Supervisor II, Quality
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Job Description
Direct and coordinate products inspection activities using knowledge of product technology, quality specifications, and procedures. Job duties:
• Direct and coordinate Quality Control Inspection on the performance of in-process and final product inspection.
• Provide feedback to QA, Operations, and R&D on quality issues.
• Assist and train QC on the build record review.
• Assist Operations and R&D with process or inspection improvements.
• Schedule and manage workflow for the Quality Control Inspection staff within the clean room.
• Assure in-process and final product inspection training is performed.
• Evaluate QC inspection resources needed for product transfers and line expansions.
• Supervise QC leads, QC Jr Supervisors, and QC Supervisor I’s.
• Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
• Perform additional job-related task as assigned by Quality Assurance Manager. Required
Qualifications:
• Bachelor's degree or equivalent experience.
• Minimum five (5) years in quality control for medical device manufacturing.
• Minimum two (2) years in quality leading role as a team supervisor or equivalent.
• Use of microscope and other hand measurement tools required to perform inspection. Desired Qualifications
• Competent at inspection techniques, solid understanding of technician documentation including mechanical drawings.
• Experience supervising other associate in quality control inspection including organizational QC leads.
• Ability to determine and plan resources regarding QC support for product transfers and line expansions.
• Strong decision-marking abilities focused on product quality and customer safety.
• Good written and oral communication skills in both Spanish and English.
• Ability to read technical documentation.
• Experience working in a controlled environment (clean room).
• Good interpersonal skills.
• Knowledge of Quality Systems for medical device manufacturing and requirements for inspection and testing. Please submit your updated resumes to dora.castro@terumo.com
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