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$189k

Per Year

Position range in Kansas City, MO-KS Metropolitan Statistical Area $78k

• $166k Per Year Director, Quality Assurance
• Technical
  Travere Therapeutics
  

Occupation:

Management Occupations

Location:

Kansas City, MO

• 64118
  

Job Type:

Full Time (30 Hours or More)

Posted:

07/18/2026

Positions available: 1

Source:

FileImport

• Travere Therapeutics
  

Web Site:

travere.wd1.myworkdayjobs.com

Expires:

10/31/2026

Job #:

R-100901MO

Job Requirements and Properties

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Full Time Schedule

Full Time

Job Description

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Department:

107100 Quality

Location:

San Diego, USA

• RemoteBe a part of a global team that is inspired to make a difference in the lives of people living with rare disease.

At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients.

Our work is rewarding

• both professionally and personally
• because we are making a difference. We are passionate about what we do. We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission
• to identify, develop and deliver life-changing therapies to people living with rare disease.

We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients.

Position Summary:

The Director, Quality Assurance

• Technical is responsible for providing technical quality and compliance support and/or oversight of the contract manufacturing, testing, storage and distribution, research and/or laboratory organizations.

Responsibilities:

• Lead, manage and perform critical Quality Assurance (QA) GMP functions providing oversight of GMP Contract Service Providers (CSPs) for Drug Substance and Drug Product activities/projects leading up to Phase 3 Process Validation and Commercialization. Leads validation efforts, projects, and action items including validations of:
• Process; Facilities, Utilities, Equipment (FUE); Shipping; Cleaning, Test Methods, and Computer System Validation Develop, execute, review, approve and/or oversee various aspects of a validation activities, including but not limited to:
• Master Plan (VMP) Validation Plan (VP) User Requirements Specifications (URS) Process Failure Mode and Effects Analysis (FMEA) of the process Process Characterization (PC) and Process Understanding (PU) studies Factory Acceptance Test (FAT) Site Acceptance Test (SAT) Commissioning Installation Qualification (IQ) Operational Qualification (OQ) Performance Qualification (PQ) Process Validation (PV) protocolseports Direct Support of contract manufacturing, testing, storage and distribution organizations including, but not limited to:

Change Control Deviations/Quality Events OOS/OOT investigations Corrective Actions and Preventive Actions Risk Management Vendor qualification and auditing Contractor qualification Collaborate closely with the Technical Operations Department for review and approval of CSP documentation for the above functionality. Provide technical input to Travere Polices, SOPs, Work Instructions, etc., assuring internal needs are defined while complying with Regulatory requirements, Guidance and/or industry standards. Review and approve Travere GxP related documents as requested. Ensure compliance with applicable laws, regulations and guidelines for Travere Therapeutics' contract manufacturing organizations. Participate in the project core teams and sub-teams as needed and assigned. Track progress versus timelines and goals. Additional duties assigned as needed.

Education/Experience Requirements:

Bachelor's degree in life science or related field of study required. A relevant technical or scientific field, Chemistry, Biology, or Chemical Engineering is preferred. Equivalent combination of education and applicable job experience may be considered. Master's degree preferred. 10 years of relevant experience working in an FDA regulated ...For full information see follow application link.

Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer