AB - Production Supervisor

Descripción y detalle de las actividades

Purpose of the position : Fully responsible for overseeing production assemblers and test technician personnel for multiple shifts. Execution of material and production plans, manufacturing scheduling and implementation of document and engineering changes into manufacturing. Key Tasks & Responsibilities : -Review and distribute daily, weekly, and monthly schedules to support MPS. -Attend all meetings related to Department performance, QIT, DMAIC, MPS, and product training. -Setup capacity plan for production, design and implement training objectives for the PFT and personnel. -Execute MPS accordingly. -Candidate must have a strong knowledge of bill of material, KANBAN and the concept of Point-of Use. -Must be self-motivated, require minimal direction and able to assist in cross functional meetings; exhibit the ability to define problems, collect and analyze data, establish facts, and recommend corrective actions. -Possess good interpersonal skills and be able to effectively present information to peers and co-workers.

Experiencia y requisitos

• Bachelor Degree in Engineering (industrial, electronic, mechanical, electrical, mechatronic, bio).-Must have at least 3-5 years’ experience in supervision of manufacturing assembly lines (medical devices and or electronic devices). _ Visa B1 / B2 for USA.-Must be able to take the lead role, especially when conducting production meeting and interaction with engineering, planning, QA and R&D. -Perform capacity analysis and generate reports in response to questions regarding production scheduling. -Lead production meetings regarding Performance Metrics, floor training and QIT. Knowledgeable in Line Clearances and compliance as it relates to FDA CFR's for medical devices. -Attainment and understanding of production schedules, material handling and lean manufacturing. Experience with ERP systems (i.e. Dataflo), MS Access, Word and Excel. Desirable : -APICS certification.-Preferred experience in a lean manufacturing environment. Preferred within a FDA regulated (Medical Device) environment.-Preferred experience with any type soldering / welding assembly.