Qc Incoming Material And Standards Management Specialist
GlaxoSmithKline
Pennsylvania, United States
Hybrid
Incoming material control
Laboratory reference standards management
Gmp records in lims/sap
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, and we support 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 control
Laboratory reference standards management
GMP records in LIMS/SAP
Certificate of Analysis review
Material reception and release processes
Nice-to-have
Interfacing with regulatory auditors
Sense of urgency and accountability
Executive capability and leadership
Committed team player
Attention to detail and accuracy
Key Requirements
Bachelor's degree in chemistry, life sciences, or related technical field
3+ years experience in high volume, rapid turnaround testing
3+ years experience in GMP/FDA regulated environment
3+ years experience in Quality Control environment