Description

COMPANY:At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at <a target="_blank" href="http://www.biocryst.com/">www.biocryst.com </a> or follow us on <a target="_blank" href="https://www.linkedin.com/company/biocryst-pharmaceuticals/">LinkedIn</a> and <a target="_blank" href="https://www.instagram.com/biocrystpharma/">Instagram.</a>JOB SUMMARY:<h3>The Director of Analytical Development will provide scientific and operational leadership for analytical development and extended characterization testing activities supporting BioCryst’s biologics portfolio. This role is responsible for overseeing phase‑appropriate product characterization and analytical method development, qualification, and execution at external Contract Development and Manufacturing Organizations (CDMOs) and Contract Test Laboratories (CTLs).</h3><h3></h3><h3>The Director will work cross‑functionally with Drug Substance, Drug Product, Quality, and Regulatory Affairs teams to ensure product quality, robust analytical strategies, and timely support of clinical and late‑stage development programs. This position requires strong technical expertise in biologics analytical sciences, a data‑driven mindset, and the ability to operate effectively in a fast‑paced, collaborative biotech environment.</h3>ESSENTIAL DUTIES & RESPONSIBILITIES: <ul><li>Provide scientific and operational leadership for analytical development and QC testing across biologics programs from early development through late stage and commercialization, primarily at external partners.</li><li>Lead comprehensive analytical characterization of compounds to understand molecular behavior, structure–function relationships, and potential impact on mechanism of action (MOA).</li><li>Drive interpretation and application of product quality data to define CQAs, QTPPs, control strategies, and characterization packages supporting regulatory submissions and process changes.</li><li>Lead analytical method development, qualification, technology transfer, and testing activities at CDMOs and contract test laboratories as pertains to extended characterization.</li><li>Author and review high‑quality analytical reports, technical summaries and other documentation to support product development.</li><li>Author and review analytical sections of CMC regulatory filings and communicate analytical risks, timelines, and data interpretations to internal teams and external partners.</li><li>Build and maintain strong relationships with CDMO and CTL partners, applying metrics to manage risk, prioritize work, and drive continuous improvement.</li><li>Stay current with evolving CMC and global regulatory strategies for biologics and small‑molecule programs through literature and external networking, ensuring alignment with industry best practices and regulatory expectations.</li><li>Provide mentorship, coaching, and leadership to internal and matrixed teams, contributing to a high‑performing analytical organization.</li><li>Partner with Quality and cross‑functional stakeholders to support analytical development strategies including extended characterization, reference material qualification, investigation of deviations, OOS/OOT events, and CAPAs.</li><li>Performs other duties as assigned.</li></ul>EXPERIENCE & QUALIFICATIONS:<ul><li>PhD in Chemistry, Biochemistry, or a related field with 8–12 years of experience in analytical development and QC supporting biologics programs from preclinical through late‑stage development.</li><li>BS/MS with 10–12 years of relevant industry experience in analytical laboratories supporting biologics development and manufacturing.</li><li>Strong technical expertise in analytical chemistry, biologics characterization, and data interpretation.</li><li>Demonstrated experience supporting regulatory submissions and interacting with Quality and Regulatory functions.</li><li>Proven ability to manage external partners and deliver results in a fast‑paced biotech environment.</li><li>Excellent written and verbal communication skills, including experience authoring technical reports and regulatory documentation.</li><li>Experience with method development and validation and GMP release and stability testing of biologics is a plus</li></ul>The statements in this position description are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. The manager may assign additional responsibilities and assignments from time to time. BioCryst is an equal opportunity employer and is committed to providing equal employment opportunities without regard to age, race, religion, sex, sexual orientation, gender identity, national origin, Veterans status, disability and/or other protected class characteristics. Additionally, BioCryst is committed to achieving its business objectives in compliance with all federal, state and local law.Equal Opportunity Employer/Protected Veterans/Individuals with DisabilitiesThis employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the <a target="_blank" href="https://www.eeoc.gov/poster">Know Your Rights</a> notice from the Department of Labor.

Director, Analytical Development

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BioCryst Pharmaceuticals

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