Sr Qa Technician: Batch Records Release (8hr Days, Mon-fri)

Thermo Fisher Scientific UK

Greenville, NC, US
Gmp compliance review
Cross-functional collaboration
Documentation issue resolution
Independently performs batch record review and collaborates with operations to resolve documentation issues

Job Summary

  • Independently performs batch record review and collaborates with operations to resolve documentation issues.
  • Gains exposure to deviation assessments and quality systems.
  • Review complex or high-risk production records for GMP compliance.

Matching Summary

Independently performs batch record review and collaborates with operations to resolve documentation issues.

Skills & Requirements

Must-have

  • GMP compliance review
  • Cross-functional collaboration
  • Documentation issue resolution
  • Regulatory and client audits

Nice-to-have

  • Positive global impact
  • Scientific advancement
  • Team environment

Key Requirements

  • Minimum 2 years of work experience
  • Experience in a cGMP environment
  • High School diploma / equivalent minimally required
  • Associates degree or higher in Science or Technology is preferred

Work Rights

Not specified

Tailored Resume

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