GMP QC Microbiology Lab Lead (Contract)

Biopharma-Consulting-Jad-Group; Fort Worth (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Biopharma-Consulting-Jad-Group seeks a QC Microbiology Supervisor to lead biological and microbiological quality control testing at a pharmaceutical site in Fort Worth, Texas.

The role oversees routine and non-routine microbiological analyses, method development and transfer, andOOS/ deviation investigations while training analysts and ensuring GMP compliance. On-site, 1st shift, ~40 hours/week, 12-month contract with potential extension.

Qualifications

• Bachelor's degree in Microbiology, Biology or related science.
• Experience in a GMP QC Microbiology lab (environmental monitoring, microbial limits, endotoxin).
• Experience with method validation/transfer and OOS/deviation investigations.
• Technical writing of SOPs, protocols and reports.

Responsibilities

• Perform routine and non-routine microbiological analyses of materials and products.
• Develop, qualify, validate and transfer microbiological methods (limits, endotoxin).
• Train analysts in microbiological procedures and assays.
• Participate in OOS and contamination investigations and recommend corrective actions.
• Write and revise SOPs, protocols, deviation reports and trend analyses.
• Review contract lab data and coordinate testing with vendors.
• Maintain lab cleanliness and biosafety; troubleshoot equipment.
• Support internal assessments, audits and regulatory submissions.

Skills

Supervisory experience

Technical writing

GMP knowledge

Training analysts

Education

Bachelor's degree in Microbiology, Biology or related science

Tools

PCR

ELISA

Flow cytometry

Job description

Biopharma-Consulting-Jad-Group seeks a QC Microbiology Supervisor to lead biological and microbiological quality control testing at a pharmaceutical site in Fort Worth, Texas.

The role oversees routine and non-routine microbiological analyses, method development and transfer, andOOS/ deviation investigations while training analysts and ensuring GMP compliance. On-site, 1st shift, ~40 hours/week, 12-month contract with potential extension.