Senior Quality Operations Lead (GMP)
Aquestive Therapeutics
Aquestive Therapeutics is seeking a Quality Assurance Lead in Portage, Indiana. This role requires oversight of manufacturing quality, adherence to GMP regulations, and expert risk management. You will lead a team ensuring compliance, managing quality operations, and working collaboratively with manufacturing and supply chain sectors. Applicants should have 7–10 years of relevant pharmaceutical manufacturing QA/QC experience, a Bachelor's degree in a related field, and strong project management capabilities. #J-18808-Ljbffr Aquestive Therapeutics
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