Associate Director, Late-Stage Drug Product & Process Development
Listed on 2026-10-13
-
Pharmaceutical
Pharmaceutical Manufacturing, Regulatory Compliance Specialist, Pharma Engineer, Pharmaceutical Science/ Research
Otsuka America Pharmaceutical Inc. is seeking a senior specialist to lead late-stage drug product development from Phase 2/3 through commercial launch, overseeing formulation optimization, process validation readiness, and robustness studies.
You will drive CMC-related NDA submissions, manage tech transfer, and ensure alignment with QbD and regulatory expectations across global frameworks.
This opening is for the Associate Director, Late-Stage Drug Product & Process Development role at Otsuka America Pharmaceutical Inc.
Join Otsuka America Pharmaceutical Inc. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Associate Director, Late-Stage Drug Product & Process Development role at Otsuka America Pharmaceutical Inc., based in Dover, DE, United States.
We are looking to fill the Associate Director, Late-Stage Drug Product & Process Development position at Otsuka America Pharmaceutical Inc. in Dover, DE, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).