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To prepare regulatory documents for submission to regulatory authorities within subject area clinical safety The Regulatory Documentation Scientist takes accountability for delivering regulatory documents working effectively and closely with key..
This role within the in-vivo biology team in the Translational Immunology department is responsible for assessing new therapies to treat serious human diseases The successful candidate will identify develop and..
Overview nJazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients u2019 lives by identifying developing and commercializing meaningful products that address unmet medical needs We are continuing to..
Purpose The Medical Director at Genentech puts patients and science at the center of all actions. They drive medical tactics aimed at maximizing medical progress for patients. They collaborate to..
Requirements Entry level No Education Salary to negotiate San Jose Description Job Description Summary: Health is everything. At CVS Health, colleagues are committed to increasing access, lowering costs and improving..
DescriptionrnrnThe Senior Regulatory Operations Associate will be responsible for functional activities related to US and global regulatory submissions as well as clinical and compliance documentation.rnrn Responsibilities:rnrnrntSupport submission activities associated with..
Biotechnology opened the door to new types of medicines based on nature's own building blocks. No company has done more to advance this revolution than Amgen & the company's broad..
u003Cbu003EPosition Overview:u003C/bu003Eu003Cbru003Eu003Cp style=MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px\u003Eu003Cspan style=mso-fareast-font-family: timesnewroman mso-ansi-language: en-us mso-fareast-language: mso-bidi-language: ar-sau003Eu003Cfont face=\ arialu003EIncumbent in this role has dual campus responsibility and is accountable for the planning and operational..
OverviewnDignity Health Medical Foundation, established in 1993, is a California nonprofit public benefit corporation with care centers throughout California. Dignity Health Medical Foundation is an affiliate of Dignity Health -..
Vice President, Regulatory Affairs Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are passionate about developing..
The Team Lead will report to the Director of Program and Delivery Management Team and will be accountable leading the delivery team for a specific channel and digital service (Media,..
Senior Director, Regulatory Affairs Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are passionate about developing..
Myriad Genetics, Inc Myriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to..
The Scientist I/II, Analytical Development will work in a biopharmaceutical analytical development group responsible for analytical method development, method qualification/validation and QC transfer of active pharmaceutical ingredients (API) and drug..
Cancel L Scientist I / Scientist II Cellular Pharmacology Lyell Immunopharma, Inc. South San Francisco , CA 94080 Posted Yesterday Apply This Job is not relevant Tell us why At..
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses..
Job Description: Intarcia Therapeutics, Inc., is a rapidly emerging biopharmaceutical company committed to developing innovative therapies that merge medicine with technology. At Intarcia, we seek to transform the standard of..
We are seeking a talented and motivated Associate Scientist in the Small Molecule Analytical Chemistry (SMAC) Department at Genentech to develop automation strategies for high-throughput experiment and pre-formulation, and analysis...
Job Description: The CMC Regulatory Affairs Project Manager will be responsible for tracking the status of key filings for clinical and commercial programs for all global markets. Other responsibilities include:..
Commercial IT Business Analyst Abbott in Santa Clara, CA, USA Core Responsibilities: Requirements Capture: Investigate, record, analyze and confirm system requirements and business processes. Identify overlapping requirements/processes across the existing..
Requirements Entry level No Education Salary to negotiate South San Francisco Description POSTDOCTORAL RESEARCH FELLOW - EARLY DISCOVERY BIOCHEMISTRY South San Francisco California, United States of America Job ID: 201903-108680..
Responsibilities: A postdoctoral position is available in the Department of Early Discovery Biochemistry to investigate molecular mechanisms underlying complex biology. Active areas of research include structure-function studies of protein complexes..
Location 217 ALMA ST , PALO ALTO, CA Apply Models and delivers a distinctive and delightful customer experience. Registers sales on assigned cash register and provides customers with courteous, fair,..
US Tech Solutions is seeking a ‚Äú CMC Regulatory Affairs Project Manager for a 6 months position with a client in Foster City/California/USA/94404 Responsibilities The CMC Regulatory Affairs Project Manager..