- Senior
- Oficina en Waltham
Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medicines that meet significant unmet medical needs. Ardelyx has two commercial products approved in the United States, IBSRELA® (tenapanor) and XPHOZAH® (tenapanor). Ardelyx has agreements for the development and commercialization of tenapanor outside of the U.S. Kyowa Kirin commercializes PHOZEVEL® (tenapanor) for hyperphosphatemia in Japan. A New Drug Application for tenapanor for hyperphosphatemia has been approved in China with Fosun Pharma. Knight Therapeutics commercializes IBSRELA in Canada.
- Develop, maintain, and manage detailed CMC project timelines across product lifecycle phases (development, validation, technology transfer, registration, and commercial supply)
- Lead and facilitate cross-functional meetings, ensuring clear communication of priorities, risks, and deliverables
- Monitor project progress and proactively identify and mitigate risks to ensure adherence to timelines and budgets
- Lead scenario planning and “what-if” analyses to support strategic decision-making
- Act as the primary operational liaison between Technical Operations, Quality, Regulatory, Analytical, and Supply Chain teams
- Oversee change controls and resolution of technical and logistical issues by partnering with external CMOs/CDMOs to align project milestones
- Support governance and communication with senior management through regular project updates and dashboards
- Ensure alignment of CMC documentation with regulatory and quality expectations (e.g., IND / NDA submissions)
- Maintain up-to-date project documentation, decision logs, and meeting summaries
- Drive process improvement initiatives to optimize CMC workflows, document review cycles, and communication with partners
- Contribute to development of best practices, templates, and metrics within the Technical Operations organization
- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field preferred with 8 - 10 years of experience in pharmaceutical or biotech industry or equivalent experience
- 3+ years in CMC project management or related technical operations role
- Strong understanding of drug substance and/or drug product development, technology transfer, and GMP manufacturing
- Experience managing external partners (CMOs/CDMOs)
- Working knowledge of regulatory CMC requirements (FDA, ICH)
- Exceptional organizational and communication skills with ability to lead through influence
- Proficiency with project management tools (MS Project, Smartsheet, or equivalent)
- Strong problem-solving, critical thinking, and risk management skills
- Ability to thrive in a fast-paced, dynamic environment with shifting priorities