R & D Jobs in Palo Alto, California

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271 Palo Alto, CA R & D jobs found on Monster.

Jobs 1 to 20 of 271
The Director of Regulatory Affairs DEA will be responsible for direct control over the company’s documentation, security, and handling of controlled substances and listed chemicals as the company’s Agent, as required by the Drug Enforcement Administration (DEA). The Director will develop a relationship and liaise with DEA on behalf of the company, facilitate the import/export of controlled substan...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
SUMMARY: The Senior Director, Medical Science Liaison (MSL) Team Leader will be responsible for building the Company’s MSL team and for developing both strategies and tactical execution plans to engage scientific thought leaders and to develop partnerships with key scientific and medical organizations. The MSL team will provide non-promotional scientific, educational, and research support for the ...
SUMMARY: Work independently in the identification and resolution of CMC method related issues. Identify, evaluate, and implement novel and viable analytical technologies for characterization of polymers. Coordinate routine testing of drug substance and product using contract service providers (CSP). Conduct method transfer between contract service providers. This position reports to an Associate D...
Title: Temporary Senior R&D Technician Purpose of Position: The Senior R&D Technician provides hands on technical support working in conjunction with Engineering and Operations staff to develop new devices and processes, and to support manufacturing and operations efforts. The Senior R&D Technician also contributes to documentation, design, test, and assembly of prototypes, as well as participa...
Our Pharmaceutical client in the East Bay Area is looking for a Manufacturing Purification Associate II to join their team! Duties: Primarily support the validation implementation. Operate in clean room. Support and ensure compliance of routine procedures following established company policies. Troubleshoot equipment and manufacturing procedures. Routine maintenance of manufacturing equipmen...
Senior Director, Clinical Drug Safety Science Description General Position Summary/Purpose: The Sr. Director of Clinical Drug Safety Science is responsible for the medical oversight of global pharmacovigilance activities of clinical trials and product development. Telecommute option is available after 3-6 months on site in Sunnyvale, CA Key Accountabilities/Core Job Responsibilities: Provide ...
Our client on the Peninsula is looking for Research Associate II to join their team! Research Associate II - QC Duties: - The Research Associate II will be responsible for the performance of a variety of routine scientific tests utilizing laboratory apparatus, including the generation, analysis and recording of data, with daily supervision - The Research Associate II will be responsible for ge...
We are a small, private, medical device start-up company launching our first product. We are looking for a hands-on Vice President Clinical and Regulatory Affairs to support the organization in support of the Company’s goals and objectives. The VP of Clinical and Regulatory Affairs is responsible for providing the strategic direction and tactical management of all Regulatory and Clinical Affairs ...
Sr Regulatory Affairs Associate (Advertising & Promotional Review) System One has engaged with a Top Client in a search for a Sr Regualtory Affairs Associate to join their team in Santa Clara CA. In this critical role, you will ensure Regulatory Labeling and Promotional Review Compliance is within guidelines set forth by cGMP (GxP) and FDA standards. Knowledge of OPDP (Formerly DDMAC) is also re...
Summary: We are seeking a highly talented and motivated Bioinformatics Scientists/Sr Bioinformatics Scientists to join our Biocomputing Team. Our group is focused on tackling some of the most challenging problems in integrative genomics spanning diverse research and clinical applications. If you are an expert in one or more of the following areas, we would like to hear from you. Responsibilities...
Big Data at AT&T comes with big opportunities for innovation. With access to one of the largest and coolest data sets available, youll gain insight into the way consumers think, feel and act. And together, well turn that knowledge into innovative solutions that change the world, day in and day out. Located in downtown Palo Alto, youll find yourself immersed in a start-up culture with the support ...
AT&T is seeking candidates for the unique opportunity to work with our massive, heterogeneous, data set. Our group has been tasked with creating a culture within a culture; a new team with a startup mentality focused on making big data and its thoughtful use a company imperative. You will not be yet another cog in a large internet company with a pre-existing big data machine. You will not be drivi...
AT&T is seeking candidates for a highly unique opportunity in the field of Data Science. The opportunity is to participate as a member of a small team with a simple objective. Given one of the largest data sets in the world â¦.. Innovate! We are assembling teams to drive new and innovative ideas to our business units. The teams will consist of Subject Matter Experts, Data Scientist, Business Anal...
This role will oversee multiple development projects within the Hematology / Oncology Therapeutic Area, providing strategic and technical strategic support and ensuring that projects are making progress consistent with strategic objectives and project plans. Job Responsibilities: Ensure leadership of the Hematology / Oncology Development Team(s) in the Research & Development Matrix structure Wo...
CCS Associates has more than 25 years of broad-ranging experience providing expert consulting services to government and industry clients concentrating on acquisition and analysis of scientific information and on providing support at key steps of drug development. We are highly qualified in regulatory affairs, clinical and preclinical studies management, quality assurance, data management, data an...
SUMMARY: The position reports to the Head of Drug Safety and Pharmacovigilance. The Drug Safety and Pharmacovigilance Operations Manager is independently responsible for the development, management and maintenance of Relypsa’s drug safety and pharmacovigilance program. This will include the evaluation, oversight and management of an external contract service provider(s), covering the receipt, proc...
This position is responsible for formulating liquid and lyophilized dosage forms consistent with preclinical and clinical needs. The candidate must be proficient in analytical techniques used for protein stability and characterization testing. This person will perform development stability studies and analytical characterization to support the development of protein therapeutics, prepare data summ...

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