Research Associate​/Associate Scientist – Innovative composite drug development

Position Summary

We are seeking a skilled and motivated Research Associate or Associate Scientist to join the R&D team s role focuses on supporting the discovery, optimization, process development, and evaluation of novel nanoporous silicon microparticle (NSMP)–based drug products. The position contributes to our translational efforts to develop robust, scalable, and effective product candidates aligned with CDMO practices to enable efficient technology transfer.

The ideal candidate will have a strong background in pharmaceutical formulation and chemistry, along with experience in pharmacological evaluation and hands‑on experimental execution.

• Support iterative product development by conducting chemical, analytical, and pharmacological experiments, collecting and analyzing data, and providing timely technical feedback to the R&D team.
• Prepare and maintain experimental protocols, technical reports, SOPs, and study documentation to support preclinical development and future technology transfer activities.
• Troubleshoot product performance and experimental issues through systematic investigation and clear documentation of findings.
• Operate and maintain laboratory instruments such as DLS, HPLC, and multimode microplate reader; ensure proper instrument use and high-quality data generation.
• Collaborate with cross-disciplinary teams (engineering, chemistry, pharmacology) to support research objectives and experimental execution; assist in coordinating activities with external manufacturing partners as needed.
• Maintain laboratory operations, including equipment upkeep, inventory management, and adherence to safety and quality procedures.
• Contribute to additional research and development activities aligned with the company’s mission and project needs.

• MS in Pharmaceutical Sciences, Chemistry, Materials Science, Biomedical Engineering, or a related field with relevant industry or translational research experience; or BS with substantial hands‑on industry experience.
• Hands‑on experience with drug delivery systems and laboratory‑scale formulation techniques.
• Practical experience operating analytical and laboratory instruments, including but not limited to DLS, HPLC, and multimode microplate reader.
• Demonstrated ability to independently execute complex experiments, follow study plans, and generate reliable, well‑documented data.
• Experience in troubleshooting experimental and formulation challenges using structured, methodical approaches.
• Strong written and verbal communication skills, with emphasis on accurate scientific documentation.

• Experience with cell culture techniques and in vitro pharmacological assays.
• Experience working with antibody therapeutics or ADCs.
• Exposure to preclinical drug product development workflows or IND-enabling support activities.
• Exposure to in vivo preclinical studies (e.g., DMPK, efficacy and safety in small animal models).
• Experience supporting technology transfer or scale‑up activities in collaboration with CDMOs.

• A mission‑driven environment focused on transforming drug delivery with novel particle technologies.
• The opportunity to build translationally relevant novel composite drug platforms from the ground up.
• Competitive compensation package.
• Access to specialized equipment and local academic and industry partnerships for extended analytical capabilities.

Applicants must be legally authorized to work in the United States on a full-time basis and must not require sponsorship for an employment visa.