Featured Job
-
Job Removed or Not Found
Related Jobs
- Merck & Co. (Rahway, NJ)
- …of all stakeholders, building an SME network, and facilitating the use of enabling tools or technologies such as SAP. The Process Steward Team members enable the business
- Merck & Co. (Lower Gwynedd, PA)
- …PDMB Regulated Bioanalytics Department is seeking a Compliane Senior Specialist and Technical Writer team within the Late Development (AdVAnce) Vaccines bioanalytical
- Merck & Co. (Rahway, NJ)
- …Rahway based Senior Specialist, Global Development Quality Operations, is responsible for independent approval of documentation to support GMP clinical supply drug
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Provide Quality oversight of all aspects of the cell therapy clinical manufacturing process.Supervise manufacturing and manufacturing support activities for cGMP
- Merck & Co. (North Wales, PA)
- …The GPAM Senior Specialist, Value & Implementation Project Manager (VIPM), is a core member of Value & Implementation (V&I) Team, partnering with team leaders
- Merck & Co. (Lower Gwynedd, PA)
- …detailed data and in-lab process reviews to ensure integrity, accuracy, and completeness of GxP data-Participate in regulatory or internal QA audits-Monitor lab
- Merck & Co. (Lower Gwynedd, PA)
- …Data Systems Senior Scientist (P3), Regulated Bioanalytics, Integrated Logistics & Sample Management (ILSM)-Description The PDMB Regulated Bioanalytics Department is
- Legend Biotech USA, Inc. (Raritan, NJ)
- …for providing quality oversight over the validation and qualification activities for equipment, systems, computer systems, and processes within a cell therapy
- Monster (Springfield, IL)
- …JOB SUMMARY: Under general supervision, use knowledge of clinical workflow and product use in assessing incoming complaints and hazards. Assist in post-market
- Health eCareers (Memphis, TN)
- …& RequirementsSpecialty: Clinical Document Improvement SpecialistDiscipline: RNStart Date: 10/01/2025Duration: 13 weeks40 hours per weekShift: 8 hours, daysEmployment