R & D Jobs in Fremont, California

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124 Fremont, CA R & D jobs found on Monster.

Jobs 1 to 20 of 124
ATR International has been a leader in the staffing industry since 1988, placing professionals in the industry's most innovative companies. We currently have an exciting opportunity for a Chemist with one of our important clients. Position Information: Job Title: Chemist Location: Fremont, CA Duration: 3 Months Compensation: DOE Contact Information: Joon An: ***** Job Description: We are...
Job summary The Clinical Research Manager (CRM) is responsible for managing and meeting the objectives of a clinical study. This position should be able to independently handle various clinical study protocols and assignments. The CRM duties will primarily support the daily in-house management of clinical studies; however, there will be a combination of both in-house and field responsibilities. In...
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 under...
Job Description: A reputable life science company in the East Bay that is central to 880, 237, 680 highways has an immediate opening for an Accounts Receivable Specialist. The accounting department is seeking an Accounts Receivable Specialist to join the team. You will work closely with the Revenue Accountant to manage and assist with billing clients, cash application, and collections; to assist w...
On March 12, 2014, SYNARC and BioClinica have completed the transaction to merge companies, creating a leading global provider of specialized outsourced clinical trial services. At our centers in the United States, Europe, and Asia, we provide our clients with the industry's highest quality of service across modalities and therapeutic areas. Synarc is looking for intelligent, creative and dedicate...
On March 12, 2014, SYNARC and BioClinica have completed the transaction to merge companies, creating a leading global provider of specialized outsourced clinical trial services. At our centers in the United States, Europe, and Asia, we provide our clients with the industry's highest quality of service across modalities and therapeutic areas. Synarc is looking for intelligent, creative and dedicate...
On March 12, 2014, SYNARC and BioClinica have completed the transaction to merge companies, creating a leading global provider of specialized outsourced clinical trial services. At our centers in the United States, Europe, and Asia, we provide our clients with the industry's highest quality of service across modalities and therapeutic areas. Synarc is looking for intelligent, creative and dedicate...
On March 12, 2014, SYNARC and BioClinica have completed the transaction to merge companies, creating a leading global provider of specialized outsourced clinical trial services. At our centers in the United States, Europe, and Asia, we provide our clients with the industry's highest quality of service across modalities and therapeutic areas. Synarc is looking for intelligent, creative and dedicate...
Duties: Accountable for the day-to-day operational oversight of 1-4 clinical trials including trail start-up, conduct, and close-out activities Mentoring and support of junior Clinical Operations staff Facilitates SMT Meeting, responsible for the timely setting of agendas, effective conduct of SMT meetings and timely issuance of meeting minutes Facilitates in all operational activities pertaining...
Responsibilities: Executes clinical trials by directing a multi-functional study team. Ensures that timelines, budget and quality are met by partnering with Clinical Operations and Project management. Actively participates in CRO, site and vendor selection to ensure that trial responsiblitites are delegated. Provides mentorship, supervision and training to Clinical Operations Staff involved in the...
The Clinical Trial Manager is responsible for: Activities ensuring high quality deliverables are within budget and timelines. Support cross-functional Study Team within Clinical Operations with minimal oversight from the CTM and/or CPL. Clinical Operations deliverables to achieve study objectives and milestones within timelines and budget. Responsible for vendor selection and management including...
Clinical Program Manager: One of Real Staffing Group's clients is seeking a Clinical Program Manager who will ensure that assigned clinical trials are executed on time, on budget, and in compliance with applicable guidelines and regulations by providing leadership to a multi-functional study team. Responsibilities: Executes clinical trials by directing a multi-functional study team. Ensures that t...
We are a large and growing food manufacturing company located in the beautiful Bay Area of California. We have experienced a tremendous amount of success over the last decade and are actively recruiting highly motivated and career minded food manufacturing professionals to help us continue to grow as our product demand increases. We are currently recruiting for a Director of Research and Developme...
In this critical role of Director of Clinical Affairs (Regulatory), the successful candidate will be part of the Regulatory Affairs management team and develop submission and clinical trial strategy for international countries to support new product development efforts, as well as expansion into new international markets. The director will manage the overall operation of clinical trials including...
Experis is seeking a Quality Control Analyst with cGMP laboratory background to start ASAP! Quality Control Analyst w/cGMP laboratory - The ideal candidate will be responsible for performing microbiological, biochemical and chemical evaluations of in-process product, equipment and manufacturing facilities, and with experience can operate as a backup for testing in the Raw Materials and Analytical...
Job Title: Quality Lab Associate I Position Description Ability to handle multiple tasks concurrently, and in a timely fashion. Computer literate. Must be detail oriented, conscientious and have high reading comprehension skills. Must have basic understanding of laboratory instrumentation. Must be able to communicate effectively with supervisors and peers. Position Responsibilities Conduct biologi...
Duties Candidates should be experienced working on PCR and handling human viral pathogens. Able to have basic molecular biology lab skills and working independently, operate automated sample prep and PCR instruments. Work in controlled and regulated environment, handle human specimens, detailed date analysis by MC Excel. After introduction to work process, candidate should begin to organize, condu...
6 month contract Responsibilities: Conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Makes recommendations to resolve problems encountered during experimental procedures. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results, and reviews conclusi...
The Device Engineer will be responsible for various devices, structures, and systems that are critical components for IC design but currently have no direct technical support. The primary responsibility of the position is fuse/anti-fuse structures and associated circuitry used for trimming and generating rules, guidelines, and CAD automation for implementation of these systems. In addition to the...
As a Technical Writer is needed for a long term assignment for semiconductor company in Milpitas, CA. The Technical Writer will be responsible for writing hardware and occasionally, software documents for both integrated and standalone products. Most documentation is written in Framemaker 7.0, and a strong working knowledge of Adobe Framemaker and Adobe Acrobat is required. Large manuals are divid...
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