What are the responsibilities and job description for the Quality Systems Specialist position at Corcept Therapeutics?
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 role is a core member of the Quality Systems team and works on activities and tasks that support various Quality Systems projects. This is a supporting role that requires an adaptable and fast learner that works under the guidance and direction of Quality Systems staff across systems used to manage controlled documents, training, and quality events. This position reports to the Sr. Manager of Document Control and Training.
This is a hybrid position, requiring on-site presence 3 days per week.
Responsibilities:
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.
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 role is a core member of the Quality Systems team and works on activities and tasks that support various Quality Systems projects. This is a supporting role that requires an adaptable and fast learner that works under the guidance and direction of Quality Systems staff across systems used to manage controlled documents, training, and quality events. This position reports to the Sr. Manager of Document Control and Training.
This is a hybrid position, requiring on-site presence 3 days per week.
Responsibilities:
- Ability to promptly respond to email inquiries and user support questions using ticketing systems like Zendesk
- Support the Quality Systems team on a variety of tasks or projects that span across document control, training, inspection management and other quality event modules (including but not limited to deviations, CAPAs, and change controls)
- Assist with training attendance records and cataloging and filing activities, as well as uploading completed forms into the Learning Management System (LMS)
- 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
- Organize, file, and catalog legacy-controlled records in Document Control’s cabinets
- Assist with uploading and certifying documents into Veeva QualityDocs to align legacy processes with current ones
- Provide support for Corcept’s continuous improvement efforts of the Quality Management System (QMS)
- Identify and escalate gaps and discrepancies in controlled documents and the processes that govern them (e.g. document formatting, SOP style consistency, clear and concise wording, document change control, etc.)
- Capture detailed meeting minutes, action items, and key decisions, and circulate
- Assist in drafting internal communications for events and status reports
- Coordinate and schedule lunch and learn training sessions, office hours, and other events
- Experience with Electronic quality systems (Veeva QualityDocs and Veeva QMS) and Learning Management Systems (ComplianceWire LMS)
- 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
- BA/BS degree in a scientific/technical/engineering field
- Minimum of 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.
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.
Salary : $86,300 - $101,500