- Cedars-Sinai (Los Angeles, CA)
- …compliance with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Maintains research ... field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures,… more
- University of Miami (Miami, FL)
- …to entities such as the Institutional Review Board (IRB) and the Food and Drug Administration ( FDA ). This role is essential for ensuring compliance and ... to track both currently enrolled as well as follow-up patients/participants. Maintains drug accountability records for study drugs. + Determines data to be collected… more
- Cedars-Sinai (Los Angeles, CA)
- …compliance with all federal and local agencies, including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Primary Duties ... field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures,… more
- Bayer (Cambridge, MA)
- …the Regenerative Medicine Advanced Therapy (RMAT) designation by the US Food & Drug Administration ( FDA ). The Phase 1 manuscript from this program was ... Disease and/or relevant neurologic diseases as well as thorough understanding of drug development process over different stages; + Adept strategic and global mindset… more
- Fujifilm (Holly Springs, NC)
- …qualified and validated per standards and regulatory requirements (eg, Food & Drug Administration ( FDA )) * Reads piping & instrumentation diagrams ... North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.… more
- Amgen (Cambridge, MA)
- …and chapters, and International Conference on Harmonization (ICH) / Food & Drug Administration ( FDA ) mentorship documents related to analytical method ... Provide analytical testing support to functions including but not limited to Drug Substance Technologies, Quality, and Manufacturing + Leverage latest advances in… more
- Charles River Laboratories (Wilmington, MA)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...about. **Job Summary** We are seeking an experienced nonclinical drug development professional to serve as a Senior Principal… more
- Abbott (Pleasanton, CA)
- …and product and technology projects + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... systems (hardware, electrical, mechanical and software) + Working knowledge of FDA 510(k) and/or EU MDR regulatory requirements + Program/Project Management… more
- Aerotek (St. Paul, MN)
- …(EMS), and other regulatory requirements. + Comply with US Food and Drug Administration ( FDA ) regulations and company policies. Essential Skills + ... and building or testing electronic assemblies. + Experience in GMP, ISO, and FDA -controlled environments preferred. + Ability to work both within a team and as… more
- Abbott (Pleasanton, CA)
- …lead quality system improvement activities. + Comply with US Food and Drug Administration ( FDA ) regulations, EUMDR, and other regulatory requirements and ... or an equivalent combination of education and experience. + Knowledge of FDA regulations and guidance, ISO 13485, ISO 14971, Software Standards (eg, 62304),… more