- Danaher Corporation (Miami, FL)
- …diagnostic tools that address the world's biggest health challenges. The Manufacturing/ Process Engineer II for Beckman Coulter Diagnostics is responsible for ... of the Manufacturing Engineering Team and report to the Manufacturing Engineering Manager responsible for providing technical support to the manufacturing lines of… more
- Kedplasma (Port Orange, FL)
- …Responsible for registering and screening donors under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice ... and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...donors. + Assists qualified donors in completing the screening process . + Assesses the self-administered health history, refers donors… more
- Kedplasma (Port Orange, FL)
- …suitability and handling donor reactions under the direction of the Center Manager , Physician Substitute Supervisor and Center Medical Director. Operates within the ... scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...suitability. + Promotes donor education of the plasma donation process to encourage a positive donor experience. + Answers… more
- MyFlorida (Arcadia, FL)
- …Regulatory Programs Standard 2 (MFRPS), Laws and Rules and Certified Food Manager certifications, as required, as implemented by the Department of Agriculture and ... in this position. NOTES: To maintain fairness and integrity in our hiring process , the use of Artificial Intelligence (AI) tools to answer qualifying questions or… more
- Highmark Health (Tallahassee, FL)
- …and testing processes in partnership with the pharmacy benefits manager . The successful candidate will possess excellent communication, analytical, and ... a fast-paced and collaborative environment. **ESSENTIAL RESPONSIBILITIES** + Monitor FDA -approvals, drug manufacturer pipelines, assess drug utilization reports, and… more
- AdventHealth (Orlando, FL)
- …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... institutional IRB approved informed consent (IC) document, according to current FDA , state, federal and institutional regulations with study candidates and/or legal… more
- Bayer (Sarasota, FL)
- …Medical Inquires in collaboration with Medical Communications; + Adherence to SOP and FDA guidance for distribution of scientific information; + Adherence to SOP and ... and collaboration with territory cross-functional stakeholders (ie Area General Manager , Area Business Unit team, Field DGOS, etc.) as...or equivalent experience is preferred; + Working knowledge of FDA , OIG requirements; + A minimum of 1 year… more
- AdventHealth (Orlando, FL)
- …in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices (ICH/GCP) ... institutional IRB approved informed consent (IC) document, according to current FDA , state, federal and institutional regulations with study candidates and/or legal… more
- Kedplasma (Orlando, FL)
- …primarily responsible for the safety and care of the donor during the plasmapheresis process under the direction of Center Manager . Operates within the scope of ... EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...safety and care of the donor during the plasmapheresis process . + Maintains alertness for donor reactions and assists… more
- Kedplasma (Pensacola, FL)
- …SUMMARY** Responsible for the day-to-day coordination and administration of the training process within the assigned plasma collection center under the direction of ... the Center Manager . Operates within the scope of EU Guidance on...scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB SUNCTIONS** Every effort has… more