Minimum experience of 4 years in Medical devices Manufacturing Engineering.
Good Experience working on Process Validations (IQ OQ PQ. .
Experience developing manufacturing processes and technologies which includes process characterization.
Experience working on PFMEAs.
Experience performing Data analysis (Minitab. .
Evaluate process and design alternatives based on Design for Manufacturability principles.
Ability to work within a team and as an individual contributor in a fastpaced 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 followup skills as well as attention to detail.
Complies with U.S. Food and Drug Administration (FDA) regulations other regulatory. requirements Company policies operating procedures processes and task assignments.
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