Manufacturing Engineer

Globus Medical•West Carrollton, OH

19d

About The Position

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. Position Summary : As a Manufacturing Engineer, you will develop, implement and maintain methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies. Support new initiatives and productivity targets for given manufacturing processes. Interface with design engineering in coordinating the release of new products. Estimate manufacturing cost, determine time standards and make recommendations for tooling and process requirements of new or existing product lines. Maintain records and reporting systems for coordination of manufacturing operations.

Requirements

Ability to effectively communicate information, both formally and informally, such as data, methods, findings, and remediation recommendations at all levels within the organization and with key contacts
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
Familiar with implementing, maintaining, analyzing data to 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, Siemens NX or Solidworks and Gage/fixture design
Typically requires a Bachelor’s degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience
Bachelor’s degree in an engineering discipline preferred
Experience in 21 CFR 820 and/or ISO 13485 regulated environment

Responsibilities

Leads projects of moderate 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)
Drives 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
Supports design for manufacturability analysis with CNC Programmers and Quality Engineers, and provide input to Development (Design) Engineers
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech 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.