Pharmatek Laboratories, Inc.
The Quality Assurance Associate, Document Control position is responsible for supporting quality systems to advance the development and manufacture of drug candidates, including document review and approval and support of GMP manufacturing.
KRS Global Biotechnology Inc.
The QA Director has the responsibility for managing key elements of Quality Management System and monitoring its effectiveness, through performing self-inspections, investigating customer complaints, reviewing batch records, reviewing deviation...
Sutro Biopharma, Inc.
We are seeking a professional to lead our Quality Systems (QS) group, which could potentially be expanding in scope and headcount over time. This group will be responsible for establishing/updating GMP quality systems including Supplier and...
South San Francisco,
Tricida, Inc. is an innovative development stage biopharmaceutical company, founded in 2013. We have recently closed Series C financing of $55M, thus raising $95M to complete our development program. We are focused on the discovery and development...
Neos Therapeutics (NASDAQ: NEOS) is looking for an experienced Chief Compliance Officer (“CCO”) to join our team. The CCO will be principally responsible for the development, coordination and implementation of the Company’s global ethics and...
GQR GLobal Markets
Dallas/Fort Worth Area,
Our client, a global Clinical Research Organization (CRO) is looking for a full-time office-based Clinical Research Manager. The successful candidate will play a key role in the Clinical Operations division. Our client covers a variety of...