Qc Incoming Material And Standards Management Specialist
GSK
Marietta, Georgia, US
Hybrid
Incoming material testing
Reference standards management
Gmp documentation
The QC Incoming Material and Standards Management Specialist is responsible for driving the creation, receipt, and control process, testing requirements, disposition and documentation of incoming raw materials and laboratory reference standards to ensure materials meet quality, regulatory and safety requirements
Job Summary
The QC Incoming Material and Standards Management Specialist is responsible for driving the creation, receipt, and control process, testing requirements, disposition and documentation of incoming raw materials and laboratory reference standards to ensure materials meet quality, regulatory and safety requirements.
This role supports QC operations by maintaining robust standards management, ensuring traceability, and partnering with Procurement, Suppliers, Manufacturing and Regulatory Affairs to enable compliant material release, qualification, and recertification.
You will gain exposure to supplier relationships, laboratory workflows, and regulatory readiness, with support for development through training, mentoring, and opportunities to lead improvement projects.
Matching Summary
The QC Incoming Material and Standards Management Specialist is responsible for driving the creation, receipt, and control process, testing requirements, disposition and documentation of incoming raw materials and laboratory reference standards to ensure materials meet quality, regulatory and safety requirements.
Skills & Requirements
Must-have
incoming material testing
reference standards management
GMP documentation
supplier documentation review
laboratory reference standards
Nice-to-have
sense of urgency and flexibility
executive capability and leadership
committed team player
attention to detail
high level of integrity
Key Requirements
Bachelor's degree in chemistry, life sciences, or related technical field
3+ years experience in a laboratory
3+ years experience in a GMP/FDA regulated environment