**Acerca de la vacante**:
**Funciones del Puesto**:
**Responsibilities**:
Support, promote and enforce safety across the campus.
Support and promote the overall EHS initiatives and programs.
Follow all Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's) as defined by MedPlast's policies, practices and procedures to ensure that FDA and ISO regulations along with Viant quality standards are met.
Identify processes improvements, meet quality specifications and productivity goals for current and/or new business and programs.
Continuously seek for process improvement projects, relevant to Lean Manufacturing and Innovation.
Drive product / process compliance investigations for non-conformances (NCs), Corrective and Preventive Actions (CAPAs) and Internal / External Audits; and ensure timely completion and effectiveness of implemented actions if is requested.
Perform other duties, tasks, or projects at the direction of immediate supervisor.
Receive and enter customer Purchase Orders (PO).
Load and maintain Customer forecasts.
Create Work Orders (WO).
Generate planning reports.
Perform other duties, tasks, or projects at the direction of immediate supervisor.
Participate on project teams if required.
Support product launch manager on management activities as required.
Understanding of customer requirements and ERP system.
Make delivery commitments on MTO/MTS products, which involve checking uncommitted material and capacity availability with Procurement and Operations.
Monitor actual output versus the Master Production Schedule (MPS).
Identify gaps and drive solutions, including metrics for production performance according to the requested production plan.
Develop inventory targets and manage production to achieve target inventory levels.
Perform other duties, tasks, or projects at the direction of immediate supervisor.
**Requisitos del Puesto**:
Education
Proficient in Microsoft Office.
Well organized
Customer service skills oriented.
Bilingual English/Spanish - Intermediate English level.
(Written and spoken).
Knowledge on ERP system.
Bachelor degree in Industrial Engineer or Business Administration.
Experience within the medical device manufacturing field or in any other regulated industry it's a plus.
**Experiência Deseada**:
Job Experience
From 3 to 5 years of experience in planning and manufacturing environment.
Experience within the medical device manufacturing or pharmaceutical fields, or any other highly regulated industry (i.e.
food, aerospace, etc.)
is a plus.
**Habilidades Deseadas**:
Competencies
Good interpersonal skills and the ability to communicate orally and in writing.
Self-motivated.
Organized and able to manage multiple tasks and priorities.
Must be able to quickly and independently make decisions.
Must be able to work and effectively communicate with others.
Highest ethical standards and professional integrity.
Able to work independently.
Teamwork oriented.
**Otros detalles**:
**Area del Puesto**:
Logística
**Ubicación del Puesto**:
Barreal de Heredia, Heredia, Costa Rica
**Nível Académico**:
Bachillerato Universitario
**Nível de Cómputo**:
Office Profesional
**Idiomas**:
**Inglés**: 80%