Manufacturing Process Engineer

hace 6 horas


Alajuela, Alajuela, Costa Rica Abbott Laboratories A tiempo completo

**About Abbott Laboratories**

A global healthcare leader, Abbott is creating breakthrough science to improve people's lives.

We anticipate changes in medical science and technology, always looking towards the future.

**Working at Abbott**

You can do work that matters, grow, and learn, care for yourself and family, be your true self, and live a full life.

At Abbott, you will have access to:

Career development with an international company where you can grow your career.

- A company recognized as a great place to work in dozens of countries around the world.

- A company named one of the most admired companies in the world by Fortune.

**The Opportunity**

This position works out of our Costa Rica - Alajuela location in the Structural Heart Division.

In Abbott's business purpose is to restore health and improve quality of life through device and management solutions for the treatment of structural heart disease.

As the Manufacturing Process Engineer, you will support the development and implementation of optimal manufacturing processes and methods in accordance with product specifications and quality standards.

You will recommend and implement improvements to production processes, methods, and controls.

Support the activities related to installation and validation of production lines as well as the lifecycle management of equipment.

**Key Responsibilities**

- Daily support to the manufacturing activities in order to meet established goals for safety, quality, cost, and production.

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

If indicators show an adverse trend, work with the functional team to plan and implement appropriate changes.

- Lead yield/productivity analysis & improvement plans.

Analyze defective material to identify probable cause.

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

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

**Required Qualifications**

- High school degree.

- 3+ years of experience in similar roles, knowledge in manufacturing process.

- Basic Command of English.

- Capable to perform data analysis and data collection in Excel or other software.

- Strong computer software knowledge (Microsoft Word, Excel, PowerPoint, Visio).

- Capable to support investigations using root cause problem-solving methodologies.

- Demonstrated knowledge/expertise in a specific technical/Engineering area.

- Willing to travel.

**Preferred Qualifications**

- 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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