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Responsibilities include :
- Communicating business-related issues or opportunities during QA Value Stream Meetings.
- Supporting internal / external audit execution and deliverables as required.
- Reviewing the effectiveness of investigations against established processes.
- Analyzing proposed changes to determine if they will result in non-compliance.
- Assessing the need for risk mitigation techniques considering potential defects, defect types, and frequency.
Requirements :
3+ years of experience in medical device quality engineering.Completion of a Six Sigma or similar industry certification.Experience in statistical analysis for quality purposes (sampling plans, trending reports, scan charts in Minitab).Additional Details :
Seniority level : AssociateEmployment type : ContractJob function : Quality AssuranceIndustry : Pharmaceutical ManufacturingThis job is currently active.
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