- Globus Medical, Inc. (Redwood City, CA)
- …and reports, and validation plans and reports. Works with Quality and Regulatory Engineers for the release and submission of technical documents. + Reviews ... Bachelor's degree, 6 years with a Master's degree, or 3 years with a PhD - related experience with development or verification in the medical device industry. (class… more
- WuXi AppTec (San Diego, CA)
- …Plan, execute, and document cGMP and non-GMP/GLP laboratory work supporting regulatory submissions; Assist with Scale up (multi-kg scale) tech transfers from ... Kilo Lab and Pilot Plant scales following cGMP compliant execution of API manufacturing processes; Research and recommend new methods and alternative synthetic sequence techniques to optimize existing processes (Process R&D); Perform job-specific tasks in… more
- AbbVie (San Francisco, CA)
- …leader. Qualifications + Doctorate degree in a related scientific field required (eg PhD , PharmD, MD). + 2+ years of drug development or Business Development work ... one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs, Chemistry Manufacturing and Controls (CMC)). + Experience with… more
- NVIDIA (Santa Clara, CA)
- …ML fairness challenges. What we need to see: + You have a Master's or PhD in Computer Science, Electrical Engineering or related field or equivalent experience. + 3+ ... Experience with multimodal and/or multilingual Content Safety, legal and regulatory compliance. + Background with Robustness including Hallucinations, Digressions,… more
- The Boeing Company (El Segundo, CA)
- …and documents certification and test results to substantiate for customers and regulatory agencies that requirements are satisfied + Supports in-service products by ... experience or an equivalent combination of technical education and experience _(eg PhD +4 years' related work experience, Master+7 years' related work experience)._ +… more
- Amgen (Thousand Oaks, CA)
- …and risk mitigation plans to improve operational consistency and ensure regulatory alignment. + Support change management and long-range strategic planning to ... / GED and 12 years of project management experience **Preferred Qualifications:** + PhD , Master's degree or MBA + Experience in strategic planning, operations, and… more
- Amgen (San Francisco, CA)
- …pharmacy directors in alignment with applicable compliance, legal, and regulatory guidelines. + Understand, integrate and effectively communicate scientific/medical ... information and commercial value of products to the medical community and other key internal and external audiences. + Prioritize and work effectively in a self-directed manner in a constantly changing environment, including ability to obtain, integrate, and… more
- Cedars-Sinai (Los Angeles, CA)
- …or patient contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of ... Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. + Responsible for sample preparation and shipping and maintenance of study supplies and kits. + Maintains research practices using Good Clinical… more
- Cytel (Sacramento, CA)
- …we're looking for:** + Master's degree in statistics or a related discipline. PhD strongly desired. + 5+ years supporting clinical trials in the Pharmaceutical or ... ICH guidelines. + Solid understanding & implementation of CDISC requirement for regulatory submissions. + Adept in ADaM specifications generation and QC of datasets.… more
- UKG (Ultimate Kronos Group) (San Francisco, CA)
- …development. Ensure that AI products comply with ethical standards and regulatory requirements, advocating for transparency, fairness, and accountability in all ... AI-related initiatives. Desired Outcomes: Advance the vision and strategy of UKG's AI business by contributing distinctly to the organization's plans and driving the execution of the AI product roadmap. Establish a culture of excellence in execution and… more