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A Japan-based company, our goal is to make people smile by delivering breakthroughs where no adequate treatments currently exist, working from drug discovery to product development and commercialization.
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Experience in development, maintenance, and production support projects. Experience in Software Development and Implementation Life Cycle. 7+ years of experience in Mainframe, COBOL, DB2, Store Procedures, MQ, CICS, SPUFI, ENDEOR, VSAM, ICETOOL.
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Act as a key stake holder in business development and financial accountability, including growing the PMG MID Pharmacy, Infusion, and Injection program. Participates in formulary management, review of medication use processes, and development and implementation of evidence-based treatment guidelines Identify programs and areas for cost reduction; specifically target drugs, and therapeutic regimens that can be changed through pharmacy intervention to reduce cost; prepare methodology of program, obtain approval, and facilitate implementation of such programs.
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Strong experience working with CHO cells with different Bioreactor volumes Perfusion cultivation experience is highly desirable Expertise in independently conducting and directing the design, execution, analysis, and documentation of all states of process development.
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Lead fish hatchery design quality control efforts which will include coordination with HDR’s quality management program, development of fisheries design standards, implementation of BIM. Serve in a fish facilities business development role by interacting with clients, developing scopes of work and fee proposals, and participating in strategic planning for business in North America.
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Intern, Accounting Development Program - 2025 Working with Us. High performing interns with interest in a full-time Accounting Development Program (ADP) position upon graduation will be given preference during the full-time application process.
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Role and Responsibilities: Work with infrastructure, Architecture, and software development teams to implement CI/CD automation on-prem and in the Azure cloud Implementation and troubleshooting of continuous build and deployment pipelines Contribute to the drive towards DevOps methodology by developing and maintaining CI/CD pipelines, automation, and API integrations.
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Maintain an overview over the relevant regulatory requirements and state-of-the-art knowledge of development in the professional regulatory environment to be able to provide guidance for timely adaptation of Otsuka’s procedures.
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Responsible for development of Integrated Statistical Analysis Plan and interpretation of integrated statistical analysis results for NDA/BLA/MAA submissions and information requests from HA. Solid understanding of development, regulatory and commercial aspects of drug development.
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QualificationsWhat we are looking forRequired Qualifications A minimum of a bachelor’s degree5+ years of Consumer Products industry experience in Category or Customer Strategy, Customer Business Development, Category Insights & Analytics, and/or Shopper Insights & analytics Extensive knowledge of omni-retail customer store operations, structure, strategy, and retail execution tactics.
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Advanced Tableau & Spotfire skills with 4+ years of development experience. Ability to lead the development of critical path analyses and support scenario planning. 5+ years Drug Safety/Pharmacovigilance experience.
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Managing costs, including use of coverage counsel and litigation costs as well as collaborating and working with the Litigation Management and Vendor Management teams ensuring cost management and the development and enhancement of the.
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Significant experience in pharmaceutical/biotechnology and extensive knowledge of drug development processes, ICH-GCP guidelines, 21 CRF Part 11, and major Health Authority regulations as they pertain to the operational aspects of clinical trials.
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Duties and Responsibilities include, but are not limited to: Work with multi-disciplinary teams on tasks such as traffic studies, concept development studies, intersection design, traffic signal design, roadway signing and pavement marking plans, signage and striping plans and traffic and roundabout and signal operations analysis.
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Supports the development of Regulatory Operations procedures and practices. Responsible for the development, implementation, and rollout of training to the organization on Regulatory Operations processes and systems, including but not limited to Starting Point Templates, existing processes or systems, the introduction of new processes and/or systems, and the training of new employees as necessary.
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development job Company: Cigna in Princeton, NJ
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