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Job description (Tasks/Responsibilities):
Performing trend analyses on quality data. Participating in nonconforming material/ Material Review Board process. Performing internal quality audits / effectiveness reviews.
Conducting supplier evaluations / audits. Run various risk analysis activities for new and existing products.
Skill Requirements:
Experience in an FDA regulated Class III electrical medical device
environment. Experience with database queries and reporting. Lean Experience and Six Sigma experience is preferred.
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