Bulletproof Documentation, Inc.
Bulletproof Documentation, Inc. specializes in high-quality consulting services for the pharmaceutical and medical device industries. With over 20 years of experience, Bulletproof can fulfill your needs on any project, large or small.
Bristol-Myers Squibb Company
· Provide strategic & operational direction to assure products are manufactured, tested, stored and distributed in accordance with regulatory & company standards, guides and procedures, and meet the requirements of worldwide regulatory...
The Quality Systems Specialist III will perform various duties essential to the implementation, maintenance and/or support of Avalanche’s quality systems including, but not limited to, Document Control, Training, Non-conformances, CAPAs, Change...
Passionate About Science
We’re passionate and rigorous about our science. For more than 30 years, Genentech has been at the forefront of the biotechnology industry, using innovative science to develop breakthrough medicines that improve the lives of...
Director, Quality Assurance
Location: Cambridge, MA
The Director, Quality Assurance provides strategic direction and leadership in the development, implementation and maintenance of quality assurance systems. They are primarily...
Help us advance the practice of medicine.
At Millennium Health, we beilieve our ability to attract the best people helps us transform the science of medication monitoring to improve patient safety and health care for those in need.
BioMarin Pharmaceutical Inc.
BioMarin leads the biotechnology industry in delivering therapies for chronic and degenerative genetic conditions that reduce patients' quality of life and shorten life spans. We target diseases that lack effective therapies and affect relatively...
This position is responsible for managing vendor qualification, external audits of clinical (GCP) and nonclinical (GLP) sites/service providers, and related activities from scheduling through finding resolution. In addition, this...
Corium International, Inc.
Menlo Park ,
This position is primarily responsible for Quality Assurance activities to support R&D development projects - including clinical and preclinical studies. This position will mainly be focused in supporting cGMP activities and...
Responsible for reviewing GMP documentation and ensuring that products and materials meet required quality standards. This position is responsible for the technical aspects of quality assurance as it relates to the products and...