R & D Jobs in Newark, California

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231 Newark, CA R & D jobs found on Monster.

Jobs 1 to 20 of 231
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 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...
Please note this is a 1 year contract position Skills: Regulatory Affairs experience, FDA Quality/ Medical Device The client is looking for a candidate with Medical Device experience. Description: Represents Regulatory Affairs on product lifecycle teams by actively contributing to the development and implementation of regulatory strategies. Independently prepares and negotiates regulatory subm...
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...
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...
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...
STATISTICAL ANALYST II Genomic Health, Inc. seeks the following position in Redwood City, CA: Statistical Analyst II. Responsible for performing data review, statistical programming and statistical analysis of clinical and genomic data for assigned projects and studies. EOE. Submit resume at www.genomichealthjobs.com. Must refer to Job ID 2014-3829. No phone calls....
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...
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...
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...
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 ...
Position Summary: Conduct routine and non-routine analysis of in-process and finished products. Perform biochemical and/or chemical analyses of product to ensure stability. Compile data for documentation of test procedures that may include biochemical and chemical assays, initial lot release and stability testing and formulation studies. Calibrate and maintain lab equipment. Participate in the pr...
Headquartered in Newark, CA, Triple Ring Technologies is an innovative technology and product development company that partners with clients to deliver complete solutions from conceptual design through product launch. Our highly interdisciplinary team includes senior professionals from industry, finance, and academia, with extensive experience in medical device, life science, clean tech, security,...
Our client in East Bay is looking to have a QC Analyst join their team! Responsibilities: Regularly apply basic theory and principles from one's expertise in biochemistry, cell biology, and cGMP to develop, optimize, and validate physico-chemical and biological assay for lot release and stability testing. Participate in the technical transfer of assays to and from contract test laboratories und...
Company: Yoh Scientist - Assay / System Integration needed for a direct hire opportunity with Yoh's client located in Fremont, CA. The Big Picture - Top Skills You Should Possess: - Troubleshooting Assay's - Chemistry knowledge (qPCR) - Validation What You'll Be Doing: - Assist in development and troubleshooting of assays and instruments on SmartChip systems. - Interface with researchers /...
This is an exciting position with a clinical laboratory offering next generation diagnostics for disease stratification and therapy selection. This company offers a comprehensive menu of specialized, advanced diagnostic testing in the areas of cardiology, oncology, reproductive disorders, endocrinology and infectious diseases. The company deploys cutting edge molecular diagnostic technologies and ...
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...
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...

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