Associate Director, GLP/GCP Quality Audits and Compliance
Acadia Pharmaceuticals Inc.(12 days ago)
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.
Required Skills
- GLP Compliance
- GCP Compliance
- Audit Planning
- Audit Execution
- Audit Reporting
- Quality Systems
- Data Integrity
- Regulatory Knowledge
- Process Improvement
- Stakeholder Management
Qualifications
- Bachelor's Degree in Life Sciences
- SQA Certification
- ASQ Certification
- ECA Academy Certification
- European Lead Auditor
About Acadia Pharmaceuticals Inc.
acadia.comAcadia 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.
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