QA Manager

Job DescriptionThe Senior Manager, Global Quality Systems provides leadership and oversight for key elements of CooperSurgical's Global Quality Management System (QMS), including Management Review, Quality System Metrics and Reporting, Regulatory Intelligence, Quality System Impact Assessments, and Quality System integration activities associated with acquisitions and strategic business initiatives. Partners closely with Quality, Regulatory Affairs, Operations, Manufacturing, R&D, Supply Chain, IT, and other functional leaders to ensure QMS remains compliant, effective, scalable, and aligned with evolving regulatory requirements and business objectives. Serves as a key partner to the Director, Global Quality Systems, helping drive quality system performance, governance, inspection readiness, and continuous improvement across the global organization.ResponsibilitiesThe Senior Manager, Global Quality Systems is responsible for the leadership, oversight, and continuous improvement of key components of CooperSurgical's Global Quality Management System. This role ensures ongoing compliance with applicable global regulations and standards, including FDA QMSR, ISO 13485, MDSAP, EU MDR, and other relevant requirements. Leads activities related to Management Review, Quality System metrics and reporting, regulatory intelligence, standards management, quality system impact assessments, and merger and acquisition integration efforts. Through effective governance, analytics, and cross-functional collaboration, this role provides visibility into QMS health, identifies compliance risks and opportunities, and ensures regulatory and standards changes are effectively assessed and incorporated into the Quality Management System.Essential Functions & Accountabilities:Support the governance, effectiveness, and continuous improvement of the global QMS.Drive harmonization, compliance, and operational excellence across global quality system processes.Partner with process owners and cross-functional stakeholders to identify and mitigate quality system risks while ensuring inspection readiness.Lead the global Management Review program, including planning, reporting, action tracking, and continuous improvement.Develop and maintain quality system KPIs, dashboards, and performance reporting to provide visibility into QMS effectiveness, compliance status, and emerging risks.Prepare executive-level reporting on QMS health, quality objectives, risks, and improvement opportunities.Monitor process effectiveness and drive improvements that enhance compliance, efficiency, and user experience.Monitor evolving global regulations, standards, guidance documents, and industry best practices impacting the Quality Management System.Lead quality system impact assessments and gap analyses to determine the effect of regulatory and standards changes on existing QMS processes.Develop and track implementation plans to ensure timely incorporation of regulatory and standards requirements into the QMS.Partner with Regulatory Affairs and Quality leadership to evaluate new or revised regulatory requirements.Lead Quality Systems due diligence, integration planning, and QMS harmonization activities associated with acquisitions and strategic business initiatives.Assess quality system maturity, identify compliance gaps, and implement integration plans that align acquired entities with CooperSurgical processes.Support implementation and optimization of electronic Quality Management Systems (eQMS) and related quality system enhancement initiatives.Support regulatory inspections, audits, and remediation activities as required.Lead, coach, and develop a team responsible for Quality Systems governance, reporting, compliance monitoring, and improvement initiatives.Establish performance expectations, prioritize resources, and foster a culture of quality, accountability, and continuous improvement.Travel: This position may require 20% domestic or international travel.QualificationsKnowledge, Skills and Abilities:RequiredStrong working knowledge of MasterControl, Veeva, Trackwise, or similar eQMS platforms.Solid understanding of 21 CFR 820, ISO 13485, EU MDR, MDSAP.Demonstrated ability to manage and develop teams.Ability to balance operational priorities with compliance requirements.Strong organizational, analytical, and communication skills.Ability to collaborate across global, cross-functional groups.PreferredExperience participating in or supporting large-scale enterprise software implementations, including data migration and data mapping activities.Advanced proficiency in Excel for data analysis and reporting.Professional certification such as Certified Quality Auditor (CQA) or similar.Work Environment:Standard office environment with regular use of computer systems and virtual collaboration tools.Experience:Required8+ years of experience in quality management systems, within a regulated med tech industry.7+ years of people leadership and team development.Experience managing quality systems with ISO 13485 and FDA 21 CFR Part 820, MDSAP, and EU MDR requirements.PreferredExposure to other adjacent quality system compliance requirements such as 21 CFR Part 210/211.Prior involvement in supporting external and internal audits.Experience with electronic Quality Management Systems (eQMS) and/or implementation of eQMS, such as Veeva, Trackwise, MasterControl.Education:RequiredBachelor's degree in a relevant field such as Engineering, Life Sciences, Quality, or a related discipline.PreferredProfessional ASQ certification (CQPA, CQA, CMQ/OE, etc.)Project Management Professional certification (PMP)