QC Microbiology Data Reviewer & GMP Documentation Specialist

QC Microbiology Data Reviewer & GMP Documentation Specialist role supporting GMP microbiology operations through independent review of microbiology data
, documentation
, and electronic records to ensure accuracy, completeness, and ALCOA+ compliance
. The role focuses on review of EM
, bioburden
, sterility
, endotoxin
, and media qualification
data
, along with writing deviations, CAPAs, SOPs
, and routine GMP reports
. Ideal for an intermediate-level professional (4–7 years) with strong LIMS/GMP experience
, working knowledge of Share Point , and exposure to SAP
.

• Perform independent and thorough review of QC microbiology data for completeness, accuracy, and cGMP compliance.
• Verify raw data, calculations, instrument outputs, electronic records for assays including but not limited to bioburden, sterility, endotoxin, media qualification, and environmental monitoring.
• Confirm adherence to SOP’s, test methods, and approved protocols.
• Ensure documentation meets ALCOA+ data integrity principles.
• Identify discrepancies, errors or atypical results and work with analysts to resolve issues and ensure right the first-time documentation.
• Review EM results and ensure proper escalation of out of trend or excursions findings.
• Write deviations, CAPAs and revise SOP’s.
• Write monthly / quarterly reports for environmental monitoring.
• Support internal and external audits by providing clear, complaint documentation.

• Minimum 4 years’ experience in GMP microbiology laboratory data review;
• Knowledge of Bioburden, Endotoxin, Sterility, Media qualification, and Environmental Monitoring;
• Experience in writing and supporting investigations, deviations, or CAPA processes and SOPs;
• Experience with Sherpa or other LIMS;
• Intermediate level MS SharePoint experience;

• Bachelor’s degree in microbiology, Biology or Biotechnology or equivalent;
• Preferred training in Quality systems, cGMP, and Data Integrity.

• SAP: 0–2 years (exposure required);
• LIMS & GMP laboratory data review: 3–5 years;
• Microsoft SharePoint: 3–5 years;
• Microbiology assays data review (Bioburden, Endotoxin, Sterility, EM, Media Qualification);
• Deviation, CAPA, SOP, and investigation writing;
• ALCOA+ data integrity compliance.

Competitive hourly rate: $47 – $55.9/hr (W-2 only, no C2C).

Working Hours:

Monday - Friday, regular business hours.

12-month contract with possible extension.

Employee referral bonus program