rapid problemsolving events.
- Support subassembly or process outsourcing initiatives
- Review and disposition discrepant material. Implement corrective actions to prevent recurrences. Implement project to improve Material Usage / reduce Scrap.
- Evaluate designs for manufacturability (with respect to tooling and assembly methods). Provide suggested change proposals, or tooling concepts during early design process phase. (All line improvements)
- Drive our Culture Strategy by fostering our mission, founding principles, individual and leadership expectations. Create Action plan for X survey.
- Support corporate Quality improvement CAPA implementations and lead QA Improvements.
- Assist engineering with Final Manufacturing Review.
- Assist budget spending preprocess and execution.
- Ensure completion of All training ISU related for associates under his supervision (CO, Lead, CO)
- Complete Payroll activities for his reports.
- Execute production plan
- Support process validations.
Qualifications:
- Education and/or Experience: Bachelor's degree on related fields.
- 3 years of either supervisor and/or engineering experience. Experience in the medical device industry is preferred, specifically in highvolume manufacturing area.
- Knowledge of Lean Manufacturing, DFT, and 6 Sigma (GB/BB highly recommended).
- Proficient in the use of personal computers to perform daily work. Familiar with the Microsoft Office suite of programs and MRP systems. SAP and Agile experience preferred.
- Able to communication skills, including written and verbal instruction.
- Intermediate English/Spanish
- Ideal knowledge on FFs, PLC, Th
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