- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and organizational needs, and performance management process incorporates learning and development metrics- Project Leadership and Collaboration- Support DSI ... (from an accredited college or university)- Bachelor's Degree Business, Communications, Project Management or HR/Learning & Development (preferred areas of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. SummaryThe purpose of the Senior Director , Forecasting & Business Analytics is to lead the forecasting and financial ... role will lead the forecasting process supporting the Business Development team through financial analysis and valuation process for...and ensure tax collaboration: work directly with the BD project lead as well as legal team to proactively… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …member of the Global Product Team in collaboration with Clinical Development , Regulatory, Project Management, Biostatistics, Pharmacology, and other departments ... be supporting early clinical safety for our Rare Disease/Specialty Medicine portfolio. SummaryThe Director , Clinical Safety, will be a product safety lead or part of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and ... and execution through RBQM activities. Accountable for the management, performance, and development , both technical and career, of direct reports, and mentors or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable ... to the highest quality standards. This position reports to the Head, Global Development and Medical Affairs QA RDPVQA, and oversees multiple levels of direct reports… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …cross functional GxP areas in the DS groupResponsible for the development of cross-functional training strategies Strategic roadmap including , infrastructure, ... programs, and document/record management principlesResponsible for the development of document and record management principles for Global GxP… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …immune disorders. Summary: Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices to enhance ... the value of our oncology pharmaceutical products.Responsibilities: CDx development : Provide critical strategic and tactical regulatory guidance for CDx/IVD … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …This position is responsible for performance of the function and the development of group members. This position also monitors trends in functional performance ... sufficient understanding of regulations and GCP requirements for drug development , advanced knowledge of Electronic Data Capture/related applications and industry… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...complexity. This position makes decisions with consultation. Responsibilities:Planning for Development : Manages multiple CMC development projects.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Experience Qualifications 7 or More Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development or ... and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary information to author the Dose Preparation… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the ... of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Responsibilities:Supports positions from Director through Vice President, as needed, and in so doing will ... provide direct assistance to the project teams, committees and the department/function.Attend GPT meetings and... administrator or similar role in a pharmaceutical drug development environment required Travel:Ability to travel up to 5%… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Director , Global Sourcing (Direct Materials) as part of the Technical Operations team ... based in Raritan, NJ.Role OverviewThe Director , Global Sourcing (Direct Materials) is responsible for leading...risk score of all BOM and other high-risk Materials.Lead development of Sourcing Score Boards, KPIs and other Metrics… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Implementation Services Lead plays a key role in overseeing the development , validation, implementation, and integration of GxP-regulated systems across the ... emerging technologies and industry trends; lead feasibility studies, prototype development , and advocate for scalable, compliant architecture and design.Collaborate… more
- Merck & Co. (Rahway, NJ)
- …late-stage pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics ... Mentoring Staff, Negotiation, People Leadership, Pharmaceutical Management, Pharmaceutical Process Development , Process Scale Up, Program Risk Management, Project… more
- Merck & Co. (Rahway, NJ)
- …a total spend of $500M+.- This role reports to the Executive Director of Global Marketing Procurement within the Indirect Sourcing & Procurement organization. ... suppliers globally, aligning sourcing execution with business strategies, as well as project management of sourcing activities to deliver the intended benefits and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionCurrently we are looking for an Associate Director Packaging Engineer. Welcome to the teamOur Packaging Technical Operations (PTO) team is where we ... lead projects from conception to implementation. Primary responsibilitiesLead the development and qualification of tertiary packaging components and processes,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director is responsible for defining sourcing strategies for Clinical Innovative and Decentralized Services in support of our Company's ... clinical development pipeline. The role will need to interact effectively...performance indicators that demonstrate improvements. Change Management: Utilizes outstanding project , program and change management skills to manage and… more
- Merck & Co. (Rahway, NJ)
- …Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage ... clinical study reports, or publicationParticipation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Director , Launch Strategy and OperationsLocation: North Wales (Upper Gwynedd), PennsylvaniaDivision: Human Health US (HH-US)Therapeutic ... are passionate about driving impactful changes. Position Overview: As the Associate Director of Launch Strategy and Operations, you will lead the enterprise… more
