Engineer II Process – Controls

## Engineer II Process – Controls Apply:
United States
- South Carolina
- Liberty:
Full time:
Posted Today:
Abbott is a global healthcare leader that helps 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. Our 122,000 colleagues serve people in more than 160 countries.##
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* JOB DESCRIPTION:

**** Working at Abbott
** 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’ll also have access to:
* Career development with an international company where you can grow the career you dream of.
* Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
* An excellent retirement savings plan with 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 around the world and named one of the most admired companies in the world by Fortune.
** Main Purpose of the Role
** Performs analyses to develop design specifications and performance requirements. Provides technical information concerning manufacturing or processing techniques, materials, properties and process (advantages/limitations) engineering planning. Selects techniques to solve problems and make sound design recommendations.
** Main Responsibilities
*** Establishes processes based on product specifications.
* Evaluates process and design alternatives based on “design for manufacturability” principles.
* Understands principles of “Cost of Goods Sold”.
* Manages program compliance with “Quality Control” requirements (i.e. Design Control, Process validation etc.).
* Understands IP issues relative to processes being developed.
* Maintains knowledge of new developments in manufacturing and design technologies.
* Understand work environment issues (i.e. OSHA regulations, etc.).
* Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
* Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
** Qualifications
* *** Education
* ** Bachelors Degree (± 16 years) - Engineering or Technical Field
** Experience/Background
*** Minimum 2 years
* 2 – 4 years manufacturing experience.
* Experience designing and testing medical devices required.
* Experience developing manufacturing processes and technologies and designing for manufacturability required.
* Experience working in a broader enterprise/cross-division business unit model preferred.
* Ability to work in a highly matrixed and geographically diverse business environment.
* Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
* Ability to leverage and/or engage others to accomplish projects.
* Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
* Multitasks, prioritizes and meets deadlines in timely manner.
* Strong organizational and follow-up skills, as well as attention to detail.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:…