R & D Jobs in Newark, California

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

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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...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
Alexza Pharmaceuticals is a specialty pharmaceutical company located in Mountain View, California, focused on the research, development and commercialization of novel proprietary products for the acute treatment of central nervous system conditions. Our product candidates are based on our proprietary technology, the Staccato® system. The Staccato system vaporizes an excipient-free drug to form a c...
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...
SUMMARY: The Senior Director, Medical Science Liaison (MSL) Team Leader will be responsible for building the Company’s MSL team and for developing both strategies and tactical execution plans to engage scientific thought leaders and to develop partnerships with key scientific and medical organizations. The MSL team will provide non-promotional scientific, educational, and research support for the ...
Title: Temporary Senior R&D Technician Purpose of Position: The Senior R&D Technician provides hands on technical support working in conjunction with Engineering and Operations staff to develop new devices and processes, and to support manufacturing and operations efforts. The Senior R&D Technician also contributes to documentation, design, test, and assembly of prototypes, as well as participa...
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...
The Director of Regulatory Affairs DEA will be responsible for direct control over the company’s documentation, security, and handling of controlled substances and listed chemicals as the company’s Agent, as required by the Drug Enforcement Administration (DEA). The Director will develop a relationship and liaise with DEA on behalf of the company, facilitate the import/export of controlled substan...
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 ...
Our client in Fremont is looking to have a Jr. Associate join their growing team! Jr. Associate Duties & Responsibilities: · Assisting with all routine unit operations in filling including change-over procedures, equipment cleaning and set up. · Able to perform in-process testing such as visual inspection, weigh checks and environmental monitoring. · Collaborates within team and department in...
Our client in Fremont is looking to have a Jr. Associate join their growing team! Jr. Associate Duties & Responsibilities: · Assisting with all routine unit operations in filling including change-over procedures, equipment cleaning and set up. · Able to perform in-process testing such as visual inspection, weigh checks and environmental monitoring. · Collaborates within team and department in...
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 ...
We are looking for a motivated, energetic, detailed-oriented professional with excellent computer software skills. The Clinical Research Assistant will provide general support to the Clinical Affairs and Regulatory Affairs Group by assisting with the execution and maintenance of clinical studies and preparation of regulatory documents. Support will include, but is not limited to the following: est...
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...
SUMMARY: The Silicon Nanophotonics Engineer is part of the Illumina R&D team creating new industry-leading genetic analysis platforms for life sciences and clinical markets. In this position, you will be responsible for the design and fabrication of micro and nanometer scale photonics devices and the integration into these instruments. The job includes working closely with design houses and semic...
Summary: The ideal candidate will have expertise in molecular biology techniques and experience working on the development of sequencing related technologies. Key responsibilities include the design, execution, and reporting of laboratory experiments; trouble-shooting sample prep protocols, and application of genomics knowledge to the design of new sample preparation products. Basic Function and...
AT&T is seeking candidates for a highly unique opportunity in the field of Data Science. The opportunity is to participate as a member of a small team with a simple objective. Given one of the largest data sets in the world â¦.. Innovate! We are assembling teams to drive new and innovative ideas to our business units. The teams will consist of Subject Matter Experts, Data Scientist, Business Anal...

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