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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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The Candidate: Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience Master of Science in Analytical Chemistry/Pharmaceutics preferred 3 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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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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Skills and Qualifications:Bachelors Degree and enrollment in a Master of Divinity program from an accredited Seminary or Divinity School. Application should be submitted on the church's website - Summary:As the Youth and Young Adult Minister, youll serve as a vital support to the First Baptist Church of Lincoln Garden ministry focusing on pastoral care tailored specifically for children, teens, young adults, and those engaged in youth and young adult ministries.
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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. 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.
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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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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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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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The Global Biologic Stability (GBS) team manages the stability programs for Bristol Myers Squibb’s commercial biologics Drug Substances and Drug Products. MS) or BS degree required with relevant cGMP experience in biopharma at BMS or other companyStrong working knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents.
$58 - $63 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Intelligent Automation Architect will work closely with cross-functional teams to identify opportunities for automation, design and implement solutions, such as automations for Clinical trial agreements, contract management, site management relates tasks, trial master file management, to streamline/speed up tasks and ensure their effective/secure utilization, faster completion, error/cost reduction and data quality improvement.
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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.
$117,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Strong business andor technical background in the areas of Master Data Management Data Quality Data Governance Data Integration ETL SoA and Data Security. Deliver endtoend master data management projects for our customers that includes but not limited to Designing data model MDM Hub configuration.
$120,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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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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trial master file jobs Title: trial master in New Brunswick, NJ
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