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A teaching facility, in affiliation with the Texas A&M University System Health Science Center College of MedicineAccredited Chest Pain CenterAccredited Joint Commission Stroke TeamThe Shoreline campus is a premiere facility housing many of the region’s most vital and renowned programs such as a Primary Stroke Center, nationally accredited Cancer Center and a nationally recognized Chest Pain Center.
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QualificationsBachelor’s degree in business management Req15 years relevant industry experience (CRO/Pharmaceutical) Req OrEquivalent combination of education, training, and experience ReqProven track record at developing mid-level and high-level contacts.
$165,500 - $281,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Drive strategy for Healthcare Packaging segment across medical device and in process pharmaceutical packaging verticals. Identifying, designing and driving longer term growth projects in Medical Device and Pharmaceutical packaging in a disciplined manner.
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Life Science Industry: Designing production facilities for Flu Vaccines, Active Pharmaceutical Ingredients (APIs) for important drugs, Blood Fractionation for the life-saving plasma industry, and more.
$118,500 - $213,500 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering, or Chemistry or closely related science field with chemistry and mathematics in coursework. Oakwood Laboratories is a privately owned specialty pharmaceutical company focused on the design, development and commercial manufacture of sterile injectable sustained release pharmaceuticals.
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Bachelor's in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field with 8+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
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Their platform is a scientist-led pharmaceutical industry publication focusing on the science of drug discovery. Bonus if you’ve worked in the biotech or pharmaceutical sales industry, but a scientific background is not required.
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These activities will be performed in cross-functional collaboration with a range of partners throughout the organization, including the US Market Access, US Medical Affairs, Medical Outcomes Science Liaison (MOSL), Public Policy & Government Relations, and US Regulatory Affairs teams.
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Business Intelligence (BI), Database Design, Data Engineering, Data Modeling, Data Science, Data Visualization, Machine Learning, Project Management, Software Development, Stakeholder Relationship Management.
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5+ years of substantive compliance and litigation experience which must include compliance program and policy experienceA blend of experience in a law firm as well as in-house experience is required; in-house at a pharmaceutical or biotechnology company and/or at a firm counseling life-science clients is strongly preferredExperience with privacy, information security, and compliance laws and regulations is required; CIPP, CIPM, and CCEP certifications are preferred.
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Master’s degree in Chemistry, Chemical Engineering, Materials Science and Engineering, or a closely related field. Two-year chemical experience in the pharmaceutical industry as a Chemist, Scientist I or in a related occupation.
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Partnering with cross functional members in Gilead Pharmaceutical Development & Manufacturing (PDM), including Quality, Supply Chain, Manufacturing, Regulatory Affairs CMC, Finance and Technical Development to ensure successful commercialization of the late-stage portfolio, as well as on time delivery of clinical and commercial products.
$237,660 - $307,560 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ph. D. with at least four years of pharmaceutical drug development experience relating to: PKPD, pharmacometrics, mathematics, statistics/ biostatistics, or chemical/biomedical engineering. Masters, with or without PharmD, or equivalent degree with at least six years of experience, where “experience” means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
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Taro is a multinational, science-based pharmaceutical company dedicated to meeting the needs of its customers through the discovery, development, manufacturing and marketing of the highest quality healthcare products.
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Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.
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