Manufacturing Engineering Supervisor

Date: Jul 26, 2022

Location: Pendleton, SC, US, 29670

Company: Arthrex

Requisition ID: 54320 
Title: Supervisor - Manufacturing Engineer - SC 
Division: Arthrex Manufacturing Inc (US02) 
Location: Pendleton, SC 

 

 

 

 

 

 

 

 

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Manufacturing Engineering Supervisor. This position will support our sutures production processes. Successful candidates must possess a Bachelor’s degree in an Engineering or Engineering Technology discipline. This position requires 10 years of applicable working experience that includes at least 3 years of supervisory experience. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

 

Main Objective:

Designs, develops, implement superior medical device manufacturing processes and systems in order to fulfill customer requirements.

Works with the Manufacturing Operations, Design Engineers, Quality Engineers and Product Managers to recommend alterations and enhancements to improve quality of processes, products and procedures.

 

Essential Duties and Responsibilities:

 

  • Supervise Manufacturing Engineering teams
  • Coach individual engineers and engineering teams in the practical application of engineering methods and processes
  • Coach individual engineers and engineering teams in the practical application of project management methods
  • Mentor a “Do it more right the first time” culture, skills and tools to enhance quality and operational excellence
  • Lead the introduction of new products, manufacturing equipment, and manufacturing processes that are superior in quality, capability, and reliability.
  • Develop and disseminate best practices for the creation, validation, and deployment of process work instructions

 

Incidental Duties:

The above statements describe the general nature and level of work being performed in this job.  They are not intended to be an exhaustive list of all duties, and indeed additional responsibilities may be assigned, as required, by management.

 

Education and Experience:

  • Mechanical Engineering Degree or other engineering or engineering technology field.
  • 10 years experience in the medical device manufacturing industry, or closely related field required
  • 3 years of supervisory experience required

 

Knowledge and Skill Requirements/Specialized Courses and/or Training:

  • Ability to work independently and effectively with cross functional teams.
  • Thorough understanding of manufacturing processes.
  • Detail oriented with strong analytical and critical think skills.
  • Descriptive statistics knowledge.
  • Strong communication skills and ability to communicate effectively with technical and non-technical staff.
  • Experienced user of MS Office Suite
  • Experience with planning and conducting tests to characterize and validate equipment and processes.
  • Experience in completing technical documentation for engineering and manufacturing.
  • Familiarity with clean room practices preferred.
  • Solidworks experience preferred
  • CAM experience preferred

 

 

 

 

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


Nearest Major Market: Greenville
Nearest Secondary Market: South Carolina

Job Segment: Manufacturing Engineer, Medical Device Engineer, Engineering Manager, Medical Device, Mechanical Engineer, Engineering, Healthcare