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Septerna

Licenses GPCR discovery platform to pharma

Staff Scientist - Pharmaceutical Development

Bioprocess & BiomanufacturingPosted on Nov 13
Full-timeSouth San Francisco, CA, USA

About the Job

Requirements

  • A PhD, MS, or BS in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or a related field, with at least 6, 10, or 12 years of relevant industry experience in small molecule formulation development, respectively.
  • Demonstrated success delivering data-driven, risk-based formulation strategies to support preclinical research studies.
  • Experience developing small molecule formulations across multiple routes of administration, including powders, solid dosage forms, solutions, suspensions, nanoparticles, and lipid-based systems.
  • Hands-on experience with UPLC/HPLC and solid-state characterization techniques, including particle size analysis, DSC, DVS, PLM, and XRPD.
  • Working knowledge and practical application of current industry and compendial standards and regulatory authority guidance and expectations, including ICH, FDA, MHRA, and EMA guidelines and USP-NF, Ph. Eur, BP, and JP compendia.
  • Ability to manage and collaborate with external partners, including consultants and CDMOs/CROs.
  • Ability to prepare high-quality technical documentation and concisely present data to peers, management, and external groups.
  • Strong organizational and critical-thinking skills, attention to detail, and data integrity to support sound, technically driven decision-making.
  • Ability to travel domestically and internationally as needed, up to 20% of the time.

Responsibilities

  • Develop early formulation strategies and serve as a subject-matter expert to deliver fit-for-purpose formulations supporting PK, PD, efficacy, and safety preclinical studies through discovery to candidate selection across research programs.
  • Design, manage, and execute early formulation screening studies, including solubility assessments, excipient compatibility, enabling approaches, and stability, to support high-quality in vivo data.
  • Implement early formulation development and preparation workflows, tools, templates, and best practices internally and with CDMOs/CROs to support preclinical studies.
  • Represent early formulation on cross-functional research teams and present data and recommendations to ensure aligned, timely support.
  • Author and review technical documents supporting early formulation activities and preclinical studies, including development reports and study protocols.
  • Manage multiple priorities and solve problems to ensure on-time supply of formulations for preclinical studies across programs.

About the Company

Septerna

Licenses GPCR discovery platform to pharma

Septerna develops and licenses a platform called Native Complex™ that enables drug discovery on G protein-coupled receptors (GPCRs) outside of cells. The platform reproduces GPCRs with their original structure, function, and dynamics, allowing scientists to design drugs based on GPCR structures and to perform ultra-large-scale screening across the full GPCR target class. This helps unlock GPCR targets that were previously hard to study and could lead to new medicines. The company differentiates itself by offering an industrial-scale, structure-based discovery workflow specifically for GPCRs, paired with a licensing business model for pharmaceutical companies. Its goal is to expand therapeutic options by turning more GPCRs—previously considered undruggable—into viable drug targets and to bring GPCR-targeted medicines to market through licensing and partnerships.

Company size
51-200
Company stage
IPO
Headquarters
South San Francisco, CA
Founded
2022

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