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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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Environment: Our client is a global leader in providing integrated services, superior drug delivery technologies and manufacturing solutions to help life science innovators develop and launch successful pharmaceuticals, biologics and consumer health products.
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Global Life Science Hub is proud to partner with a specialised Biopharmaceutical company leading the charge of next-generation drug delivery technologies and oral. biosimilar drug development.
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Requirements Minimum Valid Class B CDL License (We do accept those with a Class A CDL) Tanker and Hazmat endorsement a must TWIC Card DOT Medical Card- Able to obtain Be able to pass a pre-employment drug screen.
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Maplewood Senior Living conducts pre-employment screening including background check, drug screening and reference checks. The Resident Service Designee in concert with the Director of Nursing assumes responsibility for providing oversight of the resident health care service’s needs, including the overall medication delivery system and the coordination of in-service training for the Resident Care Services Department.
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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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The Clearinghouse is a secure online database that provides real-time information about commercial drivers license (CDL) and commercial learners permit (CLP) holders drug and alcohol program violations.
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Research & Development intern working on Evonik’s Eudragit® aqueous dispersion polymer coatings which are applied to pills, tablets, and capsules; providing a protective layer which controls drug release / delivery of the active pharmaceutical ingredients (APIs.
InternExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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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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The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.
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This position contributes significantly to the successful timely development of new pharmaceutical products utilizing oral solid formulation drug delivery systems and hot melt extrusion technology by conducting required formulation and process development activities.
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Develops formulations for compounds from drug discovery and clinical phase development programs for evaluation in pharmacokinetic (PK), efficacy, and other pharmacology studies; develops formulations that enable the delivery of water insoluble compounds in preclinical and clinical studies by providing safe and viable formulations composed of pharmaceutically acceptable vehicles and excipients dosed by multiple routes of administration.
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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 11 days ago - UpvoteDownvoteShare Job
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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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Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Process Engineering intern working on startup activities for a new chemical process, such as procedure updates, redlining P&IDs, and development of Gannt charts to track and improve process efficiency.
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delivery drug jobs in Bridgewater, NJ
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