Associate Manufacturing Engineer

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions.

Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.

As an Associate Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence, and processes in the manufacturing of parts, components, sub-assemblies, and final assemblies. Support new initiatives and productivity targets for given manufacturing processes.

Responsibilities will also include participation in design reviews, design transfer to production as it relates to the development of manufacturing processes, post-processing development, equipment and process validations, process definition for machine operation and maintenance requirements, test/inspection methods, fixturing, gauging and applying inspection and process control techniques.

• Supports and leads projects of limited scope for existing families of production
• Coordinates cross-functional teams to execute and document the manufacturing launch of new/legacy products
• Supports the development and optimization of manufacturing processes required to accurately and efficiently make spinal implants, from raw material to final cleaning and shipment
• Develops and completes manufacturing documentation (pFMEA, control plan, process flow, work instructions, and inspection plans)
• Manages machine/equipment efficiency thru cycle time reduction, waste elimination, tooling improvements, and changeover reductions
• Performs product/process analysis and troubleshooting for cost reduction, quality improvement, and improved efficiency
• Designs develops, tests, sources, and cost-justify various tools, machinery, and equipment for recommended manufacturing methods
• Participates in non-conforming material review process by supporting containment and review activities, root cause analysis, driving production disposition, and implementing corrective and preventative actions
• Adheres to the letter and spirit of the company Code of Conduct, the Adva Med Code, Med Tech Code, and all other company policies
• Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
• Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties
• Performs other duties as assigned
• Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

• Ability to determine and report critical manufacturing process and control characteristics
• Able to effectively influence others, develop consensus, and create support throughout the organization
• Support design for manufacturability analysis with CNC Programmers and Quality Engineers, and provide input to Development (Design) Engineers
• Ability to implement, maintain, analyze and react to various production performance metrics and KPIs
• Proven ability and fluency in Print Reading and GD&T, Statistical Process Control, Lean Manufacturing, Six Sigma, and Gage/fixture design
• Typically requires a Bachelor’s degree and no previous professional experience
• Bachelor’s degree in…