- Merck & Co. (Rahway, NJ)
- …#VETJOBS Required Skills: Adaptability, Adaptability, Change Control Processes, Change Management, Clinical Development, Clinical Documentation , Clinical ... E2E product development process & connectivity between functions supporting pipeline (ie clinical development, CMC, supply chain, & human health ), and balancing… more
- ALPCO (Denver, CO)
- …Applications Specialist will serve as a trusted advisor to clinical , academic, and pharmaceutical customers, functioning as both a technical problem-solver and ... research and medical diagnostic industries. Customer segments include routine clinical laboratories, biotech and pharmaceutical R&D groups, CROs, and academic… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Document Control Specialist role is an exempt level position with responsibilities...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 a QA Shop Floor Specialist II/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)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. ... for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual will be… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... KTA teams. Manages all aspects of training materials creation and documentation to ensure vendor compliance Program Compliance: Implements recommendations and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe Operations Support Specialist will be part of the Technical Operations team...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Stanford Health Care (Palo Alto, CA)
- …of America) **This is a Stanford Health Care job.** **A Brief Overview** Clinical Government Audit Analyst and Appeal Specialist II plays a critical role in ... requires strong clinical acumen, a strong understanding and application of clinical documentation standards, coding, and regulatory requirements, as well as… more
- Teleflex (Phoenix, AZ)
- Clinical Sales Specialist -Phoenix **Date:** Oct 23, 2025 **Location:** Phoenix, AZ, US **Company:** Teleflex **Expected Travel** : More than 50% **Requisition ... Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision...make a difference in patients' lives. **Position Summary** The Clinical Sales Specialist (CSS) augments the sales… more
- WesleyLife (Johnston, IA)
- …as well as the people whose lives they touch. **A Typical Day for a RN, Clinical Quality Specialist :** + You will serve the organization in a provisional status, ... Director of Health Services, Assistant Director of Health Services or MDS Clinical Resource in...and all CMS and State regulations. + Will evaluate documentation practices and assure that the clinical … more
