
Director, Drug–Device CMC Reg Affairs (Autoinjector)
Merck, Honolulu, HI, United States
A leading biotechnology firm in Honolulu is seeking a Director/Principal Scientist to oversee regulatory CMC activities for autoinjectors and device-drug combinations. The successful candidate will have a minimum of 10 years of experience in relevant biological or pharmaceutical fields and demonstrate effective leadership and communication skills. Responsibilities include leading regulatory strategies and ensuring compliance across product lifecycles. A comprehensive benefits package is available, including competitive compensation and a hybrid work model.
#J-18808-Ljbffr