• Inbound Inspector

    Fujifilm (Wayne, NJ)
    …+ Otherduties as required + 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:** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of… more
    Fujifilm (09/13/25)
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  • Assoc Endoscopic Repair Tech

    Fujifilm (Wayne, NJ)
    …safety policies and procedures. + 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. + Must follow instructions and apply to real situations in a very quick manner. + Reach monthly targets on a consistent basis. **Qualifications:** + HS Diploma or… more
    Fujifilm (09/13/25)
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  • Senior Business Analyst

    NANA Regional Corporation (Rockville, MD)
    …environment. + Agile development practices. + Prior experience with the US Food and Drug Administration (FDA) Business Analysis and regulatory process is a major ... plus. **Job ID** 2025-19142 **Work Type** Remote **Pay Range** $120,000 - $149,000 **Benefits** Regular - The company offers a comprehensive benefits program, including medical, dental, vision, life insurance, 401(k) and a range of other voluntary benefits.… more
    NANA Regional Corporation (09/13/25)
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  • Associate Project Manager-SDS

    Fujifilm (Concord, NH)
    …strategies to address challenges. + 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. + This position description contains the general duties considered necessary to outline the principal functions of the job and shall not be construed as inclusive of all… more
    Fujifilm (09/11/25)
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  • Government Operations Consultant II

    MyFlorida (Tallahassee, FL)
    …Elevator Safety - comprise a team of approximately 358 personnel fulfilling the regulatory obligations of the division throughout the state. Our Mission is to ... that must be adhered to. Analyzes all incoming plan review applications for regulatory authority and adequacy of submittal. Provides risk- based menu analysis of all… more
    MyFlorida (09/11/25)
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  • Analyst II, Network

    Fujifilm (Twinsburg, OH)
    …available help desk analysts. + 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: + 4 years of applicable experience, with a minimum of 2 years IT help desk experience. + 2 years installing and maintaining server operating… more
    Fujifilm (09/11/25)
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  • Clinical Specialist

    ConsignMed (Pittsburgh, PA)
    …industry credentialing requirements/standards. Clear and complete background investigation and drug screen, complete immunizations and pass regulatory exams. ... + Able to cover cases in local area and surrounding areas within 100 mile radius + In conjunction with Territory Sales Manager, provide case and clinical support during product evaluations to prospective customers. + Keep current on all product literature and… more
    ConsignMed (09/08/25)
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  • Principal Scientist 2 - ARD

    Cambrex High Point (High Point, NC)
    …a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (09/04/25)
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  • Clinical Training/Education Specialist

    ConsignMed (Houston, TX)
    …industry credentialing requirements/standards. Clear and complete background investigation and drug screen, complete immunizations and pass regulatory exams. ... This is a PRN/1099 role. The Clinical Specialist will do on-site support, traveling to hospitals/clinical facilities for introduction, training, and/or implementation of the device. The Clinical Specialist will work closely with physicians, nurses, educators,… more
    ConsignMed (09/03/25)
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  • Senior Scientist II, Immunosafety/Immunogenicity

    AbbVie (Worcester, MA)
    …team on project meetings, designing & coordinating IVIS studies of biologic drug candidates. + Author publication, presentations, and/or regulatory documents. ... Qualifications Qualifications + Bachelor's Degree and typically 12 years of experience OR Master's Degree and typically 10 years of experience OR PhD and typically 4 years of experience. + Ph.D. in Biological Sciences, Cellular Immunology, preferred +… more
    AbbVie (09/03/25)
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