Job Title: Drug Product Development and CMC Leader (Contract – 7 Months) Start Date: End of July/ Mid-August Duration: Until end of March 2026 Workload: Full-time (or minimum 80%) We are seeking a highly experienced Drug Product Development and CMC Leader to join our team on a contract basis. This is a unique opportunity to contribute to a late-phase small molecule development project currently transitioning from Phase 2 (capsule) to Phase 3 (tablet). You will play a key role in managing outsourced development and clinical bulk supply activities, while shaping the formulation and manufacturing strategy. Your Mission As the Drug Product (DP) Development Leader, you will: Lead the DP development and clinical supply strategy for a late-phase project. Represent CMC in the project team and align strategy, planning, and execution. Manage the CMC budget and oversee the execution of the CMC development plan. Supervise manufacturing of development and GMP batches. Evaluate formulation/process data and adjust strategies as needed. Oversee stability studies and regulatory documentation. Manage external service providers (ESPs) and ensure compliance with cGMP. Collaborate with internal Quality and Compliance teams. Support due diligence activities when required. Your Profile MSc or PhD in Chemistry, Pharmaceutical Sciences, Bio-Engineering, or equivalent experience. Minimum 10 years of experience in drug product development. Deep expertise in solid oral formulation development. Proven experience working with CROs and in cross-functional teams. Strong leadership, communication, and organizational skills. Fluent in English (written and spoken). Hands-on, pragmatic, and solution-oriented. If you're a seasoned CMC professional ready to make an impact in a dynamic, late-stage development environment, we’d love to hear from you. Apply now or reach out for more information!