Teams at Acadia Pharmaceuticals Inc.

Lead and support QMS activities for EU/EEA commercial product release and distribution. Oversee batch review, deviation/CAPA/change control, audits, supplier oversight, GDP compliance, data integrity, computerized systems governance, and cross-functional collaboration to ensure product quality, patient safety, and regulatory compliance.

Lead European cGMP QA operations for Acadia, overseeing CMO quality activities, batch record review and disposition, product release, audits, CAPA, change control, QMS maintenance, and regulatory compliance (Swissmedic/EMA/MHRA). Provide QA oversight for technology transfers, validations, investigations, and continuous improvement across global teams. Travel required.

Promote Acadia neuroscience products to HCPs, build territory business plans, deliver clinical and reimbursement education, secure patient access, track sales activity, collaborate cross-functionally, and represent the company at meetings and conferences.