Sr. FATP Supplier Quality Engineer

ABOUT THE ROLE

The Sr. FATP Supplier Quality Engineer will be working with the Peloton Quality and broader Operations teams to drive improvements and support in the management of quality processes and quality management systems at our manufacturing partners’ facilities. You will work with our partners to drive process control improvements ensuring that only qualified parts and processes are used to build our products. This will be done by evaluating that they are following best practices for inspection, providing root cause and corrective action guidance and by integrating with their teams to help identify and execute data driven process enhancements and improvements. You have the technical ability, problem solving skills, and communication skills to solve issues on the factory floor and with the Peloton technical team. You’ll act as the first line of defense to improve our product and processes. You are an individual who is independent, highly motivated, super organized, hyper-flexible and enjoy working in a collaborative team environment to improve total product quality.

YOUR DAILY IMPACT AT PELOTON

• Quality Systems: Maintain and improve company quality management systems (QMS) in compliance with applicable regulatory & Peloton requirements related to control of processes and product.
• 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.
• 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).
• Process Verification and Validation: Provide input regarding appropriate statistical methods, test facilities and equipment. This can include process validation, equipment installation/operational qualification, etc.
• 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.
• 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.
• 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.
• 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.
• Compliance: Ensures compliance with company quality policies and practices by participating in product and material reviews, assist in “troubleshooting” problems related to the manufacture, testing, validation and documentation. May be responsible for aspects of MRB, corrective actions, process control, complaints, document control, calibration & preventive maintenance programs and product/process/equipment validation activities.
• Work with Peloton Quality Control team to develop and implement inspection and escalation plans
• Coordinate disposition and cost recovery for non-conforming material from suppliers
• Drive supplier root cause analysis and corre