The Design Quality Assurance team is an integral part of developing and bringing to market innovative new products and technologies that make life more rewarding and dignified for people with challenging medical conditions.
Responsibilities
Associates within the Design Assurance team
Resource planning, allocation, and monitoring on projects and initiatives
Mentor Design Assurance team on projects and ensure completion per timelines and expectations
Support Design Assurance issues and escalate for resolution if required
Be a core team member on SPRING or Continence projects as required
Drive continuous improvement initiatives within the Design Assurance function
Support the internal and external audit program
Complete assigned Impact Assessments within the change control system
Support periodic review of assigned design control procedures
Support the development of the strategic direction for the Design Assurance function
Complete gap assessments to new standards as required
Ad hoc travel
Essential Functions of the Role**:
The successful candidate will engage with Global Team of Design Quality Assurance Engineers and cross functional partners as part of driving the new product development process.
Work Experience Requirements
8+ years of design assurance medical device experience is required.
Relevant experience in the medical device industry
Education Requirements
Degree in Engineering/Science Discipline or Quality Engineering Qualification
Specialized Skills/Technical Knowledge
Experience in Quality Systems and Design Assurance
Working knowledge of ISO 13485 and FDA 21 CFR Regulations and BS EN ISO 14971
Software: Knowledge and experience of Word, Excel, PowerPoint and Minitab
Knowledge of statistical data analysis
An ability to work independently and as part of a team. The successful candidate will be able to organize their own work on a routine basis.
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