GMP Quality Associate DirectorVirtualVocations • Charleston, South Carolina, United States
GMP Quality Associate Director
VirtualVocations • Charleston, South Carolina, United States
[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]
A company is looking for an Associate Director, Global Product Quality - GMP Processes.
Key Responsibilities
Lead global strategy and governance for Product Quality Complaints, CAPA, Deviations, and Change Control processes
Collaborate with cross-functional teams to ensure integration of quality into product lifecycle activities
Support regulatory inspections and internal audits, ensuring readiness and robust documentation of quality system performance
Required Qualifications
Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or related field (Master's or PhD preferred)
8+ years of experience in pharmaceutical quality, regulatory affairs, or technical operations
Proven expertise in managing and optimizing PQC, CAPA, deviation, and change control systems
Experience leading cross-functional teams and global projects
Strong knowledge of GMP, ICH guidelines, and global regulatory requirements
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