- Kelly Services (Sunnyvale, CA)
- Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a one-year contract opportunity with a leading molecular diagnostics ... Remote US (Pacific and Central Time preferred **)** **Position Title:** Regulatory Affairs Process Specialist **Position Type:** One-year contract… more
- Abbott (Pleasanton, CA)
- …mothers, female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Heart Failure ... Pleasanton, CA. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to...to appropriate team members. + Supports the product implementation process by creating database (GTS) licenses or reviewing and… more
- Amazon (Sunnyvale, CA)
- …Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best in ... product post-marketing approval requirements. * Supports the product release process . * Acts as an SME for internal and...dollar businesses and reporting to senior leadership - . Regulatory Affairs Certification (RAPS) - . Drug… more
- Abbott (Pleasanton, CA)
- …best place to work for diversity, working mothers, female executives, and scientists. This ** Regulatory Affairs Specialist ** **II** will work out of our ... personnel. + May interface directly with FDA and other regulatory agencies. + Supports the product release process...+ Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a… more
- Kelly Services (Sunnyvale, CA)
- **Senior Regulatory Affairs Specialist I** **Overview:** The Senior Regulatory Affairs Specialist I, NPD is responsible for evaluating and ... R&D, and Clinical Affairs , as part of client's global change control process . The position ensures regulatory compliance of product labeling and offers… more
- Stanford University (Stanford, CA)
- Regulatory Specialist **School of Medicine, Stanford, California, United States** Research Post Date Nov 12, 2024 Requisition # 105179 TheBlood and Marrow ... for patients worldwide. BMT-CT is seeking a Clinical Trials Regulatory II Specialist to support a very...in a dynamic research setting. + Strong knowledge of regulatory affairs , including FDA regulations, IRB review… more
- Stanford University (Stanford, CA)
- … regulatory requirements, or experience working with an IRB. . Knowledge of regulatory affairs , including FDA regulations, IRB review and approval process ... Clinical Trials Regulatory and Quality Specialist **School of...external policies. . Manage and oversee new study initiation process , including educating study staff and sponsors, resolving issues… more
- Stanford University (Stanford, CA)
- … regulatory requirements, or experience working with an IRB. + Knowledge of regulatory affairs , including FDA regulations, IRB review and approval process ... Clinical Events Committee Specialist I **School of Medicine, Stanford, California, United...compile research protocol documents and all materials required for regulatory submissions in compliance with University and external policies.… more
- Abbott (Pleasanton, CA)
- …team. In this role, you will work cross-functionally with teams in Quality, Regulatory Affairs , Research and Development, Manufacturing, and Global Supply Chain. ... colleagues serve people in more than 160 countries. **Product Stewardship Engineer / Specialist ** **Working at Abbott** At Abbott, you can do work that matters,… more