IQA Supervisor

作为进料质量主管，您将负责监督来料实验室的日常运营，确保符合GMP/GLP标准，带领团队进行质量改进，并参与制定质量政策

Recommend revision of specifications when indicated. Formulate or assist in formulating quality control policies and procedures. Drive quality improvement and cost reduction using Six Sigma or Lean methodology. Supervise the day-to-day activities of the Incoming Material laboratory are carried in a safe manner. Knowledge of basic principles, methods, technologies and practices of a professional/technical field. General knowledge of procedures and activities within own work area. Focus on learning the key aspects and duties of the job being performed. Apply research, information gathering and analytical skills. Handle detailed and structured problems. Work on assignments where judgment is required a majority of the time. Work under general direction, seek assistance as needed. Contribute to own team/closely related teams through quality and accuracy of own output. Convey information in a concise and professional manner. Ask effective questions and solicits feedback to understand needs. Anticipates future needs based on past transactions. Working knowledge of GMP/GLP in medical device manufacturing, with emphasis on incoming materials handling and sampling. Computer literacy and experience with ERP and LIMS systems would be advantageous. Goal Setting Initiate. Troubleshooting/resolve and recommend. Planning Execute. Provide leadership within their shift, and sometimes lead projects across multiple shifts. Develop operational direction for immediate team. Conduct route cause analysis to determine root cause.