- Gilead Sciences, Inc. (Santa Monica, CA)
- …action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the ... seeking a highly motivated individual contributor to join us as a QA Specialist III within External Quality embedded within Kite's External Quality Organization. The… more
- Gilead Sciences, Inc. (Foster City, CA)
- …team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve ... together. **Job Description** **Responsibilities:** The responsibilities of the Senior QA Specialist is to maintain commercial product specifications current in all… more
- Bayer (Berkeley, CA)
- …minds to make a real difference, there's only one choice.** **Sr. Conformance Specialist - Berkeley, Ca - Hybrid** **Sr. Conformance Specialist - Berkeley, ... who possesses the following: **REQUIRED QUALIFICATIONS** + Bachelor's Degree in a scientific or technical field, preferably biological sciences or engineering; + The… more
- Cedars-Sinai (Los Angeles, CA)
- …Review Board (IRB). Primary Duties and Responsibilities + Provides research writing activities such as developing scientific documents for abstracts, ... are NOT available for this position at this time. The Clinical Research Specialist II provides clinical research expertise by participating in the design and… more
- Stanford University (Stanford, CA)
- Regulatory Specialist (Hybrid Opportunity) **School of Medicine, Stanford, California, United States** Research Post Date Nov 19, 2025 Requisition # 107768 The Blood ... and Cellular Therapy (BMT-CT) Divisionis seeking a Clinical Trials Regulatory Specialist II position to support a very active clinical trials faculty.… more
- Kelly Services (Irvine, CA)
- We are seeking to identify a skilled **QA Validation Specialist (Contract)** to join a leading pharmaceutical team supporting critical **cGMP qualification and ... knowledge of cGMP and regulatory standards for validation. + Experience in writing and reviewing SOPs, GMPs, governmental regulations and/or protocols for accuracy,… more
- Abbott (Pleasanton, CA)
- …from routine fingersticks. **WHAT YOU'LL DO** We are recruiting for a **Regulatory Affairs Specialist II** to join our team in the Pleasanton, CA location. In this ... is preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. + Experience with Regulatory… more
- Parexel (Sacramento, CA)
- …development process, and industry guidelines and regulations, eg, ICH-GCP. + Extensive clinical/ scientific writing skills. + Scientific background essential; ... to come to a consensus. + Supervise collection of documentation by Medical Writing Support Coordinator, Document Specialist , and/or Associate Medical Writer for… more
- Parexel (Sacramento, CA)
- …as applicable) and liaising with the client, as require + Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality + ... **Medical monitoring (as applicable)** + Answering day to day medical and scientific questions, provide daily medical support to Parexel staff or site… more
- Philips (San Diego, CA)
- …product line at luminary sites in North America. + Will be the expert MRI specialist in an assigned technical or clinical application area, build a network in the ... scientific community and report and advise about new insights...experience are strongly desired. + You have proven experience writing and overseeing research grants. You have proven experience… more