Design Quality Engineer 2

At Smith+Nephew, we design and manufacture technology that takes the limits off living as the Design Quality Engineer you would be Reporting into the Quality Department, this role provides Quality Engineering support for Smith & Nephew New Product Development activities for Hardware/Software products in the Sports Medicine franchise. Works collaboratively with project team members to develop and manage project plans and activities related to new product development.

What will you be doing?

About Smith+Nephew

• Life Unlimited.
• We believe in crafting the greatest good for society.
• Our strongest investments are in our people and the patients we serve.
• Committed to Welcoming, Celebrating and Thriving., Learn more about Employee Inclusion Groups on our website ( https://www.smith-nephew.com/ ).
• Stay connected by joining our Talent Community .
• We're more than just a company - we're a community!
• Follow us on LinkedIn to see how we support and empower our employees and patients every day.
• Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You.
• Unlimited. , life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer.

Responsibilities

• Responsible for supporting the execution of design control and risk management activities in accordance with internal procedures and applicable standards/regulations.
• Risk management planning, use/design/software FMEA, risk control and mitigation, verification of effectiveness (15%) Cross-functional NPD support: Quality input to user needs, design inputs, software requirements, specifications and design outputs including CTQ features (25%) Design verification, validation and usability testing; software/system V&V including protocol/use case development, test execution and report writing (25%) Development and release of engineering design documentation; support design reviews and design history file compilation/audit activities (10%) Manufacturing quality activities including MSA, incoming inspection, control plans, process summaries and process FMEA (5%) Regulatory submission preparation and audit/inspection support (10%) Education: B.S. in engineering or technically related field

Requirements

What will you need to be successful?

• Risk Management per ISO 14971 (preferred) Medical device software development per IEC 62304 (preferred) ISO 13485 (preferred) Time management, multi-project planning
• Effective cross-functional collaboration Written/oral communication skills
• Accountability 2–5 years Quality Engineering experience in Medical Device or comparable regulated industry Y ou Unlimited.

Benefits

• Other reasons why you will love it here!
• Major medical coverage + policy exclusions and insurance non-medical limit.
• Educational Assistance.
• Flexible Personal/Vacation Time Off, Privilege Leave, Floater Leave.
• Hybrid Work Model (For most professional roles) Your Wellbeing: Parents/Parents-in-Law’s Insurance (Employer Contribution of 8,000/- annually), Employee Assistance Program, Parental Leave.
• Hands-On, Team-Customized, Mentorship.