Director, Drug Product Development

Benefits

Parental leave

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Non-birth-parent leave

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Mental health support

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Market context

U.S. role benchmark (BLS OEWS)

$116,543 U.S. median for this role

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.

Role

Role function

Engineering From the posting source

Seniority

Staff Plus From the posting source

Schedule

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Weekend work

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Application

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Assessment

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Deadline

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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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