INGENYX- Senior Quality Management Systems Manager

Expected Travel : Up to 25% Requisition ID : 14393

Ingenyx proudly launched as a new, independent company following its divestiture from Teleflex on August 3, 2026. Ingenyx is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fibers; and bioabsorbable sutures, yarns and resins. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.   For more information, please visit  Ingenyx.com Position Summary

We are seeking an experienced Senior Quality Management Systems (QMS) Manager to lead and continuously improve our global medical device Quality Management System. This role provides leadership for QMS governance, regulatory and standards compliance, Supplier Quality, internal audits, digital Quality Systems, and continuous improvement across multiple sites. The ideal candidate combines strong medical device QMS expertise with regulatory judgment, people leadership, and the ability to drive change across a global organization. Principal Responsibilities

•    Lead global QMS governance, harmonization, and continuous improvement across sites and functions. •    Lead regulatory and standards surveillance, gap assessments, and implementation of new or revised requirements. •    Provide governance of core QMS processes, including CAPA, change management, document control, training, Management Review, and quality metrics. •    Provide governance and oversight of the Supplier Quality Program, including qualification, monitoring, performance, SCARs, and supplier risk. •    Lead the Internal Audit Program, including audit planning, auditor qualification, execution, reporting, and follow-up. •    Lead implementation and optimization of electronic QMS and Document Control systems within the ERP/eQMS environment. •    Provide Quality oversight for computer software assurance/validation of quality-impacting systems. •    Drive QMS performance, inspection readiness, and continuous improvement using metrics, trends, and risk-based decision-making. •    Serve as a senior QMS SME during FDA, Notified Body, MDSAP, certification, and customer audits. •    Oversee quality processes supporting customer information requests and change notifications. •    Lead, coach, and develop the QMS team and partner with site and functional leadership to drive Quality System effectiveness.

•    Bachelor's degree in Quality, Engineering, Life Sciences, Regulatory Affairs, or related technical discipline. •    10+ years of Quality experience in the medical device or regulated life sciences industry. •    5+ years leading QMS programs or major Quality System initiatives. •    5+ years of people-management experience. •    Advanced knowledge of ISO 13485 and FDA medical device QMS requirements. •    Experience with global regulatory requirements, regulatory/standards gap assessments, and QMS implementation. •    Strong experience with core QMS processes and Supplier Quality Program governance in a manufacturing environment. •    Experience with regulatory inspections, Notified Body audits, MDSAP, and/or certification audits. •    Demonstrated ability to lead complex, cross-functional and multi-site initiatives. •    Strong leadership, analytical, communication, technical writing, and problem-solving