- Stanford University (Stanford, CA)
- …precision medicine in mental health and neuroimaging trials + Experience with FDA regulatory procedures and reporting + Demonstrated capacity to solve problems ... proactively and to be accountable for project tasks + Directly relevant experience, Examples include: -Coordination and execution of each component of a study, including set up, IRB submission, implementing protocols, implementing recruitment and scheduling… more
- Cordis (Irvine, CA)
- …Support company goals and objectives, policies and procedures, and FDA regulations. **Qualifications** **Qualifications** + Bachelor's degree in engineering ... (Mechanical, Biomedical, Chemical, or related field) + 8+ years related work experience, including 2+ years of previous supervisory experience, or equivalent work experience + 5+ years' experience in the medical device/pharmaceutical field or in a related… more
- Envista Holdings Corporation (Glendora, CA)
- …interpret 2D engineering drawings, particularly tight product tolerances. * Experiences in FDA regulated shop environment a plus. * Manage in-line production by ... verifying dimensions and visual product attributes through inspection (eye loupes, microscopes, etc.). * Good understanding of injection molding concepts. * Prior experience in manufacturing environment desired, particularly in a machining operation. * Good… more
- Envista Holdings Corporation (Glendora, CA)
- …in general shop floor practices, 5S, tidiness and cleanliness. * Experiences in FDA regulated shop environment a plus. * Experience with robotics or automation ... systems a plus. * Minimum High School graduate. Associate degree or technical certification grad a plus, molding background preferred. Physical Demands/Work Environment: The work environment characteristics described here are representative of those an… more
- Sunrun (Downey, CA)
- …+ Complies with local, state and federal regulatory agencies (ie OSHA, AIB, FDA , USDA, etc.) + Achieve consensus on operating plans. Provide reports and requested ... information to management as needed. + An active and strong contributor to the management team, he/she takes the lead in highlighting, developing and executing best in class solutions for our customers. + All other duties as assigned. **REQUIREMENTS… more
- Ascendis Pharma (Palo Alto, CA)
- …and global safety reporting regulatory requirements. + Expert knowledge of FDA safety regulations, ICH Guidelines, and other applicable regulatory guidance ... documents; working knowledge of global safety regulations. + Ability to travel up to 20% of the time domestically and internationally Benefits + 401(k) plan with company match + Medical, dental, and vision plans + Company-offered Life and Accidental Death &… more
- Cardinal Health (Sacramento, CA)
- …+ Review marketing materials related to customer services and FDA approved pharmaceuticals. + Review Business Associate Agreements, Confidentiality Agreements ... and Information Security Agreements **_Qualifications_** + 10+ years of experience preferred + Law firm or in-house healthcare experience preferred, including commercial transactions and fraud and abuse compliance expertise + Experience working with Group… more
- University of Southern California (Los Angeles, CA)
- …issues in a timely manner. Knowledge of regulatory requirements and guidelines (eg, FDA , EMA) related to cGMP. REQ20165292 Posted Date: 07/30/2025 - Thru date - ... cGMP Manufacturing Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP-Manufacturing-Specialized-Laboratory-Technician\_REQ20165292/apply) Keck School of Medicine Los… more
- Sumitomo Pharma (Sacramento, CA)
- …Bayesian Statistics + Good understanding and working knowledge of GCPs, ICH guidelines, FDA and other applicable country regulations is a plus + Advanced proficiency ... in BASE SAS and R, or other statistical software is advantageous + Effective verbal and writing skills **Education and Experience** + PhD or MS in statistics or biostatistics related field required. + PhD with 0-3 years or MS with 3 years related experience or… more
- Cedars-Sinai (Los Angeles, CA)
- …and local agency requirements including the Food and Drug Administration ( FDA ) and local Institutional Review Board. **Primary Job Duties and Responsibilities:** ... + May contribute content to standard sections of grant applications. + Monitors Time & Effort for accurate reporting and performs necessary funding corrections via direct cost transfer requests. + Responsible for grant close-out. + Finds opportunities for… more