• Spectraforce Technologies Inc (Bridgewater, NJ)
    Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ ... in Microsoft Office (Word, Excel, PowerPoint) VEEVA experience is a plus Description: The CMC Regulatory Technical Writer II authors high quality Module 2 and 3… more
    JobGet (04/20/24)
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  • Regulatory Affairs Specialist

    ConvaTec (Lexington, MA)
    …strong working relationships within RA group as well as internal/external customers. ** Regulatory Affairs Specialist work includes:** Direct submission ... The primary responsibilities of the position are to drive improvements in regulatory affairs processes, systems and infrastructure whilst supporting … more
    ConvaTec (04/06/24)
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  • Senior Regulatory Affairs

    Bausch + Lomb (Bridgewater, NJ)
    …the advancement of eye health in the future. **Objectives/Purpose of Job:** + The Regulatory Affairs Senior Specialist handles US regulatory development ... Regulatory Authorities for assigned products. + Liaise with country-specific regulatory affairs personnel for international submissions and registrations. +… more
    Bausch + Lomb (02/15/24)
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  • Sr. Specialist Regulatory

    Kedrion Biopharma, Inc. (Fort Lee, NJ)
    …Responsible for US change control assessment for assigned products. + Manage regulatory affairs activities including preparation of Annual Report, Change Control ... required, and the role will collaborate with tasks across the existing US Regulatory Affairs team Education/Experience: + BS/BA/MS degree in science. Minimum of… more
    Kedrion Biopharma, Inc. (04/02/24)
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  • Regulatory Strategist - Associate Director

    Sanofi Group (Bridgewater, NJ)
    …of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory ... pharmaceutical/biotechnology industry experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in… more
    Sanofi Group (03/07/24)
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  • Change Management Specialist

    Insight Global (Rahway, NJ)
    …largest pharmaceutical clients is looking for someone to join their Global Regulatory Affairs organization and Regulatory Information Management team ... change management initiatives, including managing a suite of documentation that supports regulatory processes and transforming this documentation with the use of the… more
    Insight Global (04/23/24)
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  • Manager, Clinical Trials & Charge Capture

    Rush University Medical Center (Chicago, IL)
    …and coding. Certifications may include Certified Professional Coder (CPC), Certified Coding Specialist (CCS) and Certified Medical Coder ( CMC ), and any other ... communicates with Revenue Cycle colleagues, study teams, patients, Office of Research Affairs , IRB, RUMC Compliance, and all partners in the Research Continuum. *… more
    Rush University Medical Center (03/07/24)
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