You have honed your knowledge and technical skills and are looking to join a fast-paced, high-performance team developing and marketing products in the genomics space to improve the human condition.
As a member of Agilent?s new business group ? Diagnostic and Genomics Group (DGG) ? you will play a key role in the success of our business through the development and implementation of novel genomics and molecular biology solutions from research to clinical applications.
We are seeking a highly motivated individual to join our cross functional team for the development and analysis of large data sets generated as we move genomic solutions into the clinical arena.
Work as part of a core team to transition Agilent?s research solutions to clinical diagnostics.
Assist with development, planning and tracking of validation experiments associated with regulatory submissions.
Analyze genomic data utilizing in-house developed software and other statistical methods for regulatory submissions.
Communicate effectively with a cross functional team
Maintain and document activities related to the analysis and management of data sets
BS/MS degrees in Molecular Biology or Bioinformatics with 5+ years of professional work experience or PhD with 3+ years of work experience.
Experience in product development and/or product support.
Experience with development or support of products sold into a regulated market, ideally in clinical diagnostics.
Knowledge and experience with genomic technologies.
Expertise in analysis of large complex data sets (e.g., Microarray and/or Next Generation Sequencing data) required.
Excellent written communication skills necessary
Working knowledge of standard statistical methods and tools
Experience operating in a IVD Regulatory environment preferred
Geo Location: Santa Clara, CA
Agilent is an equal opportunity employer.