R & D Jobs in Foster City, California

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221 Foster City, CA R & D jobs found on Monster.

Jobs 1 to 20 of 221
Role: Veeva Resource Location : Foster City , CA Duration: 6-12+ months contract Job Description: Must have knowledge of: 1. Veeva CRM a. Primary Care functionality b. Business and Person Account c. Cycle Plan d. Rep Roster e. Time Off Territory f. Survey g. Medical Forms 2. Pharmaceutical/Life Science Domain experience 3. Salesforce Customization a. User Management (including Role/Profile/Securit...
Specific Responsibilities and skills for Position : Actively manages Contract Manufacturing Organizations (CMO’s) for their assigned projects. Ensures all regulatory requirements are met in the manufacturing of bulk API. Ensures availability of raw materials at contract manufacturing sites. Manages transfer of new technology from Process Development to contract manufacturing sites. Assists in the...
Specific Responsibilities and Skills for the Position: Will have an active role in critical cross-functional projects. (e.g.) Management Reporting, Metrics Implementation). Facilitates and drives timelines for strategy, implementation, and roll-out of Biometrics operational initiatives. Maintains project timelines and deliverables. Tracks and reports on status of tasks, assigned resources, and act...
Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff of more than 5,000 people is a close com...
Specific Responsibilities and skills for Position Candidate will coordinate activities and resolution of complex issues and potential problems related to manufacturing and inventory planning/management. Ensures products are manufactured packaged and labeled according to approved procedures using approved packaging components and labels. Ensures that all manufacturing equipment is validated, calibr...
Research Associate III needed for a contract opportunity with Yoh's client located in San Carlos, CA. The Big Picture - Top Skills You Should Possess: - Support phase 3 clinical readiness and aerosol / device characterization for an inhalation product. - Functions as a team resource able to perform a variety of laboratory based tasks. - Knowledge of programming using data acquisition software a pl...
Our client on the Peninsula is looking for a Deviation Specialist to join their team! Deviation Specialist Duties: - The Deviation Specialist participates in the disposition of batches, including resolution of investigations and deviations to meet lot release time lines and disposition as designated. - Maintains the cross project support systems which may include, material receipt, QA line clearan...
Deviation Specialist, Commercial Manufacturing – 1 year contract Resolves investigations and deviations to meet lot release time lines. Performs a wide variety of activities to ensure compliance with applicable GXP requirements. Assures all operations are performed in compliance with company procedures and Quality Standards. Monitors designated phases of the manufacturing operations. Writes and re...
Overview Teva’s Global Biologics group develops protein-based therapeutics from concept to commercial launch. The successful candidate will work with a multidisciplinary team to validate drug targets and protein-based lead candidates targeting neurodegenerative conditions and refractory pain. Responsibilities Candidate responsibilities will include developing and optimizing in vitro assays for val...
Our client in Redwood City is looking to have a QC Specialist join their growing team! Responsibilities: · Perform data checks for analytical data generated during routine GMP release and stability testing, and qualification/validation experiments. · Perform data checks for lab records that support analytical testing, equipment operation, and general lab operations. · Participate in and conduct la...
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 Clinical Project Manager (Non-MD) with one of our important clients. Position Information: Job Title: Clinical Project Manager (Non-MD) Location: Redwood City, CA Duration: TBD Compensation: DOE Contact Informati...
At Codexis, we are creating sustainable chemicals, pharmaceutical processes, and renewable ingredients that make industry more efficient, productive and profitable. Industrial biotechnology from Codexis reengineers enzymes and microorganisms – nature’s catalysts – and puts them to work to solve real global challenges for the world’s largest companies. We provide our customers with optimized, faste...
Research Assistant, Quality Control At Codexis, we are creating sustainable chemicals, pharmaceutical processes, and renewable ingredients that make industry more efficient, productive and profitable. Industrial biotechnology from Codexis reengineers enzymes and microorganisms – nature’s catalysts – and puts them to work to solve real global challenges for the world’s largest companies. We provide...
Clinical Supply Manager - Project Manager Redwood City, CA. Minimum Requirements: Bachelor’s Degree required, preferably in physical science, math, engineering, or pharmacy. 3 - 5+ years total experience in the Pharmaceutical Industry. Job Responsibilities: Responsible for the project management of key Clinical Supply Chain activities at the protocol level for Phase I – IV clinical trials of varyi...
Basic Function and Scope of the Position: Provide the clinical department with technical assistance in the development of diagnostic products and collaborations as part of the global Reproductive Health and Genomics programs. Provides technical oversight on projects related to sequencing and/or new technologies for the successful conduct of clinical studies and collaborations consistent with appli...
PRINCIPAL SDTM PROGRAMMER *This remote opportunity is open to any US home-office location. Theorem Clinical Research is currently searching for experienced SDTM Programmers. In this role, the SDTM Programmer will be responsible for mapping entire studies in accordance with SDTM guidelines, as well as performing Quality Control checks. RESPONSIBILITIES: Create SAS datasets of clinical data from cli...
DESCRIPTION: Create new SKUs using SKU wizard ECO request of new part release through Agile Write processing documents Support work related to SAP and Agile database Work with various stakeholders: following up the progress of ECO, and facilitating the resolution of any issues. Support Tech Transfer group in lab testing of assays. EXPERIENCE AND QUALIFICATIONS: Familiar and experienced with SAP an...
Johnson & Johnson companies are equal opportunity employers. SENIOR ENGINEER R&D-8519140415 Description Acclarent, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior R&D Engineer position located in Menlo Park, CA. Acclarent, Inc. is a medical device company in Menlo Park, CA that was established in June of 2004. The company is dedicated to the development of inn...
Johnson & Johnson companies are equal opportunity employers. SR ASSOCIATE CLINICAL RESEARCH-5771140310 Description Acclarent, Inc., a member of the J&J Family of Companies is actively recruiting for a Senior Clinical Research Associate (CRA) to be located in Menlo Park, CA. Acclarent, Inc. is a medical device company in Menlo Park, CA that was established in June of 2004. The company is dedicated...
Johnson & Johnson companies are equal opportunity employers. SR. MANAGER, COMMERCIAL OPERATIONS-6825140321 Description Acclarent, Inc. is a medical device company in Menlo Park, CA that was established in June of 2004. The company is dedicated to the development of innovative devices providing new technologies to further meet the needs of ENT patients. Acclarent's initial focus is on achieving the...
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