Director, Technical Operations; Combination Product Development

Department: 106800 Technical Operations

Location:

San Diego, USA - Remote

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.

The Director of Technical Operations (Combination Product Development) is responsible for leading device development of a combination product program from late‑stage development (Phase
3) through regulatory approval, global commercialization, and lifecycle management. This role serves as the technical lead for device development and combination product activities, building the operational infrastructure for market readiness, and ensuring alignment with design controls, regulatory requirements, quality standards, and commercial launch objectives.

This individual will operate in a highly matrixed environment and will collaborate closely with colleagues in Technical Operations, Quality, Regulatory, Supply Chain, Medical Affairs, and Commercial supporting the corporate goals for development and commercialization of a combination product for a rare disease indication.

• Lead the device program from Phase 3 through regulatory approval, commercialization, and lifecycle management
• Drive execution against key milestones including design verification and qualification, process validation (PPQ), BLA submission, and launch readiness
• Serve as the primary technical liaison between internal stakeholders and external partners and manufacturers
• Manage packaging timelines and deliverables to align with regulatory submission and commercial launch milestones; and ensure supply chain and external partners readiness for product launch
• Assess external partners such as Contract Packaging Organizations (CPOs) and Contract Manufacturing Organizations (CMOs) based on technical capability, regulatory compliance, operational readiness, scalability, and cost effectiveness
• Oversee implementation of selected CPOs and CMOs, including onboarding, readiness assessments, and operational alignment
• Ensure alignment between clinical and commercial packaging configurations and lead transition from development to commercial manufacturing, including:
  • Design transfer and process validation
  • Supply chain readiness and launch planning
  • Final product configuration and control
  • Partner with Quality to drive complaint handling and investigation as well as post‑market surveillance and medical device reporting (e.g. root cause analysis, device malfunction and safety)
  • Author and/or review global regulatory submissions for combination product (e.g. BLA with device constituent) and ensure regulatory inspections readiness (e.g. Pre‑Approval Inspections)
  • Participate in Pre‑Approval Inspections and routine audits as device SME
  • Support contract negotiations by providing technical input on scope, capabilities, and operational feasibility
  • Drive integrated risk management across drug–device interfaces; continuously update the Post‑Market Risk Management file (ISO 14971) based on real‑world complaint data and trending
  • Support continuous improvement and lifecycle management post‑approval

• M.S. or Ph.D. degree in Biomedical Engineering, Chemical Engineering, Pharmaceutical Sciences or…