Sr. Qa Technician - Records Specialist (8hr Days; Monday-friday)

Thermo Fisher Scientific UK

Greenville, North Carolina, United States
Cgmp environment experience
Document review and compliance
Risk assessment capabilities
The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals within the Drug Product Division

Job Summary

  • The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals within the Drug Product Division.
  • Employees will perform document reviews, conduct risk assessments, and advance deviation events to maintain product quality and safety.
  • The position requires adherence to Good Manufacturing Practices (GMP) and safety standards including the use of personal protective equipment.

Matching Summary

The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals within the Drug Product Division.

Skills & Requirements

Must-have

  • cGMP environment experience
  • document review and compliance
  • risk assessment capabilities

Nice-to-have

  • leadership in quality initiatives
  • fast-paced multi-tasking ability
  • independent judgment and reliability

Key Requirements

  • Minimum 2 years QA or QC experience
  • High School Diploma required; Associate degree preferred
  • Experience in a cGMP environment

Work Rights

Not specified

Tailored Resume

Cover Letter