- GE Vernova (Wilmington, NC)
- …licensed nuclear configurations worldwide. This deep operating history reduces regulatory uncertainty, streamlines licensing, and supports confident adoption by ... Build and maintain relationships with key stakeholders, including industry partners, regulatory bodies, and potential clients. + Coordinate and participate in… more
- VTI Life Sciences (Raleigh, NC)
- …years Location: North Carolina, USA (On-Site) Duration: Through the end of the year + (Initial Contract ) Job Description + Past work in a CDMO or a drug product ... candidate needs to have current industry Cleaning Validation knowledge, including autoclaves, for drug products. + The candidate needs to be able to work across… more
- Actalent (Durham, NC)
- …responsible for executing and validating ELISA assays to support pharmacokinetic and anti- drug antibody analysis. This role is integral in ensuring data integrity ... and regulatory compliance within a fast-paced R&D environment. Responsibilities +...Execute established MSD-based ELISA assays for pharmacokinetic (PK) and anti- drug antibody (ADA) analysis. + Perform GLP-level assay validation… more
- GE Vernova (Wilmington, NC)
- …+ Ensure work is performed with high quality in accordance with regulatory rules and regulations, customer requirements, and business quality assurance standards. ... Experience with BWR technology and BWR Stability analysis to support applicable regulatory requirements + Knowledge of plant operational support in the Stability… more
- GE Vernova (NC)
- …applicable nuclear guidance, and industry standards. + Remain current on nuclear regulatory issues and system, component, and equipment product knowledge. + Use ... testing and qualification. + Experience in US and international nuclear regulatory affairs, licensing, laws, rules, regulations, guidance, etc. applicable to power… more
- Lilly (Greenville, NC)
- …oversee day-to-day operations and the technical agenda for a parenteral drug product process. **Key Objectives/Deliverables:** + **Support JPT Operations:** + Become ... improvement opportunities. + Model safety behaviors. **Relationships:** + Engage with contract manufacturers, Lilly TS/MS, QA, Auditing groups, and laboratories. +… more
- Cambrex High Point (Durham, NC)
- …global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
- CDM Smith (Raleigh, NC)
- …updates design requirements as necessary. Prepares technical specifications and front-end contract documents for publicly bid design projects. Reviews draft designs ... and local regulations and signs off on completed designs. Contributes to regulatory compliance programs and ensures that firm policies and practices are followed… more
- CDM Smith (Raleigh, NC)
- …budgets, and schedules. - Forecast workload and schedules. - Prepare contract documents including drawings, specifications, design documentation and criteria, cost ... and design of reinforced concrete and structural steel hydraulic structures under the regulatory authority of state and federal dam and levee safety agencies such as… more
- Fujifilm (Holly Springs, NC)
- …strategies and procedures. This role facilitates improvement initiatives, supports regulatory agency, and third-party inspections, as needed. **Company Overview** ... North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.… more