Associate Principal Scientist, Long-Acting Injectable Sterile Product Development

Job Description

Overview:
The Sterile Product Development group is responsible for the development of parenteral dosage forms, including long‑acting injectables (LAIs), across small molecules, peptides, and biologics from preclinical development through commercialization. Our teams enable robust and scalable drug product and delivery solutions through deep scientific understanding of formulation, drug‑excipient interactions, delivery system performance, and manufacturing processes, ensuring product quality, safety, efficacy, and patient‑centric design.

• Serve as an LAI formulation scientist, providing scientific leadership for the design, development, and lifecycle management of long‑acting injectable drug products, including depot, sustained‑release, and controlled‑delivery parenteral dosage forms
• Lead LAI formulation and delivery development for one or more programs, including selection and optimization of release mechanisms (e.g., polymer‑based depots, suspensions, microspheres, in situ forming systems), excipient systems, and delivery approaches to meet target product profiles
• Provide technical leadership on cross‑functional program teams, ensuring alignment of formulation, drug substance properties, delivery system performance, container/closure systems, manufacturability, and clinical use considerations throughout development
• Design and interpret studies to understand and control release kinetics, stability, and performance, including:
  • Drug‑excipient and drug‑polymer interactions
  • In vitro and in vivo performance relationships
  • Physical stability, aggregation, and particle size control
  • Syringe ability, injectability, and device compatibility
• Support early‑ and late‑stage development programs, including:
  • Selection of scalable manufacturing processes for LAIs
  • Definition of formulation and process design space
  • Support for clinical and commercial process scale‑up and validation
  • Technology transfer to GMP manufacturing facilities
• Partner closely with Clinical, Non‑Clinical, Quality, Regulatory, Manufacturing, and Engineering teams to:
  • Define critical quality attributes (CQAs) and critical process parameters (CPPs) relevant to LAI performance
  • Support clinical strategy through formulation design and risk mitigation
  • Contribute to CMC regulatory submissions and health authority interactions
• Provide scientific oversight and mentoring to junior scientists on project teams, fostering capability development in LAI formulation science, experimental design, and data‑driven decision making
• Maintain awareness of emerging LAI technologies and delivery platforms, contributing to internal capability assessments, external collaborations, and innovation initiatives aligned with portfolio and organizational strategy
• Enhance our Company's professional image and competitive advantage through generation of patents, external presentations, publications, and professional organizations related to sterile product development and/or long‑acting injectables

• Ph.D. with 4+ years industry experience, or
• M.S. with 8+ years, or
• B.S. with 10+ years

in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Biochemical Engineering, Chemistry, Materials Science, or a related discipline

• Deep expertise in parenteral drug product development, with demonstrated experience in long‑acting injectable or sustained‑release formulations
• Strong scientific understanding of:
  • Controlled‑release mechanisms and LAI delivery systems
  • Drug‑polymer and drug‑excipient interactions
  • Formulation stability and performance characterization
• Experience applying Quality by Design (QbD) principles and DOE approaches to formulation and process development
• Experience supporting process scale‑up,…