Senior Quality Engineering Manager

We anticipate the application window for this opening will close on - 17 Aug 2026   Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life                       Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results…the right way.   That’s   the Medtronic Mindset — our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.    Medtronic is   seeking   a highly skilled and innovative   Senior Quality Engineering Manager   to join the  Acquisition & Integration Center of Expertise ,   reporting to the leader of the Center of   Expertise.   This role plays a critical part in supporting Operating Units   (OU)   throughout the   acquisition   lifecycle, including due diligence,   post-acquisition   assessments, and integration planning and execution.      This role is ideal for candidates who thrive in dynamic environments, enjoy cross-functional collaboration,   strategic thinker   and are committed to upholding the highest standards of quality and compliance during periods of organizational growth and transformation.     At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work.   We’re   working   a   minimum of   4   days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.       Responsibilities may include the following, with other   duties as   assigned.   Perform patient safety and technical assessments of acquisition targets during the Due Diligence and Post-Acquisition Assessment periods per procedure 042-P026, to identify quality system, product, process, design control, and risk management gaps that may impact patient safety, regulatory compliance, product performance, or successful integration. Leads the quality functions on how to create a cost model $ to support integration and remediation upon acquisition of a target acquisition. Supports quality partners to develop and execute a risk and time-based integration plan that covers: CAPA’s addressing compliance findings QMS and IT Integration Remediation Activities Establish and track high risk key process indications that drive patient safety, technical and compliance risk reduction. Builds collaborative relationships with cross-functional stakeholders, ensuring all teams have the information and resources needed for effective integration. Coordinates and collaborates remotely with multidisciplinary teams across various time zones and geographies to support global acquisition initiatives.   Must Have:

To be considered for this role, please   ensure   the   minimum   requirements are   evident   in your applicant profile.    Bachelor’s degree with 7 years of work experience in Quality and/or experience in a regulated industry plus 5 years of leadership experience OR advanced degree with 5 of work experience in Quality and/or experience in a regulated industry plus 5 years of leadership experience     Key Skills & Experience   Strong knowledge in one and/or all of the following areas: Design Controls Manufacturing Quality Supplier Quality Global