• Deerfield Beach Multi-Modality Technologist 2

    University of Miami (Deerfield Beach, FL)
    …including but not limited to: Joint Commission, AHCA, ACR, FL DOH and FDA /MQSA. + The multi-modality technologist must rotate in the department "on call" schedule ... where applicable. + Travel to UM facilities may be necessary. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. Department Specific Functions Spends a… more
    University of Miami (10/11/25)
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  • Senior Manager, Validation and Aseptic Processing

    ThermoFisher Scientific (Miami, FL)
    …corporate QMS, GMP, GxP, and relevant regulations/standards (eg, ISO 13485, MDSAP, FDA /ICH). + Partner with Operations, Engineering, MSAT, and QC on tech transfers, ... change controls, deviations, and investigations with validation impact. + Review regulatory trends; update policies/SOPs and training to maintain compliance. + _Leadership & Partner Management_ + Lead a matrixed cross-site team; provide mentoring, workload… more
    ThermoFisher Scientific (10/11/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Tallahassee, FL)
    …and perseverance to achieve results + Understanding of medical terminology, and FDA and ICH regulations/guidance documents specific to clinical research and general ... product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute to content as… more
    Sumitomo Pharma (10/11/25)
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  • Environmental Specialist III

    MyFlorida (Kissimmee, FL)
    …assurance activities to ensure that the lab is in compliance with FDA requirements. Provides and/or assists with quarterly Division evaluations of the laboratory ... for conformity with the National Shellfish Sanitation Program Model Ordinance Laboratory Checklist. Conduct non-routine laboratory work and help coordinate any special projects. Responsible for ensuring that lab has operational procedures and processes which… more
    MyFlorida (10/11/25)
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  • Clinical Quality Operations Manager- FSP

    Parexel (Tallahassee, FL)
    …be assigned as Point of Contact (POC) for a specific area of regulations (eg FDA , EMA, NMPA, etc.). As such, the Clinical Operations Manager (COM) is responsible for ... monitoring, interpreting and communicating key regulatory developments within CQO. + Collaborate with other therapeutically aligned CQOM to provide comprehensive oversight of the TA. Maintain contemporaneous awareness of filing schedules, potential future… more
    Parexel (10/11/25)
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  • Senior/Vice President, Technical (Clinical…

    Parexel (Tallahassee, FL)
    …of regulatory applications. + Previous experience with a regulatory agency (such as the FDA or MHRA) as a Senior / Master Medical Review Officer, Team Lead, etc. ... or a related medical role is required. _Depth of experience will be considered when determining the level of Senior Vice President Technical or Vice President Technical_ + Extensive Endocrinology, Neuroscience, Rare Disease, or Immunology experience is… more
    Parexel (10/11/25)
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  • Senior Regulatory Affairs Consultant - Regulatory…

    Parexel (Tallahassee, FL)
    …executing regulatory strategies for NCEs and biologics * Deep knowledge of FDA , ICH, and global regulatory frameworks * Experience with international clinical trials ... and regulatory documentation * Strong communication, leadership, and collaboration skills * Detail-oriented mindset with a proactive approach to problem-solving * Willingness to travel 15-20%, if needed, in a global work environment Why You'll Love Working… more
    Parexel (10/11/25)
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  • Credit & Collections Specialist

    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. **Qualifications** Experience: + 3+ Years Collection experience preferred. Educational requirements: + Bachelor's Degree or equivalent work experience required. Special skills or other job requirements: +… more
    Fujifilm (10/11/25)
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  • Senior Product Manager, Women's Health Marketing

    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** + Bachelor's degree required,… more
    Fujifilm (10/11/25)
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  • Associate Scientist II, QC

    Catalent Pharma Solutions (St. Petersburg, FL)
    …help train colleagues; contribute to continuous improvement within the group, comply with FDA , EPA and OSHA regulations, performing all work in a safe manner and ... maintain proper records in accordance with all SOP's and policies. Shifts: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch This position is 100% on-site at the St. Petersburg site. Catalent is committed to a Patient First… more
    Catalent Pharma Solutions (10/10/25)
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