Head of Analytical Development : NYC
Position Overview
We are seeking a Director or Senior Director of Analytical Development to lead and expand the analytical development function. This individual will play a pivotal role in supporting late-stage programs, ensuring robust analytical strategies for drug substance and drug product, and driving method development, validation, and transfer activities.
This is a hands-on leadership role for someone who thrives in a dynamic environment, enjoys rolling up their sleeves, and is committed to building best-in-class analytical capabilities. The ideal candidate will be comfortable commuting to the New York site four days per week and collaborating cross-functionally with CMC, Quality, and external partners.
Key Responsibilities
- Lead the Analytical Development team responsible for method development, qualification, validation, and transfer for drug substance and drug product.
- Develop and implement analytical strategies to support late-stage development, scale-up, and commercialization.
- Oversee characterization studies, stability programs, and specification setting in alignment with regulatory requirements.
- Partner closely with Process Development, Quality, and Regulatory teams to ensure seamless integration of analytical deliverables.
- Manage relationships with CDMOs and external testing labs, ensuring timelines and quality standards are met.
- Provide technical leadership and mentorship to a growing team, fostering a culture of scientific excellence and accountability.
- Contribute to regulatory submissions (IND, NDA) and represent Analytical Development in health authority interactions as needed.
Qualifications
Ph.D. or M.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.10+ years of experience in analytical development within the biotech or pharmaceutical industry, with a strong focus on small molecule late-stage development and commercialization.Proven track record of leadership in method development, validation, and transfer for complex modalities (biologics experience strongly preferred).Deep understanding of ICH guidelines, regulatory expectations, and CMC requirements for global filings.Excellent communication and collaboration skills; ability to work effectively in a fast-paced, matrixed environment.Willingness and ability to be onsite in New York 4 days per weekWhy Join?
Opportunity to shape analytical strategy for a late-stage pipeline with high-impact programs.Work in a well-funded biotech with strong pharma partnerships and a clear path to commercialization.Collaborative, science-driven culture where your contributions make a tangible difference.