Abbott Manufacturing Process Engineer in St. Paul, Minnesota
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.
We are seeking an experienced, high caliber Process Development Engineer I. This position will design and develop manufacturing processes and support production and service activities in order to meet daily production schedules while enhancing productivity, cost and product quality.
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.
Troubleshoot manufacturing process and equipment using understanding of electronics, software, circuits and systems
Design and develop manufacturing processes, in order to meet daily production schedules while enhancing productivity and product quality
Identify and execute cost reduction activities
Evaluation of production equipment
Production support and process validation
Interface with vendors for incoming components
Understand Lean manufacturing concepts like Value Stream mapping, 5S and Visual Workplace to improve quality, labor efficiency, and throughput.
Protocol and report writing
Generate and modify manufacturing process documentation
Work with cross functional teams as required
Develop and implement process improvements
Resolves and/or facilitates resolution of problems including identifying causes to prevent re-occurrence
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.
Minimum Experience, Education and Knowledge:
Bachelors of Science degree in Mechanical, Biomedical, Chemical Engineering, or equivalent
0-3 years of relevant engineering experience
Experience working in medical device or other regulated industry
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
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
Ability to travel approximately 5%, including internationally
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email firstname.lastname@example.org