Associate Director

Associate Director, Formulation Design Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients. We employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA. Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community that’s focused on innovation and are driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast. 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. Application Requirements When applying for a position with Quotient Sciences to be able to work in our organisation you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organisation. As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. Specifically we will not discriminate on the basis of race, colour, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and / or local laws. This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.