Sr Manufacturing Engineer - Heredia, Costa Rica - TE Connectivity

TE Connectivity

Empresa verificada

Heredia, Costa Rica

hace 1 semana

Publicado por:

Andrea Rodríguez

beBee Recruiter

Descripción

About the position:

Responsabilities

Daily support to the manufacturing activities in order to meet established goals for safety, quality, cost and production.
Based on key performance indicators data such as yield, nonconforming material or Leadtime, takes action to maintain indicators under control.
Uses statistical techniques to facilitate decision making and to draw conclusions from available data.
Understands product cost components and its interactions, (direct & indirect material costs, labor, overhead).
Prepares product and process reports by collecting, analyzing, and summarizing information and trends.
Performs installation/validation activities for new or existent production lines, meeting regulatory requirements. That includes equipments, process, product and test method validations.
Estimates validation activities cost and assures it is budgeted withing financial cycle.
Identifies, selects, and purchases equipment/fixtures according to production requirements, due to obsolescence, redundancy or line capacity expansion.
Has direct relation with vendors to define equipment suitability.
Keeps equipment operational by coordinating calibration, maintenance and repair services; following manufacturer's instructions and established procedures; requesting special service when needed.
Analyzes equipment data, trends, and performance to assure correct lifecycle management. Identifies and mitigates risks associated to equipment technical knowledge, spares availability and external technical service
Evaluates the financial, process or quality impact, derived from product & process changes.
Assures that production lines output meet the specifications of the product.
Has clear criteria of conforming/ non conforming product and the test methods used for verifying conformance.
Able to navigate and excecated activities on manufacturing systems for example, update routers, BOM's or to generate new part numbers.
Coordinates the activities related to new part numbers implementation.
Maintains MP's current and compliant to regulations. Ensures practices at the manufacturing floor adhere to them.
Supports DL's & IDL's training process.
Participates in the identification and investigation of Nonconforming products.
Uses Root cause problem solving techniques to identify and eliminate causes, implements controls and define preventive activities.
Leads or supports CAPA investigation processes, or exception documents such as complaints investigations.

Qualifications

Bachelor's Degree. STEM careers.
6+ years of manufacturing/process development experience
Computer software knowledge (Microsoft Word, Excel, Power Point).
Willing to travel.
Experience with continuous improvement methodologies. Such as lean manufacturing techniques, value stream mapping, or similar.
Knowledge of FDA, GMP, and ISO guidelines is required.
Experience leading validation plans for medical industry products and processes and leading root cause problem solving methodologies.
Experience in project management.
Advance command of English (written and speaking). Required

years prior experience in medical devices manufacturing.