This person applies technical and regulatory compliance knowledge daily.
Flexibility in problem solving, providing direction and work hours to meet business objectives. Good verbal and written communication skills. MS Office skills; equipment...
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...
Kite Pharma, Inc. is focused on the development and commercialization of novel cancer immunotherapy products designed to harness the power of a patient’s own immune system to eradicate cancer cells. We believe our immunotherapy is a...
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...
Supports the culture of “Quality” by ensuring that the analytical methods, and validations, used to test raw materials and finished products are current and meet regulatory and internal requirements. The Scientist II will assist...
The LTS Chemist III supports the culture of “Quality” by ensuring that the analytical methods, and their validations, used to test raw materials and finished products within the QC laboratory are current and meet regulatory and...
Cook Pharmica, LLC
Primary Function: To plan, supervise and evaluate the activities of the QC Microbiology laboratory and to oversee the environmental control program and/or product testing program to ensure safe and effective products are manufactured in compliance...
Zosano Pharma, Inc.
Description and Responsibilities
• Reports to the QC Manager.
• The QC Analyst will be assigned either day shift or night shift on an as-needed basis.
• Performs sampling (analytical test samples and retains) and various analytical testing on raw...
Momenta Pharmaceuticals, Inc.
This position will help drive analytical development strategies and activities for our biosimilar / biologic products. Included in these activities will be acting as a technical resource for both internal and external organizations. This is an...
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...