• Manufacturing Associate II

    Endo International (Horsham, PA)
    …are looking for talented individuals to join our team. **Job Description Summary** The Manufacturing Associate II , Manufacturing Support Services works ... cGMP production and authors and revises SOPs and forms applicable to manufacturing and process equipment documentation. This role supports necessary production and… more
    Endo International (01/14/25)
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  • Manufacturing Associate II

    Actalent (Philadelphia, PA)
    Job Title: Manufacturing Associate II **Shift Options** -Monday - Friday 8:00am - 4:30pm - Sunday - Tuesday with alternating Wednesday: 7:00am - 5:30pm - ... Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). Responsibilities + Manufacture Master and Working Cell Banks.… more
    Actalent (01/11/25)
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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 (01/06/25)
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  • Quality Excellence Associate II

    Insight Global (Malvern, PA)
    …of our large pharmaceutical clients is looking to hire a Quality Excellence Associate to join their growing team. This individual will be leading Continuous ... technical discipline. -5 years of industry experience in a regulated manufacturing environment, preferably in biotechnology or pharmaceutical industry, is required… more
    Insight Global (01/08/25)
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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 (10/18/24)
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  • Associate Director, Cell Therapy Process…

    J&J Family of Companies (Spring House, PA)
    Johnson & Johnson is recruiting for an Associate Director, Cell Therapy Process Development based in Spring House, PA. At Johnson & Johnson, we believe health is ... all belong. We are looking for an energetic and highly motivated Associate Director candidate with demonstrated expertise in autologous cell therapy process… more
    J&J Family of Companies (01/08/25)
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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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