Travere Therapeutics

Senior Quality Specialist, Technical

Travere Therapeutics$95K — $124K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences or related field; preferred in Chemistry, Biology, or Chemical Engineering.
  • 5+ years of quality experience in solid oral drug and/or biologics in biotech or pharmaceutical industry.
  • 5+ years of experience in GMP Quality Assurance, Qualification/Validation of Process and/or Test Methods.
  • Knowledge of electronic Quality Management Systems; familiarity with Veeva QMS is a plus.
  • Broad knowledge of cGMPs and international regulations.

Responsibilities

  • Assist in monitoring and progressing technical documents through review workflows using the Quality Management System (Veeva).
  • Support data review for internal and external protocols and reports as required.
  • Review and electronically approve interim stability reports in the QMS.
  • Cross check regulatory submission data against approved source records to find discrepancies.
  • Develop and maintain knowledge of validation requirements and manufacturing processes for Travere products.
  • Proactively develop technical skills through training, coaching, and mentoring within the team.
  • Support QA with various technical projects as needed.

Benefits

  • Premium health and wellness offerings for employees and dependents.
  • Financial benefits including retirement plans with employer match.
  • Employee support programs and wellness initiatives.
  • Life insurance and disability coverage.
  • Generous paid time off.
Full Job Description
Department:
107100 Quality

Location:
San Diego, USA- Remote

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:
$95,000.00 - $124,000.00

*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.

About Travere Therapeutics

Travere Therapeutics is a biotechnology company that develops treatments for rare diseases. The company's products are focused on the treatment of kidney diseases, including focal segmental glomerulosclerosis (FSGS) and Alport syndrome. Travere Therapeutics was founded in 1998 and is headquartered in Alameda, California.
Learn more about Travere Therapeutics
Size
300 employees
Market Cap
$1.2 billion
Industry
Net Income
-$169.4 million
5 Year Trend
+11.2%
Revenue
$198.3 million
NASDAQ

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