- 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 ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Valvoline Global (Lexington, KY)
- …on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory guidelines. Responsible for review and compilation of results ... and data comparison against SOP acceptance criteria, methodology, protocol, and product specifications. Write reports summarizing data, suggests improvements to work processes and test procedures, proactively communicate with formulators, peers, and managers.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …within company policies, procedures, and all applicable regulations.Key Responsibilities Review documentation for all manufacturing activities executed in accordance ... with Good Documentation Practices (GDP). Review documentation for miscellaneous activities executed in accordance with Good Documentation Practices (GDP).Work in a… more
- Applied Research Solutions (Bedford, MA)
- …prepare, review and develop acquisition reports, including statutory and regulatory acquisition report and milestone review documentations identi?ed in DoDI ... and Contract Data Requirements List (CDRLs), and other RFP products + Review acquisition documents and provide comments with programmatic perspective to ensure… more
- Formation Bio (New York, NY)
- …implement a comprehensive quality assurance strategy that ensures compliance with regulatory requirements and industry best practices to support drug development ... of risks associated with product quality. Build strong relationships with regulatory agencies and other stakeholders, representing the company's interests and… more
- Legend Biotech USA, Inc. (Philadelphia, PA)
- …from early research through IND-enabling studies and into clinical development, ensuring regulatory compliance and scientific rigor in support of our pipeline of ... AAV, lentiviral, gene editing, cell-based therapeutics), a strong understanding of regulatory requirements, and the ability to work cross-functionally in a… more
- AUROBINDO (Durham, NC)
- …with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a ... the investigations are conducted and written in compliance with all cGMP regulatory as well as facility requirements. This individual will be responsible… more
- Houston Methodist Willowbrook Hospital (Houston, TX)
- …compliance with ethical and legal business practices and accreditation/ regulatory / government regulations. PEOPLE ESSENTIAL FUNCTIONS Performs management ... competent and engaged employee group by conducting regular department meetings to review policies and procedures and operational matters, rounding on all employees,… more
- Energy Northwest (Richland, WA)
- …technologies, support progressive design/build contracts and construction efforts, interpret and review NRC (Nuclear Regulatory Commission) regulations, NEI and ... use of available Probabilistic Risk Assessment (PRA) standards and regulatory guidance, and other related PSA activities. Provide independent engineering… more
- MUSC (Charleston, SC)
- …work with the team to ensure adherence to protocol requirements and regulatory guidelines contributing to excellence in patient care, research, teaching, and ... clinical research Participates in and supports accreditation, compliance, and regulatory activities of the organization Demonstrates responsibility for professional… more
