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

PPD (Thermo Fisher)

Greenville, North Carolina, United States
Cgmp environment experience
Document review and determination
Risk assessment execution
The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals

Job Summary

  • The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals.
  • Employees perform document reviews to determine if work meets current procedures and regulatory expectations.
  • The position involves advancing deviation events to the appropriate area and quality management while conducting risk assessments.

Matching Summary

The role provides direct quality support to ensure compliance with regulations governing pharmaceuticals.

Skills & Requirements

Must-have

  • cGMP environment experience
  • document review and determination
  • risk assessment execution

Nice-to-have

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

Key Requirements

  • Minimum of 2 years QA or QC experience
  • High School Diploma required
  • Associates degree preferred in Science or Technology

Work Rights

Not specified

Tailored Resume

Cover Letter