Associate Director, Analytical Development
- Location: Rhode Island
- Working situation: On-Site
- Level: Associate Director
Our client is a clinical stage, global pharmaceutical company looking for an Associate Director with a passion for curing and enhancing lives of patients with degenerative diseases and being at the forefront of groundbreaking discoveries and drug development. As the Associate Director of Analytical Development, you will be a key architect in shaping the future of patients worldwide.
Associate Director, Analytical Development will:
- Develop and execute a visionary analytical development strategy aligned with our mission and goals, driving us closer to commercialization
- Define and plan out strategies for mid- to late -stage development in the drug product lifecycle
- Harness your mastery in method development, validation, HPLC, LCMS, and GC to ensure the analytical rigor of NDA products
- Leverage your proficiency in molecular biology, PCR, ELISA, and assay development to guide the implementation of advanced analytical techniques
- Lead cross-functional project teams of 4-6 to drive and execute CMC development plans
- Partner with CMC and Quality, to support cGMP manufacturing
The Associate Director - Analytical Development has the following qualifications:
- Bachelor's Degree with 10+ years of experience, OR Master's Degree with 8+ years of experience, OR Ph.D. with 5+ years of industry experience
- Experience in contributing to CMC efforts from Phase I to Phase III (desired)
- Experience with biologics and has supported or reviewed BLA submissions
Company Benefits:
- Competitive 401K program, health insurance, and HSA accounts
- LTI's offered at this level
If you are interested, please apply by clicking here.
