Validation Engineer I

Arthrex

16h

About The Position

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. Arthrex is actively seeking a Validation Engineer I to join us at our growing Pendleton, SC location. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™. Main Objective: Responsible for supporting the AMI Validation Manager with all process validation related support for the life cycle development and manufacturing of Class I, II and III medical devices.

Requirements

Bachelor’s degree in Engineering or Engineering related technology required.
Experience in a Quality Control, Quality Assurance or Validation position in a Medical Device Company preferred.
Knowledge of testing equipment, statistical methods, control plans.
Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), QAD or similar inventory software.

Nice To Haves

Experience in a Quality Control, Quality Assurance or Validation position in a Medical Device Company preferred.

Responsibilities

Responsible for writing of protocols and conducting validations of special processes, including laser marking, passivation, laser welding, molding, etc.
Responsible for reviewing and approving validations of special processes performed at all Arthrex facilities
Facilitate the execution of protocols by working closely with Engineering, Operations, Quality Control, and other manufacturing functions.
Responsible for measuring validation parts and perform analysis of data generated from validations to evaluate process capability.