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.
Position Summary:
The Associate Director, Technical Operations CMC Strategyis responsible for the creation and execution of the CMC strategy for a diverse portfolio of small molecules in development, ensuring test article and study drug are developed and manufactured on time, within budget & scope.
This individual will collaborate closely with Quality, Regulatory Affairs, Clinical, and Supply Chain to ensure alignment, risk management, and successful achievement of program milestones. The successful candidate will bring substantial experience in small molecule API development and manufacturing, including an ability to drive CMC strategy for a late-stage development asset.
Responsibilities:
Provide strategic and technical leadership for technology transfer, scale-up, and cGMP manufacturing activities, ensuring timely resolution of technical issues across Phase I-III clinical and commercial products.
Oversee formulation development of current approved drugs and new drug candidates.
Manage and provide technical oversight of formulation development and cGMP manufacturing activities at contract manufacturing organizations (CMOs).
Support creation of integrated CMC development plans, timelines, budgets, risk assessments, and mitigation strategies to support clinical and commercial milestones.
Managing CMOs to develop and maintain methods for clinical/commercial production of finished dosage forms
Review and approve technical and GMP documentation, including specifications, Master Batch records, validation documents, change controls, and technical reports.
Author, edit, review, and contribute to CMC sections of regulatory submissions, responses, and health authority interactions.
Partner closely with Regulatory Affairs, Quality, Supply Chain, Clinical Operations, and Program Management to ensure alignment of CMC activities with development and commercialization goals.
Support regulatory inspections, partner audits, and ongoing compliance with applicable cGMP and global regulatory requirements.
Provide technical leadership, mentorship, and strategic guidance across Technical Operations and cross-functional teams.
Support launch readiness and commercialization planning to ensure reliable product supply.
Education/Experience Requirements:
Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related discipline required. Equivalent combination of education and applicable job experience may be considered
8+ years of relevant experience in cGMP related CMC drug development and manufacturing with emphasis on late-phase clinical development, scale-up, and commercialization
Expert knowledge and extensive CMC experience advancing small molecule APIs from process development through process characterization, PPQ, commercialization, and tech transfers in support of solid oral dosage form programs
Demonstrated leadership experience in CMC: preferably in more than one related CMC area, and drug development experience with small molecules (both oral and injectable), peptides, and biologics of varying degrees of complexity
Extensive experience managing global CMOs, third-party manufacturers, and testing labs.
Broad knowledge and experience with phase-appropriate cGMP requirements and applicable US, EU, and ICH guidelines
Demonstrated ability to prepare and review CMC sections of regulatory filings, including INDs, IMPDs, and NDAs
Manufacturing experience with oral solid dosage forms
Expert knowledge in process validation and technology transfer procedures
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 professional experience in a similar role within the pharmaceutical industry, preferably in small molecule development and manufacturing for solid oral dosage forms
Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes
Team player and strong interpersonal and organizational skills and excellent verbal and written communication skills
Excellent decision-making and collaboration skills with strong attention to detail
Six Sigma and statistical knowledge is a plus
Ability to travel 10-20% 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... For full info follow application link.
Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer
