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12+ years of experience in the biopharma industry in non-clinical development (toxicology, pharmacology, pharmacokinetics, bioanalytical sciences, or related discipline) Comprehensive knowledge of GLP regulations, including previous GLP experience in pharmaceutical or biotechnology industry or equivalent GXP transferable experience.
$265,000 - $300,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Gator Bio is a pre-IPO bioanalytical technology company located in Palo Alto, CA. We are creating innovative technologies to solve difficult problems facing today’s biopharma industry. Spectroscopy instrumentation a plus (UV/VIS / Fluorescence / IR /FTIR / Raman.
$48 - $53 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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RequirementsYou hold a relevant academic degree – preferably a master’s degree, but not necessarily – and 5+ years of experience as a System Manager, Application Manager, Solution Architect, Validation Manager or a similar role from a biotech, pharmaceutical company or consultancy catering to the pharmaceutical industry.
$155,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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BioPharma: Monoclonal Antibody Characterization. Electronics, Power: Ionic impurities in High Purity Water and ReagentsSUMMARYReporting directly to the Director of Operations, Sunnyvale, CA, this position directs and coordinates activities of personnel engaged in Manufacturing Planning, Purchasing, Warehouse Operations, Inventory Control, Customs Compliance, Order Management of plant manufacturing operations.
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These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
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BA or BS and 12+ years’ experience in compliance and trial master file in pharmaceutical/biotechnology industry. BA or BS and 12+ years’ experience in compliance and trial master file in pharmaceutical/biotechnology industry.
$191,335 - $247,610 a yearExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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We have a highly automated lab in San Francisco running on our custom software (Python/Django, JavaScript/React, PostgreSQL), and are currently testing relapsed/refractory cancer patients as well as samples from a variety of biopharma partnerships.
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3-5 years' experience in Pharmaceutical Manufacturing and/or Analytical Development and/or Quality Control or equivalent. This position, reporting to the Senior Director of Analytical Development, will be responsible for supporting analytical development and quality control activities for pharmaceutical drug substances and products.
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As an expression host for production of enzymes for Pharmaceutical Manufacturing & Life Science applications. The Senior Fermentation Scientist will join our Upstream Bioprocess Development team and will be responsible for the design & execution of fermentation experiments for development of new bioprocesses.
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The TAS is a critical role in our unique customer model to execute the BMS aspiration to be the BioPharma that delivers the most impactful engagement with Health Care Providers (HCPs), driving adoption of new and existing medicines for appropriate patients.
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PhD scientist with a minimum of 7 years of relevant experience is required, preferably in biotechnology or pharmaceutical sectors. PhD scientist with a minimum of 7 years of relevant experience is required, preferably in biotechnology or pharmaceutical sectors.
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Prior relevant therapeutic area experience: rare disease, liver, or immunologyUS launch experience in a competitive market spaceSub-part H materials pre-clearance experienceThe successful candidate will be highly collaborative, coachable, perceptive and an analytical problem solver with a track record of success in the pharmaceutical or biopharmaceutical industry.
$191,335 - $247,610Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a minimum, Ph. D. in Toxicology, Pharmacology, Pathology, Biochemistry or Biology with extensive pharmaceutical industry experience in drug development toxicology. As a minimum, Ph. D. in Toxicology, Pharmacology, Pathology, Biochemistry or Biology with extensive pharmaceutical industry experience in drug development toxicology.
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Lead the development of new fermentation bioprocesses utilizing E. coli as an expression host for production of enzymes for Pharmaceutical Manufacturing & Life Science applications. Experience utilizing graphical software (JMP, R, Python, or similar) and motivated in handling large data sets from high throughput fermentation platforms to make data-driven decisions.
$140,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Our products and capabilities are sought after by civilian and military organizations spanning numerous global markets, including Aviation, Communication, Electronic Warfare (EW/ECM/CIED), Industrial, Missile/UAV, Radar, Satcom, Space, and Test and Measurement.
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biopharma pharmaceutical jobs in Palo Alto, CA
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