• Careers Integrated Resources Inc (Princeton, NJ)
    …manager and current Compounder in the role. 2nd round would be with Director and Perfumer's current technician. Compounding Technician, Perfumery Main Tasks: . Small ... weighing accurate formulae ingredients using automated system . Ensuring all ingredients are quality and within expiration date . Perform other lab and project tasks… more
    JobGet (09/15/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop new ... and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal stakeholders… more
    HireLifeScience (09/13/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... difference? The Position The Scientific Director (SD) functions as a subject matter expert to...works closely with the TA Leadership Team and Medical Director team to identify and execute key projects in… more
    HireLifeScience (08/28/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …this leader enables all activities related to the successful acquisition of high- quality goods/services at the best possible prices and business terms for NNI. ... adversity Operational mindset and continuous improvement: Considers compliance, regulatory, quality assurance and other requirements when supporting all Procurement… more
    HireLifeScience (09/04/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …and Strategic Sourcing activities. This position will ensure the acquisition of high- quality goods/services at the best possible prices by negotiating and monitoring ... improvements and seek agreement through consensus management.RelationshipsReports to an Associate Director / Director within the NNI Procurement Team and… more
    HireLifeScience (09/12/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop new ... is expected to drive initiatives to improve working procedures, quality , and people development. Essential Functions Lead the Medical...Proven track record in senior Leadership roles, such as Director or Senior Director of a drug… more
    HireLifeScience (09/04/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …2 days remote. Approximately 20-30% overnight travel. Global Job level: Director Development of People Ensure that reporting personnel have individual development ... metrics/ROI) Outstanding planning and organizational skills with exceptionally high attention to quality of detail and proven track record of results and follow up… more
    HireLifeScience (09/06/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …environment. Relationships This position will report to the Associate Director , Strategic Market Intelligence. Working relationships with pipeline business unit ... Python, Tableau, Power BI, R, or similar Strong attention to detail, quality control and problem-solving using big data General coding experience highly preferred… more
    HireLifeScience (09/05/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... at Novo Nordisk, Inc. RelationshipsThe fellow will report to the Fellowship Director throughout the two-year program and will also have a reporting relationship… more
    HireLifeScience (09/05/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …and compliance. Relationships This role reports to the Associate Director -Patient CRM Product Owner. Collaborates cross-functionally with internal teams, such ... vendor engagement and collaboration, maintaining adherence to project objectives and quality benchmarks Curate, manage, and expedite the product backlog, informed by… more
    HireLifeScience (08/01/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross Functional Team ... research organizations, and study investigatorsManage vendor budget and activitiesOversee the quality and timeline of vendor workCollaborate with study medical lead… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …team resources, issues, risks as well as achieving overall project level quality metrics. An ideal Associate Director , Program Management must have ... centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for effectively planning,… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs (GMA) Oncology- Medical Content and Training works ... and GMA Oncology TA/franchise in developing and reviewing global high- quality medical information and training materials/programs, ensuring accuracy and scientific… more
    HireLifeScience (09/14/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …guide the successful completion of promotional initiatives. Relationships Reports to Director , Marketing Operations. Primary interaction is with teams that submit ... and processes to ensure the efficient development, planning, and review of high- quality marketing materials Member of PRB Working Group along with leaders from… more
    HireLifeScience (08/23/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …ensure fact-based decisions are generated. Relationships Reports to the Senior Director , Rare Value Communications & Pricing. Interacts internally with team ... Shape the payer value story, supported by credible clinical, health economics and quality of life messages as the market and the NNI asset develops. Interfaces… more
    HireLifeScience (08/23/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for producing scientifically ... accurate, high- quality clinical regulatory documents while adhering to regulatory guidelines....strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, ... that CMC documentation is complete, well organized, scientifically sound, of a high quality , aligned with the current regulations, and presented in a manner that… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.Summary The Associate Director of ERP Applications is responsible for overseeing and enhancing designated ... from all Daiichi Sankyo regions in scope.- Responsible for developing high quality solutions based on Functional Design documents. Perform system customization and… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical Affairs' ... projects are delivered on time, within budget, and meet high- quality standards. Ensure effective communication and issue resolution.Communication and Collaboration:… more
    HireLifeScience (09/14/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program. This Clinical Science (CS) Group Lead will ... is expected. The CS Group Lead will also ensure the writing of high- quality clinical trial protocols, review of clinical data and Clinical Study Reports… more
    HireLifeScience (09/14/24)
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