Senior Systems Engineer - Limerick

Senior Systems Engineer - Limerick.

About the Role
As part of the Systems Engineering group, the Senior Systems Engineer will have a phenomenal opportunity in providing their system knowledge to lead and contribute to the portfolio of products. This role entails utilising your detailed understanding of system design and system integration tools and methodologies to connect pieces across the different functional elements i.e. Software, Mechanical, Electrical, Fluidics, Biochemistry and Optical engineering. You will ensure the product requirements are defined/maintained and the lower-level functional design teams deliver them to those requirements.

Job Responsibilities:
o Coordinate system-level product development, system architecture, integration, and system characterization testing
o Exercise strong communication and leadership skills to collaborate with worldwide teams, including external partners.
o Provide technical support to a wide range of problems pertaining to specific programs and projects.
o Consistently apply Systems Engineering Techniques such as requirements management, traceability, risk management, verification and validation.
o Work effectively in a multi-functional team in a collaborative manner to identify, communicate and mitigate project/program needs based on lifecycle phase.
o Apply focused work methodologies utilising scientific and statistical methods (six sigma) in resolving problems, devising tests and setting specifications.

Education and Experience requirements:
o Minimum of a Bachelor's Degree required, ideally in BioEngineering, BioMedical, Biology, Chemical Engineering.

Masters or PhD degree an advantage.
o Minimum of 5 years' experience in systems engineering, product development, or product design with Bachelor's degree, or 3 years with Master's degree, or 2 years with PhD
o Experience developing and executing System Level Characterization, Integration or Test Procedures.

Knowledge and Skills:
o Experience with Flow Cytometry is desirable for this role
o Experience or good understanding of immunology is a plus
o Experience in Product Development for In-Vitro Diagnostic and/or medical devices in ISO 13485 environment.
o Experience with Risk Management methodology
o Proficiency in the use of traceability tools such as JIRA, DOORS or Azure.
o Good understanding of Structured Product Development Process and methodology.
o Experience with Engineering Change Management procedures post commercialisation of products such as ECO's, engineering change impact assessments, regression testing assessments etc.
o Software and script language programming skills is a plus.