• Regulatory Technical Writer

    Cardinal Health (Trenton, NJ)
    …for purpose of meeting objectives May act as mentor to less experienced colleagues The Regulatory Technical Writer (RTW) plays an important role in the ... Writing bring to Cardinal Health:_** Full-service product development and regulatory affairs consulting team that enables pharmaceutical, medical and biotechnology… more
    Cardinal Health (12/06/24)
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  • CQV Technical Writer / Validation…

    Sokol Materials & Services (Skillman, NJ)
    CQV Technical Writer / Validation Engineer Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1) ​ Job Type Validation Engineer ... science or engineering. + 1-3 years of experience in technical writing, with 3+ years in the pharmaceutical industry...proficiency in Microsoft Office Suite; experience with Blue Mountain Regulatory Asset Manager and Veeva Vault is a plus.… more
    Sokol Materials & Services (11/22/24)
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  • Technical eCommerce Copywriter & Editor

    Cardinal Health (Trenton, NJ)
    …OVERVIEW:** The Cardinal Health Pharma eCommerce Operations team is looking for a technical content writer , preferably with UX copywriting experience, to lead ... by the eCommerce Operations Content Supervisor. **RESPONSIBILITIES:** + Own technical eCommerce content execution and process management, including writing,… more
    Cardinal Health (12/05/24)
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  • Sr. Scientist, Medical Writing and Product…

    Cardinal Health (Trenton, NJ)
    **_What Medical Writing and Product Development ( Regulatory ) contribute to Cardinal Health_** For over four decades, our industry-trained regulatory consultants ... biotechnology, and medical device companies get their products to market. Our regulatory and product development strategies are designed to reduce the risk of… more
    Cardinal Health (11/22/24)
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  • Director, Biostatistics

    Taiho Oncology (Princeton, NJ)
    …analysis and reporting of data, and authoring/review of scientific and regulatory documents. The Director, Biostatistics will have responsibility for CRO oversight, ... for clinical trials and related activities (eg-DMC). + Writes (as primary writer or through management of biostatistician vendor) and finalizes statistical sections… more
    Taiho Oncology (12/20/24)
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  • Qualification Engineer

    Teva Pharmaceuticals (Edison, NJ)
    …provide root cause analyses and corrective/preventative actions + Act as a primary technical writer and reviewer for engineering turnover packages and design ... overseeing equipment, utility, and facility qualification activities, while providing technical expertise for complex engineering process improvement projects. Moreover… more
    Teva Pharmaceuticals (12/11/24)
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