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Associate Director, Quality Assurance – Technical
Travere TherapeuticsAssociate Director for Quality Assurance in a biopharmaceutical company specializing in rare disease therapies. Leading analytical qualification and compliance support for product testing and validation.
Posted 7/17/2026full-timeSan Diego • California • 🇺🇸 United StatesSenior💰 $150,000 - $195,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in analytical qualification, validation, and transfer of methods for drug and biologics development, with a strong focus on GMP Quality Assurance and regulatory compliance.
Highest-signal resume keywords
Analytical QualificationAnalytical ValidationGMP Quality AssuranceCGMP KnowledgeRegulatory Submissions
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Analytical Method DevelopmentRisk AssessmentData ReviewProtocol ApprovalAnalytical Review
Soft Skills
Cross-Functional CollaborationCommunication
Industry Keywords
BiotechnologyPharmaceutical IndustryCFRICHQuality Systems
About the role
Key responsibilities & impact- Lead and support analytical qualification, validation, and transfer of analytical methods for small and large molecules
- Review, approve and/or oversee various aspects of analytical validation activities
- Serves as the primary point of contact for Travere cross functional groups and contract vendors for analytical questions
- Provide subject matter expertise in aiding risk assessment activities
- Support product(s) stability program with review and approval of protocols
- Support the analytical review of data for regulatory submissions
Requirements
What you’ll need- Bachelor’s degree in life science or related field of study required
- 8+ years of experience in an analytical function supporting drug/biologics development and commercialization in the biotechnology or pharmaceutical industry required
- Direct experience in GMP Quality Assurance, Analytical Qualification/Validation and/or Quality Systems
- Broad knowledge of cGMPs (CFR/ICH) and applicable international regulations and guidelines
Benefits
Comp & perks- 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
- generous paid time off