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Background in pharmaceutical systems strengthening and/or supply chain management in the health sector desiredUnderstanding of USAID and field Missions; USG audiences, trends, and requirements.
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CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists.
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Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science and QA team members, both internally and externally. Our East Coast Global Development Hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.
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A minimum of 15+ years’ experience as the Head of Drug Safety/Patient Safety/ Product Safety & Pharmacovigilance for a bio-pharmaceutical/pharmaceutical company. This position reports directly to the GVP Global Medical Affairs and will be evaluating, refining, updating, and growing the Drug Safety & Pharmacovigilance function at Kiniksa.
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We are looking for a Senior Scientist to join the Manufacturing Sciences and Technology (MSAT) organization at a large pharmaceutical client based out of Andover, MA. This upstream cell culture and fermentation team supports late stage development and commercial biopharmaceuticals and vaccines, and responsible for process troubleshooting, process improvements, and second generation process development.
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MSc or PhD in Skin Biology, Dermatology, Pharmaceutical science, Bioengineering, Cosmetic science, or a related discipline with a focus on skin-related research; MSc with 3+ relevant experience, PhD with 0+ relevant experience.
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We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally.
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We are currently seeking an experienced immunogenicity scientist to join this highly innovative team and collaborate with key stakeholders across Pfizer’s Research and Development, including Protein Engineering, Clinical Pharmacology, Drug Safety and Pharmaceutical Sciences.
$166,500 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. 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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PharMerica is a closed-door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long-term care and senior living clients. PharMerica is a closed-door pharmacy where you can focus on fulfilling the pharmaceutical needs of our long-term care and senior living clients.
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Identify and establish strategic partnerships with large pharmaceutical companies, MNCs, and medium-sized biopharma companies to secure licensing agreements. The ideal candidate will have extensive experience in the biopharmaceutical industry, particularly in establishing partnerships with large pharmaceutical companies, multinational corporations (MNCs), and medium-sized biopharma companies in the US, Europe, and China.
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Basic Qualifications Requires 3-5 years with a BS degree in a related scientific discipline ( chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.
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Mechanical Design Engineer Bedford, MA FORMULATRIX®, a world leader in robotic automation for life science and pharmaceutical research, is seeking ambitious junior to mid-level mechanical design engineers to join our team at our Bedford site.
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Relationships Reports to the Senior Director, Clinical Pharmacology for the U.S. East Coast Hub. Will interact with Medical Specialists, Clinical Operations, Medical writing, Regulatory, Data Science (statistics, pharmacometrics), Research and Early Development, Global Translation, Global Medical Affairs, Global Safety (GS), Bioanalysis, CMC and occasionally with leadership in Medical and Science.
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Typically requires 3-5 years with a BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.
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pharmaceutical job Company: Charles River Laboratories in Wilmington, MA
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