R & D Jobs in Mountain View, California

RSS

322 Mountain View, CA R & D jobs found on Monster.

Jobs 1 to 20 of 322
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 ·...
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...
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...
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...
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...
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...
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...
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 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...
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...
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...
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...
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...
Responsibilities: Manage cross-functional global development teams and commercial brand teams Establish and maintain comprehensive project plans and budgets Organize interdepartmental activities to ensure completion of the project within scope, on schedule and within budget constraints Prepare meeting agendas and minutes and track action items Work jointly with team leader to guide and motiva...
The Clinical Project Assistant will be a member of the Jazz Pharmaceuticals Clinical Operations team. The Clinical Project Assistant’s responsibilities include (but are not limited to) the following: General administrative support to the Clinical Project Teams Assist project teams with study specific tasks Ensure trial master files are current and maintained Co-ordination of Investigator paym...

Get new jobs by email for this search
We'll keep looking and send you new jobs that match this search.
email me

Upload your resume and let employers find you!
It's that simple!

Popular R & D Articles

5 Critical Elements of Any Résumé Article Rating
Including these five résumé elements will help you clarify your thinking, focus on key skills and accomplishments, and craft a résumé that will help you stand out from the crowd.
Steer Clear: Three Coworkers to Avoid Article Rating
Even if you try to get along with everybody, there are some coworkers you should just plain avoid. But what can you do when avoiding them not an option?...
For Employers: Post Jobs | Search Resumes | Advertise
About Monster | Work for Monster | Advertise with Us | AdChoices | Partner with Us | Investor Relations | Social Media
Terms of Use | Privacy Center | Accessibility Center | Help | Security | Contact Us | Sitemap | Mobile
©2014 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2014.4.50.56-320
eTrustLogo