Watson Health - Design Assurance Engineer
Watson Health - Design Quality Assurance Engineer
It's time to transform health with new ways of working to improve approaches to care, productivity and well-being. Watson Health's cognitive systems understand, reason and learn - helping to translate information into knowledge that can help drive more informed decision-making. With cognitive computing, we can see and analyze more data than ever before - and achieve more than we ever thought possible.
As a Design Quality Assurance Engineer and member of the Watson Health Compliance Organization you will work in a multi-disciplinary group, contributing to the design and development of Software Systems and verification processes for the development of Class I, II and III medical devices, including new product development and maintenance of released product. You will use your knowledge of FDA Pharmaceutical and Medical Device compliance regulations and international standards to provide design quality assurance support for Clients, Project Leaders, Development, Operations, and other cross-functional team members and personnel. You will support post market surveillance processes for Watson Health. This will include participation in resolving CAPAs, complaints, MDRs, recalls, serving and non-conforming products. You will interface with the Business and Marketing leaders, the solution reams, compliance organization, the legal department and other stakeholders to maintain compliance of Watson Health Offerings.
You will be responsible for:
Providing design quality assurance support in the development of medical device software products, and facilitating the application of design controls and V&V system/software validation.
Providing design assurance support for post market surveillance processes when design changes are required.
Ensuring development activities are planned, documented, and executed to satisfy regulatory, customer and designated internal requirements.
Ensuring development is compliant with internal and external standards
Actively supporting product development projects by coaching teams to create Project Development Plans, Design Inputs and Outputs, Design Reviews, Design History Files, Risk Management, V&V Plans, V&V Protocols, Traceability matrices, etc.
Participating in risk management assessment efforts, including hazard analysis and design failure mode effect analysis
Ensuring changes to existing products are conducted in compliance with the FDA Quality System Regulations, ISO 13485 Regulations, and other applicable standards.
Participating in continuous improvement of design control process
Ideally, you will be:
Current in knowledge of applicable federal regulations and international standards including 21 CFR 820, 21 CFR 803, 21 CFR 806, ISO 13485, ISO 14971, IEC 62304 and the Medical Device Directive
Experienced with standards for the design, verification, and validation of medical device products
Skilled in requirements analysis, including testable and measurable specifications
Join us and be part of a diverse and global team of thinkers and doers - people who want to make an impact, cultivate their expertise and collaborate with some of the world's top business and technology professionals.
Required Professional and Technical Expertise
5 years of quality systems experience in a healthcare device or life sciences pharmaceutical company
2 years of design quality assurance experience in a regulated software development company, preferably in a cloud or mobile platform industry segment
Required Technical and Professional Expertise
- At least 5 years of w ork experience in a healthcare device or life sciences pharmaceutical company
Preferred Tech and Prof Experience
- 5 years of w ork experience in a healthcare device or life sciences pharmaceutical company
- 2 years of quality assurance compliance work experience in a regulated SW development company, preferably in a cloud or mobile platform industry segment
IBM is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. IBM is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
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