Monday, 10 February 2014

South San Francisco, California
Job ID: 00429577

Who We Are

At the Roche Group, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 30 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. The headquarters for Roche pharmaceutical operations in the United States, Genentech has multiple therapies on the market for cancer and other serious illnesses. Please take this opportunity to learn about Genentech, where we believe that our employees are our most important asset and are dedicated to remaining a great place to work.

The Position

An Scientist is a highly motivated and creative individual who develops, evaluates and implements state of the art bioanalytical methods to support biopharmaceuticals in the product development pipeline at Genentech.

The Scientist will develop bioanalytical strategies to support protein therapeutics, will manage timelines and resources to meet project goals, and will present these strategies to various scientific review committees. Working with Research Associates, this individual develops, characterizes, and validates in vitro assay methods to quantify biotherapeutic levels in various species and biological matrices, to detect and characterize immune responses evoked by the biotherapeutic, to measure biomarkers, and to do biological characterization of biotherapeutics in support of regulatory filings. This will involve manual laboratory work, the use of automation systems and various assay platforms, and participation in compliance and safety related activities. Scientists in the Assay Development and Technology department are expected to contribute to departmental activities, and they may also be expected to help train colleagues. Responsibilities may also include supervision of one or more Research Assistants/Associates.

This individual may also be responsible for writing sections of regulatory filings related to bioanalytical methods and characterization of biological activity. This individual may be involved with the assessment and implementation of new bioanalytical technologies and methods. This individual also works in fast-paced cross-functional project team settings to help design and support pre-clinical and clinical studies, lead Bioanalytical Working Groups,
and may be expected to lead pharmacology subteams or other cross-functional teams.

Who You Are

A Ph.D. in Biochemistry, Immunology, or a related field or an equivalent credential is required, with at least two years of relevant postgraduate experience. Background knowledge and practical experience in developing quantitative analyte and anti-therapeutic antibody assays for protein therapeutics, along with a proven track record of publications solving complex bioanalytical problems are essential. Familiarity with standard text, graphic, and presentation software is required, and familiarity with database/data archival software systems is helpful. A background in ophthalmology, oncology, and/or vascular biology is helpful. Excellent communication, interpersonal and organizational skills are required. Pharmaceutical or biotechnology industry experience is a real advantage.

The next step is yours. To apply today, click on the "Apply online"

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