Engineer II - Manufacturing - Sutures 1 at Arthrex

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. We are a privately held company that strives to accomplish our corporate mission of Helping Surgeons Treat Their Patients Better™. We are committed to delivering uncompromising quality to the health care professionals who use our products, and ultimately, the millions of patients whose lives we impact.

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 Lunch
Tuition Reimbursement Program
Trip of a Lifetime
Paid Parental Leave
Paid Time Off
Volunteer PTO
Employee Assistance Provider (EAP)

Please note, most benefits are for regular, full time employees.

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.

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Design, develop, implement and improve manufacturing processes for medical textiles to produce cost effective quality medical device products and systems. Provide manufacturing engineering expertise to create, document and implement required procedures and documents. The ideal candidate must have at least two years of post-graduate work experience. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Essential Duties and Responsibilities:

• Work with project teams to identify issues and risks. During new product development integrate with Engineers, Design Engineers, Quality Engineers and the Production Department to ensure cost effective new product development and introduction into manufacturing.
• Develop a continuous improvement culture, skills set and tools to enhance quality and operational excellence.
• Lead/support process improvement initiative.
• Introduce new equipment, products, and processes. Present process and equipment recommendations to Leadership Team with equipment reviews and plans for implementation.
• Initiate new projects and be the Project Leader for key improvement initiatives, identifying best practices.
• Develop an understanding of the current manufacturing processes and identify targets for improvement in operation efficiencies.
• Develop manufacturing Work Instructions.
• Provide process support on manufacturing technical issues.
• Provide process and equipment expertise and support for daily braid and textile manufacturing, assembly, and clean-room sterile packaging efforts/and or production efforts.
• Develop action plans to achieve short and long-range efficiency goals, selection of new production methods, designs of production fixtures, and methods to monitor efficiencies.
• Lead and/or assist with implementation of textile product specifications into manufacturing.
• Monitor timelines and project deliverables to ensure adherence with approved project plans for manufacturing process development.
• Develop protocols and coordinate validation of equipment and processes.
• Stay current with methods used in the medical device industry to advance technologies.
• Participate in defining Preventive Maintenance programs for production equipment.
• Investigates and test in time reliability and quality improvements
• Ensure Information and documentation is consistently accurate
• Analyze and plan workforce utilization, space requirements, and workflow, and designs layout of equipment and workspace for maximum efficiency.
• Confer with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards.
• Estimate production times, staffing requirements, and related costs to provide information for management decisions.
• Apply statistical methods to estimate future manufacturing requirements and potential.
• Provide process and equipment expertise and support.
• Identify issues and risks to ensure cost effective new product development and introduction into manufacturing.

Education and Experience:

• Bachelor’s degree in Engineering, Science, Textile Management or Mathematics or equivalent Arthrex experience required
• 2 years of manufacturing process improvement experience.
• Proven experience in leading process improvement projects.
• Medical device manufacturing environment preferred along with experience working within textile production environments and/or manual assembly environments, preferably in suture assembly or other medical device assembly.
• Experience in workflow optimization, work measurement, efficiencies.
• Recognized process improvement training (Lean, Six Sigma) preferred.
• Industrial Engineering experience is a plus, but not essential.
• Understanding of BOMs and routings.

 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 skills.

Strong communication skills and ability to communicate effectively with technical and non-technical staff.

Experienced user of MS Office Suite and CAD.

Experience with planning and conducting tests to validate equipment and processes.

Experience in completing technical documentation for engineering and manufacturing.

SPC (Statistical Process Control) knowledge.

Familiarity with clean room practices preferred.

Project management knowledge preferred.

Machine, Tools, and/or Equipment Skills:

Metal cutting equipment, finishing equipment, printing equipment, sealing equipment and custom fixturing.

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. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock. The noise level in the work environment is usually moderate.

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.