Senior Quality Specialist, Technical

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 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 Senior Specialist, Quality Assurance Technical, will assist the Quality team with qualification/validation documents including product transfer activities supporting solid oral dose and biologic product programs to ensure quality and compliance of the Travere product(s) to the Regulatory requirements and applicable guidance.  This role works with the cross functional Travere team to ensure safe and effective products are produced by Travere’s contract vendors for use in ongoing clinical studies and through commercial operations.

Responsibilities:

• Assist and support the monitoring and progression of technical documents through structured review and approval workflows working with cross functional teams and utilizing the Quality Management System (Veeva}:
  • Protocols and Reports for validation of:
    • Manufacturing Processes
    • Test Methods
  • Change Controls related to supplier changes
  • Manufacturing and Laboratory Investigations
    • Associated CAPA and Effectiveness Checks
• Support data review for internal and external protocols, reports, and other document types where needed.
• Assist with the review and electronic QMS approval of interim stability reports.
• Cross check regulatory submission data against approved source records to identify any discrepancies. 
• Develop and maintain knowledge of validation requirements, manufacturing processes and analytical testing applicable to Travere products.
• Maintains and proactively develops technical skill sets while working with cross function team members through knowledge sharing, training, coaching, and mentoring with the goal of professional development and enhanced job performance.
• Support QA with various technical projects as needed.

 Education/Experience Requirements: 

• Bachelor’s degree in a life science or related field of study.  A relevant technical or scientific field, Chemistry, Biology, or Chemical Engineering is preferred. Equivalent combination of education and applicable job experience may be considered.
• 5+ years of experience in quality working with solid oral drug and/or biologics in the biotechnology or pharmaceutical industry. 
• 5+ years of experience in GMP Quality Assurance, Qualification/Validation of Process and/or Test Methods or other applicable Quality Systems. 
• Knowledge of electronic QMS systems, understanding of Veeva QMS is a plus.
• Broad knowledge of cGMPs (CFR/ICH) and applicable international regulations and guidelines. 

Additional Skills/Experience: 

• The ideal candidate will embody Travere’s core values: Courage, Community Spirit, Patient Focus and Teamwork.
• Driven, intelligent, passionate about making a difference for patients with rare diseases.
• Strong interpersonal and organizational skills and excellent verbal and written communication skills are required.  
• Adept problem-solving skills, a strong sense of urgency, keen attention to detail, ability to work independently and be able to effectively manage multiple priorities in an environment under time and resource pressures.
• Excellent technical writing, communication, and organizational skills.
• Strong attention to detail and ability to manage multiple priorities.
• Ability to travel 10% 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 candidate’s 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 accommodations@travere.com. 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.