skill

BS Degree in Engineering or Technical Field or equivalent experience.

2-5 years Software Quality Engineering experience.

Detailed knowledge of FDA GMP IEEE 1012 and ISO 13485. Advanced computer skills including statistical/data analysis and report writing.

Advanced Information Technology and data mining skills.

Prior medical device experience preferred.

ASQ CSQE certification desired.

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. Ability to travel including internationally. Ability to maintain regular and predictable attendance