Job Description

Description

About New World Medical

Founded in 1990, New World Medical is a mission-driven company focused on preserving and enhancing vision through innovative ophthalmic surgical devices, including the Ahmed Glaucoma Valve and Kahook Dual Blade. We partner closely with eye care professionals to deliver tools that improve clinical outcomes and patient care. Guided by our core values - Integrity, Accountability and Innovation, we strive to make a meaningful impact in eye health worldwide. In support of our global mission, we proudly donate surgical equipment to charitable organizations to expand access to quality eye care.

Benefits starting Day One:

• Medical, Dental, and Vision Insurance
• 401(k) with Profit Share
• Bonus Opportunities
• Flexible Work Schedules
• Free Onsite Daily Lunches to foster team connection
• Career Development Program
• Tuition Assistance (after 1 year of service) 
• Cell Phone & Home Office Stipends
• Wellness & Employee Assistance Programs
• Company Events & Recognition
• And more!

Be part of something meaningful—join the team at New World Medical.  

JOB SUMMARY: 

The Principal Engineer, Quality-Software is responsible for all QMS software validation activities and identifying and leading software integration and improvement initiatives. The Software Quality Engineer will own and oversee all QMS software and supporting systems. 

ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: 

• Key contributor and leader for QMS software projects. 
• Create, design and upkeep of QMS software URFS documents. 
• Design, write and execute QMS software validation test scripts for quality system affecting software. 
• Assess and implement changes to QMS software during update reviews. 
• Assists with the selection, evaluation, and implementation of QMS software solutions. 
• Identifies, plans, and executes new software integration initiatives to improve the QMS. 
• Identifies, plans, and executes software improvement initiatives to streamline QMS software workflows. 
• Lead cross functional collaboration teams to design, write and execute software validation test scripts for Manufacturing, R&D, or other equipment which have a software component. 
• Review and identify gaps in relevant published/updated standards that may affect compliance. 
• Other job duties as assigned.

Requirements

 KNOWLEDGE, SKILLS AND ABILITIES: 

• Very strong background in software structure and computer usage (including MS applications). 
• Strong background in software validation and URFS development. 
• Strong presentation, written, and verbal communication skills and interpersonal skills. 
• Strong work ethic, ability to work in a team environment and independently on projects as needed. 
• Proficient in technical report writing and review. 
• Knowledge of ISO 13485, 21CFR, MDSAP, MDD, and MDR preferred. 
• Project Management and problem-solving skills highly preferred. 

EDUCATION AND EXPERIENCE: 

• Bachelor’s degree in Computer science, engineering, or other scientific discipline. Advanced Degree preferred. 
• 7+ years’ experience in the medical device industry or equivalent with an emphasis on validation, system-level software implementation, and integration project management. 
• SAPByD, EtQ Reliance, and API experience preferred. 
• Experience with QMS software preferred. 

PHYSICAL REQUIREMENTS: 

• Must be able to remain in a stationary position at least 50% of the time, including sitting at a desk and working on a computer. 
• Occasionally move about inside the office and travel to and from office buildings. This may include, but is not limited to, bending and walking. 
• Must be able to operate a computer and other office productivity machinery, such as a computer printer, computer keyboard, calculator, etc. 
• Occasionally lift up to 15 pounds. This may be performed with reasonable accommodation. 
• View and type on computer screens for long periods of time. 

This description reflects management’s assignment of essential functions, it does not proscribe or restrict the tasks that may be assigned.