Seasoned manufacturing professional with extensive experience spanning over 15 years. Recognized for a keen eye for detail and proficient technical skills, consistently delivering quality results. Committed to personal and professional growth, always striving for enhanced efficiency and effectiveness. Known for unwavering dedication, hard work, and loyalty in contributing to organizational success. Eager to continue this journey of learning and development within a supportive and collaborative environment.
• Quality Process development and implementation
• Annual process document review and updates
• Monitoring standard work for QC Team
• Final review and sign off for inspections, FAI's, deviation waivers, material review and alternate material review approvals
• Scheduling all internal audit activities
• Development of ISO 9001 internal process audit procedures.
• Conducting QMS required manufacturing process audits, ISO 9001and PED Pressure Equipment Directive required internal audits.
• Lead auditor for regulatory compliances (CSA, UL, ISO 9001, PED Pressure Equipment Directive)
• Managing and monitoring Quality activities an objectives, Customer complaints, calibrations, daily incoming inspection level, Incoming FAI's, Vendor related non conformances, supplier corrective actions, quality alerts,
• Performing 8D root cause analysis (internally and externally)
• Coordinating and facilitating quarantining and containment actions for products with potential risk.
• Providing manufacturing support when issues or discrepancies arise to identify issue.
• Performance evaluation testing on customer RGA's, determining root cause of failure and assigning actions as needed.