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Director, Pharmaceutical Sciences

Job in Germany, Pike County, Ohio, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-02-03
Job specializations:
  • Healthcare
  • Pharmaceutical
Job Description & How to Apply Below
Location: Germany

Role Summary

Centessa Pharmaceuticals is seeking an experienced Director of Pharmaceutical Sciences to establish and lead a critical function supporting early-stage drug development. This role will provide technical expertise in physicochemical characterization, pre-formulation development, and dose formulation analysis across the portfolio. The Director will ensure robust analytical and formulation support from Candidate Selection through IND-enabling studies, bridging gaps between Non-Clinical and CMC teams to drive efficiency and compliance.

Responsibilities
  • Lead early-stage physicochemical characterization of drug candidates during Candidate Selection through IND stages.
  • Oversee pre-formulation activities to support pharmacology, DMPK, and toxicology studies.
  • Manage dose formulation analysis for non-clinical studies, ensuring accuracy and compliance with regulatory expectations.
  • Develop and implement processes for analytical verification of formulations, including stability and concentration checks for research and GLP/non-GLP toxicology studies.
  • Collaborate closely with Non-Clinical and CMC teams to optimize resource allocation and ensure timely delivery of formulation and analytical data.
  • Serve as subject matter expert for pharmaceutical sciences, advising on formulation strategies and analytical methodologies.
  • Support regulatory submissions by providing high-quality data and addressing formulation-related questions.
  • Build and maintain relationships with CDMOs and external partners to ensure best practices and scalability.
Qualifications
  • Advanced degree (Ph.D. or M.S.) in Pharmaceutical Sciences, Chemistry, or related discipline.
  • 10+ years of experience in pharmaceutical development, with a focus on analytical and formulation sciences.
  • Proven track record in early-stage drug development, including IND-enabling activities.
  • Strong understanding of dose formulation analysis, stability studies, and regulatory requirements for non-clinical and clinical phases.
  • Experience managing cross-functional teams and external vendors (CDMOs).
  • Excellent problem-solving, organizational, and communication skills.
Education
  • Advanced degree (Ph.D. or M.S.) in Pharmaceutical Sciences, Chemistry, or related discipline.
Additional Requirements
  • Remote role based in the US with approximately 15% travel.
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