Quality Control Data Review Specialist

Harrow, Inc.

Nashville (TN)

On-site

USD 65,000 - 95,000

Full time

5 days ago
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Job summary

Harrow, Inc. is seeking a Quality Control Data Reviewer to ensure data integrity and compliance across QC laboratory operations. The role performs second-person review of chromatographic data and reports, ensuring adherence to validated methods and cGMP requirements.

Ideal candidates bring a BS in a life sciences field and 4–5 years of lab experience, with familiarity in Chromeleon, HPLC, GC, and FTIR. Strong writing and communication skills are essential for documenting findings and supporting

Qualifications

  • BS in Chemistry, Biology, Pharmaceutical or related sciences (minimum).
  • 4–5 years lab experience in pharma/chemical/food labs preferred.
  • Experience with data review and quality systems (21 CFR Part 11/ GMP).
  • Knowledge of USP-NF and deviation/CAPA investigations.
  • Strong written and verbal communication; ability to work independently.

Responsibilities

  • Review QC data and analytical reports for compliance with specs and GMP.
  • Examine chromatographic data, notebooks, and results for accuracy and traceability.
  • Review instrument logs for correct, contemporaneous entries and compliance.
  • Verify audit trails and electronic data integrity per 21 CFR Part 11.
  • Document data review findings clearly and timely; escalate issues when needed.
  • Support investigations and continuous improvement of data review practices.

Skills

Attention to detail
Written communication
Independent worker
Computer literacy (Word/Excel)
Data integrity & GMP awareness
Quality systems knowledge (Veeva/etc)

Education

BS in Chemistry/ Biology/ Pharmaceutical or related sciences

Tools

Chromeleon
HPLC
GC
FTIR

Job description

Harrow, Inc. is seeking a Quality Control Data Reviewer to ensure data integrity and compliance across QC laboratory operations. The role performs second-person review of chromatographic data and reports, ensuring adherence to validated methods and cGMP requirements.

Ideal candidates bring a BS in a life sciences field and 4–5 years of lab experience, with familiarity in Chromeleon, HPLC, GC, and FTIR. Strong writing and communication skills are essential for documenting findings and supporting

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