- Gilead Sciences, Inc. (Foster City, CA)
- …knowledge of the drug development process and GVP, including global regulations ( FDA , EMA, ICH) and their application to cross-functional drug development. + ... Proficient in GxP Auditing with a successful track record of leading pharmacovigilance audits. + Thorough knowledge of standards, systems, policies, and procedures that enable QMS operations and compliance within the biopharma industry, specifically those… more
- Gilead Sciences, Inc. (Foster City, CA)
- …manufacturing sector and trends in that sector. + Familiarity with FDA and ICH guidelines relating to registration, quality, and compliance concerning ... drug substance, drug product, and devices. + Experience in managing organizational cross-functional initiatives and/or business operations programs. + Strategic thinking and ability to influence and constructively challenge the status quo. + Ability to manage… more
- Fujifilm (Sacramento, CA)
- …+ 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:** Baseline Qualifications: + Bachelor's Degree, Trade School Certification (Industry related), or Industry Experience Equivalent + One or more industry-specific certifications in relevant… more
- Curia (Camarillo, CA)
- …environments + Prefer knowledge of cGMP and regulatory agencies (OSHA, EPA, FDA , JP, EU, etc.) requirements Pay Range $26.44/hr. - $31.45/hr. Education, experience, ... location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to… more
- Abbott (Sylmar, CA)
- …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. + Conduct code reviews and enforce best practices in software engineering. + Mentor junior and… more
- Chipotle Mexican Grill (Newport Beach, CA)
- …professionals and professional groups such as LGMA, etc. + Familiar working with FDA , USDA, State and local agencies. + Bilingual in English/Spanish preferred + ... Proven ability to develop and implement programs that improve food safety and quality monitoring. + Ability to analyze data, perform statistical analysis, proficient in MS Office. **PAY TRANSPARENCY** A reasonable estimate of the current base pay range for… more
- Cedars-Sinai (Beverly Hills, CA)
- …research staff and ensure compliance with federal and local regulations, including FDA and IRB requirements. + Develop and implement strategies to increase patient ... enrollment, improve efficiency, train personnel, and identify new research opportunities. + Specimen and Clinical Services: + Coordinate study participant tests and procedures as required, and handle research specimens (processing, shipping, tracking). +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …strategy, and early clinical trial design. + Regulatory knowledge: Familiarity with FDA /EMA guidance for preclinical and early clinical phases. + CMC awareness: ... Understanding of drug substance/product development and manufacturing timelines. + Possess strong business acumen to align drug development and launch strategies with commercial goals, assess financial implications, and support data-driven decision-making… more
- Boehringer Ingelheim (Palm Springs, CA)
- …Manager. + Performs all Company business in accordance with all regulations (eg, EEO, FDA , DEA, OSHA, PDMA, EPA, PhRMA, etc.) and Company policy and procedures. When ... violations are noted/observed they are to be immediately reported to management. Demonstrates high ethical and professional standards with all business contacts in order to maintain BIPI's excellent reputation within the medical and pharmaceutical community. +… more
- Abbott (Alameda, CA)
- …industry and/ or quality systems are required. + Strong working knowledge of FDA Code of Federal Regulations as it applies to medical device manufacturing, including ... cGMP, ISO14971, as well as complaint handling systems. + Proven track record of managing projects from initiation to completion in a timely manner. + Strong technical writing skills and excellent oral and written communication skills Apply Now… more