Director, Drug Product Development
Iambic Therapeutics - San Diego HQ, San Diego, California, United States
Posted Mar 3, 2026
Benefits
- Parental leave
- Not verified
- Non-birth-parent leave
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- Family-building benefits
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- Fertility benefits: Not verified
- Adoption assistance: Not verified
- Surrogacy assistance: Not verified
- Mental health support
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- Relocation assistance
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- Childcare support
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- Learning budget
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- Verification
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- Salary
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- 401(k) match
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Market context
- Median wage (BLS OEWS)
- $116,543 national median
- Projected growth (BLS Employment Projections)
- +9.8% - Much faster than average
Matched to SOC 15-1252 - Software Engineering aggregate by role bucket.
Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.
Schedule
- Shift type
- Not verified
- Weekend work
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Application
- Cover letter
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- Assessment
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- Deadline
- Not stated
Where they hire
State eligibility is not yet verified.
About this role
Director, Drug Product Development San Diego HQ, San Diego, California, United States JOB SUMMARY Iambic Therapeutics is seeking a Director , Drug Product Development to lead formulation and process development for small molecule programs from late discovery/IND-enabling through clinical phases, with a clear path to later-stage development, global registrations, and commercialization. This role will set drug product strategy within CMC and drive execution, oversee scale-up, technology transfer, and manufacturing readiness at CDMOs, and ensure high-quality CMC documentation to support global regulatory filings. The successful candidate brings deep subject matter expertise in formulation design and process development to deliver robust, scalable, patient-centric, and cost-effective drug products from early through late phases of clinical development. This role will partner closely with Discovery, Analytical Development, Process Chemistry, Project Management, Quality, Regulatory, Clinical Pharmacology, Clinical Operations, and Supply Chain teams to align development plans, manage risk, and deliver on program timelines. This position will be on-site at our San Diego Headquarters. KEY RESPONSIBILITIES - Serve as the drug product lead in a cross-functional matrix team, defining and driving execution of formulation and manufacturing process strategies in alignment with key stakeholders to meet program objectives. - Lead small-molecule formulation design and development from late discovery through clinical stages, translating biopharmaceutic requirements into patient-centric, clinically viable dosage forms that are manufacturable, stable, and compliant with global regulatory expectations. - Partner with Chemical Process R&D on the DS-DP interface to advance APIs with optimal physicochemical properties (such as solid form, PSD/morphology, pH-solubility, and stability) into clinical development.
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