Qc Incoming Material And Standards Management Specialist

GlaxoSmithKline

Marietta, Georgia, US
Hybrid
Incoming material testing
Laboratory reference standards
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 join a team focused on quality and patient safety, 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 testing
  • Laboratory reference standards
  • GMP records in LIMS/SAP
  • Certificate of Analysis review
  • Material reception and control

Nice-to-have

  • Auditor interfacing
  • Team-based culture
  • Attention to detail
  • High integrity
  • Flexibility and accountability

Key Requirements

  • Bachelor's degree in chemistry, life sciences, or related technical field
  • 3+ years experience in high volume testing
  • 3+ years experience in GMP/FDA regulated environment
  • 3+ years experience in Quality Control

Work Rights

Not specified

Tailored Resume

Cover Letter