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Manufacturing Quality Engineer
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- Responsibilities: Responsible for ensuring percent quality and regulatory compliance in accordance with documented procedures for all aspects of functional responsibility.
- Supports continuous product and process improvement through detailed failure analysis for non-conformances, and investigates, develops, and implements effective and compliant solutions for product or process corrections, action plans, and for corrective and preventive actions (CAPA Program).
- Utilizes risk management tools and aids for use by the organization in accordance with documented procedures, including but not limited to PFMEA, DFMEA, Failure Mode Analysis, etc.
- Develops process mitigation plans and strategies that are designed to mitigate the risks identified through the Risk Management process.
- Responsibilities: Bachelor's degree years Quality Assurance/Quality Engineering experience in the medical device or pharmaceutical industry.
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