R & D Jobs in Sunnyvale, California

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90 Sunnyvale, CA R & D jobs found on Monster.

Jobs 1 to 20 of 90
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,...
JOB TITLE: Product Development Chemist RESPONSIBLE TO: President, VP Operations, Lab Manager GENERAL DUTIES: •Immunoassay reagent development and production. Tasks will also include maintenance of laboratory, instruments, and cold rooms. SPECIFIC DUTIES: •Quality control/quality assurance duties involving the testing of retain lots or cross-reactivity testing. •Inventory management of finished goo...
About Remilon Remilon is a technology company on a mission to make education accessible. We own and operate EducationPortal.com, which is the destination for millions of students to improve their grades and earn college credit. Education Portal offers self-paced, online video courses that cover every subject taught in high school and junior college. Our team has built these courses from the ground...
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...
. A QA Chemist I position in Mountain View, CA is available courtesy of Adecco Engineering and Technical. The QA Chemist I should have working knowledge of GLP with an understanding of equipment calibration and willingness to support other functional groups. The individual will be responsible for in-process and final product test and disposition. Additionally, the individual is expected to approve...
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...
Hello, My name is Jacqueline and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Regulatory Affairs Associate for a prominent client of ours. This position is located in Santa Clara, CA. Details for the positions are as follows: Job Description: Responsible for filing necessary applications and handling all government interactions pertaining to the regul...
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...
Chemist 100,000-105,000 San Jose, CA SUMMARY Responsible for researching, developing and validating rubber polymer based recipes/processes related to the creation of rubber products. EDUCATION and/or EXPERIENCE: Bachelor’s degree in Chemistry or related field; 10-12 years proven experience developing recipes based on multiple base polymers along with other raw materials used to meet performance re...
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...
This unique role offers you the opportunity to conduct long-term scientific research used to develop future Canon Products and work for one of the world’s most admired companies. As a Scientist, you will work in the Computational Imaging area and join a close-knit team of talented and experienced Scientists and Researchers. This is an exciting opportunity to join: you’ll be stepping into the Innov...
Responsibilities: Responsible for the medical writing of abstracts, posters, manuscripts from Jazz sponsored clinical trials. Responsible for leading publication planning teams, development of a comprehensive publication plan and its implementation. Work with external authors, speakers on oral presentations, posters, abstracts, slide sets and publications. Identify and screen appropriate publicati...
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