Associate Director, Antisense Oligonucleotide Analytical Development

The Associate Director, Antisense Oligonucleotide (ASO) Analytical Development will provide scientific and people leadership for analytical development activities supporting ASO drug substance and drug product programs. This role leads the development of analytical methods and control strategies, oversees cross-functional execution, and contributes to regulatory filings. The position establishes priorities, timelines, budgets, and resource plans while partnering across CMC functions and with external organizations.

The Associate Director will also build team capability, foster innovation and automation, and support portfolio and career-development goals.

The ASO Analytical Development team develops analytical methods, control strategies, and supporting data packages for ASO drug substances and drug products. The team partners with process development, Quality Control, Manufacturing Sciences, Regulatory CMC, asset teams, and external laboratories to support development programs, GMP activities, and regulatory submissions. The team emphasizes scientific rigor, innovation, collaboration, operational excellence, and talent development.

• Lead day-to-day analytical development activities for ASO drug substance and drug product programs, aligning project requirements with portfolio priorities for development and GMP support.
• Develop and implement phase-appropriate analytical methods and control strategies for the release, stability, characterization, and comparability assessment of ASO materials and products.
• Provide technical leadership for analytical strategy, method development, qualification, validation, transfer, specification setting, and lifecycle management.
• Represent Analytical Development on cross-functional CMC and asset teams, contributing to program strategy, risk assessment, planning, timelines, and decision-making.
• Author, review, and approve analytical content for regulatory submissions, technical reports, briefing packages, and responses to health authority questions.
• Collaborate with process development, Quality Control, Manufacturing Sciences, Regulatory CMC, portfolio management, and asset leadership to align analytical plans with process understanding and program needs.
• Oversee outsourced analytical work performed by contract research, development, manufacturing, and testing organizations, including review of protocols, data, reports, timelines, and technical issues.
• Manage, mentor, and develop scientists and associates, fostering inclusive teamwork, accountability, innovation, and achievement of portfolio and career-development goals.
• Develop the strategic roadmap for ASO Analytical Development, including capability building, hiring, capital investment, external services, automation, and budget planning.
• Represent the function in external consortia, technical working groups, publications, and scientific conferences to advance analytical science and help shape relevant industry and regulatory practices.

• You have a proven track record in ASO analytical development for drug substances and/or drug products, along with strong scientific judgment and people leadership.
• You have current knowledge of analytical control strategies, comparability assessments, product development, and regulatory expectations.
• You are a clear communicator and possess the ability to effectively collaborate across scientific, quality, regulatory, manufacturing, and external partner organizations.

• Ph.D. in analytical chemistry, pharmaceutical sciences, chemistry, biochemistry, chemical engineering, or a related scientific discipline with 6 or more years of relevant analytical development experience; or M.S. in a relevant scientific…