Biotech Jobs in Mountain View, California

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228 Mountain View, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 228
Our Client in the South Bay is looking for a Manager of Budgets & Proposals to join their team! Manager of Budgets & Proposals Duties: - The Manager of Budgets and Proposals reports directly to the Director of Business Development and will interface with Finance and Client Management teams. - The Manager of Budgets and Proposals is responsible for working with Business Development in managemen...
Company Confidential Sunnyvale, CA, 94086
Purpose of the Job: Ensure that the company is adhering to its Quality Policy and Quality System. Provides Quality Assurance support to new product development projects from the Concept Phase through the Market Release Phase. Most important responsibility is ensuring that product used for human use has undergone the requisite quality control checks. Major Duties and Responsibilities: · Function...
The Senior Manager/Associate Director, Clinical Trial Supply Management will work as an integral member of Jazz Pharmaceuticals’ team, assisting in the development of new products. The Senior Manager/Associate Director, Clinical Trial Supply Management will manage clinical trial supplies in support of the development pipeline and other clinical and non-clinical studies. May also provide general CM...
The Biostatistician/Senior Biostatistician will be acting as a study statistician. This role assumes responsibilities for statistical aspects of study designs, planning and execution of statistical analyses and providing any statistical contributions necessary for Jazz clinical study. This position will work collaboratively with clinicians, biostatisticians, and statistical programmers as well as ...
Company: Yoh Research Assistant needed for a Contract opportunity with Yoh's client located in Palo Alto, CA. What You'll Be Doing: - Primary responsibilities will be to design and construct vectors, transformation of microbial strains, and evaluation of gene expression and protein production. - Candidate will also be expected to process data, in addition to recording and communicating results...
Job Summary: At the Howard Hughes Medical Institute (HHMI), creativity and excellence are fundamental to our success. As one of the world's largest philanthropies, HHMI is a major force in advancing biomedical research and science education in the U.S. and abroad. We have an exciting opportunity for a Bioinformatics Specialist to join the research team in the Bergmann Lab at Stanford School of Me...
Regulatory Affairs Project Manager System One has engaged with a global client in Santa Clara CA in seeking a Regulatory Affairs Project Manager. In this opportunity the regulatory affairs professional must possess a broad knowledge of all aspects of the regulatory space. The incumbent will develop new regulatory policies and SOPs and ensure the proper people are trained on them. Providing key re...
BioPhase Solutions specializes in recruiting top talented professionals for California's Scientific community. We are recruiting for a direct hire full-time Quality Engineer to work with our medical device client located in Menlo Park. Responsibilities: Review new and modified product designs and process documentation for quality attributes, including manufacturability, serviceability, testabili...
The function of a Regulatory Affairs Associate Director is to combine knowledge of scientific, regulatory l and business issues to enable products that are developed, manufactured or distributed to meet required legislation. The individual has department level influence and is generally recognized as an expert resource both within our company and externally. The individual may comment on changing ...
Company: Hitachi America, Ltd. Division: R&D – User Experience Design Lab Location: Santa Clara, CA Status: Regular, Full-Time Summary: Hitachi America, Ltd. (www.hitachi-america.us) is looking for a User Interface Designer to join our new laboratory in Santa Clara, CA. We are looking for an experienced candidate that has the background and skill set needed to create graphical user interface ...
IMMEDIATE NEED: for a R&D Engineer who is creative, passionate and a hands-on researcher with a solid background in speech processing and acoustics. MS/Phd in Electrical Engineering, Electronics, Physics or Digital Signal Processing. Ideally you have built up solid experience with algorithm research in the speech domain with your PhD thesis, or equivalent from industry for this 4+ month contract a...
Director of Clinical Affairs Job Description The Director of Clinical Affairs is responsible for all U.S. and international clinical trials conducted by CapsoVision and assures compliance to all relevant local, national, and international regulations, guidelines, and ethical standards. The Director works closely with senior management to assess business objectivesand develop a clinical strategy ...
Experis is seeking a Quality Engineer II with ISO 13485 and CAPA to start ASAP!! Quality Engineer II with ISO 13485 and CAPA An intermediate engineering level between entry level and qualified engineer. Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Assignments have clear and specified objec...
Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a non-absorbed potassium binder, which is being developed for the treatment of hyperkalemia. The company was formed in 2007 and is b...
POSITION SUMMARY The Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results. ACCOUNTABILITIES • Performs and reports laboratory testing on clinical laboratory samples used to aide physicians in the diagnosis and treatment of patients. • Selects, implements, and evaluates results for Quality Control materials used in statistical process control of lab...
POSITION SUMMARY The Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results. ACCOUNTABILITIES • Performs and reports laboratory testing on clinical laboratory samples used to aide physicians in the diagnosis and treatment of patients. • Selects, implements, and evaluates results for Quality Control materials used in statistical process control of lab...
Company Confidential Redwood City, CA
Overview Pearl Therapeutics is hiring an Associate Scientist responsible for conducting laboratory studies for the quantitative and qualitative characterization of active pharmaceutical ingredients and related substances, excipients, and other quality attributes of metered dosage inhalers. The ideal candidate is technically oriented and has a strong background in quantitative HPLC and LC-MS. This ...
Johnson & Johnson companies are equal opportunity employers. PRINCIPAL ENGINEER - HUMAN FACTORS, DRUG DEVICE DEVELOPMENT-00000TOF Description Janssen R&D, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Principal Engineer, Human Factors – Drug Device Development, to be located in either Fremont, CA, Spring House, PA, Raritan/Titusville, NJ, Schaffhausen, Switzerla...
Our client in the South Bay is looking for a Clinical Research Assistant to join their team! Job Duties · Support Clinical Research team members · Obtains, reviews, processes, and tracks study related documents such as CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc. · Maintains and distributes basic study tracking information including: Visit Reports, Regulatory D...
Overview: The Product Transfer Scientist will combine knowledge of basic molecular biology, real-time PCR, fluidics, and a technical understanding to play a key role in product sustaining and support within the Product Transfer group. Lead the Manufacturing, Quality and Planning Departments in assuring the continued production of cost-effective quality products. Identify and implement streamlined...

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