Engineer II, Process

Job description

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

JOB DESCRIPTION:

We are seeking an experienced, high caliber Process Engineer. Responsible for developing new manufacturing processes, equipment and materials for use in production of medical devices. Works on process engineering problems of diverse scope. Exercises judgment and defines methods and criteria in conducting process engineering experiments and reports results. Develops networks with internal/external working relationships in area of expertise.

Each employee can make a difference at Abbott and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals.

Impact this role will have on Abbott:

• 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.

Basic Qualifications:

• BS degree in Mechanical Engineering or other Technical Field
• 2 or more years of experience in a manufacturing environment
• Experience developing manufacturing processes and technologies and designing for manufacturability required

Preferred Qualifications:

• advanced degree preferred

• Experience working in a broader enterprise/cross-division business unit model preferred
• experience in a microelectronics assembly environment
• Experience designing and testing medical devices a plus
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to travel approximately 10%, including internationally.

JOB FAMILY:

DIVISION:

LOCATION:

ADDITIONAL LOCATIONS:

WORK SHIFT:

TRAVEL:

MEDICAL SURVEILLANCE:

SIGNIFICANT WORK ACTIVITIES: