Engineering Maintenance Supervisor

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You?ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeAs a Engineering Maintenance Supervisor in our Billerica, MA facility, you'll lead and develop a high-performing team responsible for the construction and maintenance of equipment used to manufacture life changing products in our growing cardiac ablation portfolio.You will play a critical role in daily operations?driving safety, quality, delivery, and productivity while fostering a culture of inclusion, innovation, and continuous improvement. Your leadership directly contributes to the devices and systems that help clinicians improve patient outcomes worldwide.Responsibilities may include, but are not limited to:- Promote an inclusive and safe workplace by modeling Medtronic's values and reinforcing positive team behaviors.- Supervise, coach, and develop a team of equipment maintenance technicians within a fast- paced, regulated manufacturing environment.- Ensure production schedules, quality standards, and compliance requirements are met through strong daily floor presence and communication.- Lead problem-solving and root cause analysis for equipment, process, and quality issues; implement robust corrective actions.- Collaborate cross-functionally with Engineering, Quality, Supply Chain, EHS, and Operations to optimize production performance and support new product introductions.- Utilize Lean, Six Sigma, and continuous improvement tools to streamline workflow and eliminate waste.- Drive team engagement through recognition, feedback, training, and opportunities for career growth.- Maintain accurate documentation, metrics, and reporting aligned with internal and external audit requirements (FDA, ISO, etc.).Must Have: Minimum RequirementsBachelor's degree and minimum of 1 year of relevant experienceNice to Have- Bachelor?s degree with 2+ years of technical supervisory experience, or an Associate degree with 4+ years of supervisory experience in manufacturing, operations, or technical production environment.- Demonstrated experience in medical device, aerospace, or other regulated industry.- Strong communication, organizational, and problem-solving skills.- Experience leading equipment maintenance teams.- Working knowledge of Lean Manufacturing, 5S, Six Sigma, or continuous improvement methodologies.- Familiarity with ERP systems (Workday, SAP, etc.) and production scheduling tools.- Familiarity with CAD (Computer-Aided Design) Tools including SolidWorks.- Familiarity with Good Manufacturing Processes (GMP) and Good Documentation Practices (GDP)- Familiarity with FDA Quality System Regulation, 21 CFR Part , ISO , and ISO - Proficiency in MS Office and manufacturing documentation systems.- Ability to build trust and engagement across diverse teams.- Proven track record of developing team members and fostering inclusive leadership practices.

Created: 2025-11-24