Confirmed on the employer's own hiring board on Nov 14, 2026. First seen by Alion on Nov 11, 2026. QCS Staffing scores A on the Alion truth index.
Lead CMC programmes from development through regulatory submission, approval and implementation.Develop and maintain the integrated programme plan, critical path, milestones, budget and resource requirements.Coordinate formulation, analytical development, stability, process development, validation, manufacturing readiness and regulatory activities.Partner with Regulatory Affairs to drive submission readiness, health-authority responses and approval timelines and clear risk communication.
Experience required:
Bachelor's or advanced degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering or related discipline.Significant pharmaceutical industry experience, including leadership of complex CMC or product-development programmes.Strong understanding of pharmaceutical development, GMP, CMC requirements and global regulatory submissions.Demonstrated experience coordinating multidisciplinary teams through major development and regulatory milestones.Strong programme planning, risk management, stakeholder management and executive communication skills.
If this assignment is of interest, apply now! #LI-JS5

