Amgen Sr Scientist in Thousand Oaks, California
Amgen is seeking a Senior Scientist to work out of their Thousand Oaks, CA location. This position reports to the Director Preclinical.
The department of Pharmacokinetics and Drug Metabolism (PKDM) within Amgen is dedicated to the discovery and development of novel effective, safe medicines. PKDM 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.
We are seeking a Senior Scientist who will contribute to developing, validating and implementing robust bioanalytical methods for the measurement of large molecule biotherapeutics. These methods will be used to support both nonclinical and clinical studies.
The primary responsibilities of the Senior Scientist will include:
Design and manage 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 novel protocols to address specific issues and/or troubleshoot and improve current existing assay platforms towards being more robust and transferable. Key contributor to an independent research/project team and capable of initiating productive collaborations outside of the department or company.
Doctorate degree and 2 years of pharmaceutical-biotechnology and/or CRO industry and/or Scientific experience
Master's degree and 5 years of pharmaceutical-biotechnology and/or CRO industry and/or Scientific experience
Bachelor's degree and 7 years of pharmaceutical-biotechnology and/or CRO industry experience
Knowledgeable in any of the following areas: immunology, immunochemistry, biochemistry or cell biology.
Demonstrated experience contributing as a lead author on external peer review publications.
Experience in transferring methods or assay knowledge internally or to an external lab.
Excellent written and oral presentation skills.
Ability to work in a team environment and to identify solutions for complex technical bioanalytical challenges.
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.
Experience mentoring fellow scientists and leading projects.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.