Manufacturing Engineer II

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

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. You will have access to:

• Career development with an international company where you can grow the career you dream of.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

This position works out of our Costa Rica – Alajuela location in the  EP Division.  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.

As the Manufacturing Engineer II, you will develop and implement optimal, cost-effective manufacturing processes and methods in accordance with product specifications and quality standards; recommends and implements improvements to production processes, methods and controls; is also responsible for the activities related to installation and validation of production lines as well as the lifecycle management of equipment.

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

• →Maintains systems that support the monitoring of key performance indicators such as yield, nonconforming material or Leadtime. If indicators show an adverse trend, works with the functional team to plan and implement appropriate changes.
• →Prepares product and process reports by collecting, analyzing, and summarizing information and trends. Uses basic statistic tools.

• →Performs installation/validation activities for new or existent production lines, meeting regulatory requirements. That includes equipment, process, product and test method validations.

• →Identifies, selects, and purchases equipment/fixtures according to production requirements, due to obsolescence, redundancy or line capacity expansion.

• →Participates in the identification and investigation of Non-conforming products. Uses Root cause problem solving techniques to identify and eliminate causes, implements controls and define preventive activities.

• →Keeps equipment operational by coordinating calibration, maintenance and repair services; following manufacturer's instructions and established procedures; requesting special service when needed.

• →Has knowledge and expertise on product requirements and specifications. Understands potential risks related to product malfunctions.

• →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.

• →Maintains manufacturing systems such as SAP routers and BOM's current.

• →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 Non-conforming products. Uses Root cause problem solving techniques to identify and eliminate causes, implements controls and define preventive activities.

• →Leads or supports continuous improvement projects for any of the main key areas: safety, quality and production.

• →May supervise and provide technical assistance to non-exempt personnel, being accountable for their correct training and performance management.

• Bachelor’s Degree in STEM careers.
• Participant of Abbott internship program or technician with 100% courses completed of a STEM career bachelor’s degree program, and currently studying (final project in process).   
• 0-2 years of manufacturing/process.
• Statistical techniques knowledge (DOE, SPC) is required. PE license is a plus.Computer software knowledge (Microsoft Word, Excel, Power Point). 
• Willing to travel.
• Intermediate command of English language.

• Desired experience in validation plans for medical industry products and processes and root cause problem solving methodologies
• Knowledge of FDA, GMP and ISO guidelines.
• US Visa and passport up to date.

• B: Monday to Friday 3:30 pm to 10:00 pm & Saturday 8:00 am to 3:30 pm
• Works 100% on site

Apply Now

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

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In specific locations, the pay range may vary from the range posted.