Supply Quality Professional
hace 2 meses
Abbott Laboratories is a globally renowned healthcare leader, pioneering groundbreaking science to improve people's health.
We're constantly looking towards the future, anticipating innovations in medical science and technology.
Working at Abbott LaboratoriesAt Abbott Laboratories, you can do meaningful work, grow, and learn, care for yourself and family, be your true self, and live a full life.
As an Abbott Laboratories employee, 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 Alajuela location in the Structural Heart Division. Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.
As the Sr Supply Quality Engineer, you'll be responsible for activities related to supplier selection and evaluation, material qualification, supplier performance, and receiving inspection. Contribute to the development, establishment, and maintenance of supplier quality engineering methodologies, systems, and practices that meet Abbott and regulatory requirements. This position will be responsible for personnel facilitation, training, and development.
Key Responsibilities:
- Contributes to the development, maintenance, and improvement of Abbott supplier development quality program policies, procedures, and forms.
- May provide mentoring for team personnel.
- Supervises personnel and supports the work, projects, and tasks associated with quality systems for the different business units.
- Reviews and approves all supplied product drawings and component quality plans.
- Manages development of supplied product inspection procedures and first article requirements.
The ideal candidate will possess:
- B.S. in Engineering or Technical field (STEM careers).
- 5-7 years of experience, with preferably 3+ years in quality engineering roles. Preferably in supplier quality engineering roles.
- Prior medical device experience.
- Demonstrated use of Quality tools/methodologies, such as: (Root Cause Analysis, Fishbone, Is/Is Not, etc.), Six Sigma or Process Control & Monitoring (SPC).
- Knowledge of FDA, GMP, QSR CFR 21 Part 820, and ISO 13485.
- Experience implementing various product and process improvement methodologies, such as Lean Manufacturing.
- Technical writing experience.
- Quality Auditor training for ISO 13485 or 9001.
- Ability to travel approximately 10-40%, including internationally.
The ideal candidate will also possess:
- Master's Degree.
- Demonstrated supervisory experience.
- ASQ CQE, CQA, or CSQP certification.
- Previous Supplier Quality engineering or Receiving Inspection experience.
- Experience with SAP (or ERP system) in supply chain modules.
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