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The Candidate: Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience Master of Science in Analytical Chemistry/Pharmaceutics preferred or more years of applicable industry experience in support of pharmaceutical product development Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing.
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The DTS Business Process Owner will promote a manufacturing process excellence culture by identifying, developing and implementing program initiatives focused on manufacturing process improvement solutions within the highly integrated platform of SAP S4/HANA, SAP-ME, & LIMS. The individual will lead and direct the activities of Process Experts, Super Users, Specialists and Trainers (where they exist) and directly manage DTS process experts and master data stewards.
$70 - $80 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The CMC Regulatory Associate Director, Biologics is responsible for content development, compilation, maintenance, and review of the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & background packages (including participating/leading HA meetings); and/or post-approval submissions.
$200 - $250Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Review/approve creation/modifications to Master Stability Protocols (MSP) and Study-Specific Protocols (SSP), batch-specific enrollment documentation, and LIMS stability studies. Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you.
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The Stability Senior Scientist reports to the Senior Principal Scientist or Associate Director of GBS and is responsible for end-to-end oversight of product stability programs. The Global Biologic Stability (GBS) team manages the stability programs for Bristol Myers Squibb’s commercial biologics Drug Substances and Drug Products.
$58 - $63 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The New Jersey Judiciary consists of: the Supreme Court, the Superior Court including the Appellate Division and the Trial Court of the 15 vicinages in New Jersey, the Tax Court and the Municipal Court System.
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Minimum 4 years of relevant work experience in Pharmaceutical Manufacturing System Processes (GxP) Systems environment and related Master Data Management. Develop and implement robust site Governance around E2E ERP Master Data, including defining and authoring local standardizations, SOPs, and work instructions.
$76,000 - $121,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Join us as an Outsourcing Manager/BioMarker Operations Manager and play a crucial part in advancing our clinical biomarker and bioanalytical activities. If you meet these qualifications and are eager to contribute to a dynamic team, apply now and help us advance our clinical biomarker and bioanalytical initiatives.
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Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System (e.g. TrackWise or Veeva), JMP, etc. Our client, a leading pharmaceutical company, is hiring a Stability Associate Scientist, on a contract basis.
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The Sample Management (SM) Manager, Clinical QC reports to the Associate Director of Clinical QC and will manage the daily operations of the QC Sample Management team and is r esponsible for QC SM scheduling, routine management of in-process, final product and stability samples as well as QC data throughout the sample lifecycle from receipt to disposition.
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A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility. MS) or BS degree required with relevant cGMP experience in biopharma at Client or other company.
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The Global Biologic Stability (GBS) team manages the stability programs for Client’s commercial biologics Drug Substances and Drug Products. Job Title: Manufacturing - Stability Associate Scientist. Working knowledge of biologics drug substance manufacturing and drug product filling operations and good understanding of analytical and microbiological methods.
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MS) or BS degree required with relevant cGMP experience in biopharma at COMPANY or other company. The Global Biologic Stability (GBS) team manages the stability programs for COMPANY’s commercial biologics Drug Substances and Drug Products.
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Professional Counselor License or NJ Licensed Clinical Social Worker or Marriage and Family Therapy,Professional Counselor. providing direct clinical services to youth and young adults with co-occurring behavioral health and substance use treatment needs.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.
$74,000 - $104,000 a yearExpandApply NowActive JobUpdated Today
clinical trial master file jobs Title: trial file in Somerset, NJ
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