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8+ years of experience as a product owner, product manager, senior business analyst in Global Drug Safety and Pharmacovigilance areas, with at least 3 years in a delivery leadership role.
$190,625 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Monitor assay development, assay validation and sample analysis processes, ensure timely delivery of quality results in compliance with regulatory guidance. Act as the project manager to support the externalization and operationalization of clinical biomarkers and bioanalytical activities for pre-clinical and clinical drug development.
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Requirements : A BS, MS in Pharmaceutics, Chemistry, or a related field, with experience in nanoparticle drug formulation and characterization techniques such as (DLS, NTA, HPLC, etc. Requirements : A BS, MS in Pharmaceutics, Chemistry, or a related field, with experience in nanoparticle drug formulation and characterization techniques such as (DLS, NTA, HPLC, etc.
$37 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of Drug Safety and Pharmacovigilance function. Maintenance and delivery of systems supporting the PV business unit, the primary focus is the Argus Safety Systems. Validates and implements annual, periodic and ad-hoc reports in the Drug Safety systems.
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Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting.
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Drive planning for key drug development stage-gate decision points after Phase 1 and co-chair stage-gate committee for Rare Disease franchise. Successful candidate will have a strong understanding of the drug development process from preclinical pharmacology through to regulatory approval and the principles, concepts, practices, and standards of pharmaceutical program management.
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RN night shift , Rotating weekends, Rotating holidays, RN day shift , Rotating weekends, Rotating holidays, Job Overview: The Registered Nurse is expected to ensure the delivery of safe and quality patient care.
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Experience: Prefer experience working in retail, hotel, restaurant, grocery or drug store environments. Helps in the unloading of merchandise from delivery trucks, organizes merchandise, and transports merchandise from stockroom to sales floor.
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Be responsible for release or rejection of GMP materials and utilize QA staff to manage the timeline and assure on time delivery of approved materials. In addition, responsible for facilitating transition from drug development to commercial product.
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Catalent in Somerset, NJ is home to oral solid dose manufacturing operations as part of the Oral and Specialty Delivery (OSD) business unit. serves as the champion of ensuring the health and safety of our employees, environmental compliance and implementation of our environmental sustainability strategy.
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The QC Microbiology Data Reviewer is an exempt level position with responsibilities for reviewing microbiology data and documentation generated from the Environmental Monitoring program, drug product and intermediates testing from the manufacturing facility utilized for cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
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Drive the development of and deliver the vision, strategy and road map, in partnership with the CORM LT, to build a holistic and integrated Risk Management and Central Monitoring capability and processes to drive proactive risk-based management and related data insights that enable BMS Drug Development to accelerate in performance and safeguarding the well-being of our trial participants.
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Efficient delivery of all aspects of business operations including but not limited to Commercial Operations, Patient Services, Clinical Development, Sales & Marketing, Market Access, Corporate Communications/Patient Advocacy, Sales Training, Commercial Digital Analytics, Medical Affairs, Regulatory Affairs, Sales Ops, Supply Chain, Drug Safety and Finance, Legal and Quality Assurance.
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The position acts as a subject matter expert for drug delivery systems, suppliers and related materials providing expertise globally, as needed, for Combination Products related Supplier Quality activities and issues.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago
delivery drug jobs in Hillsborough, NJ
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