- Philips (Ontario, CA)
- …areas. The role is site based in Ontario, CA - an air-conditioned FDA regulated manufacturing environment for Medical Devices and Pharmaceutical drugs (ISO 13485). ... **Your role:** + Effectively work in a high volume, fast paced FDA regulated manufacturing environment providing safety orientation and trainings to employees,… more
- Stanford Health Care (Palo Alto, CA)
- …Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved indication (off-label use) ... and coordination of community resources. + Ensures compliance with legal, regulatory and clinical policies and procedures. + Participates in quality improvement… more
- Stanford Health Care (Palo Alto, CA)
- …Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA -approved indication (off-label use) ... and coordination of community resources. + Ensures compliance with legal, regulatory and clinical policies and procedures. + Participates in quality improvement… more
- Highmark Health (Sacramento, CA)
- …responsibilities will include clinical review, assisting in navigating a complex regulatory environment, working with claims data, performing financial analyses, and ... a fast-paced and collaborative environment. **ESSENTIAL RESPONSIBILITIES** + Monitor FDA -approvals, drug manufacturer pipelines, assess drug utilization reports, and… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). **Primary Duties and Responsibilities** + ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research practices using Good… more
- Charles River Laboratories (Northridge, CA)
- …accelerate their critical programs from basic research and proof-of-concept to regulatory approval and commercialization. Utilizing this broad portfolio of products ... the development of 100% of the current commercially available FDA -approved immunocellular therapies. Our mission is to provide a...drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to… more
- Stanford Health Care (Redwood City, CA)
- …Ordering, Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA - approved indication (off-label ... and coordination of community resources. + Ensures compliance with legal, regulatory and clinical policies and procedures. + Participates in quality improvement… more
- Takeda Pharmaceuticals (Los Angeles, CA)
- …The role is essential in ensuring that all quality-related activities meet regulatory standards and uphold Takeda's commitment to excellence. The incumbent will work ... Quality Systems procedures across departments, driving consistent compliance + Ensure regulatory conformance across multiple operational areas + Identify and resolve… more
- Medtronic (Irvine, CA)
- …requirements for business continuity, operations security, cryptography, forensics, regulatory compliance, internal counter-espionage (insider threat detection and ... knowledge of cybersecurity regulations and standards specific to the medical device industry ( FDA , HIPAA, IEC 62443, NIST, NIS 2, etc.). + Drive improvements in the… more
- Abbott (Alameda, CA)
- …of clinical projects. Internally interfaces with data management, biostatistics, regulatory , clinical research associates, Finance, field clinical specialists, and ... ensure contracts are written in accordance to associated Abbott and regulatory protocols, obtain necessary approvals from senior management for clinical agreements.… more