ABOUT THE ROLE
The Sr. FATP Supplier Quality Engineer will be focused on our component supply. This position is critical for ensuring the delivery of quality components from established suppliers and developing new suppliers to meet Peloton’s quality
requirements. You will manage all quality-related communication between Peloton and suppliers to manufacturing and distribution centers. As a main technical interface for our component suppliers, you will be responsible for driving
problem-solving accountability (8Ds), reviewing and approving the implementation of process/part changes, and identifying opportunities for continuous improvement. You will be the responsible escalation point for internal and field
concerns regarding component quality. As an individual, you are independent, highly motivated, super organized, hyper-flexible, and enjoy working in a collaborative team environment to protect and improve 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.