- HCA Healthcare (Charleston, SC)
- …quality control, handling of radiopharmaceuticals, usage of adjunctive medications, in vitro diagnostic testing, radionuclide therapy, and radiation safety. ... **What qualifications you will need:** + ARRT(N) and/or NMTCB. SCRQSA Required, BLS + Graduate of an AMA approved Nuclear Medicine Program. Nuclear Medicine Technologist may complete a one- or two year certificate program, a two year associate's degree, or a… more
- US Fertility (Westhope, ND)
- …a timely manner. + Coordinate and develop care for assigned physicians' In- Vitro Fertilization (IVF), Embryo Transfer (ET/FET), Egg Vitrification and Mock Cycle ... education including but not limited to medication teaching, resources and diagnostic testing. + Provide emotional/compassionate support to patients through their… more
- Veterans Affairs, Veterans Health Administration (San Francisco, CA)
- …providing a wide range of specialized nuclear medicine procedures, including diagnostic imaging, therapy with unsealed radioactive materials, radio-assay, in-vivo or ... in- vitro cell labeling, evaluating abnormal results; using and maintaining...System (NMIS). Perform a full range of nuclear medicine diagnostic imaging, non-imaging, in-vivo, and therapeutic procedures, including highly… more
- Teleflex (Maple Grove, MN)
- …code of federal regulations. * Understanding of the Medical Device and In Vitro Diagnostic Regulations (MDR & IVDR). * Excellent collaboration, communication, ... leadership, influencing, and presentation skills. \#LI-LM1 **Specialized Skills / Other Requirements** Teleflex, Inc. is an affirmative action & equal opportunity employer. D/V/M/F. Applicants will be considered without regard to age, race, creed, color,… more
- HP Inc. (Vancouver, WA)
- …The lab team supports an R&D organization engaged in development of novel in vitro diagnostic systems. The combined organization drives development of IVD system ... hardware, software, and assays as well as whole-system integration and performance optimization. The successful candidate will work on assignments that are highly complex in nature where a strong degree of good judgment, initiative, and scientific and… more
- Tufts Medicine (Boston, MA)
- …a myriad of cross-disciplinary approaches in its research, including: in vitro cell-based assays, intravital microscopy, flow cytometry, state-of-the-art in vivo ... research purposes. 9. Contributes to the development and validation of new diagnostic tools, treatments, and interventions. 10. Participates in the preparation of… more
- Actalent (Branford, CT)
- …Time Registered Nurse to join the team at one of the top fertility and in vitro fertilization programs in the state and nation in Branford, CT . Their mission is to ... documentation . Telephone triage and patient call-backs, prior authorizations, order diagnostic testing . Participates in the research process as appropriate,… more
- Sanofi Group (Cambridge, MA)
- …diverse team supporting the medical device, combination product, digital health and in- vitro diagnostic products within the Sanofi portfolio of products. The ... team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within Global R&D. This critical and highly visible position offers the successful candidate the opportunity to support a wide range of combination products, from pre-filled… more
- Boston University (Boston, MA)
- The position will involve working on projects aim to identify new diagnostic and prognostic biomarkers of AD because preventative and therapeutic strategies depend ... studies in experimental models. CORE DUTIES IN DETAILS: + Assist in in vitro functional studies of ncRNAs biomarker candidates in neuronal and glial cells… more
- BD (Becton, Dickinson and Company) (Warwick, RI)
- …+ Three (3) years Regulatory Affairs experience with medical devices or in vitro diagnostic devices with proven success in the preparation and completion ... of regulatory submissions (PMA, 510(k), IDE, Pre-submissions) to the FDA and other global regulatory agencies,ORFive (5) years experience with medical devices in other functions (eg, QA, R&D, etc.) with demonstrated support of regulatory submission development… more