- Grifols Shared Services North America, Inc (Goldsboro, NC)
- …of operational priorities, and provides direct support to the Center Manager in driving performance, donor satisfaction, and continuous improvement. **Primary ... Responsibilities** + Serves as acting leader in the absence of the Center Manager as assigned. Maintains the ability to perform any/all tasks within the plasma… more
- Kedplasma (Greenville, NC)
- …suitability and handling donor reactions under the direction of the Center Manager , Physician Substitute Supervisor and Center Medical Director. Operates within the ... scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...and meeting(s) in a timely manner as instructed by supervisor/ manager . + Cooperate with department personnel, as well as… more
- Medtronic (Charlotte, NC)
- …in the operating room, so healthcare/surgical setting experience + Familiarity with FDA product requirements and regulatory guidelines + Experience with robotics ... 20-40% _\#MDTsurgicalOU_nowhiring #MDTSurgicalOUHiringEng_ **Qualifications - External** **Must Have: Minimum Requirements ** + Bachelors degree required + 3+ years of… more
- Fujifilm (Raleigh, NC)
- …. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements , applicable ISO 13485 standard requirements ... on systems within a service area as directed by the Area Service Manager . **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to… more
- Kedplasma (Hickory, NC)
- …Responsible for registering and screening donors under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice ... and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...and meeting(s) in a timely manner as instructed by supervisor/ manager . + Cooperate with department personnel, as well as… more
- Cambrex High Point (Durham, NC)
- …of cGMP requirements .* Strong understanding of basic lab techniques* Good understanding of FDA , EU and ICH requirements and implementation for GLP and GMP in ... workflows for drug substance and drug product. Reporting to the ( Manager , Associate Director, or Director), the Analytical Services Supervisor will provide… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager . Primary responsibilities for this position will be: perform QC analysis in ... products. + Assist in the monitoring of changes in the monographs Pharmacopoeia requirements , Regulatory agencies recommendations and implement the same in QC Lab. +… more
- ThermoFisher Scientific (Greenville, NC)
- …Position will support to the Greenville, NC, site and will report to the Sr Manager , Validation. The Drug Product Division - North America (DPD-NA) is one of the ... + Host and coordinate regulatory inspections performed by the FDA , MCA, and other regulatory agencies. + Defend policies,...workplace. Align with all job-related safety and other training requirements . + Perform other duties as assigned. **Keys to… more
- Grifols Shared Services North America, Inc (Goldsboro, NC)
- …Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. ... ** ** **Summary:** Under the direct supervision of the Quality Systems Manager , perform quality assurance and Training functions to ensure compliance with internal… more
- BioLife Plasma Services (Greensboro, NC)
- … (in state of licensure) for basic IV therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years ... customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to… more