As a key member of the Software Quality Group, the incumbent will support the process development activities related to the design, development, or reliability of Fresenius Medical Care’s products.
Familiarity with the FDA’s Quality System Regulation (QSR) 21 CFR Part 820.
Understanding of ISO13485 (Medical devices – Quality management systems) and ISO 14971 (Application of risk management to medical devices)
Knowledge of QMS principles and practices
Expertise in risk management processes, including hazard analysis, risk assessment, risk control
Understanding of design control processes, including design input, design output, design verification, design validation, design transfer, and design changes
Strong problem solving and analytical skills.
Lead major efforts, or phases of projects, to resolve Software Quality-related problems
Support the product development teams in the adoption and use of best practices, Quality tools, and Software Design Control methodologies
Develop and execute systems level and functional area tests
Monitoring and developing software reliability improvements to existing & new design
Strong analytical and problem-solving skills, ability to multitask in an environment with changing priorities
Support Software Quality System sub-systems as directed by senior management, i.e. CAPA, Internal Audits, et
Assist with various projects as assigned.
Other duties as assigned.