Drimva

GSK

OQ Team Lead (Quality Oversight)

USA - North Carolina - Zebulon · On-site · Full-time · Posted Oct 30, 2026

Experience
6+ years of manufacturing experience in the stated fields.
Education
Bachelor’s degree in science, pharmacy, engineering, or a related discipline, or equivalent pharmaceutical industry experience.

About the job

Leads an Operational Quality team providing GMP and Quality Management System oversight across manufacturing to protect product quality and patient safety.

What you'll do

  • Lead and coach the quality team; monitor quality metrics and trends, escalate risks, and support corrective action plans.
  • Oversee investigations, root cause analysis, batch record and quality-document review, and quality decision-making across GMP areas.
  • Support product changes and introductions, audits and inspections, and continuous improvement through real-time oversight and CAPAs.

What they ask for

  • Bachelor’s degree in science, pharmacy, engineering, or a related discipline, or equivalent pharmaceutical industry experience.
  • 6+ years of manufacturing experience in the pharmaceutical industry, biologics manufacturing, distribution, supplier quality, or quality operations.
  • Experience with quality systems including deviations, CAPA, change control, and document control.
  • Experience with data trending, statistical analysis, root cause analysis tools, and multiple dosage forms, packaging, or device assembly activities.

Nice to have

  • Leading or supervising a quality team in operations or supplier quality; working knowledge of Good Manufacturing Practices and applicable U.S. regulatory expectations.
  • Familiarity with inspection readiness and supporting regulatory inspection responses.

Tools

Quality Management System (QMS), CAPA, Good Manufacturing Practices, ALCOA++

Model-written summary · the original posting is authoritative

First seen Oct 31, 2026 · Last verified Nov 5, 2026 (UTC)