Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a System Engineer II , who will be part of the system development team focusing on the development of a cutting edge next-generation sequencing (NGS) system for RUO & IVD applications.
Experience and Responsibilities:
Experience in RUO or IVD product design and development is essential.
Specific experience in Requirements Management and Analysis as well as Design Verification process for biomedical systems is highly desirable.
Knowledge of Risk Analysis methods, Reliability Engineering, Design Transfer activities for product manufacturing is desirable.
Experience with all phases of technology development is highly desirable.
Nucleic acid based technology background and next-generation sequencing experience are highly desirable. Other system development experience in complex diagnostic development environments is a plus.
Knowledge of NGS workflows and data analysis is desirable. Experience with NGS systems development is a plus.
The individual responsibilities are:
Works under general supervision, to conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding
Work with cross-functional teams to determine and document appropriate design requirements
Summarizes experimental results, and reviews conclusions with supervisor/project leader
Develops test plans, writes test cases, and implements and executes automated tests to verify the hardware, software and system performance.
Hands-on with a strong instrument/platform development background, the candidate will be asked to troubleshoot systems, identify opportunities for quality improvements, provide root causes of complex HW-SW interaction problems, and communicate test results and corrective recommendations to the team. He or she will work closely with internal design teams to understand and resolve product performance issues.
Required Bachelors in Biomedical Systems Engineering or related field
Required 2-5 years relevant industry experience; MS with 2+ years of experience preferred.
Experience working on the development of medical devices under design control processes, experimental design, versatile laboratory practice, data analysis, and data and concept presentation.
Please respond with your updated resume and contact information to .
DAWAR CONSULTING, INC.
Dawar Consulting, Inc.