Clinical Genomics Scientist

Organization: 
Agilent Technologies, Inc. US
Job Location: 
Santa Clara, CA
Job Description: 

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.
Responsibilities:
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

Requirements:

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.

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