Biotech Jobs in Palo Alto, California

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159 Palo Alto, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 159
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...
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 o...
Are you a strong Network Engineer ready to step up your game? This opportunity might be right the career move you've been waiting for! The Network Architecture leader is the primary contributor amongst a team of Infrastructure members in terms of the future state of the company's global business network. This person will bring experience and industry best practices to areas such as LAN, WAN, DMZs,...
Our client, a fast-growing specialty pharmaceutical and biotech company, has an immediate need for HRIS Analyst. Industry experience is strongly preferred. This is a contract position, and is expected to last up to six months. This values-based organization is recognized as being one of the best places to work in the area. Under direction, provides HRIS support and analysis to meet the needs of th...
The Position The Director, IT Operations partners with stakeholders and vendors to develop strategies and roadmaps to deliver technology solutions, manage desktop support and oversee build-out, implementation and maintenance of enterprise-wide system tools. The role will also work to establish and approve operating policies to mitigate risk and drive execution of plans that meet business objective...
The Position This position will be responsible for oversight of Quality Control activities performed by contract testing laboratories and contract manufacturing companies, including method development, validation, method transfer, GLP and GMP analytical testing and troubleshooting. The candidate will proactively seek issue resolution to ensure timelines, technical/scientific validity and GLP/cGMP...
The Cancer Clinical Trials Recruiter, Spanish Bilingual, will be a key participant and leader in the clinical trial recruitment strategies and programs focusing on the Hispanic population. The Recruiter will focus on developing recruitment initiatives for disease areas based upon Stanford Cancer Institute (SCI) priorities. The Recruiter will interact with patients on the phone and in-person to inf...
The Stanford University NCI Designated Cancer Center seeks a Cancer Clinical Trials Financial Specialist. This position will report to the Cancer Clinical Trials Office (CCTO) Financial Manager. The Cancer Clinical Trials Financial Specialist is the Institutional Representative for sponsored cancer clinical trials and is the primary point of contact for sponsor and University clinical research gra...
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 Work...
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...
BS or MS in Mechanical Engineering with hands-on design experience in a product development or manufacturing environment. About the Job: Responsibilities: PARC is seeking a talented and driven mechanical design engineer. In this position, you will be responsible for the design and integration of complex systems and parts across a wide range of applications. The ideal candidate will be able to perf...
The Position The Associate Director will manage Chemistry, Manufacturing and Control (CMC) activities for projects at all development stages, interfacing with relevant functional groups (e.g. Quality, Device, Regulatory, Clin Ops) and with external vendors. The successful candidate will plan and coordinate the timely execution of CMC activities and contingencies. In partnership with the VP of Manu...
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...
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...
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...
Our client in the South San Francisco Bay Area is looking for a Senior Electro-Mechanical Technician to join their team! Duties: Calibrate, inspect, and maintain lab equipment Preventative maintenance and system repair Work with lab personnel and vendors to repair and support in set up and maintenance of equipment Work with engineering and production teams to develop and document procedures Suppor...

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