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New · posted Oct 16

Corcept Therapeutics · Pharmaceuticals

Quality Systems GxP Training Specialist II

  • Redwood City, CA
  • Hybrid
  • Full-time
  • Senior & Principal
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EmploymentFull-time
Deadline

Open until filled

The role

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.

This role is a core member of the Quality Systems team and works on activities and tasks that support the GxP training program. This role requires an adaptable, self-starter that can independently assess issues and propose solutions for systems like ComplianceWire used to manage training compliance. This position reports to the Sr. Manager of Document Control and GxP Training.

This is a hybrid role that typically requires on-site presence three days per week.

What you need

Preferred Education and Experiencenice to have

  • BA/BS degree in a scientific/technical/engineering field
  • 5+ years of experience in pharmaceutical or life sciences organizations

 Applicants must be currently authorized to work in the United States on a full-time basis.

Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

Preferred Skills, Qualifications and Technical Proficienciesnice to have

  • Experience with electronic Learning Management Systems (ComplianceWire LMS and Veeva Training preferred)
  • Experience supporting GxP training programs for life sciences
  • Proficient in the use of MS Office applications (Excel, Word, Visio, Teams)
  • Excellent organizational skills and the ability to manage multiple competing tasks
  • Excellent communication skills with the ability to collaborate with a wide range of stakeholders in various departments

What you'll do

  1. Perform administrative tasks in the LMS including creation of training items or curricula, support for system enhancements, troubleshooting issues with user accounts or training access, and monitoring and sharing reports to drive training compliance
  2. Support cross-functional GxP Training Leads in strengthening training compliance using instructor led training, reports and metrics, and education on GxP training matrix
  3. Assess training qualification materials, including but not limited to SOPs and work instructions, ensuring they are appropriately added into training curricula across various GxP departments
  4. Assess existing curricula to determine if additional training items, like work instructions, should be added to support learning
  5. Support onboarding activities by working with HR, IT, and managers to identify training roles and requirements prior to making assignments in the LMS
  6. Support hiring managers in their understanding of the GxP training matrix and work with GxP Training Leads to determine if revisions are required
  7. Support supplemental training activities including on-the-job training and instructor-led training
  8. Collect and report training metrics using reporting functionality in the LMS
  9. Design dashboards to expand visibility on training compliance at the department level
  10. Identify and escalate gaps and discrepancies in the GxP training program and propose solutions for remediation
  11. Assist with training attendance records and cataloging and filing activities, as well as uploading completed forms into the Learning Management System (LMS)
  12. Assist in the implementation of new LMS enhancements or systems
  13. Capture detailed meeting minutes, action items, and key decisions
  14. Assist in drafting internal communications for events and training status reports
  15. Coordinate and schedule lunch and learn training sessions, office hours, and other supplemental training events
  16. Promptly respond to email inquiries and user support questions using ticketing systems like Zendesk

Pay

$106,200 – $124,900 a year

Employer provided
How this compares

The pay range that the Company reasonably expects to pay for this headquarters-based position is $106,200-$124,900; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Where you'll work

Redwood City, CAHybridOpen in Maps (opens in a new tab)

More jobs in Redwood City, CA
Equal opportunity, accessibility and legal noticesCorcept Therapeutics's statements, word for word

Corcept is an Equal Opportunity Employer

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Job intelligence

The context around this role

Live data · October 16, 2026

Salary intelligence

How the pay compares

This role's midpoint is 6% below the US median for Quality Assurance roles at this level.

This roleEmployer provided

$106,200 to $124,900 a year

Senior & Principal roles in California85 roles publishing pay

Middle half $117,500 to $158,500, median $135,000

Senior & Principal roles in the US285 roles publishing pay

Middle half $104,000 to $137,500, median $122,500
Annual base pay
Annual base payLowMedianHigh
This role$106,200—$124,900
California$117,500$135,000$158,500
All US$104,000$122,500$137,500

This role: Corcept Therapeutics's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 866 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $79K median239 open
  2. This role

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $123K median359 open
  3. Next step

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $154K median137 open
  4. Later

    Director

    Often: Director, Quality · Associate Director, Quality Assurance

    $209K median115 open
  5. Later

    VP & Executive

    Often: Vice President, Quality Assurance · AVP

    $306K median16 open

Skills DNA

What this role leans on

How many of the posting's 30 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 9 linesDocumentation and SOPs: 7 linesValidation and qualification: 1 lineQuality systems and risk: 1 lineData and digital systems: 2 linesCollaboration and leadership: 20 linesGMPDocumentationValidationQuality systemsData systemsTeamwork
  • Collaboration and leadership20
  • GMP and compliance9
  • Documentation and SOPs7
  • Data and digital systems2
  • Validation and qualification1
  • Quality systems and risk1

Company hiring pulse

Corcept Therapeutics on Regulatory Jobs

8
Open roles
8
Distinct roles
1
Locations

By discipline

  • Regulatory3 38%
  • Quality3 38%
  • Compliance & Safety2 25%

By level

  • Manager3 38%
  • Director2 25%
  • Senior & Principal2 25%
See all 8 Corcept Therapeutics roles

More roles at Corcept Therapeutics

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Similar Quality Assurance roles elsewhere

Quality Systems GxP Training Specialist II at Corcept Therapeutics

Open until filled. $106K–$125K a year, employer provided.

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