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Ph. D. or postdoctoral fellowship in Chemical Engineering or a related pharmaceutical science with 3+ years of relevant industry experience. Master's degree in Chemical Engineering or a related pharmaceutical science with 9+ years of relevant industry experience.
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O Familiarity with pharmaceutical informatics standards like CDISC and MedDRA. o Familiarity with pharmaceutical informatics standards like CDISC and MedDRA. o Electronic data captures (EDC) solutions, e.g., REDCap, Encapsia, Oracle Clinical, Medidata Rave.
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Bachelor's degree in Chemical Engineering or a related pharmaceutical science with 11+ years of relevant industry experience. Review, interpret and communicate data cross functionally within pharmaceutical sciences and project teams.
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We have expertise in a wide range of disciplines including adult and pediatric medicine, data science, demography, epidemiology, health economics, health systems strengthening, and pharmaceutical policy.
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MS/PhD/PharmD in chemical or biomedical engineering, pharmaceutical sciences, mathematics, physics, or equivalent area. As a PK/PD and QSP modeler, Neuroscience – Senior Scientist in DMPK & Modeling, you will be empowered to interface between biology/pharmacology, chemistry/biologics, nonclinical safety assessment, drug metabolism, translational medicine, clinical pharmacology and clinical research, to influence drug discovery and development.
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We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. This is an exciting opportunity to join our Digital and Cloud Team to help leading pharmaceutical and biotech companies adopt cutting edge scientific R&D technology.
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PhD in Immunology or related discipline with 3-5 years drug discovery experience in pharmaceutical industry or biotech. Knowledge of biomarker discovery and analysis is highly desirable while experience with in vivo pharmacology is preferable.
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PhD in chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 7+ years relevant industry experience. Master's degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 13+ years relevant industry experience.
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Familiarity with pharmaceutical R&D processes and one or more diseases areas of interest of Takeda (neuroscience, gastrointestinal and inflammation) desired. PhD in computational biology, bioinformatics or similar discipline with 2+ years of postdoctoral experience in human genetics research.
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Apnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime.
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Production, purification, and lyophilization of Shiga toxins using anion-exchange and analog affinity chromatography for research and pharmaceutical use. The Specialist will be responsible for the production, purification, and lyophilization of Shiga toxins using anion-exchange and analog affinity chromatography for research and pharmaceutical use.
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We work with some of the largest professional services, insurance, consulting, hospitality, retail, and pharmaceutical brands in the world including Circle K, Starbucks, BSH, Travelers, Zurich Insurance, Oliver Wyman, PwC, Boehringer Ingelheim.
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3+ years’ experience in the pharmaceutical or biotech industry, focusing on process and product development, and analytical method development for oligonucleotide drug substances and products. Strong experience in small molecule, peptide and/or oligonucleotide method development, characterization, and analytical control strategy especially having mass spectroscopy (MS) experience.
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Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP or GLP. DPS Group is a global EPCMV firm offering full-service solutions within the Life Sciences (pharmaceutical, biotechnology, and medical technology) and Advanced Technology (semiconductor, data center, and solar) industries.
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Minimum of 15 years of experience in the pharmaceutical and biotech sectors, with considerable management experience in the development and manufacturing of protein therapeutics. Experience in technology transfer to Contract Development and Manufacturing Organizations (CDMOs) for both non-Good Manufacturing Practices (non-GMP) and Good Manufacturing Practices (GMP) manufacturing, encompassing cell line development, process development, and scale-up.
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pharmaceutical job in Boston, MA
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