Senior Manufacturing Process Engineer

18 hours ago


Santa Clara, California, United States Abbott Full time

At Abbott, we're committed to helping people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.

Working at Abbott

We offer a dynamic work environment where you can grow, learn, and care for yourself and your family. You'll have access to:

  • Career development with an international company where you can grow the career you dream of.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Santa Clara, CA location in the SH division. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.

As the Senior Manufacturing Process Engineer, you'll have the chance to be responsible for providing support to the Manufacturing organization to facilitate efficient operations within the production area, to optimize existing processes, and to ensure that production goals are met. You will monitor performance of equipment, machines, and tools and corrects equipment problems or process parameters that produce nonconforming products, low yields, or product quality issues. Interfaces with Quality and Research and Development organizations to integrate new products or processes into the existing manufacturing area.

Key Responsibilities

  • Interacts cross-functionally and with internal and external customers.
  • Serves as a consultant for engineering or scientific interpretations and advice on significant matters.
  • Develops processes for manufacturing or testing of the product.
  • Understands business environment and relates extensive knowledge of internal and external technological activities to trends.
  • May lead a project team. Provides technical leadership to business units. Acts as a mentor to less-experienced staff and may provide work direction or supervise other technical employees. Exercises judgment independently.

Requirements

  • Bachelor's degree preferably in Biomedical Engineering or Mechanical Engineering, or a closely related discipline or equivalent combination of education and work experience.
  • 6+ year of significant engineering experience in the medical device field.


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