• Merck & Co. (North Wales, PA)
    Job DescriptionRole SummaryThe Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease ... study sites and identifies potential investigators to participate in phase II -IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects… more
    HireLifeScience (01/10/25)
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  • Manufacturing Associate II

    Insight Global (Philadelphia, PA)
    …current Good Manufacturing Practices (cGMPs). Responsibilities vary based on Manufacturing Associate level, but key responsibilities will include: Collects, ... document practices Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs) and starts to understand why behind the regulation… more
    Insight Global (01/23/25)
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  • Manufacturing Associate II

    WuXi AppTec (Philadelphia, PA)
    …products, and final product fills according to current Good Manufacturing Practices (cGMPs). **Responsibilities** **Essential Job Functions:** * Understands aseptic ... * Understands the concept of and has performed or experience with manufacturing processes and methods * Identifies and understands acceptable and unacceptable… more
    WuXi AppTec (11/26/24)
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  • QA Associate II

    Kelly Services (Malvern, PA)
    **Quality Assurance Associate II ** Montgomery Country, PA Every day, Kelly Science & Clinical connects professionals with opportunities to advance their careers. ... We are currently interviewing and hiring immediately for an experienced **Quality Assurance Associate II ** to join a global pharmaceutical, R&D, and medical… more
    Kelly Services (01/08/25)
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  • Training Associate II

    WuXi AppTec (Philadelphia, PA)
    **Overview** The Training Associate II will have the responsibility for performing a variety of tasks related to learning and development in a Good ... Manufacturing Practices (GMPs) facility. The position requires providing classroom...+ Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs) and understands 'why' behind the regulations.… more
    WuXi AppTec (01/23/25)
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  • Quality Inspector II

    Cadrex (Southampton, PA)
    …Description OVERVIEW Cadrex is searching for a Quality Inspector II to directly support site manufacturing practices through ... the production floor by assisting with interpretation and development of manufacturing related documentation and providing proper measuring techniques + Assist with… more
    Cadrex (01/17/25)
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  • Field Service Engineer I/ II - Southern

    BD (Becton, Dickinson and Company) (Trenton, NJ)
    …the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the ... and support customer base. **Qualifications:** + High School diploma required. Associate degree in electrical, mechanical or similar engineering or Biomed program… more
    BD (Becton, Dickinson and Company) (11/18/24)
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  • Training Associate I

    WuXi AppTec (Philadelphia, PA)
    **Overview** The Training Associate II will have the responsibility for performing a variety of tasks related to learning and development in a Good ... Manufacturing Practices (GMPs) facility. The position requires providing classroom...* Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs) and understands 'why' behind the regulations.… more
    WuXi AppTec (01/06/25)
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  • Oncology Regional Medical Scientific…

    Merck (North Wales, PA)
    **Job Description** **Role Summary** + The Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic ... study sites and identifies potential investigators to participate in phase II -IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects… more
    Merck (01/10/25)
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  • Quality Assurance Specialist (Regulatory)…

    University of Pennsylvania (Philadelphia, PA)
    …clinical trials in immunotherapies. Main duties include: + Review of manufacturing batch records and product release documentation under tight deadlines with ... impact on patients and clinical teams for early phase I/ II first-in-human clinical development. Verify calculations, chain of custody, and all applicable records… more
    University of Pennsylvania (12/08/24)
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