R & D Jobs in Emeryville, California

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159 Emeryville, CA R & D jobs found on Monster.

Jobs 1 to 20 of 159
Job Title: Method Validation Scientist Location: Emeryville, CA Duties: Responsible for developing, optimizing, and validating release, in-process, raw materials and cleaning methods in support of Diagnostic Solutions immunodiagnostic intermediates. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that...
Our client in the Peninsula area is looking for an Associate Research Scientist II to join their team! Duties: · As a member of a product development team, performs research and development on inhalation drug products and delivery devices. · Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. · Exercises judgment within defined proc...
The Life Cycle Assessment (LCA) team conducts assessments to evaluate and communicate the life cycle impact of manufactured products. To meet increasing demand for these services, SCS is seeking a Technical Associate to join our LCA team. The successful candidate must have a strong quantitative background with the ability to analyze and interpret complex technical data. This is a great opportunity...
Responsibilities: Provide animal husbandry (feeding, cleaning, watering, observing, handling, and moving of animals ) to mice, rats, cotton rats, hamsters, and rabbits. Keep accurate records. Follow SOPs and protocols. Operate laboratory equipment as pertaining to the work environment. Maintain a clean, organized, and safe work environment. Carry out assigned projects in a timely manner. Perform o...
Responsibilities: Required to operate cage washing and sterilizing equipment, process soiled caging and vivarium equipment, prepare clean caging and vivarium equipment. Able to Validate and troubleshoot cage washing equipment dispose of waste (general waste, carcass, sharps, biohazard, chemical) and lift/move more 50 lbs. Must receive and maintain/stock supplies and sanitize work areas. The job is...
Job details: Working in a team setting, performing a variety of different procedures on Laboratory mice and rats. Work schedule will be M-F 7:00am to 3:30pm, with some weekend work available as OT Skills: · Must be familiar with a variety of techniques for COLLECTING AND tissue samples. · Must have strong computer skills · Must have strong communication skills · 2-4 years’ experience working in a...
Leading pharma client seeks a Buyer for a 6 month contract. Duties: - Must follow processes outlined in SOP's. - Support Master Production Plan. - Resolve/manage material change controls issues. - Place orders based on safety stock levels. - Work with QC Raw Materials, QC Inspection, QA and Planning toexpedite materials. - Review MPS and ensure material availability. - Manage material expiry. - Mo...
This position supports production for cGMP peptides and HRP conjugates to meet production schedules and lifecycle validation activities. Responsibilities include peptide synthesizer set-up for the cGMP production of three synthetic peptides using an ABI peptide synthesizer, cleavage and purification of crude peptides using reverse phase HPLC as well as conjugation of recombinant antigens to larger...
As a Senior Associate in the Manufacturing Science & Technology Analytical group, you will play a key role in providing scientific leadership and laboratory support for all analytical testing to support Fermentation and Purification studies, QC or Manufacturing deviation investigations, and Process Characterization studies. This position will also be responsible for performing laboratory-based Ana...
The Biostatistician will be responsible for providing statistical consultation and advice in quantitative/statistical issues in support of Clinical Affairs, R&D, antigen Manufacturing, and quality operations of the diagnostics blood screening division. The Biostatistician II position will: Review protocols and develop appropriate statistical design and analysis plans Develop and build SAS program...
The Manager, Global Regulatory Affairs will be responsible for carrying out logistical activities in relationship to global regulatory submissions for IVD systems (assays, instruments, software). The Manager will also serve as regulatory subject matter expert for design control, development and compliance projects. The Manager will prepare and maintain regulatory documentation for submission to US...
We are looking for several Experienced Sales Reps with background in the medical industry. This position is for the city on posting but we have openings across the state. The medical industry is changing and along with it the stability of having a long term pharmaceutical or medical device jobs. What do we have as sales representatives? We have great relationships and experience, so why not get pa...
AMEC is a focused supplier of consultancy, engineering and project management services to its customers in the world's oil and gas, mining, clean energy, environment and infrastructure markets. With annual revenues of some £4.2 billion, AMEC designs, delivers and maintains strategic and complex assets and employs over 29,000 people in around 40 countries worldwide. See amec.com. AMEC shares are tr...
please email your resume to ***** Global Study Manager Berkeley, CA (Onsite) 1 year + Contract MAJOR DUTIES OF POSITION: Participates in strategic discussions regarding the design of global clinical programs and in reporting the progress of clinical programs by working collaboratively with the global Core Team and sub-teams. Negotiates study timelines during project developme...
As a member of the Analytical Development team, this role will support the early to late stage drug development programs including oligonucleotides, proteins, and oligonucleotide-protein conjugates. Duties will include but not be limited to development, transfer, validation and life cycle management of analytical methods for drug substance and drug product release, stability and characterization....
Responsibilities: Responsible for conducting clinical programs consistent with applicable regulations, guidelines, and policies. Ensures study adherence to ICH/GCP and SOPs Research, prepare, and revise the study protocol, Monitoring Plans, Informed Consent/Assent Forms, Case Report Forms, etc., in consultation with the cross-functional project team, investigators, data management, and biostatisti...
Responsibilities: Directs a multi-functional study team in the day-to-day execution of clinical trials Partners with Clinical Operations management and Project Management to define study milestones and deliverables and executes to ensure timelines, budget and quality are met. Actively participates in CRO, site and vendor selection in order to ensure that trial responsibilities are appropriately de...
Laboratory Asst II (9603C) #18250 UC Berkeley - Main Campus The University of California, Berkeley, is one of the world’s most iconic teaching and research institutions. Since 1868, Berkeley has fueled a perpetual renaissance, generating unparalleled intellectual, economic and social value in California, the United States and the world. Berkeley’s culture of openness, freedom and acceptance—academ...
Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: CA - Berkeley Req ID: 134655 Position Title: Sr. Regulatory Technical Specialist (IVD) Experience Level: Senior Level Education Required: Bachelors Degree Travel Required: No Company Description: Siemens Healthcare Diagnostics is a global leader in in vitro diagnostics, providing healthcare professionals in hospita...
Our client in East Bay area is looking for a Sr. Medical Writer to join their team! SENIOR MEDICAL WRITER The Sr. Medical Writer will be responsible for writing and reviewing; clinical documents, protocols/amendments, investigator brochures, statistical analysis plans, consent forms, annual reports, final study reports, and clinical sections of INDs and NDAs. DUTIES: · Write high-quality clinical...
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