• Merck & Co. (North Wales, PA)
    …the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
    HireLifeScience (10/31/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionJob Description:The Associate Director, Marketing, HPV Scientific Strategy plays a critical role in supporting the HPV vaccine franchise.- The HPV ... and resources to address the opportunities.Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center… more
    HireLifeScience (11/09/24)
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  • Merck & Co. (North Wales, PA)
    …under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) organizations ... forecasting and analytical support to our Research & Development Division, Global Regulatory Affairs & Clinical Safety (GRACS), and QA organizations.Forecast… more
    HireLifeScience (11/07/24)
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  • Associate Director, CMC Regulatory

    J&J Family of Companies (Spring House, PA)
    Associate Director, CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director, CMC Regulatory ... the product and is in alignment with the strategies of global regulatory affairs , the therapeutic area, commercial, regional functions and the Quality Target… more
    J&J Family of Companies (11/07/24)
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  • Associate Principal Scientist,…

    Organon & Co. (Plymouth Meeting, PA)
    …**The Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist ( Associate ... will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and… more
    Organon & Co. (10/08/24)
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  • Associate Director, Advertising & Promotion…

    Merck (North Wales, PA)
    …Director/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
    Merck (10/31/24)
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  • Director, Global Regulatory Affairs

    Merck (Upper Gwynedd, PA)
    **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help ... drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs Liaison is responsible for development...labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice… more
    Merck (10/31/24)
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  • Senior Principal Scientist (Senior Director)…

    Merck (North Wales, PA)
    …Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation… more
    Merck (10/31/24)
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  • Supervisory Business Manager - Pharmacy

    Veterans Affairs, Veterans Health Administration (Philadelphia, PA)
    …as collecting data and tracking risk management indicators. Represents the Chief and Associate Chiefs, Pharmacy Service, in their absence or conflict in schedule, in ... assure that administrative activities follow appropriate standards and applicable regulatory entities. Financial and Resource Management: Typical duties include… more
    Veterans Affairs, Veterans Health Administration (11/06/24)
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  • Quality Assurance Specialist ( Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …resources, and much more. Posted Job Title Quality Assurance Specialist ( Regulatory ) CVPF(Center for Cellular Immunotherapy) Job Profile Title Research Coordinator ... to help with raw materials release, new hire QA Associate train. Position contingent upon funding. Qualifications + Bachelor...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
    University of Pennsylvania (10/27/24)
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  • Sr Associate , Communications

    Pfizer (Collegeville, PA)
    …digital communication boards, visuals / posters / signage, etc.). The Sr Associate will serve on cross-site projects and provide communications support related to ... operations, data management, and procurement activities. As a Sr Associate , your knowledge and skills will contribute towards the...the goals and objectives of the Pfizer Collegeville Site Affairs team. Your focus and ability to meet team… more
    Pfizer (10/30/24)
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  • Associate Director, Project Management

    Organon & Co. (Plymouth Meeting, PA)
    …and development operations across the functions (Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs ) and the drug ... of industry experience​ in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.) + At least… more
    Organon & Co. (10/30/24)
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  • Associate Director, Marketing - HPV…

    Merck (North Wales, PA)
    **Job Description** **Job Description:** The Associate Director, Marketing, HPV Scientific Strategy plays a critical role in supporting the HPV vaccine franchise. ... resources to address the opportunities. + Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center… more
    Merck (11/09/24)
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  • Associate Director, Real World Value…

    J&J Family of Companies (Horsham, PA)
    Associate Director, Real World Value and Evidence Oncology Solid Tumor - 2406221056W **Description** Johnson & Johnson is currently recruiting an Associate ... humanity. Learn more at https://www.jnj.com/. In this in-house position, the Associate Director, RWV&E, will be responsible for conducting real-world evidence… more
    J&J Family of Companies (11/06/24)
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  • Senior Specialist, Financial Planning & Analysis

    Merck (North Wales, PA)
    …under the guidance of the Associate Director who supports the Global Regulatory Affairs & Clinical Safety (GRACS) and Quality Assurance (QA) organizations ... Provide financial planning, forecasting and analytical support to ourResearch&DevelopmentDivision, Global Regulatory Affairs & Clinical Safety (GRACS), and QA… more
    Merck (11/07/24)
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  • Associate Principal Scientist, General…

    Merck (Upper Gwynedd, PA)
    …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... **Job Description** The Associate Principal Scientist, General Medicine Publications Medical Writing,...other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our… more
    Merck (11/01/24)
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  • Vpse C2l PHL Associate Director

    University of Pennsylvania (Philadelphia, PA)
    …programs and resources, and much more. Posted Job Title VPSE C2L PHL Associate Director Job Profile Title Associate Director B, Student Services, Student ... Job Description Summary Reporting to the Director of VPSE C2L-PHL, the Associate Director is responsible for leading, developing, articulating, and implementing best… more
    University of Pennsylvania (10/27/24)
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  • Associate Scientist

    Fujifilm (Warminster, PA)
    …+ Collaborate effectively with cross-functional teams, including researchers, quality control, and regulatory affairs , to meet project goals and timelines. + ... America Corporation reporting to FUJIFILM Holdings Corporation. We are hiring an Associate Scientist. The Associate Scientist will conduct protein purification… more
    Fujifilm (11/08/24)
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  • Associate Principal Scientist, Nonclinical…

    Merck (West Point, PA)
    …drug metabolism, process chemistry, analytical chemistry, manufacturing, and regulatory affairs . Other responsibilities include conducting literature/database ... **Job Description** Associate Principal Scientist to support mutagenic and non-mutagenic risk assessment activities as well as perform in silico assessments to… more
    Merck (10/01/24)
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  • Associate Director Project Management Oligo…

    WuXi AppTec (Philadelphia, PA)
    …in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC dossiers to ... support global filings for TIDES new drug applications. **Job Summary:** Responsible for managing projects within WuXi-TIDES, WuXi's API development and manufacturing division for Oligonucleotides and Peptides. Leads the orderly progression of projects from… more
    WuXi AppTec (10/18/24)
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