Manufacturing Engineer I
hace 1 mes
The Opportunity
Abbott's Electrophysiology (EP) Division is seeking a skilled Manufacturing Engineer I to join our team in Costa Rica - Alajuela. As a key member of our manufacturing team, you will play a critical role in developing and implementing optimal manufacturing processes and methods to meet product specifications and quality standards.
Key Responsibilities
- Develop and implement cost-effective manufacturing processes and methods in accordance with product specifications and quality standards.
- Recommend and implement improvements to production processes, methods, and controls.
- Responsible for the activities related to installation and validation of production lines as well as the lifecycle management of equipment.
- Assure that production lines output meet the specifications of the product.
- 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, nonconforming material, or leadtime.
- Prepare product and process reports by collecting, analyzing, and summarizing information and trends.
- Use basic statistical tools.
- Keep equipment operational by coordinating calibration, maintenance, and repair services.
Requirements
- Bachelor's Degree in STEM careers or participant of Abbott internship program or technician with 100% courses completed of a bachelor's degree STEM career program and currently studying (final project in process).
- 0 to 2+ years of working experience on similar roles.
- Intermediate Commands of English to Advance Commands of English.
- Statistical techniques knowledge (DOE, SPC) is required.
- Computer software knowledge (Microsoft Word, Excel, Power Point).
- Willing to travel.
Preferred Qualifications
- Desired experience in validation plans for medical industry products and processes and root cause problem solving methodologies.
- Knowledge of FDA, GMP, and ISO guidelines.
- Previous experience supporting NCMR/CAPA investigations.
- Experience with the use of SAP, Minitab, Infititive QS, and INFOR (or equivalent systems).
- New product validation is a plus.
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