Qc Compliance Specialist

GlaxoSmithKline

United States
**
Investigate qc deviations
Dmaic process for root cause
Author qc technical documents
** GlaxoSmithKline is seeking a QC Compliance Specialist to serve as a Lead Investigator for QC deviations and lab investigations, utilizing the DMAIC process. The role emphasizes quality control in a cGMP-regulated environment, requiring strong technical writing and communication skills, along with a background in scientific disciplines. **

Job Summary

  • You will serve as the Lead Investigator and SME for QC Deviations and Lab Investigations using the DMAIC process to investigate true root causes and identify CAPA to address them.
  • This role will provide YOU the opportunity to lead key activities to progress YOUR career.
  • We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive.

Matching Summary

Match Score: 75

** GlaxoSmithKline is seeking a QC Compliance Specialist to serve as a Lead Investigator for QC deviations and lab investigations, utilizing the DMAIC process. The role emphasizes quality control in a cGMP-regulated environment, requiring strong technical writing and communication skills, along with a background in scientific disciplines. **

Skills & Requirements

Must-have

  • Investigate QC Deviations
  • DMAIC process for root cause
  • Author QC Technical Documents
  • GMP documentation
  • Data integrity principles (ALCOA++)

Nice-to-have

  • Continuous improvement culture
  • Cross-functional team collaboration
  • Facilitating team environment
  • Safety culture
  • Ambitious for patients

Key Requirements

  • Bachelor’s degree in scientific discipline
  • 4+ years cGMP-regulated environment
  • 4+ years Quality Control laboratory experience
  • Previous UPLC/HPLC experience
  • Must obtain GSK Orange Belt certification

Work Rights

Not specified

Tailored Resume

Cover Letter