Lead Qa Technician (8hr Days, Monday-friday)

Thermo Fisher Scientific UK

Standard onsite (monday-friday, 8-hour days)
Gmp manufacturing operations oversight
Batch record review and compliance
Deviation investigations and capa
Thermo Fisher Scientific is seeking a Lead QA Technician to ensure product quality and regulatory compliance in pharmaceutical manufacturing. The role involves oversight of GMP operations, batch record reviews, and collaboration with cross-functional teams

Job Summary

  • Join the Drug Product Division to ensure product quality and regulatory compliance in sterile injectable and oral solid dose drug production.
  • You will provide independent quality oversight of GMP manufacturing operations including aseptic processing and lead batch record reviews.
  • The role involves mentoring QA technicians, supporting regulatory inspections, and utilizing electronic quality systems like TrackWise.

Matching Summary

Match Score: 85

Thermo Fisher Scientific is seeking a Lead QA Technician to ensure product quality and regulatory compliance in pharmaceutical manufacturing. The role involves oversight of GMP operations, batch record reviews, and collaboration with cross-functional teams.

Skills & Requirements

Must-have

  • GMP manufacturing operations oversight
  • Batch record review and compliance
  • Deviation investigations and CAPA
  • TrackWise and Documentum proficiency
  • Aseptic processing knowledge

Nice-to-have

  • Cross-functional team collaboration
  • Regulatory inspection support experience
  • Continuous improvement mindset
  • Technical guidance and mentorship
  • Data integrity standards application

Key Requirements

  • High School Diploma required
  • Minimum 3 years pharmaceutical QA experience
  • Knowledge of aseptic manufacturing controls

Work Rights

Not specified

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