• Director of Product Marketing, Enterprise Imaging

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... all other applicable laws, regulations, and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. Key Performance Indicators: + Revenue and sales… more
    Fujifilm (08/11/25)
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  • ENDOSCOPY Clinical Specialist or Advanced GI…

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... all other applicable laws, regulations, and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. **Qualifications:** While this position is listed as a… more
    Fujifilm (08/09/25)
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  • Clinical Research Monitoring and Auditing…

    University of Pennsylvania (Philadelphia, PA)
    …research. + Provide preparation support for inspections by external bodies such as the FDA , EMA, the NCI and CTEP. + Produced deliverables and take actions following ... centers. Additional experience in clinical research ie Data Management, Project Management, Drug Safety are a strong plus. The appropriate candidate will possess a… more
    University of Pennsylvania (08/03/25)
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  • Sr. Director Engineering-NPI

    PCI Pharma Services (Philadelphia, PA)
    …new or improvement/expansion of existing assembly and packaging processes to deliver FDA compliant production capacity on time and within budget according to ... and utilities to accommodate new equipment and meet all regulatory requirements. + This position may require overtime and/or...skills. + Lean/Six Sigma training + GAMP5 experience with drug -device assembly processes \#LI-LM1 Join us and be part… more
    PCI Pharma Services (08/02/25)
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  • Regional Director, Cardiovascular Sales…

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... all other applicable laws, regulations, and standards. **Qualifications:** Experience + 5+ years of progressive experience in the Medical Informatics Sales. + Broad functional expertise in sales and experience in the areas of sales and marketing, strategic… more
    Fujifilm (08/02/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... all other applicable laws, regulations, and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. **Qualifications:** + BA/BS or equivalent, preferably… more
    Fujifilm (07/24/25)
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  • Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …experience working in the **medical device industry** with a strong understanding of regulatory requirements ( FDA , ISO 13485, GMP) would be an advantage. + ... or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening. \#LI-9394 more
    West Pharmaceutical Services (07/18/25)
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  • Global Director, Continuous Improvement

    Catalent Pharma Solutions (Philadelphia, PA)
    …understanding of financial and business concepts. + Experience working to regulatory standards: FDA , Good Engineering Practice (GEP), Good Manufacturing ... **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving… more
    Catalent Pharma Solutions (07/08/25)
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  • Medical Director, Interventional Urology…

    Teleflex (Wayne, PA)
    …resources. * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, ... and all other international regulatory requirements with which NeoTract complies. TRAVEL REQUIRED: 35-50% (Variable) The pay range for this position at commencement… more
    Teleflex (07/08/25)
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  • Specialist, Clinical Apps - MRI

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... all other applicable laws, regulations, and standards. **Qualifications** + Experience + Minimum three (3) years clinical MR experience. + Educational requirements: + Degree from accredited Radiology Technologist Program. + Certification/Licensure: +… more
    Fujifilm (07/02/25)
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