- LifeCenter Northwest (Bellevue, WA)
- …transplant recipients. This role oversees donor safety initiatives, adverse event management , and patient safety risk reduction strategies while aligning practices ... with CMS, OPTN/UNOS, FDA , AATB and other applicable regulatory requirements and best...goals, including reducing adverse events, enhancing donor evaluation and management practices, and improving recipient outcomes. + Participate in… more
- Abbott (Columbus, OH)
- …relevant customs regulations and trade laws and regulations, including 19CFR, 15CFR, FDA , USDA, and other US regulatory agency requirements. + Operates with general ... confidential financial information and must work within the scope of attorney/ consultant and client privilege, where deemed appropriate. The proper balance between… more
- Olympus Corporation of the Americas (Westborough, MA)
- …+ Providing expertise and guidance to Olympus Engineers, Marketing, Manufacturing, and Management Project leader on Exploratory, Discovery, TRP and TDP Projects. + ... and ongoing production. + Prepares and acts as a consultant to marketing on technical brochures, training programs, and...for new and existing products. + Working knowledge of FDA requirements, including 820CFR, ISO14971, IEC60601, GMP and other… more
- Charles River Laboratories (Reno, NV)
- …assigned section to ensure effective performance. Assist the Director in department management functions as required and serve as acting department head in ... to the sites needs. + Serve as advisor to management in technical matters as they relate to the...other efforts as identified + Assist Director as a consultant to Study Directors and/or sponsors regarding study design… more
- Charles River Laboratories (Reno, NV)
- …Administration ( FDA ) standards and regulations. * May assist in management of the activities of assigned section, including supervising employees, scheduling, ... assigned section to ensure effective performance. Assist the Director in department management functions as required and serve as acting department head in… more
- Abbott (Sylmar, CA)
- …and process development from concept through sustained manufacturing of FDA regulated products. Responsible for production support, maintenance support, performing ... specifications. *Support equipment validations *Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS),… more
- HCA Healthcare (Las Vegas, NV)
- …regulatory compliance, drug utilization, clinical education and staff development, management of appropriate drug utilization, drug spend analysis, and quality ... in this role: + Provide guidance to facilities regarding JCAHO, CMS, NQSF, FDA standards, and State Board of Pharmacy Requirements. + Analyze and evaluate detailed… more
- UPMC (Pittsburgh, PA)
- …Work collaboratively with researchers holding them accountable for product, timeframes and management of their specific projects. + Routinely monitors all trials for ... compliance with FDA , UPMC and IRB compliance; promptly and effectively reports...and successful conduct of research to our patients. + Consultant to all physicians, researchers, specific work groups, and… more
- J&J Family of Companies (Titusville, NJ)
- …and the Clinical Team. Team matrix interactions may include project management , finance, legal, quality assurance, quality monitoring & compliance, clinical supplies ... unit, TA strategy, regulatory affairs, data management , medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health… more
- Cedars-Sinai (Los Angeles, CA)
- …May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all ... federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities:** +… more