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Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 billion.
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Successfully completes manufacturing engineering project work on Value Improvement Process (VIP), Strategic Activity Review (STAR) projects, or new product development. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.
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Coordinates the full software development lifecycle (SDLC) in a scientific environment, including defining technical and functional requirements, quality control planning, implementation, upgrades, and integration with existing NCBI systems through Agile Process methodology.
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The Logic Technology Development (LTD) organization delivers the latest process technology innovations to drive Intel's amazing product roadmap. from semiconductor process development and manufacturing, through yield improvement to packaging, final test and optimization, and world class Supply Chain and facilities support.
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5+ years experience post Master's degree in biology, Biochemistry, Molecular Biology or 8 -10yrs equivalent experience in quality control testing, analytical development, or GMP; OR a; OR a PhD degree in a relevant scientific discipline with 2+ years of experience.
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The PM is responsible for creating, managing and communicating the program development workflow plan and providing the Scientific Director (SD) and Strategic Account Director or Manager (SAD/SAM) with the timing and process information required for them to effectively and efficiently manage their departments, programs and the client.
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Requires a thorough knowledge of the drug development process, good knowledge of worldwide GxP compliance regulations, sound research and development practices, scientific and quality terminology, company quality assurance procedures and policies, and quality evaluation techniques.
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Understands the life sciences industry (e.g., CROs, pharma/biotech, medical device), scientific & clinical data/terminology, and the drug development process. MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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The Director of Business Development is responsible for the sales of Astrix Technology Groups Scientific Informatics Services portfolio within a defined territory, serving customers across a wide variety of industries including Pharma, Life Sciences, Food & Beverage, Oil & Gas and Chemical.
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We are currently looking to strengthen our Business Development team through the recruitment of a Director, Business Development to support our business development activities. This position is primarily remote, non-office based, with the expectation to travel up to 50.
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Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct advantage. 5+ years of related experience, including 3 years of relevant industry experience, preferably in data services (data management and biometrics) or a clinical research environment.
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This individual oversees clinical guidelines, assessing appropriateness and outcomes of care; develops interdisciplinary, individualized plan of care for each patient assigned, utilizing a scientific problem solving approach and in collaboration with the patient, family, physician, and other care team members; coordinates the discharge process to promote continuity of care and optimal outcomes; makes timely referrals to various disciplines; and facilitates patient and family education.
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Directs and manages product/process development and commercialization activities (as a technical leader of junior and senior level scientists and Team Leaders), interfacing with cross-functional departments to ensure products can be produced with scientific rigor in a manner that is efficient, safe, and compliant with FDA and company regulatory standards.
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This is what you will do:Alexion’s Product Development and Clinical Supply (PDCS) organization is seeking an innovative expert in process analytical technology (PAT) & chemometrics to enable development, optimization, monitoring, and control of continuous processes for the manufacture of synthetic drug substances.
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As an Institutional Account Sales Specialist, Acute Care, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives within our Acute Care Hospital Sales Team. You will help lead the growth and expansion of our innovative and unique product portfolio, following FDA approval, for providers addressing life-threatening bleeds for patients on Direct Oral Anticoagulants (DOACs.
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