Sr Manufacturing Engineer
Job in
Memphis, Shelby County, Tennessee, 37544, USA
Listed on 2026-10-16
Listing for:
Medtronic
Full Time
position Listed on 2026-10-16
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer, Process Engineer, Validation Engineer -
Manufacturing / Production
Quality Engineering, Manufacturing Engineer, Validation Engineer
Job Description & How to Apply Below
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 At Medtronic Neuroscience, we bring innovation, expertise, and purpose together to improve outcomes and transform lives for people living with neurological, spine, and chronic pain conditions.
At Medtronic CST, we bring together innovative technologies that empower surgeons and improve outcomes in complex spine and cranial procedures. Check us out on Linked In:
Medtronic CSTThis role provides engineering support for released spinal products with a focus on manufacturing operations, technical project management, process improvement, and change implementation. The position serves as a key technical resource supporting manufacturing partners, product transfers, process validations, quality initiatives, and continuous improvement efforts while ensuring compliance with Medtronic requirements. At Medtronic CST, we bring together innovative technologies that empower surgeons and improve outcomes in complex spine and cranial procedures.
In this exciting role, you will provide critical manufacturing engineering expertise to Spine product development teams with an emphasis on New Product launches. Assess drawings and other design output to identify potential manufacturing, assembly and inspection challenges along with proposing alternate solutions. Activities include review, feedback and approval of design changes, print updates, suitability of manufacturing and inspection equipment, use of PLM tools to process change requests, approval of instrument and implant rework requests, product transfers, support all aspects of manufacturing operations, CAPA mitigation, and assist Supply Chain in backorder resolution.
This position will be based at our Memphis TN location.
Responsibilities Manage technical aspects of product and process transfers to manufacturing partners.
Lead design and process change activities through Product Lifecycle Management (PLM) systems and change control processes.
Provide technical guidance and engineering support to manufacturing partners for production and process-related issues.
Develop, coordinate, and execute process validation and qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).Partner with cross-functional teams on Measurement System Analysis (MSA), process capability assessments, and continuous improvement initiatives.
Support manufacturing operations through corrective and preventive action (CAPA) activities, rework evaluations, and product sustainment efforts.
Collaborate with Supply Chain and Operations teams to resolve manufacturing constraints, backorders, and supplier-related technical issues.
Ensure adherence to product specifications, regulatory requirements, quality standards, and manufacturing best practices.
Required Qualifications Bachelor's degree in Engineering and 4+ years of manufacturing engineering experience OR Master's degree in Engineering and 2+ years of manufacturing engineering experience OR PhD with 0+ yeas of experience required.
Preferred Qualifications Experience supporting manufacturing processes, process improvements, and production operations.
Experience with engineering change management, design changes, or process changes in a regulated environment.
Experience developing or executing process validations, qualifications, or manufacturing process controls.
Experience working with cross-functional teams and external manufacturing partners.
Experience with and effective application of Design for Inspectability, Validation Protocol and Report creation, SPC, Process Control Plans, MSA, GR&R, Gauging applications, Gauge design, and Gauge construction, Sampling methodologies, Data Analysis, VAVE, and IQ/OQ/PQMedical device related experience with and understanding of Machining, Molding, Grinding, Forming, Assembly, Welding, Finishing, Cleaning, Passivating, Anodizing, Shot Peening, Mass Media Operations, Coatings, EDM, Casting, Forging,…
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