Stoke Therapeutics is seeking an Associate Director of Quality Systems to lead the QMS, drive regulatory readiness, and partner with IT for system improvements. The role demands 10+ years of biotech/pharma experience, strong GMP knowledge, and a track record in audits and inspections.
The role is hybrid in Bedford, MA, with a move to Waltham, MA, and offers a comprehensive benefits package including bonus and equity participation.
#J-18808-LjbffrQuality Systems Lead, Biotech (QMS, GMP) in bedford at Unknown Company
This position is listed as full time and hybrid.