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Familiarity with NJDOT, PennDOT and AASHTO design standards is a plus. The candidates will work under the supervision of Senior Project Managers with responsibility for providing civil/highway design for projects with minimal supervision.
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Experience with FDA regulatory processes and medical device design is a plus. Experience with electrical and optical simulation tools is a plus. Python, and Matlab is a plus.
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The purpose of the role is to provide crucial insights on Novo Nordisk, Inc. (NNI) & North America Operations (NAO) performance from a consolidated P&L perspective, including regular reporting to senior stakeholders in NAO and HQ, proactive monitoring of financial impact and market dynamics.
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ServiceNow Certified System Administrator (CSA), Certified Application Developer (CAD) or Certified Implementation Specialist (CIS) certification is a plus. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.
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5-7 years of pharmaceutical and or life sciences marketing experience; additional pharmaceutical experience in sales, medical affairs, and market access a plus Experience with marketing and/or selling biologics within at least two of the following disease areas is REQUIRED : dermatology, immunology, rheumatology.
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Maintenance mechanic strong on the HVAC side with a minimum of a High Pressure Black Seal License. Change filters, change out belts, grease bearings and motors, troubleshooting skills, experience with vacuum pumps and compressors is a plus, experience with R/O and DI water systems, is again a plus.
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The Senior Process Engineer will lead as a process engineer and a process supervisor in developing design packages, studies, and technical proposals. More than ten (10) years refining/petrochemical industry experience plus demonstrated ability to work on multiple assignments independently; assume role of Lead Engineer and process supervisor.
$145,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A demonstrated ability to perform Phase I ESAs and limited environmental compliance reviews of complex industrial sites, with the ability to travel on short business trips. Join our global M&A Environmental Due Diligence Practice and work with us to close the gap to a sustainable future.
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Otsuka researches, develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for the maintenance of everyday health.
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JD or LL.M. from an accredited law school with at least 3-8 years of relevant work experience in the life science industry or in a law firm servicing life science clients. Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.
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Serve as a subject matter reference in analysis of transplant contracts and provide guidance to the TPA/Case Managers in the selection of the best transplant contract for their client.
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Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.
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Certifications:Series 07 - FINRA, Series 66 - FINRA Company Overview Fidelity Investments is a privately held company with a mission to strengthen the financial well-being of our clients.
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Dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than €12 billion. As a vital member of the Indirect Procurement team, your contribution to shaping our vision and mission, driving the overall agenda, and being accountable for the team’s success is needed.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. Hands-on experience with flow, PCR and cell-based assays is a plus.
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