Taniushka M. Horn

• Secret US Security Clearance - Active
• Represent Quality as part of cross-functional team integrating contractual and Boeing QMS requirements into all aspects of proposals, POs, program processes and documentation
• Quality APQP focal
• Lead reviews to ensure quality attributes and requirements are incorporated by suppliers
• Perform Supplier Quality Engineering and Quality Planner functional roles and responsibilities
• Lead internal preventive and corrective actions. Advise and train management on preparation for audits.
• Analyze data and develop quality metrics reports like CoRRS, non-conformance trends to evaluate effectiveness of corrective actions, etc
• Action owner for NOEs, internal and external Corrective Actions, and supplier support activities

• Hired as Level 2 on Oct 2018, Promoted to Level 3 on May 2019
• Programs: Weapons- Direct Attack (LJDAM, JDAM, B61, SDB)
• Interim Lead Quality Engineer. On-boarded new members of the team including Lead QE.
• Analyze data and develop quality metrics reports for Weapons Programs & the St. Charles site. Lead meetings presenting quality metrics to customers, DCMA and upper management.
• St. Charles site Quality Metrics focal.
• Conduct capability assessments and process validations to support supplier selection activities.
• Lead Root Cause Corrective Action (RCCA) team to address Corrective Action Records (CAR) issued by DCMA.
• Recommend, lead and track corrective actions to address non-conformances and support Cut the CoRRS 2.0 project as part of St. Charles site quad team.
• Direct Attack quality focal responsible for scheduling, performing, originating and tracking surveillances performed by Quality team. Work with senior management on preparation for internal and 3rd party audits.
• Provide interpretation of quality, customer and engineering requirements and technical solutions to a wide range of operational challenges.
• Develops solutions that are imaginative, thorough, practical, and consistent with organization objectives.
• Lead interactions with inter-organizational personnel, external customers and DCMA.
• Take initiative to provide innovative solutions to difficult technical issues associated with customer-specific projects and addressing DCMA requests.

• Oversight, document review and audits at third-party packaging company
• In charge of making critical decisions at third party location - approvals to protocols, deviations and investigations as Customer Representative
• Established 5S project to Incoming Area reducing time locating samples by 90%

• Internal audits, problem analysis, problem-solving, support to investigations and root cause analysis for CAPA and Change Controls.

• Provide support to manufacturing supervisors managing internal audit observations, metrics and follow up
• Participated in validation processes and in evaluation of protocols and major change controls for operations.

• Manufacture of validation, experimental, clinical and commercial products, including Controlled Substances products.
• Improvement to Quality records

• Directed inspection and testing of medical device products with established company quality standards while meeting customer specifications.

Courses: Advance Statistics & Quality Improvement, Operations Planning & Control, Lean Manufacturing, Foundations in Quality Learning, Six Sigma, Assessment Tools to Improve Business, Project Management, Audit Program Management, Research Methodology, Professional Writing and Presentations, Measuring and Managing Customer Satisfaction, and Managerial Finance and Cost Accounting.