South San Francisco,
A hands-on position responsible for performing a wide variety of quality activities with emphasis managing a phase-appropriate quality system and QA operations in support of internal GXP activities and at contract service providers....
GMP Quality Assurance (QA) Manager with in depth experience in small molecule drug substance manufacturing. Reporting to the Director of Quality Assurance, The GMP QA Manager will provide Quality oversight and support to the Technical Operations...
We are seeking a talented and self-motivated Document Control Specialist to be responsible for administration and maintenance of the document control system that supports our quality system in compliance with good manufacturing...
DaVinci Biosciences LLC
Who we are
DaVinci Biosciences, LLC is engaged in the discovery and development of cell-based therapeutics and tools that aid in the research for treatment of human degenerative disorders. We have three business units:
• DV Biologics focuses on...
NovaBay Pharmaceuticals, Inc
- Manage Document Control and Change Control: Process controlled documentation and change orders while mentoring other departments to utilize the change control process. As the gate keeper of the controlled documents, ensure that both paper and...
Kite Pharma Inc. is an innovative, rapidly growing company located in beautiful Santa Monica, CA dedicated to the development and commercialization of new cancer immunotherapies with exciting early trial results. These therapies harness the power of...
AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott.
AbbVie Biotherapeutics (ABR) is AbbVie’s Center of Innovation in Oncology Research and Development, located in Redwood City,...
BioRestorative Therapies, Inc.
Biorestorative Therapies (BRT) develops innovative biologics, primarily involving adult stem cells. The lead therapeutic product, brtxDISC™ (Disc Implanted Stem Cells), is an autologous cell therapy for the non-surgical treatment for protruding and...
The Senior Validation Engineer will be responsible for activities related to the lifecycle of validated equipment and systems, including execution of validation, and ensuring calibration and maintenance activities meet requirements to maintain GMP...
Plans, coordinates, and executes the quality assurance program associated with creation and maintenance of GMP related change controls in Trackwise to ensure consistency with established standards, by performing the following...