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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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Document Preparation: Draft, review, and file legal documents related to trust and estate matters, such as wills, trusts, powers of attorney, advance directives, and probate petitions. Court Filings: Prepare and file documents with probate courts and other relevant agencies, ensuring compliance with court rules and deadlines.
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Proven experience as a Scrum Master and Business Analyst within the financial services industry, specifically with Loan IQ systems. We are looking for a seasoned Scrum Master/Business Analyst with extensive experience in Loan IQ to facilitate the delivery of complex projects.
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Requires minimal managerial oversight and guidance from the Managing Trial Attorney (MTA) and NTD Leadership in all aspects of core duties and job responsibilities. Reporting Relationships: Managing Trial Attorney.
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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.
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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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Certification in project management (PMP), Six Sigma Black Belt, and/or RJG Master Molder. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. This position is part of the Manufacturing Engineering Department (Plastics Operations) and will be onsite in Lodi, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions.
$117,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Scientist, Clinical QC Bioanalytical will be a subject matter expert supporting method transfer/validation and routine testing of in-process, final product, and stability samples. Title: Senior Scientist, Clinical QC Bioanalytical.
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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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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.
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Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing.
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Use computer software/programs: Microsoft Office applications, SAP, LIMS, Quality Management System (e.g. TrackWise or Veeva), JMP, etc. 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.
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Our client, a leading pharmaceutical company, is hiring a Stability Associate Scientist, on a contract basis. The Global Biologic Stability (GBS) team manages the stability programs for commercial biologics Drug Substances and Drug Products.
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MS) or BS degree required with relevant cGMP experience in biopharma at Client or other company. The Global Biologic Stability (GBS) team manages the stability programs for Client’s commercial biologics Drug Substances and Drug Products.
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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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clinical trial master file jobs Title: trial master file in New Brunswick, NJ
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