Job Description:
The Senior Software Engineer in the Systems Engineering team will develop and support software and middleware for in-vitro diagnostics (IVD) and clinical diagnostics systems. As a development lead in cross-functional project teams, he/she shall work as a subject matter expert in architecting, developing and commercializing software and middleware systems by utilizing expertise in software and systems engineering and analysis Major Activities: -Lead or contribute to development of software, from requirements through design, implementation, and validation and release to customers. • Contribute to the architecting of software systems solutions for in-vitro diagnostic systems and interfaces to other diagnostic lab systems and LIS. -Interact with outside partners and vendors work and progress towards specifying and developing software products, including architecture, design, prototype testing, defect reviews, design reviews, V&V and UAT. • Develop system level product requirements and software/component requirement documents using requirements management methodologies including change management. -Partner with Global Marketing to develop customer requirements; work with other internal stakeholders to facilitate the collection of business and regulatory requirements. • Define and prepare a schedule of development tasks, deliverables and timelines. • Conduct patient safety risk management activities according to FDA and ISO regulations. • Establish product configuration management. • Plan and perform system, integration and unit testing. • Support verification and validation activities. • Document and present work product to project team and business stakeholders. - Mentor others on software engineering best practices and procedures. Requirements: -Bachelors Degree in a technical discipline such as Software Engineering or equivalent. Advanced degree preferred. 9+ years of relevant experience developing software based diagnostic products. -Ability to solve complex software issues and problems, for both application and networking software. Experience with Laboratory Information Systems (LIS) is a plus. -Experience with leading development efforts in a cross functional environment. -Experience in database based software development. -Experience in graphical user interface design and development. -Knowledge of molecular biology is a plus. -Experience with Next Generation Sequencing (NGS) software and bioinformatics is a plus. -Demonstrated software product development experience using lifecycle methodologies and under FDA design control. -Possesses project management skills in managing priorities, delegating, and influencing others. -Experience in a cross functional environment. -Ability to convey complex information in both written and oral form. -Experience with external vendor relationships. -Ability to influence others, gain acceptance and build consensus. -Excellent communication and interpersonal skills.
Additional Info:
Grifols is a global healthcare company whose mission is to improve the health and well being of people. Our three divisions –Bioscience, Diagnostic and Hospital–develop, produce and market our innovative products and services to medical professionals in more than 100 countries. We are committed to fostering an environment that creates continuous learning opportunities and encourages professional development and growth. As a company devoted to improving the health and well-being of people, we are looking for talented professionals worldwide. Make a difference and join us in this challenging and rewarding enterprise. EEO Minorities/Females/Disability/Veterans[Click Here to Access the Original Job Post]
The Senior Software Engineer in the Systems Engineering team will develop and support software and middleware for in-vitro diagnostics (IVD) and clinical diagnostics systems. As a development lead in cross-functional project teams, he/she shall work as a subject matter expert in architecting, developing and commercializing software and middleware systems by utilizing expertise in software and systems engineering and analysis Major Activities: -Lead or contribute to development of software, from requirements through design, implementation, and validation and release to customers. • Contribute to the architecting of software systems solutions for in-vitro diagnostic systems and interfaces to other diagnostic lab systems and LIS. -Interact with outside partners and vendors work and progress towards specifying and developing software products, including architecture, design, prototype testing, defect reviews, design reviews, V&V and UAT. • Develop system level product requirements and software/component requirement documents using requirements management methodologies including change management. -Partner with Global Marketing to develop customer requirements; work with other internal stakeholders to facilitate the collection of business and regulatory requirements. • Define and prepare a schedule of development tasks, deliverables and timelines. • Conduct patient safety risk management activities according to FDA and ISO regulations. • Establish product configuration management. • Plan and perform system, integration and unit testing. • Support verification and validation activities. • Document and present work product to project team and business stakeholders. - Mentor others on software engineering best practices and procedures. Requirements: -Bachelors Degree in a technical discipline such as Software Engineering or equivalent. Advanced degree preferred. 9+ years of relevant experience developing software based diagnostic products. -Ability to solve complex software issues and problems, for both application and networking software. Experience with Laboratory Information Systems (LIS) is a plus. -Experience with leading development efforts in a cross functional environment. -Experience in database based software development. -Experience in graphical user interface design and development. -Knowledge of molecular biology is a plus. -Experience with Next Generation Sequencing (NGS) software and bioinformatics is a plus. -Demonstrated software product development experience using lifecycle methodologies and under FDA design control. -Possesses project management skills in managing priorities, delegating, and influencing others. -Experience in a cross functional environment. -Ability to convey complex information in both written and oral form. -Experience with external vendor relationships. -Ability to influence others, gain acceptance and build consensus. -Excellent communication and interpersonal skills.
Requeriments :
Skills :
Additional Info:
Grifols is a global healthcare company whose mission is to improve the health and well being of people. Our three divisions –Bioscience, Diagnostic and Hospital–develop, produce and market our innovative products and services to medical professionals in more than 100 countries. We are committed to fostering an environment that creates continuous learning opportunities and encourages professional development and growth. As a company devoted to improving the health and well-being of people, we are looking for talented professionals worldwide. Make a difference and join us in this challenging and rewarding enterprise. EEO Minorities/Females/Disability/Veterans[Click Here to Access the Original Job Post]