Research Assistant, Cancer Companion Diagnostics

Agilent Technologies•Carpinteria, CA

1d•$28 - $44•Hybrid

About The Position

Agilent's Companion Diagnostics Business (CDx) partners closely with leading pharmaceutical companies to develop, manufacture and commercialize in vitro diagnostic devices, which are a critical part of precision medicine. The CDx business serves to support the development of targeted cancer therapies. Be a part of the future of Precision Medicine! Our mission is to improve the human condition by bringing the power of precision medicine to labs, partners and patients globally. We are looking for a hardworking and dedicated representative level research assistant to join our CDx Research and Development Department. You will provide research support to develop accurate, robust, and precise assays. Your challenge will be to create value for Agilent through innovative ideas that either create new businesses or enhance existing ones. You will work in a cross-functional team dedicated to the design and development of CDx assays in a highly regulated environment.

Requirements

BS/BA or MA in Biology, Biochemistry or related field
Ability to follow Quality System regulations including Design Control
Experience with immunohistochemistry and microscopy
Demonstrated problem-solving skills
Detail-oriented and organizational skills
Analytical skills and creativity
Proficient with Microsoft Office
Demonstration of excellent verbal and written communication
Ability to work both independently and within a team setting

Nice To Haves

Background in biology techniques including immunohistochemistry, in situ hybridization, fluorescent techniques, protein biochemistry; cell biology and molecular biology
Background in one or more of the following: tumor biology, immunology, and histology
Experience with assay/protocol development

Responsibilities

Working in a cross-functional team that supports clinical trials testing new targeted anti-cancer drugs, by developing tailored companion diagnostic assays.
Performing project-related research and/or development in collaboration with others to develop immunohistochemistry assays, in situ hybridization assays, and possibly molecular biology-based assays.
Assisting in defining and designing the optimal development path for each product within our workflow.
Leading development projects, as applicable, requiring coordination with other functions or suppliers.
Carrying out technical design tasks which require use of planning and judgment.
Understanding and implementing our quality management system framework.
Writing scientific protocols and reports.
Carrying out experiments including planning, execution, quantitative data analysis and reporting.
Making detailed observations, analyzing data and interpreting results.
May participate in scientific conferences and contribute to scientific journals.
Ensuring success through collaboration with your team.