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Scientist - Bioanalytical Sciences

Posted on Apr 13, 2021 by Amgen

Newbury Park, CA 91319
Immediate Start
Annual Salary

Let's do this. Let's change the world. The department of Translational Safety & Bioanalytical Sciences (TS&BA) within Amgen is dedicated to the discovery and development of novel effective, safe medicines. TS&BA scientists work closely in partnership with disciplines such as protein therapeutics, medicinal chemistry, pharmacology, toxicology, pharmaceutical sciences and clinical pharmacology and regulatory to design promising clinical therapeutic candidates, conduct preclinical development studies, support clinical evaluation and contribute to regulatory submissions.

In this vital role you will contribute to developing, validating and implementing robust bioanalytical methods for the measurement of large molecule biotherapeutics. These methods will be required to support both nonclinical and clinical studies. The primary responsibilities of the Scientist will include:

Design and execution of innovative scientific experiments for development, validation and implementation of robust bioanalytical methods for large molecule biotherapeutics, including Oligonucleotides in clinical and nonclinical study samples.
Develop and implement new and novel protocols to address specific issues and/or troubleshoot and improve current existing assay platforms towards being more robust and transferable.

We are all different, yet we all use our unique contributions to serve patients. The qualifications professional we seek is a Scientist with these qualifications.

Basic Qualifications:
Doctorate degree

Master's degree and 4 years of pharmaceutical-biotechnology and/or CRO industry and/or Scientific experience

Bachelor's degree and 6 years of pharmaceutical-biotechnology and/or CRO industry and/or Scientific experience

Preferred Qualifications:
2+ years of laboratory experience.
Experience in any of the following areas: immunology, immunochemistry, biochemistry, cell biology or equivalent.
Experience in developing and validating of ligand binding assays.
Working knowledge of the regulatory (GxP) requirements for bioanalysis in drug development and possess critical thinking skills with an ability to integrate data and information to solve complex problems to advance drug discovery and development programs.
Experience communicating complex ideas to audiences with varying degrees of knowledge.
Demonstrated ability to drive scientific excellence and innovation.
Demonstrated experience of contributing as lead author on external peer review publications.
Ability to work in a team environment with excellent verbal and written communication skills

Reference: 1162846441

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