Acadia Pharmaceuticals Inc.

Associate Director, GLP/GCP Quality Audits and Compliance

Acadia Pharmaceuticals Inc.

2 months ago
Princeton, New Jersey, United States
Hybrid
Full Time
Director
2 applicants
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Acadia Pharmaceuticals Inc.
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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
Acadia Pharmaceuticals Inc.

About Acadia Pharmaceuticals Inc.

acadia.com

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.

About Acadia Pharmaceuticals Inc.

Headquarters

San Francisco, CA

Company Size

201-500 employees

Founded

2018

Industry

Technology

Glassdoor Rating

4.2 / 5

Leadership Team

Sarah Johnson

Chief Executive Officer

Michael Chen

Chief Technology Officer

Emily Williams

VP of Engineering

David Rodriguez

VP of Product

Jessica Thompson

Chief Financial Officer

Andrew Park

VP of Sales

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