R & D Jobs in Sunnyvale, California

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

Jobs 1 to 20 of 303
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 ...
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...
Our client in the South Bay is looking to have a Manufacturing Technician II join their growing team! Responsibilities: · Perform daily production processes including wet processing, chemical vapor deposition, resist coating, mechanical assembly, and visual inspections using high powered microscopes · Perform preventative maintenance on processing equipment · Assists with ordering materials ·...
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...
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...
Our client in the South Bay is looking to have a Research Associate II join their growing team! Responsibilities: Perform chemical and physical assays on drug substance and drug products. Collect, calculate, and compute data, analyze and submit interpreted results to supervisor for disposition; report abnormalities immediately; investigate and analyze and resolve problems within prescribed scop...
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 ear...
The Director, Medical and Scientific Writing, is responsible for writing and managing the completion of a broad range of documents in support of company products and projects. As a writer, this individual will craft document messages and write, substantively rewrite, and edit documents companywide for sense, clarity, accuracy, and effectiveness. As a director, this individual will manage project d...
As part of the iCAD/Xoft Clinical Affairs team, the Clinical Affairs Project Manager will be responsible for the coordination of all activities associated with the conduct of multiple clinical trials (develops study protocols, CRFs; supervises study tasks and mentors other CRAs; assists in the generation and oversight of trial budgets and contracts; and communicates trial status to management). In...
Assist in monitoring and collecting data from sponsor initiated clinical study. RESPONSIBILITIES: Travel to clinical research sites to collect clinical data for publication Check the data for compliance with study/site protocol, consistency and quality assurance Post-process, analyze the collected data using various software tools Document and report the analysis results Work with Investigat...
The Staff Biostatistician performs data analysis, statistical experimental, design, sampling techniques, and sample size determination in support of product development, clinical trials, regulatory submissions, and product quality. The qualified candidate exercises independent judgment in developing methods, techniques, and evaluation criteria for obtaining results and will develop specialized sta...
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...
Our Pharmaceutical client in the East Bay Area is looking for a Manufacturing Technician II/III to join their team! Duties: · Support equipment start-up and validation efforts of commercial fill/finish line. · Responsible for cGMP commercial fill/finish line. · Working knowledge of final formulation and fill/finish procedures, materials, and equipment. · Support validation of equipment and pr...
Our client in the South Bay Area is looking for an Organic Chemist to join their team! Duties: · Work with charged organic molecules · Purify small molecules and peptides by means of reverse phase HPLC · Create molecules for specific target sites · Basic bench work duties Requirements: · BS in Chemistry or related field and/or higher level of education · 1-5 years' experience in a lab envi...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Lab Technician Mountain View, CA Full-Time $40,000 - $70,000 Apply Apply Lab Technician Mountain View, CA Full-Time $40,000 - $70,000 Apply Job Details If you are a Lab Technician with experience, please read on! Top Reasons to Work with Us 1. Just received a round of funding that will help ta...
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...
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 th...
Experis is looking for a Test Operator (Deposition), to join our client in Santa Clara CA for a short term contract working on 2nd shift. Essential Functions & Responsibilities Will conduct developmental tests, including sample fabrication and testing. May compile and analyze test data from performed testing and review results with engineering personnel to improve efficiency and stability of ph...
Position: Research Associate, Hadoop / Big Data Computer Science Location: Santa Clara, CA Duration: 10-12 months Job Description: This particular position is for someone with a deep more complete skill set in big data technologies and focused more on computer science. We are seeking an enthusiastic, experienced and skilled researcher to work as part of an international innovative multidiscip...
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 P...

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