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Corcept Therapeutics

Associate Director, Supply Chain

Reposted 7 Hours Ago
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In-Office
Redwood City, CA
175K-206K Annually
Senior level
Easy Apply
In-Office
Redwood City, CA
175K-206K Annually
Senior level
Lead and manage the global commercial supply chain infrastructure, ensuring compliance with serialization and regulatory requirements during product launches, while overseeing budgeting and performance.
The summary above was generated by AI

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators.

In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome).

Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation.

What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease.

This position will provide leadership and management in the build-out of the commercial supply chain infrastructure and operations in the US and globally. 

The ideal candidate will be experienced in EU serialization requirements and processes. This individual will provide end-to-end commercial supply chain expertise.

This is an exciting role working in a dynamic, complex, fast-paced environment during a period of significant growth and global expansion.

Responsibilities:

  • Implement serialization for Corcept’s products globally; ensure serialization and onboarding readiness for global launches
  • Assist in the set-up of new 3PL's and integration with internal processes
  • Support supply chain planning and launch of new commercial products, ensuring compliance with artwork and serialization requirements
  • Defines label requirements; controls inventory; manages shipping/receiving (including import/export), storage, and destruction
  • Generate and review documents such as work orders, contracts, purchase orders, material transfer requests, and shipping documentation
  • Works with QA to ensure supplies are prepared in accordance with the applicable global GxP regulations; supports QA vendor qualification and auditing process
  • Develop, maintain, and implement supply chain policies, procedures, techniques, standards, and systems with a focus on continuous improvement
  • Monitor and report cost, schedules, and performance of contracts, ensuring budgets and timelines are on track
  • Assist in the preparation of the department budget. Manage budgets and collaborate with Finance to address budget variance
  • Other responsibilities as defined
  • Position requires 10-15% travel

Preferred Skills, Qualifications and Technical Proficiencies:

  • Demonstrated knowledge of global pharmaceutical distribution requirements
  • Proven experience of global pharmaceutical regulatory / registration requirements
  • Ability to think strategically to anticipate risk to uninterrupted supply
  • Demonstrated skill in successful international shipments

Preferred Education and Experience:

  • Bachelor of Science degree in Life Sciences or Business (Operations Management or Supply Chain Management) or equivalent experience; Certifications in APICS CPIM or CSCP
  • 10+ years’ experience in pharmaceutical industry, 7+ years’ experience in supply chain
  • Successful experience in implementing and managing serialization for the EU
  • Successful vendor management experience

The pay range that the Company reasonably expects to pay for this headquarters-based position is $174,700 - $205,600; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

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

For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link. 

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.

 Please visit our website at: https://www.corcept.com/

Corcept is an Equal Opportunity Employer

Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview.  Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

 

Top Skills

Apics Cpim
Cscp
Eu Serialization Requirements
Gxp Regulations
Qa Regulations
Supply Chain Planning
HQ

Corcept Therapeutics Menlo Park, California, USA Office

149 Commonwealth Dr, Menlo Park, CA, United States, 94025

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