Industrial Engineering Manager for Medical Devices
hace 3 días
**About Abbott Laboratories**
We're a global healthcare leader, pioneering breakthrough science to enhance people's lives.
Ours is a culture of innovation, where we continuously anticipate and respond to changes in medical science and technology.
**Why Work at Abbott?**
At Abbott, you'll have the opportunity to do meaningful work that drives positive change, while growing and learning alongside talented colleagues who share your passion for making a difference.
You'll have access to:
Career development opportunities with an international organization that empowers you to achieve your career aspirations.
A company recognized as one of the best workplaces globally, known for its commitment to diversity, equity, and inclusion.
**The Opportunity**
This role is part of our Electrophysiology Division, based in Costa Rica, where we're pushing the boundaries of heart disease treatment through cutting-edge medical technologies.
As the Manufacturing Engineering Section Leader, you'll be responsible for providing strategic leadership to engineering teams to drive business results.
The ideal candidate will have expertise in developing and implementing efficient manufacturing processes and methods, ensuring compliance with product specifications and quality standards.
Key responsibilities include:
- Ensuring production lines meet product specifications
- Developing and maintaining clear criteria for conforming/non-conforming products
- Collaborating with cross-functional teams to navigate and execute activities on manufacturing systems
- Coordinating new ZFIN implementation activities
- Maintaining MP's current and compliant to regulations
- Leading or supporting local cross-functional team activities
Requirements
- Bachelor's Degree in a STEM field
- 7+ years of experience in manufacturing/process development or equivalent combination of experience/skills
- Fluency in English and Spanish
- Experience with statistical techniques (e.g., DOE, SPC)
- Proficiency in computer software (Microsoft Word, Excel, PowerPoint)
- Experience with continuous improvement methodologies (e.g., lean manufacturing techniques, value stream mapping)
- Solid knowledge of FDA, GMPs, and ISO regulations
- Experience leading validation plans for medical industry products and processes
Preferred Qualifications
- 5 years prior experience in medical device manufacturing
- Performance management experience
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