- Merck & Co. (Rahway, NJ)
- …(Bulk Drug Product and Clinical Finished Goods). Responsible for authoring clinical supply documentation in support of labeling and packaging activities as ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...well as supply chain documentation to support critical CMC activities . Responsible for… more
- Merck & Co. (Rahway, NJ)
- Job Description Specialist - Prep Lab Engineer Job Description: The Enabling Facilities (EF) group within the Chemical Engineering Research & Development (CERD) ... provides a high degree of technical and project management responsibility. The Specialist -Prep Lab Engineering position will report to the Director, Engineering and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA, Document Control Specialist (1st Shift) as part of the Quality team based in Raritan, NJ. ... Role OverviewThe QA Document Control Specialist (1st shift) role is an exempt level position...within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionGlobal Clinical Supply Operations is seeking a highly motivated individual to support the clinical supply operations packaging organization; ... is responsible for providing day to day tactical direction to the team of Clinical Packaging Technicians, ensuring that business objectives are met and that a high… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Maintenance Specialist I (3rd shift) as part of the Facilities & Engineering team ... 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)
- …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist (Contractor) as part of the Technical Operations team based in Raritan, ... for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... facility equipment readiness with respect to repair, cleaning (including documentation and execution), batch execution, building housekeeping, and consumable… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Experience with Quality Assurance oversight and support for all phases of Clinical and Production documentation and processes Knowledge, Skills, and Abilities: ... is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and… more
- SSM Health (MO)
- …of nursing, PA, NP, or medical school, or Associate's degree and Certified Clinical Documentation Specialist (CCDS) certification from the Association of ... LICENSE AND/OR CERTIFICATIONS State of Work Location: Illinois + Certified Clinical Documentation Specialist (CCDS) - Association of Clinical … more
- UNC Health Care (Smithfield, NC)
- …improve the health and well-being of the unique communities we serve. Summary: The Clinical Documentation Specialist will be responsible for analyzing and ... clinical valid, complete, and compliant. In addition, the Clinical Documentation Specialist will be responsible for educating physicians, non-physician… more
