QC Microbiology Supervisor

BioPharma Consulting JAD Group; Fort Worth (TX); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

12-month contract

1st shift - 40 hours/week

On-site in Fort Worth, TX

Job summary

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

You will oversee routine and non-routine analyses, develop and transfer methods, train analysts, investigate OOS and contamination, and maintain biosafety standards while supporting audits and regulatory submissions. On-site, 1st shift, ~12 months with possible extension.

Qualifications

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

Responsibilities

• Conduct and oversee routine and non-routine microbiological analyses of raw materials, in-process, environmental, finished goods and stability samples.
• Develop, qualify, validate and transfer microbiological and biological methods (microbial limits, endotoxin, cell-based assays).
• Train analysts in microbiological procedures and biological assays.
• Participate in OOS and contamination investigations and recommend corrective actions.
• Write and revise SOPs, protocols, deviation reports and microbial trend analyses.
• Review contract laboratory data and coordinate testing with contract labs and vendors.
• Maintain lab cleanliness and biosafety standards; troubleshoot incubators, autoclaves and biosafety cabinets.
• Support internal assessments, audits and regulatory submissions.

Skills

Supervisory experience

Education

Bachelor's degree in Microbiology

Tools

PCR

ELISA

Flow cytometry

Job description

We are seeking a QC Microbiology Supervisor to lead biological and microbiological quality control testing at a pharmaceutical manufacturing site in Fort Worth, Texas.

Key Responsibilities

• Conduct and oversee routine and non-routine microbiological analyses of raw materials, in-process, environmental, finished goods and stability samples
• Develop, qualify, validate and transfer microbiological and biological methods (microbial limits, endotoxin, cell-based assays)
• Train analysts in microbiological procedures and biological assays
• Participate in OOS and contamination investigations and recommend corrective actions
• Write and revise SOPs, protocols, deviation reports and microbial trend analyses
• Review contract laboratory data and coordinate testing with contract labs and vendors
• Maintain lab cleanliness and biosafety standards; troubleshoot incubators, autoclaves and biosafety cabinets
• Support internal assessments, audits and regulatory submissions

Requirements

Required Qualifications

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

Preferred Qualifications

• Supervisory or lead experience, including training analysts
• Experience with PCR, ELISA or flow cytometry
• Experience managing contract laboratories
• Statistical trending of microbiological data

Benefits

• Contract position: approximately 12 months, starting November 2026, with possible extension
• Shift: 1st shift, 40 hours/week
• On-site in Fort Worth, Texas