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Demonstrated success in managing clinical pharmacology activities and quantitative drug development (population PK, mechanistic PK/PD modeling/systems pharmacology, and clinical trial simulations.
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Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
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Amgen is currently seeking a Sr. Scientist - Analytical Chemist in our Pivotal Attribute Sciences Department in Thousand Oaks, CA. This team plays a crucial role in pivotal phase analytical development, including method development, validation, transfer, process and product development support, and GMP testing of drug substances and drug products.
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Amgen Clinical Pharmacology Modeling and Simulation (CPMS) is seeking a Principal Scientist in our Thousand Oaks, CA location. The Principal Scientist will support Amgen clinical development and translational sciences programs across multiple therapeutic areas with emphasis on oncology.
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In this vital role, you will be part of an innovative Medicinal Chemistry team with responsibilities centering around using Medicinal Chemistry principles to support the design and discovery of novel compounds for potential clinical drug development.
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2) Knowledge and experience in capital project lifecycle management including conceptual design, scope, resource estimate & cost estimate development, business case development, detailed design, engineering, commissioning, validation, and project execution, as it relates to Plant Automation and process control systems with GMP biopharmaceutical production facility equipment/systems in support of Drug Substance, Drug Product and Supply chain plant operations.
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2) Represent ATA Plant Automation team during the development of project plan, business case, and cost estimates in partnership with key customers and stakeholders - ATO MCS Plant Operations, Engineering, Operations Information Systems (OIS), Global Construction Project Management (GCPM), and provide necessary support to obtain funding approval.
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Manage a team of Medicinal Chemistry research scientists within a collaborative environment to drive drug discovery process. Lead small molecule drug discovery programs and determine Medicinal Chemistry team direction to advance one or more projects.
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As part of the Clinical Pharmacology, Modeling and Simulation department, the Modeling and Simulation Senior Scientist will support Amgen clinical development and translational sciences programs across multiple therapeutic areas.
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All job offers are contingent upon successful completion of certain background checks which unless prohibited by applicable law may include criminal history checks, employment verification, education verification, drug screens, credit checks, DMV checks (for driving positions only) and fingerprinting.
$81,500 - $120,500 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Principal Scientist - Drug Substance. At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
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4) Represent Plant Automation team during the development of project plan, business case, and cost estimates in partnership with key customers and stakeholders – ATO MCS Plant Operations, Engineering, Operations Information Systems (OIS), Global Construction Project Management (GCPM), and provide necessary support to obtain funding approval.
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Principal Scientist - Clinical Pharmacology Live. Amgen Offers a Total Rewards Plan Comprising Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities Including.
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Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. The Engineer will apply cell culture process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology.
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Responsibility will include hardware circuit design, PCB layout, managing the project through development phase to production release. Required Skills Bachelor’s in electrical engineering or related field, or equivalent work experience Minimum of 8 years of relevant hands on experience in hardware design Demonstrated track record of success project development from design to production PCB layout experience, knowledge with Mentor Expedition is a plus Experience in managing outsourced hardware ODM/OEM development projects.
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pharmacology drug development jobs in Thousand Oaks, CA
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