• The Senior Principal Engineer, Infusion Systems leads the development and revision of all product risk documentation per current industry standards and regulatory requirements.
• Collaborates with cross-functional team members to build Use and Design Failure Modes and Effects Analyses (FMEAs) and Risk Assessments
• Identifies, and verifies effectiveness of, risk control measures throughout the product lifecycle.
• Reviews risk management processes with other business units and leads adoption of best practices.
• Reviews Process FMEAs developed by contract and internal manufacturing teams.
• Participates in Risk Management Committee meetings, preparing information to be presented and capturing and tracking action items to closure.
• Leads compliance with, and continuous improvement of, internal risk processes
• Develops and updates the Safety Assurance Case in collaboration with Clinical Product Specialist, Human Factors Engineering and Regulatory Affairs.
• Performs additional R&D system engineering activities as needed including requirements management, architecture review, V&V strategy, and post-market surveillance
• Leads post-market surveillance activities to maintain accurate, updated risk management files including responsibility for MAUDE database reviews, complaints analysis and CAPAs ownership
• Uses computer-based tools to manage versions of risk objects and traceability to requirements and specifications.
• Displays advance understanding of theories/practices utilized by own discipline and other disciplines outside the primary area of expertise to identify coverage of risks, requirements, architectural components, functions and performance
• Evaluates results relative to product requirements, definitions and/or program goals. Applies standard techniques to solving difficult problems.
• Work independently with latitude for individual judgment. Exercises judgment within defined procedures and practices to determine appropriate action.
• Guides the conceptualization of new methodologies, materials, machines, processes or products. Generates innovative solutions to complex problems through the use of multiple disciplines and technical principles. Advise senior management regarding appropriate action.
• Works on solving complex issues within department, where analysis of situations or data requires an in-depth evaluation of variable factors. Erroneous decisions or failure to achieve goals may result in additional costs and serious delays in overall schedules.
• Routinely provide advice and assistance to team members regarding routine and unique problems. May supervise or direct Sr engineers and lower-level engineers on assigned projects.

The requirements listed below are representative of the knowledge, skill, and /or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Bachelor's Degree in Engineering or similar related degree.

• 8 years' experience in a related role achieving similar responsibilities within the medical device industry.

• Comprehensive understanding of the medical device development process.

• Excellent interpersonal skills including ability to work effectively in a matrix environment.

• High attention to detail and excellent oral and written communication skills.

• Excellent problem solving and organizational skills.

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company match, andwellness program.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.