Manufacturing Engineering Technician

hace 2 meses


Alajuela, Alajuela, Costa Rica Abbott Laboratories A tiempo completo

**Job Opportunity**


At Abbott, we're always looking towards the future, anticipating changes in medical science and technology.


This position works out of our Alajuela, Zona Franca Coyol location in EP Business. In Abbott's Electrophysiology (EP) business, we're advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives.


**Job Responsibilities**


This position executes documentation control activities which includes:


Supporting daily operations to meet established goals for safety, quality, cost, and production.


Maintaining systems that support the monitoring of key performance indicators such as yield, per operators, reject parettos, etc.


Leading yield/productivity analysis and improvement plans, analyzing defective material to identify probable cause.


Executing installation/validation activities for new or existent production lines, meeting regulatory requirements.


Supporting the identification, selection, and purchasing of equipment/fixtures according to production requirements.


Keeping equipment operational by coordinating calibration, maintenance, and repair services.


Interpreting product requirements and specifications, understanding potential risks related to product malfunctions.


Driving/executing change requests process within the area as required, supporting DL's training process.


Working in a cross-functional team environment, participating in the identification and investigation of non-conforming products.


**Requirements**


High school degree, 3+ years of experience in similar roles, knowledge in manufacturing process.


Capable of performing data analysis and data collection in Excel or other software, strong computer software knowledge (Microsoft Word, Excel, PowerPoint, Visio).


Capable of supporting investigations using root cause problem-solving methodologies, demonstrated knowledge/expertise in a specific technical/Engineering area.


Willing to travel, basis English level to Intermediate Commands of English, technical/Engineering Studies are preferred.


5+ years in a Medical Device Manufacturing or similar environment is preferred, knowledge of FDA, GMP, and ISO guidelines, desired experience in validations execution.



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