THE LARGEST COLLECTION OF PHARMACEUTICAL JOBS ON EARTH
Supports PDF, DOC, DOCX, TXT, XLS, WPD, HTM, HTML files up to 5 MB
The Biologics Upstream Process Development and Manufacturing group is responsible for developing recombinant protein production processes, with a great emphasis on product quality, and the subsequent technology transfer to cGMP..
Job Description 6 to 8 years of experience in Regulatory Affairs in the biotechnology or pharmaceutical industries, including an in-depth knowledge and understanding of the regulatory environment. International regulatory experience..
The Stanford University Department of Orthopaedic Surgery in the Division of Pediatric Orthopaedic Surgery is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of various..
u003Cbu003ERequisition ID: u003C/bu003ELAB000917u003Cbr/u003Eu003Cbr/u003Eu003Cp style=MARGIN-BOTTOM: 0px; MARGIN-TOP: 0px\u003Eu003Cfont size=2 face=Arial\u003EMerck u0026amp; Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader..
For Current Gilead Employees and Contractors: Please log onto your Internal Career Site to apply for this job. Job Description Specific Responsibilities: The clinical research physician will play a key..
Job Title: Research Scientist I: FibrosisrnrnJob Type: Regular, Full-TimernrnLocation: Foster City, CArnrn rnrnSpecific Responsibilities:rnrnWe are seeking an exceptional scientist to join the Fibrosis Biology group at Gilead. This individual will..
Clinical Program Director The Clinical Program Director plays a critical role in developing and managing the clinical operations team and infrastructure for a given project(s). This position will provide strategic..
Job Description Coram/CVS Health is looking for customer service oriented professionals to join our team as a Pharmacy Clerk! In this fast-paced and dynamic role, you will work alongside our..
Title: QA Compliance Manager II - Global Quality Agreements Location: Foster City, CA Type: Contract Responsibilities: The Manager, QA Compliance will report to the Associate Director, QA Compliance – Global..
Neurology Account Specialist - Raleigh, NC The Neurology Account Specialist (NAS) engages with targeted customers and effectively communicates the value proposition for GOCOVRI for approved indications. The NAS achieves this..
Job Objectives * In accordance with state and federal regulations, assists the pharmacist, under direct supervision, in the practice of pharmacy. Assists the pharmacist in the performance of other Pharmacy..
OverviewJazz Pharmaceuticals is an international biopharmaceutical company focused on improving patientsu2019 lives by identifying, developing and commercializing meaningful products that address unmet medical needs. We are continuing to expand our..
Responsibilities Responsible for executing QA operations and overseeing junior team members as they assess, evaluate, and review operations on the floor (as defined above) against cGMPs to assure real-time observation..
At UCSF Health, our mission of innovative patient care, advanced technology and pioneering research is redefining whatu2019s possible for the patients we serve u2013 a promise we share with the..
Pharmacyclics is committed to the development and commercialization of novel therapies intended to improve the quality and duration of life and to resolve serious unmet medical needs for cancer patients...
11872 – Senior Global Project Manager (Drug Development) – South San Francisco, CA Type: Full-time direct employment with Vitaver Staffing Client. Salary: $175,000 to $185,000 range depending on your level..
Principal Engineer, New Product Quality J&J Family of Companies • Milpitas CA Job #750027619 Johnson & Johnson Vision Care, a member of Johnson & Johnson's Family of Companies, is recruiting..
u003Cpu003Eu003Cbu003EResponsibilitiesu003C/bu003Eu003C/pu003Eu003Culu003Eu003Cliu003EResponsible for processes are validated to required standards. Manage all moderate troubleshooting efforts for protocol discrepancies.u003C/liu003Eu003Cliu003EResponsible for developing moderate complex protocols using a risk-based approach that meets current regulatory requirements..
Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years..
About Us: Eureka Therapeutics is a privately-held biotechnology company focused on developing novel T cell-based immunotherapies for hematological malignancies and solid tumors. Our unique platform is aimed at developing safe..
Qualifications: Bachelor’s degree in business, finance, computer science or a related field from an accredited institution. MBA preferred. Minimum 2-4 years relevant business experience preferred. 2-3 years in reporting or..
in Santa Clara California Under indirect supervision, provides ambulatory pharmaceutical care services using approved protocols in collaboration with other health professional, including managing patient drug therapy, providing patient education, and..