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Ensure timely communication of any variances to budget forecast to the Sr. Director or Director of Clinical Operations. Overview Responsible for the implementation and oversight of clinical study or program operations by organizing and coordinating with other relevant parties the planning, implementation, management, execution and completion of clinical studies or programs according to applicable regulations and guidance, ICH and GCP, and Bausch Health Companies Research & Development SOPs within agreed-upon timeframes and budget.
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Works with Operations Planning team to ensure visibility of shipping schedule to Warehouse group. Acts as a backup to lead warehouse operations in Warehouse Supervisor's absence.
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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Assist with completion of forms, insurance referrals (to be sent to Referral Specialist if patent has insurance and requires pre-authorization), notes for work or school and other paperwork.
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The Managing Director of Technical Activities (MD of TA) oversees the strategic direction, activities, and business operations of the organizational units (OU) relating to forty-six (46) technical societies, councils and communities of the IEEE. These groups collectively engage a multitude of technical professionals and support over 350K memberships, over 200 publications, approximately 1,000 conferences, numerous webinars, educational events, and over 1,000 standards.
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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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Continuous Improvement Initiatives: Collaborate with 3PL partners to identify and implement standard processes that enhance warehouse operations and efficiency to deliver FTG goals Analyze performance data to pinpoint areas for process optimization and cost reduction Lead the adoption of innovative technologies and methodologies to improve inventory management, throughput, and service levels Monitor industry trends and benchmark against best-in-class operations.
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Posting Summary Rutgers, The State University of New Jersey is seeking a Postdoctoral Fellow for the Center for Advanced Biotechnology and Medicine (CABM) located on the Rutgers Biomedical and Health Sciences Campus in Piscataway, NJ. The Oldenburg Laboratory at CABM is seeking an outstanding Postdoc to join an exciting neuroscience project developing and utilizing new optical and molecular tools to study neural circuits.
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10+ years of experience in a GMP environment in pharmaceutical, biologics, vaccines, cell or gene therapy operations, including solid experience in Quality Systems and Regulatory CMC. This individual will be responsible for Quality oversight and support of cell therapy manufacturing operations, in full compliance with established cGMP requirements.
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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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Blue Seal Or Black Seal High Pressure steam license+ Ability to document findings+ Articulate boiler operations processes. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees.
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While primarily focused on self injector launch, this individual will also work on base product (vial and syringe) as needed including supporting performance management (both vial & syringe and self injector) as well as strategy and operations for the immunology portfolio.
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Job Purpose The Director of Global Metals Planning & Master Production Scheduling will be an integral part of the Supply Chain Team, orchestrating the complex interplay between production processes, capacity constraints, and material availability to ensure efficient operations and meet customer demands effectively.
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Qualifications Minimum of a high school diploma or GED Valid NJ criminal history letter Negative tuberculosis test obtained within 6 months of initial employment About ESS As leaders in the education staffing space since 2000, ESS specializes in placing qualified staff in daily, long-term, and permanent K-12 school district positions including substitute teachers, paraprofessionals, and other school support staff.
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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. Minimum 5+ years of industrial biologics CMC development or manufacturing experience, Cell therapy manufacture experience is desirable.
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school operations director of campus jobs in Raritan, NJ
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