To provide technical / scientific support to both internal and external clients. To assist in the delivering and monitoring of consistent deliverables for Global Scientific Affairs.
Maintain and configure testing and assay summary information in the Test Master application of the ICOLIMS system.
Configure test codes within the STARLIMS system.
Assist all other ICL departments with Global Scientific Affairs related issues and questions.
Utilize the internet, journals, internal validation documentation, etc to update specimen requirements, stability, and transport information within departmental databases.
Follow SOPs relevant to Global Scientific Affairs issues.
Attend meetings with both internal and external clients on behalf of Global Scientific Affairs.
Provide notifications and technical documentation to the Global Validation Department and ultimately Global Client Services.
Maintain CLSI documents library.
Performs additional relevant responsibilities as requested by management.
Recognize, exemplify and adhere to ICONs values, which centers around our commitment to People, Clients and Performance.
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

What you will need:

BS Degree in Medical Technology, preferred.
Experience in Analytical Platforms such as Siemens, Roche, Abbott, Beckman is preferred.
More than 5 years relevant experience
Knowledge of clinical laboratory concepts and terminology
Knowledge of Microsoft Word and Excel

Scientific Affairs Specialist I