• Supervisor Clinical Research RN Transplant

    AdventHealth (Orlando, FL)
    …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... guidelines. The Supervisor functions as a clinical study coordinator and serves to assist in the mentoring and developing of clinical study coordinators and research staff in the conduct of clinical research within the AdventHealth research enterprise at the… more
    AdventHealth (10/08/25)
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  • Medical Support Specialist EMT-P/LPN/RN (Open…

    BioLife Plasma Services (Casselberry, FL)
    …(in state of licensure) for basic IV therapy + Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist + Two years in ... a clinical or hospital setting **What Takeda can offer you:** ** ** Every day at Takeda, we feel good knowing that what we do helps improve the lives of patients with rare diseases. At BioLife, while you focus on our donors, we will support you. We offer a… more
    BioLife Plasma Services (10/08/25)
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  • Principal Therapy Development Rep - Miami/Orlando

    Medtronic (Jacksonville, FL)
    …in a manner that adheres to ethics & compliance guidelines and FDA requirements **Communication:** + Work with internal functions (marketing, customer service, ... finance, etc.) to meet targets (ie, Inventory management audits, customer service protocols, etc.) + Communicate market intelligence/competitor activity promptly, including potential sales leads, information regarding product pricing or account activity to… more
    Medtronic (10/07/25)
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  • Installed Base Specialist

    Canon USA & Affiliates (Tallahassee, FL)
    …is a remote, home office role. + Consistent with CMSU policy and FDA requirements, monitor the data integrity of multiple databases containing serialized diagnostic ... imaging equipment, peripherals and parts installed at every customer location. + Within 24 hours or less, investigate and correct (or request correction of) any discrepancy that impacts the ability to close the request and/or the timely billing. Issues are… more
    Canon USA & Affiliates (10/07/25)
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  • Director of Global Regulatory Affairs

    Danaher Corporation (New Port Richey, FL)
    …of ISO 9001 and AS9100 / CAA Part 145/CAA Part 21 standards. GMP, FDA knowledge and other ISO standards an advantage. + Good understanding of applicable regulatory ... requirements covering Food Contact, Product Compliance (Ce Marking, ATEX, ASME etc.), Product Environmental Compliance (ROHS/REACH) and airworthiness (CAA/FAA) The salary range for this role is 155,000 - 180,000. This is the range that we in good faith believe… more
    Danaher Corporation (10/07/25)
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  • Manufacturing Technician

    Mirion Technologies (Melbourne, FL)
    …environment. * Able to work overtime as required. * Experience in an ISO/ FDA /FAA work environment. * Flexible with work assignments. * Other duties as assigned ... by the team leader/manager. Must demonstrate strong decision-making and leadership skills. * Experience in handling delicate components using ESD practices. * Must have good hand and eye coordination. * AS in Electronic Technology but not required, or 2 years… more
    Mirion Technologies (10/05/25)
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  • Regional Sales Manager (Western Territory)

    Fujifilm (Tallahassee, FL)
    …+ 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** Experience: + 8+ years of progressive… more
    Fujifilm (10/04/25)
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  • MS&T Specialist II

    Teva Pharmaceuticals (Davie, FL)
    …the ANDA lots. + Participation in internal (Corporate and QA audits) and external ( FDA , MHRA) audits. + Remediation of the audit related observations (if any) and ... timely completion of the action items (if any) + Maintenance of appropriate documentation of protocols, reports and laboratory note books as required by Standard Operating Procedures (SOPs) and internal policies. + Actively participate in commercial… more
    Teva Pharmaceuticals (10/03/25)
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  • Mammography Technologist PRN

    AdventHealth (Tampa, FL)
    …questions or concerns with professionalism and compassion. Follows all MQSA, FDA , and ACR guidelines, including quality control testing, equipment performance ... checks, and documentation requirements. Collaborates with radiologists and breast imaging team to ensure accurate imaging and timely communication of results or next steps. Participates in patient tracking and follow-up processes, assisting with recalls,… more
    AdventHealth (10/03/25)
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  • Regional Catheter Supply Chain Manager

    Jabil (St. Petersburg, FL)
    …assembly. + Develop catheter supplier capabilities to meet ISO 13485 and FDA regulatory standards. + Implement supplier development plans focused on improving ... catheter quality, yield, and cost competitiveness. + Collaborate with engineering and quality teams to resolve catheter-specific technical challenges and drive continuous improvement. + Develop a Regional Commodity infrastructure that supports Jabil's business… more
    Jabil (10/02/25)
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