Manager, Supplier Engineering

Company DescriptionIt started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our technologies—like the da Vinci surgical system and Ion—have transformed how care is delivered for millions of patients worldwide.We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare, you’ll find your purpose here.Job DescriptionPrimary Function of Position Manage and lead a team of Supplier Engineers responsible for ensuring supplier manufacturing processes are capable, stable, compliant, and scalable across the product lifecycle. This role plays a critical part in protecting the validated state of medical devices, enabling safe and timely product launches, and driving sustained improvements in supplier quality, capacity, and risk reduction.The Supplier Engineering Manager leads complex, cross‑functional problem solving at the intersection of supplier manufacturing processes, design constraints, quality systems, and business priorities. Success in this role requires strong engineering judgment, the ability to operate effectively in ambiguous environments, and the authority to influence decisions that directly impact patient safety, product performance, and business outcomes.Essential Job Duties Team Leadership and Development. Lead and develop a team of Supplier Engineers accountable for driving measurable quality and performance improvements at suppliers, ensuring deep understanding of process inputs, outputs, and sources of variation through hands‑on engagement, data‑driven analysis, and on‑site problem solving.Coach, train, and performance‑manage the team by setting clear expectations, building technical depth, and holding engineers accountable for results through regular feedback, development plans, and outcome‑based goals.Develop the team’s engineering judgment by coaching decision‑making under ambiguity and effective tradeoff evaluation across quality, cost, risk, and schedule.Partner closely with Design, Quality, Supply Chain, Manufacturing, and supplier leadership to align on technical requirements, risk, and priorities, influencing decisions to ensure supplier processes meet quality, cost, delivery, and compliance objectives.Component and Process QualificationPromote Design for Manufacturability (DFM) by engaging suppliers and Engineering early in the development cycle to provide actionable feedback on manufacturability improvements prior to production.Own and govern supplier component qualification, holding suppliers and internal teams accountable for robust execution of FAIR, test method development and validation, PFMEA / spFMEA, capability studies (Cp/Cpk, GR&R), and complete, compliant documentation to support safe launch and sustained production.Component QualityLead supplier non‑conformance management by driving rigorous root cause analysis (e.g., 8D, 5‑Why, Fishbone) and ensuring timely, effective corrective and preventive actions to prevent recurrence.Drive sustained reduction of supplier defects using data‑driven insights, trend analysis, and supplier leadership engagement to improve process capability, quality performance, and regulatory compliance.Lead or support CAPA and SCAR activities arising from recurring supplier qualification issues or field complaints attributable to component performanceProcess Maturity through Supplier Capacity and Risk Management. Own supplier manufacturing process maturity across the product lifecycle, ensuring processes remain capable, stable, and scalable beyond initial qualification.Lead proactive supplier and component risk identification and mitigation, using data and engineering judgment to prioritize effort on high‑severity and high‑impact areaPartner with suppliers and Supply Chain to assess and improve manufacturing capacity, scalability, and tooling readiness to support volume ramps without compromising quality or validated state.Own and govern Supplier Change Requests (SCRs) ensuring changes are well planned, risk‑assessed, executed on time with authority to recommend approval, rejection, prioritization, and escalation of supplier actions based on risk, data, and business impact.Ensure supplier changes do not compromise the validated state by driving appropriate impact assessments, validation strategy alignment, and cross‑functional approvals to maintain product quality, compliance, and supply continuity.QualificationsRequired Skills and ExperienceProven ability to lead and scale engineering teams to solve increasingly complex technical and manufacturing process problems by applying data‑driven analysis and strong engineering judgment.Demonstrated experience hiring, developing, mentoring, and retaining high‑performing engineering talent.Comfortable operating in ambiguous environments, balancing competing priorities, incomplete data, and cross‑functional tradeoffs to drive timely, high‑quality decisions.Demonstrated ability to apply broad supplier manufacturing process knowledge to assess tradeoffs and make risk‑based decisions affecting product quality, cost, capacity, scalability, and supplier performance.Demonstrated ability to read and interpret engineering drawings and GD&T, with sufficient depth to evaluate manufacturability, inspection strategy, and risk, and to guide technical decision‑makingProficiency in PFMEA / spFMEA, process validation, root cause investigation, inspection, and test methodologies.Experience with document management systems and ERP platforms; Agile and SAP preferred.Excellent written and verbal communication skills, including the ability to present effectively to executive‑level management.Demonstrated project management skills.Ability to travel domestically and internationally to supplier sites as needed.Required Education and Training BA or BS degree in engineering12 or more years related experience in Manufacturing, Operations, Supplier Engineering, or related field with significant medical or medical device experience preferredMinimum 5 years of experience leading engineering teams, or leadership of equivalent areas.Working Conditions NonePreferred Skills and Experience Knowledge of 21 CFR part 820 and ISO 13485 preferredFinancial knowledge and ability to calculate Net Present Value (NPV)Ability to create dashboards (Smartsheets or Confluence) to track and management projects and deliverables for accountability and transparency. Additional InformationDue to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.Mandatory NoticesU.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employeeswho are nationals from countries currently on embargo or sanctions status.Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process). For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’sstart date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee.This position may be filled at a different job level than listed here depending on business need and/or on the selected candidate’s experience, knowledge and skills. Compensation will be based primarily on the job level at which the role is filled and the candidate’s qualifications, consistent with applicable law.We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target compensation ranges are listed.SummaryType: Full-timeFunction: ManufacturingExperience level: AssociateIndustry: Medical Device