Quality Technical And Validation Manager

GSK

Gxp oversight of validation
New product introduction oversight
Process and analytical tech transfer
This key member of the site quality leadership team has a responsibility and accountability of a team that ensures the highest standards of GxP compliance in the validation and qualification of processes, equipment, and systems within GSK's manufacturing and analytical environments

Job Summary

  • This key member of the site quality leadership team has a responsibility and accountability of a team that ensures the highest standards of GxP compliance in the validation and qualification of processes, equipment, and systems within GSK's manufacturing and analytical environments.
  • The role is both inward facing to the site, and outward facing to the GSK network and as an SME to regulators during regulatory inspections.
  • We create a welcoming work environment where people can do their best work.

Matching Summary

This key member of the site quality leadership team has a responsibility and accountability of a team that ensures the highest standards of GxP compliance in the validation and qualification of processes, equipment, and systems within GSK's manufacturing and analytical environments.

Skills & Requirements

Must-have

  • GxP oversight of validation
  • New Product Introduction oversight
  • Process and analytical tech transfer
  • Equipment validation protocols
  • Change control management
  • Validation data analysis
  • Regulatory inspection participation

Nice-to-have

  • Continuous improvement methodologies
  • Welcoming work environment
  • Commitment to inclusion
  • Integrity and respect
  • Adaptability and learning

Key Requirements

  • Bachelor's degree in relevant discipline
  • 10+ years pharmaceutical/biotech experience
  • 5+ years leadership experience
  • Experience with lifecycle management programs
  • Experience with validation protocols and reports

Work Rights

Not specified

Tailored Resume

Cover Letter