Manufacturing Engineering Director

Medtronic plc

WarsawFull-timeMid LevelOn-site

Job Description

We anticipate the application window for this opening will close on - 17 Apr 2026Chez Medtronic, vous pouvez entamer une longue carriĂšre d’exploration et d’innovation tout en aidant Ă  soutenir l’accĂšs aux soins de santĂ© et l’équitĂ© pour tous. Vous dirigerez avec dĂ©termination en surmontant les obstacles Ă  l’innovation dans un monde davantage connectĂ© et compatissant.**JournĂ©e type**Today, we’re partnering across the industry to confront systemic healthcare challenges – this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us.

Help us bring the next generation of life-changing medical technology to patients worldwide. At Medtronic, we must work with a sense of purpose and ownership, knowing there is a human life on the other side of every decision. 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. This role is based in Warsaw, Indiana with an expectation of working 5 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.The Manufacturing Engineering Director role is critical to leading the Engineering organization through the Warsaw Operations’ planned growth and expansion. The position is responsible for driving innovation and New Product Introduction (NPI) initiatives, while establishing a clear vision for developing a world-class manufacturing site in Warsaw, Indiana.

This leader will serve as the primary point of contact with Medtronic R&D teams, representing the needs, capabilities, and strategic priorities of the Warsaw Operation.At Medtronic, Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and guidance you need to continue to develop your expertise.As the **Manufacturing Engineering Director**, you will:* Guide, deploy, and execute the Medtronic Performance System (MPS), our “one best way” methodology and tools that support our holistic operational excellence program.* Lead, form, mentor, develop and coach an engineering team on meeting / exceeding performance expectations.* Schedule and coordinate multiple projects to drive the resolution of line-down situations.* Participate in establishing project objectives, timelines, milestones, and budgets.* Lead or participate in the appropriation of funds for projects through the preparation and approval of capital expenditure requests.* Communicate and lead meetings with internal /external suppliers and stakeholders.* Interface with Senior Management to communicate/report progress and receive strategic updates impacting projects.* Conceive and propose creative solutions to solve difficult external manufacturing constraints.* Oversees the investigation and evaluation of existing processes and technologies to find opportunities for improvement and develop action plans for execution.* Organize the coordination of activities with outside suppliers to improve yield or reduce quality risks.* Ensure the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.**Must Have: Minimum Requirements***To be considered for this role, please ensure the minimum requirements are evident on your resume.** Bachelor’s degree in Engineering and 10 years of relevant manufacturing engineering experience with 7+ years of managerial experience OR* Advanced Degree and 8 years of relevant manufacturing engineering experience with 7+ years of managerial experience.* Ability to be on site at the Warsaw, IN manufacturing facility 5 days/week with up to 20% travel.**Nice to Have:****Leadership & Change Management*** Demonstrated ability to lead, energize, and influence change at all levels of a complex organization.* Proven experience leading cross‐functional, multi‐site, or multi‐regional initiatives.* Track record of driving organizational change resulting in measurable improvements in Safety, Quality, Delivery, and Cost (SQDC) KPIs.**Manufacturing & Technical Expertise*** Strong foundation in machining complex geometry products using Milling, Mill‐Turn, and Swiss machining platforms.* Solid working knowledge of Geometric Dimensioning and Tolerancing (GD&T).* Experience with 3D metal printing or additive manufacturing technologies is a plus.**Operational Excellence*** Green Belt or Black Belt certification preferred.* Demonstrated ability to lead or support Lean transformation initiatives.* Experience applying continuous improvement methodologies in a manufacturing environment.**Quality & Regulatory Experience*** Experience working in an FDA‐regulated or similarly regulated manufacturing environment.* Working knowledge of quality systems and associated documentation requirements.* Experience with preventative and corrective action (CAPA) processes.* Understanding of equipment and process qualification protocols (IQ/OQ/PQ).**Industry Experience*** Prior experience in the medical device industry preferred.Pour les diplĂŽmes de baccalaurĂ©at obtenus en dehors des États-Unis, un diplĂŽme qui satisfait aux exigences de la rĂ©glementation 8 C.F.R. § 214.2 (h) (4) (iii) (A) est requis.**Exigences physiques du poste**Les dĂ©clarations ci-dessus visent Ă  dĂ©crire la nature gĂ©nĂ©rale et le niveau du travail effectuĂ© par les employĂ©s affectĂ©s Ă  ce poste, mais elles ne constituent pas une liste exhaustive de toutes les responsabilitĂ©s et compĂ©tences requises pour ce poste.Les exigences physiques dĂ©crites dans la section ResponsabilitĂ©s de cette fiche de poste sont reprĂ©sentatives de celles auxquelles un employĂ© doit satisfaire pour remplir correctement les fonctions essentielles du poste.

Des ajustements raisonnables peuvent ĂȘtre apportĂ©s pour permettre aux personnes en situation de handicap de remplir ces fonctions essentielles. RĂŽles administratifs : dans l’exercice de ses fonctions, l’employĂ© est rĂ©guliĂšrement appelĂ© Ă  se dĂ©placer de façon autonome. Il est Ă©galement amenĂ© Ă  utiliser un ordinateur et Ă  communiquer avec ses pairs et ses collĂšgues.

Contactez votre responsable ou votre service RH local pour connaĂźtre les conditions de travail et les exigences physiques spĂ©cifiques Ă  chaque rĂŽle.**Autorisation de travail et parrainage** Chez Medtronic, nous nous engageons Ă  favoriser un environnement dans lequel les employĂ©s peuvent s'Ă©panouir et avoir un impact significatif. ConformĂ©ment Ă  notre approche de planification de la main-d'Ɠuvre Ă  l'Ă©chelle de l'entreprise, le parrainage d'autorisation de travail aux États-Unis (H-1B, TN, J, etc.) est proposĂ© exclusivement pour les postes de niveau Principal et supĂ©rieur, oĂč l'expertise spĂ©cialisĂ©e s'aligne sur les besoins mĂ©tier Ă  long terme. Les postes en dessous du niveau Principal exigent que les candidats possĂšdent une autorisation de travail amĂ©ricaine sans restriction au moment de l'embauche et pour la durĂ©e de l'emploi.

Rejoignez-nous et aidez-nous Ă  accomplir notre mission, Ă  savoir soulager la douleur, rĂ©tablir la santĂ© et prolonger la vie, en valorisant votre expĂ©rience et votre perspective uniques.**Avantages sociaux et rĂ©munĂ©ration****Medtronic offre un salaire compĂ©titif et un ensemble d’avantages sociaux flexibles** Le cƓur de nos valeurs est animĂ© par un engagement envers nos employĂ©s. Nous saluons leurs contributions et partageons avec eux le succĂšs qu’ils ont contribuĂ© Ă  crĂ©er. Nous offrons un large Ă©ventail d’avantages, de ressources et de rĂ©gimes de rĂ©munĂ©ration concurrentiels conçus pour vous soutenir Ă  chaque Ă©tape #J-18808-Ljbffr

Posted 2 weeks ago

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