• Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Associate Director , GMP QA Process Excellence is accountable to collect ... information, analyze quality related process, define strategies to lead to the...strategies to lead to the development and implementation of quality improvement initiatives across the organization.This role will focus… more
    HireLifeScience (03/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …global markets are also met.Cross-Functional Team Participation: Responsible for working with Quality Leaders in each operating site to influence and affect the ... timely manner activity and a protective solution to avoid any risk to the quality and safety of commercial and investigational drug products supplied through DSI and… more
    HireLifeScience (02/27/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …direction to Biostats Data Mgmt & Data Ops for EDC, edit checks, data quality listings, SAP, Data Mgmt plan; Reviews patient population and protocol compliance for ... Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with Delivery Lead eg review Tables/Listings/Graphs before… more
    HireLifeScience (02/13/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Global Labeling Operations and Compliance Leads to produce high quality labeling documentation.Establishes Processes and Best Practices: Reinforces labeling best ... practices at cross-functional meetings. Assists in the development of Standard Operating Procedures (SOPs) and process improvements. Follows agreements with external partners.Department Coordination: Builds cross-functional and cross-regional… more
    HireLifeScience (02/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …of statistical activities; collaborates closely with data manager to ensure high quality data.- Drug Development Strategy: Provides input to multiple aspects of the ... development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.- CRO / Vendor Oversight: Review CRO/vendor proposal and budget.… more
    HireLifeScience (01/30/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …relevant advancements to optimize system performance and functionality. - Data Quality , Testing and Release ManagementEstablish and enforce robust data governance ... test, audit and validate HR data to maintain high data quality standards.Conduct system audits, optimize performance, and troubleshoot technical issues.Develop… more
    HireLifeScience (01/14/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …smooth transition with other sub projects with respect to supply, product quality and stakeholder satisfactions. Responsible to communicate and escalate to Senior ... CMC Lead regarding the activity status and potential critical issues, or to the governance bodies. Responsibilities - Accountability to lead teams within overall CMC development project(s), to support Sr CMC Lead. In case no Sr CMC Lead is established, take… more
    HireLifeScience (01/03/25)
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  • Merck & Co. (Rahway, NJ)
    …a lead GCS Planning program representative ) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines ,- strategies and ... software . - Familiarity with Good Manufacturing Practices (GMP) requirements, quality procedures, and Standard Operating Procedure (SOP) execution. - GCSCareer25… more
    HireLifeScience (03/13/25)
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  • Merck & Co. (Rahway, NJ)
    …CSS team with IS&O initiatives and daily operations, adopting high- quality change practices and embodying our Companys Enterprise Leadership Skills.Stakeholder ... trust through effective communication and relationship management.Execution Excellence: Deliver high- quality outputs within deadlines while navigating ambiguity.Business and Technology… more
    HireLifeScience (03/12/25)
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  • Merck & Co. (Rahway, NJ)
    …journey to become the premier "Data First" commercial biopharma organization.In this Associate Director Data Product Management role, you will be part ... a plusTranslate use cases into implementation roadmaps to deliver high quality data productsEstablish common performance expectations and processes for data product… more
    HireLifeScience (03/07/25)
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  • Merck & Co. (Rahway, NJ)
    …creative and innovative real estate and workplace solutions aligned with corporate strategy.The Associate Director of Real Estate Strategic Planning will play a ... skills and meticulous attention to detail, with a commitment to delivering high- quality work.Leadership experience with a demonstrated ability to mentor and guide… more
    HireLifeScience (03/01/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... scientific background, excellent communications skills, and project management skills to derive high- quality reference data to meet the diverse needs of the business… more
    HireLifeScience (02/25/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Manager role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... primary accountability for operational study level time, cost and quality deliverables.Lead the development of the clinical study plan...share with study team, Operations Program Lead, and Sr. Director for the compound, on regular basis and ensure… more
    HireLifeScience (02/05/25)
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  • Merck & Co. (Rahway, NJ)
    …for traceability / lineage and make them available for business consumption; Monitor data quality report and work proactively with IT on data issues as part of daily ... reconciliation process; Check the accuracy of the master and operational data which impacts dashboard reporting.Responsible for Data Management, that entails: Maintain Standard pricing across all species at multiple Units of Measure and load all Special… more
    HireLifeScience (03/04/25)
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  • Merck & Co. (Rahway, NJ)
    …with understanding of Design Controls (21 CFR 820.30)Familiarity with the following standards: Quality Management - ISO 13485, Risk Management - ISO 14971, EU MDR, ... ISO 11608 Needle-based injection system for medical use.Familiarity with Design Verification (DV) strategies and mechanical tests with validations, including engineering studies, design verification protocols, stability studies and validation protocols,… more
    HireLifeScience (02/26/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …assignment and oversight of the group. This position reports to the Associate Director Data Management Operations. Business administration activities within the ... and maintaining new SOPs, Work instructions, templates, and other quality documents.Responsibilities:Leadership, Direction, and Strategy: Establish and manage accountability… more
    HireLifeScience (02/05/25)
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  • Merck & Co. (Rahway, NJ)
    …Analytical Enabling Capabilities Department has an exciting opportunity for a Director of Nuclear Magnetic Resonance (NMR).- The NMR Lead provides strategic ... partners across Discovery Chemistry, Process Development, and Pre-Clinical Development.The Director reports to the Executive Director , Structural Elucidation… more
    HireLifeScience (03/11/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    Legend Biotech is seeking Associate Technical Lead as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe Associate Technical Lead will ... Responsibilities This individual with provide direct support to the Director of Manufacturing Excellence by providing technical expertise to Technical… more
    HireLifeScience (02/14/25)
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  • Merck & Co. (Rahway, NJ)
    …of regulatory submissions. -Under the general scientific and administrative direction of Director in the CCFS group and working in conjunction with internal and ... a cross-functional team.-Ensures project results meet requirements regarding technical quality , reliability, schedule, and cost.Monitors performance and recommends schedule… more
    HireLifeScience (03/11/25)
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  • Merck & Co. (Rahway, NJ)
    …new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific ... and ethical standards.-The Distinguished Scientist (Executive Director ) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary… more
    HireLifeScience (02/22/25)
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