
Senior Software Quality Assurance Analyst IRC273259
- Украина
- Постоянная работа
- Полная занятость
- 2-5 years of experience in Quality Assurance of class II or III with embedded software in the medical device field.
- Demonstrated competency of 21 CFR 820, ISO13485, ISO 14971, and other international standards.
- Electro-mechanical engineering experience and the ability to take on technical challenges through resolution is a huge plus.
- Bachelor’s Degree in an applied science or engineering field is highly desirable.
- Exceptional problem-solving skills.
- Understands and can subsequently explain complex quality details to non-experts.
- Exceptional organizational skills.
- Knowledge and experience with ERP/MRP systems and their applications.
Our work environment is a fast-paced, innovative, and collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We put the patients we serve first in everything we do. We are looking for like-minded individuals to join our team today!Specific job responsibilities include:
- Responsible for assuring projects meet customer expectations, quality goals, and regulatory requirements including FDA Quality System Regulations, ISO13485, EU MDR requirements, and Risk Management per ISO 14971.
- Apply knowledge of IEC 60601-1 Medical Electrical Equipment and collateral standards, IEC 62366 Usability, and IEC 62304 Software Lifecycle to product development and design improvement and sustaining projects.
- Serve as a Quality Engineering representative on teams engaged in new product development, quality processes improvements, business system implementations or other special projects
- Apply knowledge in Quality Systems to execute overall project assignments and ensure robust adherence to Design Control requirements.
- Reviews and approves product documentation, drawings, process and design verification/validation
- Serve as a technical resource for assessing validation requirements, solving test related problems, and developing preventive strategies
- Perform and lead risk assessment exercises in support of validation activities.
- Plans, develops, implements, and maintains the document change control system.
- Assist and participate in internal and external audits as the subject matter expert.