Senior Engineer, Supplier Quality

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: Reporting to Director, Supplier Quality the Senior Engineer, Supplier Quality will support key operational pillars of the Supplier Quality Program: Supplier Change Notification Program, Supplier Qualification, Quality Technical Agreements, Supplier GxP Certificate Management, Scorecard Assessments & Performance Monitoring, and to ensure the delivery of high-quality materials and services. The scope of this role includes commercial and development (clinical) GMP. You will be responsible for assisting in day-to-day management of the Supplier Quality Processes. You will partner with cross-functional stakeholders and external suppliers to support qualification and monitoring activities, drive regulatory compliance, reduce risk, and implement continuous improvements that strengthen supplier performance across the product lifecycle. What You'll Do: In this role, you'll have the opportunity to partner with cross-functional SMEs and Business owners in selection, qualification, and onboarding of new suppliers. You will also: Lead the Supplier Change Notification program by reviewing, assessing, and coordinating Supplier Change Notifications with internal stakeholders and external suppliers. Assess potential impacts on product quality, compliance, and supply continuity, and ensure appropriate documentation and follow-up in the quality management system. Own and support lifecycle management of the global Quality Technical Agreement program to ensure alignment with internal policies and applicable regulatory requirements. Facilitate development, negotiation, execution, and periodic review of Quality Agreements with suppliers and Insmed SMEs to define quality expectations, responsibilities, and compliance requirements. Monitor agreement status and effectiveness to confirm documents remain current, compliant, and aligned with business and regulatory expectations. Manage assignment and timely completion of Scorecards and ensure accuracy, appropriate risk allocation, and level of control are established. Where required, work with the Supplier & Insmed functional SME’s to create corrective action plans to address failures in supplier’s material and services provided. Trend and analyze supplier performance data to identify systemic risks and improvement opportunities. Participate in supplier audits as required, including routine, for cause, and qualification audits. Ensure supplier quality documentation is complete, accurate, inspection ready, and maintained in accordance with company procedures and regulatory expectations. Assist with development, maintenance, and monitoring of approved supplier list, as well as maintenance of supplier files. Generate action items from supplier KPI’s for system enhancements and improvements i.e. External deviations trending, Supplier Notifications, audit reports and observations to implement value add system enhancements. Assess potential suppliers for capability, quality systems, and compliance with regulatory and Insmed standards. Collaborate with procurement, supply chain, functional SME’s and quality assurance teams to evaluate supplier capabilities and performance history. Maintain supplier escalation programs to ensure that issues are getting elevated to the right levels at Insmed and within the Supplier’s organization to ensu ... (truncated, view full listing at source)