Quality Control Supervisor, Instruments

• Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities
• Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
• Provides technical support and process improvement to minimize cost and increase productivity
• Plays a key role in Lean Manufacturing Implementation
• Supervises difficult inspection processes problems through a well and sound solution methodology
• Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
• Reviews inspection, labeling, and release logistic for appropriate process flow and documentation
• Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
• Oversees supplier quality metrics including but not limited to first pass yield
• Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components
• Supervise personnel in incoming inspection area to assure control, adherence to safety, quality, and schedule requirements
• Coordinates subordinate work to achieve result associated with daily business schedule and goals as assigned
• Support and execute quality goals and initiatives
• Interacts with suppliers, vendors, and/or customers when needed to support business needs
• Develops, establish and continuously improve the necessary controls around incoming inspections when needed to support new and existing products
• Motivates, supervises and develops personnel in a team environment
• Investigate and manage NCMRs including investigation, additional testing, test analysis, disposition, and ERP inventory management reconciliation and follow up on issued Corrective Actions
• Ensures results are recorded on inspection forms and reports number of defects found
• Maintains department files for readily retrievable access of records
• Ensures good documentation practices during document review and inspection
• Ensure incoming parts are inspected according to blue-print & drawing specifications
• Other duties as assigned

• Bachelor's Degree in Life Science or Engineering discipline
• 5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree, preferred
• 8 years of relevant experience required with an Associate Degree, preferred
• 2 years of relevant Manufacturing Operations leadership experience, preferred

competitive salary and benefits package