Manufacturing Engineer Sr 

Kinetic Concepts, Inc. is a publicly traded (NYSE: KCI) global medical technology company based in San Antonio, Texas with direct operations in 15 countries. With over 5,000 employees and 2004 revenues of approximately $1 billion, KCI is one of the fastest growing and most exciting companies in the medical technology sector, with a market capitalization of approximately $5 billion. KCI has provided a wide range of innovative medical devices for over 25 years, including leading-edge innovation in Wound Care, Pulmonary Care and Bariatric Care to patients in all care settings. More details on KCI can be found at www.kci1.com.

Job Description:

The Senior Manufacturing Engineer is responsible for the management of resources to support large-scale programs and manages medium to large size projects for the Manufacturing Engineering Department and Global Operations. In addition, the Senior Manufacturing Engineer performs work that involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unconventional materials and difficult coordination requirements.

 

 

Job Requirements:

Basic Qualifications: 

    

�         Bachelor Degree in Biomedical, Mechanical, Electrical Engineering or related field.

�         At least 8 years of experience in engineering supporting manufacturing process

�         Experience with MS Office application including:  Word, Excel, and OutLook

 

Other Qualifications:

 

�         Experience in New Product Development Processes.

�         Experience in Manufacturing Processes.

�         Demonstrated project management experience.

�         Ability to deal with all employees and external business contacts while conveying a positive, service oriented attitude.

�         Demonstrated communication and presentation organization.

�         Ability to maintain confidentiality and discretion in business relationships and exercise sound business judgment.

 

Preferred Qualifications:

�         Experience in regulated design environments a plus � specifically medical device development, Federal Drug Administration (FDA) or ISO registered.