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Corcept Therapeutics
Specialist II, Quality Compliance
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What they do
A Quality Assurance Auditor regularly evaluates the quality control systems in place and verifies compliance with quality and safety standards.
$57,451 / year median in California
-4% projected decline
Job Description
For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Quality Specialist II of Quality Compliance will be a core team member of the Quality Compliance department to perform day-to-day Quality operations as instructed and trained to support success of the clinical studies sponsored by Corcept. The Specialist II, Quality Compliance supports the Clinical Quality Compliance function by assisting with GCP compliance activities, vendor oversight processes, audit program administration, quality system activities, inspection readiness efforts, and continuous improvement initiatives. This role partners closely with Clinical QA, Clinical Operations, Pharmacovigilance, Biometrics, and external vendors to help maintain compliance with applicable GCP regulations, industry standards, and internal procedures. The Specialist will support the planning, coordination, execution, and follow-up of audits and quality system activities and may participate in audits under the guidance of experienced QA auditors. This is a hybrid role typically requiring on-site presence at least 3 days per week.