Industrial Process Optimization Specialist
hace 1 día
About Abbott Laboratories
Abbott Laboratories is a global leader in the healthcare industry, dedicated to creating innovative medical technologies that improve people's lives.
We strive to anticipate and adapt to changes in medical science and technology, ensuring our products and services meet the evolving needs of patients and healthcare professionals.
Working at Abbott Laboratories
At Abbott Laboratories, you have the opportunity to do meaningful work, grow and learn, take care of yourself and your family, be your authentic self, and live a full life.
You will have access to:
• Career development opportunities with an international company where you can grow your career and achieve your goals.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies globally by Fortune.
• A company committed to diversity, equity, and inclusion, providing a supportive and inclusive environment for all employees.
The Opportunity
This role is based in Costa Rica - Alajuela, working in the Electrophysiology (EP) business unit.
In this division, we are advancing the treatment of heart disease through cutting-edge medical technologies in atrial fibrillation, enabling people to restore their health and resume their lives.
Job Responsibilities
As an Industrial Process Optimization Specialist, you will develop and implement optimal manufacturing processes and methods, ensuring compliance with product specifications and quality standards.
You will also recommend and implement improvements to production processes, methods, and controls, as well as oversee the installation and validation of production lines and equipment lifecycle management.
Your key responsibilities will include:
• Providing daily support to manufacturing activities to meet established goals for safety, quality, cost, and production.
• Maintaining systems for monitoring key performance indicators such as yield, nonconforming material, or lead time.
• Preparing product and process reports by collecting, analyzing, and summarizing information and trends, using basic statistical tools.
• Performing installation/validation activities for new or existing production lines, meeting regulatory requirements.
• Identifying, selecting, and purchasing equipment/fixtures according to production requirements, due to obsolescence, redundancy, or line capacity expansion.
Required Qualifications
To succeed in this role, you will need:
• A Bachelor's Degree in a STEM field.
• At least 2 years of experience in similar roles.
• Intermediate-level English language proficiency.
• Knowledge of statistical techniques (DOE, SPC).
• Familiarity with computer software (Microsoft Word, Excel, PowerPoint).
• Willingness to travel.
Preferred Qualifications
Prior experience in validation plans for medical industry products and processes, root cause problem-solving methodologies, knowledge of FDA, GMP, and ISO guidelines are desirable.
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