Senior Quality Assurance Associate GMPGDP Auditing

Department:

Location:

Be 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 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 Senior Quality Assurance Associate GMP/GDP Auditing is responsible for executing GMP and GDP audits supporting supplier qualification compliance oversight and inspection readiness activities across Traveres external partner network. This role serves as a Quality Assurance subject matter expert for supplier audits risk assessments and external quality management ensuring compliance with applicable regulatory requirements and company standards.

The position partners closely with Technical Operations Supply Chain Regulatory Affairs Clinical Operations Pharmacovigilance and other cross-functional teams to support a robust supplier qualification and audit program.

Responsibilities:

GMP/GDP Auditing

• Conduct risk-based GMP and GDP audits of contract manufacturers testing laboratories distribution providers logistics partners and/or medical device manufacturers.
• Plan execute and document on-site remote and hybrid interna/external audits.
• Assess compliance with applicable FDA EU ICH ISO and other regulatory requirements.
• Prepare audit reports observations and risk assessments.
• Review supplier responses and evaluate corrective and preventive action (CAPA) plans.
• Track audit findings and quality actions through closure.
• Support audit schedule preparation audit metrics trending and management reporting.
• Communicate significant audit findings and compliance risks to Quality leadership and relevant cross-functional stakeholders.

Supplier Qualification & Oversight

• Perform supplier qualification requalification assessments and risk-based recommendations.
• Review supplier documentation inspection histories quality metrics and compliance records.
• Maintain supplier qualification records risk assessments and Approved Supplier Lists (ASLs).
• Monitor supplier performance quality events change notifications and assess their potential impact on product quality patient safety and regulatory compliance.
• Escalate significant quality or compliance risks as appropriate.

Quality Systems & Compliance

• Support GxP inspection readiness activities.
• Utilize electronic Quality Management Systems (e.g. Veeva Vault Quality Suite) to manage quality events and actions.
• Support the development revision and maintenance of quality procedures work instructions and related documentation.
• Participate in regulatory inspections partner audits and due diligence activities.

Continuous Improvement

• Contribute to quality system enhancements and process improvement initiatives.
• Support departmental and cross-functional quality objectives.
• Perform additional duties as assigned.

Education/Experience Requirements:

• Bachelors degree in Life Sciences Engineering Pharmacy Chemistry Biology or a related scientific discipline required. Equivalent combination of education and applicable job experience may be considered.
• 5 years of Quality Assurance experience within an FDA-regulated industry required.
• 3 years of GMP and/or GDP auditing experience.
• Experience auditing pharmaceutical biologic medical device and/or GxP service providers.
• Experience with supplier qualification supplier oversight and regulatory inspections.
• Experience with electronic Quality Management Systems; Veeva Vault Quality Suite preferred.
• Lead Auditor certification (ASQ IRCA Exemplar Global or equivalent) preferred.

Additional Skills/Experience:

• The ideal candidate will embody Traveres core values: Courage Community Spirit Patient Focus and Teamwork.
• Driven intelligent passionate about making a difference for patients with rare diseases.
• Strong knowledge of U.S. and EU GMP/GDP regulations and industry standards.
• Demonstrated ability to evaluate compliance risks and make sound risk-based decisions.
• Excellent technical writing communication and organizational skills.
• Strong attention to detail and ability to manage multiple priorities.
• Ability to work independently and collaboratively in a virtual manufacturing environment.
• Effective relationship-building skills with internal stakeholders and external partners.
• Ability to travel 25-40% domestically and internationally.
• All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote.

Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse equitable people-centric and pay-for-performance organization.

Benefits: Our benefits include premium health financial work-life and well-being offerings for eligible employees and dependents wellness and employee support programs life insurance disability retirement plans with employer match and generous paid time off.

Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock) designed to recognize retain and reward employees.

Target Base Pay Range:

*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidates experience education skills and location.

Travere will accept applications on an ongoing basis until a candidate is selected for the position.

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

If you require a reasonable accommodation to complete the application or interview process please contact us by sending an email to . Please note that this email address is to be used exclusively to request an accommodation with the online application interview or hiring process only. Travere HR will not reply to emails sent to this address for any other reason.