Executive Director, Pharmaceutical Development, Small Molecule

For our client, we are seeking a Executive Director, Pharmaceutical Development, Small Molecule to join the team of a leader in the Pharmaceuticals & Biotech space.

This role will lead the strategy and execution of CMC pharmaceutical development across the product lifecycle, with a strong focus on formulation, process development, and drug product readiness. The Executive Director will collaborate closely with regulatory, clinical, manufacturing, and external partner teams to advance programs from discovery through commercialization. This is a highly visible leadership opportunity for a seasoned pharmaceutical development expert who can drive technical innovation, strengthen regulatory readiness, and support both clinical and commercial objectives.

Location: Remote - US based candidates only, no visa sponsorship available

Compensation: $247,000 – $337,000 annually

Responsibilities

• Define and execute CMC strategy for pharmaceutical development aligned with corporate objectives
• Lead formulation and drug product process development, including technology transfer and manufacturing readiness
• Support global CMC regulatory strategies in line with clinical and commercial goals
• Drive innovation and collaboration through emerging technologies and partnerships
• Enhance pharmaceutical development capabilities and regulatory readiness
• Oversee development strategies for various dosage forms, including oral and combination products
• Foster strategic relationships with CDMOs and industry partners while representing the organization externally

Qualifications

• PhD with 10 years of CMC experience, or equivalent MS/BS with 12/15 years of experience in the pharmaceutical industry
• Extensive expertise in formulation and process development for solid and liquid dosage forms
• Strong commitment to experimental work and complex problem-solving skills
• Thorough understanding of regulatory requirements, including cGxP, CMC, and ICH standards
• Proven experience authoring CMC sections of regulatory submissions such as INDs and NDAs
• Demonstrated ability to manage multiple programs from discovery to commercialization
• Recognized leader in pharmaceutical development and formulation sciences

Benefits

• Comprehensive medical, dental, and vision coverage with mental health support
• Generous paid time off policy and flexible work schedules
• 401(k) plan with competitive company match and equity awards
• Access to a Learning Institute for professional development and mentorship
• Employee resource groups and community service opportunities

Our client is an equal opportunity employer. We encourage you to apply even if you don’t meet every qualification—your background could be exactly what this team needs.