- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Maintenance Technician Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift. This… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Specialist , QA Process Excellence as part of the Quality team based in Raritan, ... NJ.Role OverviewThe QA Process Excellence Specialist III role is an exempt level position with...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …quality systems and cGMP requirements.Review and approve SOPs, and other documentation .Drive continuous improvement .Have advanced computer skills to increase ... in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ.Role OverviewThe… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... position will be responsible for providing operational support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will partner… more
- Merck & Co. (Rahway, NJ)
- …Company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical , and Early Development to rapidly develop processes for diverse ... biotherapeutics and efficiently produce material to supply clinical trials. We are also responsible for commercial process development, and development and… more
- Adecco US, Inc. (Bradenton, FL)
- Adecco Healthcare & Life Sciences is assisting our client hire a Clinical Documentation Improvement Specialist in Bradenton, Florida! This role is in ... 8am to 5pm **Pay:** $64,000 to $81,000 yearly **Responsibilities of the Clinical Documentation Improvement Specialist ** . Facilitates appropriate … more
- Geisinger (Danville, PA)
- …expected risk of mortality and complexity of care of the patient. The role of the Clinical Documentation Improvement Specialist (CDIS) is to assist the ... Job Summary The Clinical Documentation Improvement Program...this position. Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement… more
- Veterans Affairs, Veterans Health Administration (Grand Junction, CO)
- …level certification is required for all positions above the journey level; however, for clinical documentation improvement specialist assignments, a ... for a mastery level certification. GRADE REQUIREMENTS Medical Records Technician ( Clinical Documentation Improvement Specialist (CDIS-Outpatient… more
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