Biotech Jobs in Sunnyvale, California

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70 Sunnyvale, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 70
Description Our Client is looking for Sr MDM/Data Integration Engineer who will provide technical expertise to successfully deliver Master Data Management and Data Integration solutions. As a Sr MDM/Data Integration Engineer, the resource will be involved in all phases of system development, including requirements, analysis, design, development, test and support. Key Accountabilities/Core Job Resp...
Our Client is looking for a Tableau Expert with experience in Biotech / Pharma industry. 5+ years Industry experience with 1-2+yrs of Strong Tableau Development Skills Ability to work with Business directly and build very rich visualization on Tableau Good communication and Self-driven Consultant Ability to deliver from concept to report and dashboard with limited supervision Thank you, Sai Kumar,...
BioPhase Solutions specializes in recruiting top talented professionals for California's Scientific community. We are recruiting for Clinical Trial Associates, junior and senior level, to support our exciting pharmaceutical client located in Sunnyvale. Responsibilities: Set up CTMS system, as appropriate Assist in preparation of documents including regulatory document templates, study binders, stu...
BioPhase Solutions specializes in recruiting top talented professionals for California's Scientific community. We are recruiting for Senior Clinical Research Associates for our pharmaceutical client located in Sunnyvale, CA. These positions are direct hire with an exciting and growing company. Relocation is possible. Responsibilities: Lead multifunctional team through clinical studies activities t...
Our client has an immediate opening for a Project Coordinator working with the Discovery team in Mountain View. Ideal candidates will be responsible for assisting the project management team on administrative items related to planning, scheduling and reporting. They are seeking someone strong in coordination, taking minutes, scheduling, tracking, billing, advanced spreadsheet formulas and budget c...
Job Purpose Manage the upstream process development activities and support CMC strategies across the product development cycle, including strain development, fermentation process development, process scale up, tech transfer and analytical implementation. Ensure that products manufactured to support pre-clinical and clinical studies are in compliance with the requisite regulations and guidelines. P...
Job Description: The Senior Clinical Research Associate will design, plan and implement the overall direction of clinical research projects. The primary responsibility is to assist the study team with all operational activities for new and/or on-going infectious disease and cancer diagnostic test product clinical evaluations. Responsibilities: •Independently responsible for all activities of the c...
The Regulatory Affairs Specialist will maintain Cepheid change control process to provide input and supply documentation on whether changes require new regulatory submissions with the United States FDA and International Regulatory Agencies. This individual will prepare the appropriate regulatory submissions and interact with health authorities to obtain and maintain product approvals in the United...
CANDIDATE MUST SPEAK CHINESE AND WRITE MANDARIN Populates, compiles and verifies required agreements (based on templates approved and provided by Legal) in order to ensure timely clinical trial start and compliance to internal and external regulations. • Negotiates Master Clinical Trial Site Agreements (“MCTSA”), Facility Use Agreements, Statements of Work and accompanying amendments and assignmen...
Prepares, edits, files, assembles documentation such as reports or technical documents, records, or correspondence. Maintains numerical, alphabetical, chronological and/or subject filing system Responsible for file maintenance and record keeping; locates and removes file material upon request Educational Requirements HS Diploma, some college, AA in Computer Systems preferable or equivalent experie...
Company: Hitachi America, Ltd. Division: R&D Location: Santa Clara, CA Status: Regular, Full-Time Summary: Hitachi America, Ltd. (www.hitachi-america.us) has an opening for a Researcher in Big Data solution technologies in our newly established Big Data Laboratory in Silicon Valley. The mission of this laboratory is to help create new solution businesses in big data analytics by doing PoC (Proof o...
Company: Hitachi America, Ltd. Division: R&D Location: Santa Clara, CA Status: Regular, Full-Time Summary: Hitachi America, Ltd. (www.hitachi-america.us) has an opening for a Researcher Scientist in Big Data solution technologies in our newly established Big Data Laboratory in Silicon Valley. The mission of this laboratory is to help create new solution businesses in big data analytics by doing Po...
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:...
The Director of Regulatory will develop strategies for worldwide regulatory approval and introduction of the current generation and future generations of this clients medical device to market. Responsibilities: This position is responsible for, but not limited to, the following: Develop a sense of regulatory leadership in the division on how the company will have a top notch regulatory system for...
MUST LIVE IN CALIFORNIA OR NEVADA We currently have an opening for Medical Science Liaison in the West Coast(territory: California, Nevada, Utah, Oregon, Washington & Hawaii). The Medical Science Liaison will function as a medical and scientific expert in Dermatology, and interact with healthcare decision makers to communicate and advance the scientific platform in alignment with goals and objecti...
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 and d...
THE POSITION The Manager, Regulatory Strategy will be responsible for registration and regulatory support of US commercial and development projects. This position may be located in either Palo Alto, CA or Philadelphia, PA. RESPONSIBILITIES Participate as an active member of a multi-disciplinary team to establish development and regulatory strategies for commercial products, late stage, and early s...
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...
Posting date: May 2, 2014 Summary The LCMS Senior Applications Scientist will be a high performance dynamic individual who will be part of the LSMS Environmental & Food Safety (EFS) factory marketing group. The incumbent will support Applications activities for Product Development and growth of the LSMS business. The position will require frequent interaction with various groups within the company...
The Associate Director of HEOR will support health economic and outcomes research activities in support of products across Jazz’s diverse portfolio. The Associate Director will report to and work closely with the Senior Director of HEOR to design and implement studies that are aligned with the data generation strategy for each brand. Job Function Design, implement, and manage outcomes research pro...
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