- Cedars-Sinai (Los Angeles, CA)
- …for compliance with regulatory requirements (federal and local agencies, including the Food and Drug Administration and Local Institutional Review Board) for ... the assigned study and/or clinical trial. **Primary Duties and Responsibilities:** + Submits continuations and amendments to ensure compliance with regulatory requirements and institutional polices. + Completes forms and generates reports from multiple data… more
- Cedars-Sinai (Los Angeles, CA)
- …initiatives. + Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. + ... Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality according to HIPAA regulations and applicable law. + Participates in required training and education programs. **Qualifications**… more
- Abbott (Sylmar, CA)
- …Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Performs other related duties and… more
- Abbott (Sylmar, CA)
- …Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. EDUCATION AND EXPERIENCE YOU'LL BRING Required… more
- Abbott (San Jose, CA)
- …reports, scheduling appointments, and making travel plans. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... company policies, operating procedures, processes, and task assignments. + Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Interacts with customers and assigned… more
- Abbott (Pleasanton, CA)
- …forecasts divisional and product and technology projects + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. **Required Qualifications** + Bachelor's degree in… more
- Fujifilm (Sacramento, CA)
- …with established policies and procedures. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, ... applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. **Qualifications** + Associates degree in Electrical/Mechanical Engineering or other related field with a minimum of 5 years technical or military related… more
- Fujifilm (Sacramento, CA)
- …assist out of territory whenever necessary. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, ... applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards. **Qualifications** + Bachelor's degree in related technical field or accredited NDT certification, or equivalent NDT work experience within the Oil and Gas… more
- Bio-Techne (San Marcos, CA)
- …processes, and equipment; ensure systems, utilities, and processes comply with the Food and Drug Administration (FDA) and industry standards. . Participate ... in management review meetings and/or prepare information and trending data to be shared in the meeting. . Enable positive communication channels internally and externally to ensure the highest level of customer satisfaction. . Develop, prepare, and implement… more
- Abbott (Pleasanton, CA)
- …Support audits and lead quality system improvement activities. + Comply with US Food and Drug Administration (FDA) regulations, EUMDR, and other regulatory ... requirements and Abbott policies, processes, and procedures. **Required Qualifications** + Bachelor's degree, or equivalent experience, in a scientific, technical, or engineering discipline. + Minimum 8 years of Software Development and Design Quality… more