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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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Bristol Myers Squibb currently markets a product in Neurology and plans to re-enter the Psychiatry market with a focus on patients suffering with schizophrenia. Bristol Myers Squibb has a rich history in Neuroscience focused on developing innovative medicines to help people living with Neurodegenerative and Neuromuscular conditions.
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The TAS liaises with other BMS functions as needed to deliver an overall higher Customer Experience (Cx) - by meeting HCP needs in a timely and scientific manner. But working at Bristol Myers Squibb is anything but usual.
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To meet the HCPs expectations, the TAS engages them with a differentiated Customer Experience (Cx) through deeper scientific dialogue on and consistent with label, leveraging new ways of working and CE^3.
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Organizes external speaker programs, selecting speakers from list approved by Speakers Bureau and facilitating scheduling and logistics. The primary role of the TAS is to drive demand for BMS medicines within their portfolio for the appropriate patients.
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Minimum Experience:Minimum Requirement: Bachelor's degree with 7+ years experience in relevant scientific area (e.g., GMP: chemistry, biology, chemical engineering, analytical chemistry, biotechnology; ECTL: cellular biology, molecular biology, immunology, biochemistry.
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B.S, M.S or Ph. D in Biology, Biochemistry, Biotechnology, Biophysics or related field. 2-5 years of experience in protein purification (Affinity purification, IEX purification, Size exclusion purification.
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Experience of working under own initiative and in planning and prioritizing workloads University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Manage audit observations and audit reports through the internal audit database and CAPA process.
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Plan, conduct, and lead complex clinical study audits (Sponsor, Investigator Sites and Clinical Suppliers) (either remote or on site) in accordance with all applicable regulations, standards, guidance, and the established procedures, maintaining a high standard of service delivery that ensures effective customer relationships.
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We believe that the human element, across our global teams, is what allows us to continually evolve. We have an excellent new opportunity for a Medical Device Lead Auditor to join our global organization.
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PhD in Molecular Biology, Biochemistry, Chemical Engineering, Biotechnology, or related field. The Biotechnology Discovery Research (BioTDR) organization within Lilly Research Laboratories spans target identification to clinical candidate selection.
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Panitch Schwarze Belisario & Nadel LLP, a renowned intellectual property boutique, seeks to hire a highly qualified mid-level associate or patent agent to join our IP Biology/Biotechnology Practice Team. The position will primarily involve patent counseling, procurement, and opinions, with opportunities for licensing and enforcement, as well.
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To meet the stringent needs of biotechnology research and production customers, the company's cell culture sera and bioprocess liquid manufacturing facilities are segregated between animal origin-free cGMP manufacturing and animal component cGMP manufacturing.
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biotechnology job Title: platform Company: Genomatica
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