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The corporate safety director needs to be available 24/7 to address emergencies or priority health and safety related issues. The corporate EHS director reports directly to ownership and works with the individual affiliate company safety directors to develop and maintain a safety program that establishes the core operational environmental, health, and safety Ferreira Group standards.
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Sanofi is recruiting a new Global medical Director to support post- regulatory authorization clinical trial program for dupilumab in the Global respiratory Franchise for the respiratory indications including asthma and Chronic Obstructive Pulmonary Disease (COPD) for dupilumab and itep.
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The role reports to the IEEE Executive Director and Chief Operating Officer and is a member of the Management Council, IEEE's executive staff leadership team. In addition, they oversee management and planning for special projects and new initiatives as assigned by the IEEE Executive Director and Chief Operating Officer.
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Ensure timely communication of any variances to budget forecast to the Sr. Director or Director of Clinical Operations. Supervise clinical staff to ensure all study activities are completed in accordance with applicable regulations and guidance, ICH, GCP and Bausch Health SOPs. Responsible for the quality of all study-related documentation (e.g., Trial Master File, site qualification and initiation visits reports, interim monitoring visit reports, clinical monitoring plan, informed consents, CRF completion guidelines, pharmacy manual, etc.
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Johnson & Johnson, is recruiting for a Director, Medical Safety Officer, Immunology to be located in Titusville, NJ; Raritan, NJ; or Horsham, PA. The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned Janssen products and will strategically lead cross-functional matrix teams responsible for product safety and benefit risk oversight and represents Global Medical Safety (GMS) as the product spokesperson regarding overall benefit/risk.
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This position reports to the Senior Director of Indirect Procurement and is responsible for developing and implementing category management strategies and procurement processes specifically for Capital and MRO-related categories, ensuring optimal cost efficiency, supplier relationships, and operational effectiveness along with promoting collaboration across categories and business.
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Director - Reinsurance Claims Quality Assurance / Warren, NJ. Reinsurance Claims Quality Assurance Director. Assist the Vice President Quality Assurance maintain a Reinsurance Claims Quality Assurance Program focused on assessing quality of technical claims handling, ensuring high quality claims handling for Everest, and identifying areas for improvement across the Global Reinsurance Claims Department.
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Legend Biotech is seeking a Senior Manager/Associate Director, External Manufacture as part of the Global Manufacturing Supply team based in Raritan, NJ. Manage the CMO tech transfer and clinical/commercial manufacture: trouble shooting problems, conducting investigations, track timeline and KPIs, overseeing capacity expansion, monitoring budget, driving cost reduction and quality improvement and serve as Person in Plant.
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By leveraging planning tools, continuous improvement methodologies, and cross-functional collaboration, the Director of Global Metals Planning & Master Production Scheduling plays a pivotal role in optimizing production workflows, reducing costs, and enhancing overall business performance.
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The Associate Director, Global Cell Therapy Commercial Operations will report directly to the Senior Director, Global Cell Therapy Commercial Operations and will be responsible for key priorities across the Janssen Cell Therapy business, including Global CARVYKTI Operations, enabling launches and operations across all Janssen regions and leading key global strategic cross-functional initiatives to enable a seamless end-to-end customer and patient experience.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Report directly to the Administrator, Executive Director or Patient Care Manager Senior and function under the direction, instruction and supervision of the Registered Nurse and/or Clinical Supervisor.
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Senior Group Director, Change ManagementAbout the RoleCHANEL is looking for a Senior Group Director to join our dedicated Project team in New Jersey. US support currently includes Annual sponsorship of the MoMA film program, Tribeca Film Festival programs and Through Her Lens, Support of the Academy Gold Fellowship for Women and Sponsorship of the BAAND Together Dance Festival at Lincoln Center.
$166,000 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Overview Within the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large molecule quantitative assay development of biological samples.
$140,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You will work closely with the Creative Services Director, Vice President of Marketing, and other senior stakeholders to understand the business goals (typically brand awareness, mental availability and demand generation), target audiences, and value propositions of SHIs products and services, and then translate them into compelling and consistent visual stories across all channels and media.
$85,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated Today
director job in Raritan, NJ
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