Sr. Supplier Quality Engineer

<h4 style="margin-top: 0pt; margin-bottom: 0pt;"><strong><span style="font-size: 11pt; font-family: Arial, sans-serif;">ABOUT THE ROLE</span></strong></h4> <h4 style="margin-top: 0pt; margin-bottom: 0pt;"> </h4> <p style="margin-top: 0pt; margin-bottom: 0pt;">The FATP Supplier quality Engineer (SQE) is responsible for driving continuous improvement within our supply chain amp; business partners. The primary focus is to work with our key contract manufacturers and sub suppliers to ensure product quality and timely deliveries as well as to develop new suppliers. The SQE will implement and manage continuous improvement programs with our suppliers’ senior and executive management to drive measurable and lasting improvements. The SQE is a data driven position supported by the correct usage of QMS assessment, quality improvement tools, risk assessment, complex project management, and leadership.<br><br></p> <h4 style="margin-top: 0pt; margin-bottom: 6pt;"><strong><span style="font-size: 11pt; font-family: Arial, sans-serif;">YOUR DAILY IMPACT AT PELOTON</span></strong></h4> <ul> <li> Quality Systems: Maintain and improve company quality management systems (QMS) in compliance with applicable regulatory amp; Peloton requirements related to control of processes and product</li> <li>Management: Responsible for representing overseas quality team onsite, training, and ongoing support of staff. Required to effectively communicate project goals to Suppliers. Provide technical guidance and training (mentorship) to suppliers to their ongoing development to reach company goals. manage supplier audit program and suggest new suppliers to audit</li> <li>Product Development: Be a key member of the Peloton product development team onsite representing the Supplier Quality function. Steer and support the design control aspects of product quality, program management, and quality planning from product design through manufacturing. Assess, support and process supplier approvals and re-approvals in the approved supplier list (ASL)</li> <li>Process Verification and Validation: Provide input regarding appropriate statistical methods, test facilities and equipment. This can include process validation, equipment installation/operational qualification, etc.</li> <li>Production: May develop and implement quality inspection procedures including sampling plans, for production level components, sub-assemblies and finished goods. May also be responsible for the development and implementation of inspection methodologies, fixtures, measurement systems and calibration of such. Monitor, support and resolve production related quality issues with material suppliers</li> <li>Auditing: Responsible for overall audit program execution. Developing, implementing, and auditing risk-based annual quality control audit plans and schedules. Conduct and lead supplier, internal and external GMP(Good Manufacturing Practice) and ISO compliance audits. supports production line qualification initiatives, continuous improvement, and regulatory compliance across all supplier sites. Reports results and recommendations for changes as required. Confirms acceptable follow up action on audits. Monitors performance to audit schedules, execution, reporting and audit finding closures within established audit plans and timelines</li> <li>Documentation: Create, review, and approve controlled documents on an electronic document control system (e.g. supplier audit plans and reports, nonconformance reports, Quality Manual, work instructions, quality specifications, engineering specifications, lot history and device master records, procedures and validation protocols and reports, etc.). Generate and complete supplier records for approvals in the ASL</li> <li>Training: Coordinates and/or provides training to staff in GMP/ISO, Quality Systems, Supplier Quality, and Safety awareness. Provides ongoing development and maintenance of training materials and records</li> <li>Compliance: Ensures compliance with ... (truncated, view full listing at source)