Supplier Quality Manager

Asks for

• Advanced Product Quality PlanningThe ad says“Are responsible for overseeing supplier partners' high-quality performance by applying Advanced Product Quality Planning (APQP) in product industrialization, driving continuous quality improvement throughout the product lifecycle, ensuring regulatory compliance, and identifying improvement opportunities through CoNQ data analysis.”
• APQPThe ad says“• Supervises, monitors, and controls APQP (Advanced Product Quality Planning) plans as part of both the NPI and sustaining change processes, ensuring consistent quality throughout the product lifecycle. Manages talent across the team, while driving employee selection, performance management, compensation management, career development, and ensuring effective operational management.”
• CAPAThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Continuous Improvement TechniquesThe ad says“8+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Continuous Improvement Techniques or equivalent.”
• Critical to QualityThe ad says“• Ensures Critical to Quality (CtQ) characteristics are effectively communicated to suppliers and incorporated into their processes, supporting consistent quality output. Oversees Part Submission Warrant (PSW) plans, deliverables, line releases, and completion, ensuring all parts meet specified quality requirements before production approval.”
• Data AnalysisThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Design for ExcellenceThe ad says“• Fosters collaboration between R&D and suppliers through Design for Excellence (DfX) initiatives, promoting innovative designs that meet quality standards.”
• DFX MethodologyThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• medical device regulationsThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Part Submission WarrantThe ad says“• Ensures Critical to Quality (CtQ) characteristics are effectively communicated to suppliers and incorporated into their processes, supporting consistent quality output. Oversees Part Submission Warrant (PSW) plans, deliverables, line releases, and completion, ensuring all parts meet specified quality requirements before production approval.”
• PPAPThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Process EngineeringThe ad says“8+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Continuous Improvement Techniques or equivalent.”
• Process ValidationThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Quality EngineeringThe ad says“8+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Continuous Improvement Techniques or equivalent.”
• Safety EngineeringThe ad says“8+ years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, Process Engineering, Continuous Improvement Techniques or equivalent.”
• Supplier Corrective Action RequestsThe ad says“• Manages the quality relationship with key suppliers, negotiating Supplier Quality Agreements, conducting defect analyses to determine supplier responsibility, and serving as an independent reviewer for Supplier Corrective Action Requests (SCAR), while providing guidance and leadership in specific SQ functional areas such as APQP and SCAR. Initiates supplier improvement and development initiatives within the APQP framework, including supplier performance monitoring, quality risk assessment, and mitigation strategies, while supporting the development, execution, and maintenance of supplier audit schedules.”
• Supplier Evaluation MethodologiesThe ad says“We prefer 3+ years of Management experience with Supplier Quality Management, APQP (PPAP) and Process Validation, medical device regulations and standards, Supplier Evaluation Methodologies, Data Analysis, DFX Methodology. CAPA.”
• Supplier Quality AgreementsThe ad says“• Manages the quality relationship with key suppliers, negotiating Supplier Quality Agreements, conducting defect analyses to determine supplier responsibility, and serving as an independent reviewer for Supplier Corrective Action Requests (SCAR), while providing guidance and leadership in specific SQ functional areas such as APQP and SCAR. Initiates supplier improvement and development initiatives within the APQP framework, including supplier performance monitoring, quality risk assessment, and mitigation strategies, while supporting the development, execution, and maintenance of supplier audit schedules.”