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Salary
≈ $73k – $137k per year (Estimated)
Location
In office (Naples)
Seniority
Senior · 5+ years exp
Visa
H-1B filings in 12 months: 19 · green card filings: 2

Confirmed on the employer's own hiring board on Oct 28, 2026. First seen by Alion on Oct 16, 2026. Arthrex scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Arthrex is a privately held American medical device company that develops and manufactures products for arthroscopy, sports medicine, joint replacement, trauma and orthobiologics, along with surgical imaging systems. Founded in 1981, it runs extensive surgeon education programs and has operations in Florida, Germany and many other countries. It hires orthopedic sales representatives, credit and collection coordinators, helpdesk supervisors and engineering staff. The company is headquartered in Naples, Florida, United States.

Requisition ID:

66476

Title:

Senior Sterilization Specialist

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 Senior Sterilization Specialist for our Global Headquarters in Naples, FL. The Senior Sterilization Specialist is responsible for Arthrex Inc’s Sterilization and end-user reprocessing projects, validations, and monitoring programs in accordance with quality systems requirements. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Essential Duties and Responsibilities:

  • Participate in design review meetings and as a key member of product design teams to assess and validate devices for proper sterilization methods, e.g., radiation, ethylene oxide, and end-user reprocessing etc.;
  • Direct and maintain global corporate programs for sterilization cycle maintenance and end-user cleaning and sterilization instructions;
  • Ensure Arthrex’s corporate sterilization programs are maintained in accordance with all relevant international standards, e.g., ISO 11135, ISO 11137, ISO 17665, etc. as well as domestic and foreign regulatory requirements;
  • Coordinate all activities related to validations and/or testing, and directly interact with external and corporate laboratories, and sterilizers personnel to accomplish the assigned tasks;
  • Perform documented assessments, and validations as required of product and process changes for impact to sterilization process efficacy;
  • Act as lead auditor and/or subject matter expert for quality management system audits of Arthrex’s global supplier base including critical contract manufacturers, sterilization service providers, and laboratories in accordance with applicable standards, e.g., ISO 13485, ISO/IEC 17025, and international regulatory directives;
  • Support manufacturing organizations in defining requirements for and ensuring infrastructure systems are efficacious in controlling and preventing potential contamination from device contacting materials, utilities, environments, etc.;
  • Ensure proper maintenance of files demonstrating internal and vendor compliance and performance including authoring and/or reviewing sterilization validations and product assessments into existing cycles, routine product and environment monitoring reports, non-conformances, CAPA’s, etc.;
  • Mentor teams, share experience, and provide best practices to sterilization / quality staff related to sterilization systems, corporate policy, and regulatory requirement;
  • Encourage and foster an environment based upon a foundation of continuous process improvement and industry benchmarking;
  • Support and lead Arthrex’s business and expansion goals;
  • Must be able to travel up to 10% of the time.

Education and Experience:

  • Bachelor’s Degree in Biology/Microbiology, Chemistry, or related science field required.
  • 5 years relevant experience
  • Knowledgeable of FDA and ISO guidelines for the sterilization assessment of medical devices required.
  • Manufacturing process knowledge preferred.
  • Project management and communication skills training preferred.
  • Working knowledge of terminal sterilization methods required.
  • Hands on experience performing laboratory testing activities.
  • Test protocol and report writing experience preferred.
  • Working knowledge of device clinical use and associated harms and hazards
  • Knowledge of orthopedic surgery principles, theories, and products preferred.

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

Specialized training in manufacturing operations, system design and development, terminal sterilization methods, industrial statistics, and technical writing preferred. Experience in project management tools are highly desirable. Experience in working with Medical Device Risk Management (Specifically ISO 14971), CAPA, Complaint Management, and Nonconformance Reporting preferred.

Machine, Tools, and/or Equipment Skills:

Proficiency in the use of Personal Computers and computer programs, particularly the Microsoft Office Suite; Excel, Word, PowerPoint (or equivalents if changed by the Company). Solidworks, Minitab, and SAP or corporate ERP systems experience desirable.

Reasoning Ability:

Ability to define problems, identify opportunities, collect data, analyze established facts, draw valid conclusions, and implement change. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

Mathematical Skills

Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements.

Language and Communication Skills:

Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to sit, use hands and fingers to handle or feel, and reach with hands and arms. The employee must occasionally lift and/or move up to 10 pounds.

Vision Requirements:

Visual acuity necessary to do the job safely and effectively.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The area that this job is performed in is a general office or open cubicle/workstation environment. The noise level in the work environment is usually low to moderate.

Arthrex Benefits

  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)

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

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