We’re looking for an Associate Director, Formulation Design to join our growing US team. Based in Philadelphia, you’ll play a pivotal role in shaping and delivering early development strategies for our clients, ensuring their molecules progress efficiently and effectively through the development pipeline.

The Role

Lead the implementation of our US Translational Pharmaceutics® strategy, aligned with global objectives. Oversee early development and clinical programs, ensuring seamless execution across R&D, GMP, and clinical operations. Act as a key technical leader and subject matter expert, guiding cross-functional teams and mentoring scientific staff. Collaborate closely with Business Development to support client engagement, site visits, and proposal development. Drive innovation by identifying and integrating new technologies that enhance our service offering. Manage resources effectively balancing project timelines, team capacity, and equipment utilization. Ensure scientific and regulatory excellence in all documentation, including batch records, protocols, and technical reports.

Skills and experience

A minimum of 10 years’ experience in pharmaceutical development, with a strong focus on oral solid dosage forms. Deep expertise in modified release and solubility enhancement technologies (e.g., matrix systems, functional coatings, spray drying). Proven ability to apply QbD principles and design space methodologies. Strong leadership and client-facing skills, with a track record of building high-performing teams. Experience working in a GMP-regulated environment and navigating complex program challenges. Proficiency in Microsoft Office and scientific documentation.