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Associate Director, GLP/GCP Quality Audits and Compliance at Acadia Pharmaceuticals Inc. - ApplyBlast

Associate Director, GLP/GCP Quality Audits and Compliance

Acadia Pharmaceuticals Inc.

9 months ago

Princeton, New Jersey, United States

Hybrid

Full Time

Director

2 applicants

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About this role

The Associate Director, GLP/GCP Quality Audits and Compliance at Acadia leads the planning and execution of internal and external GLP/GCP audits to ensure data integrity and regulatory readiness across nonclinical and clinical programs. The role partners with internal teams and contract service providers to maintain inspection-ready operations and drive continuous improvement in quality systems. This position serves as a subject matter expert on GLP/GCP compliance and supports regulatory inspections and quality oversight.

Skills

Qualifications

Bachelor's Degree in Life SciencesSQA CertificationASQ CertificationECA Academy CertificationEuropean Lead Auditor

About Acadia Pharmaceuticals Inc.

acadia.com

Headquarters

San Diego, California, United States

Company Size

501-1000 employees

Founded

1993

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Acadia Pharmaceuticals is a biopharmaceutical company focused on advancing care for underserved neurological disorders and rare diseases. The company works to translate scientific promise into meaningful innovation by progressing novel therapies from research through clinical development and commercialization. Acadia’s portfolio and pipeline prioritize conditions with high unmet medical need, emphasizing patient-centered development and collaboration to accelerate access to new treatments.