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Quality Control Microbiologist

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Kelly Science, Engineering, Technology & Telecom
Full Time position
Listed on 2026-01-17
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 35 - 45 USD Hourly USD 35.00 45.00 HOUR
Job Description & How to Apply Below

Kelly Science, Engineering, Technology & Telecom provided pay range

This range is provided by Kelly Science, Engineering, Technology & Telecom. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$35.00/hr - $45.00/hr

Direct message the job poster from Kelly Science, Engineering, Technology & Telecom

Professional science & clinical recruiter helping experienced professionals get noticed and get hired

Quality Control Analyst – Microbiology (Senior Analyst I)

Schedule:

Monday–Friday, 8:00 AM–5:00 PM

Contract Role

Pay: $35–$45/hour (depending on experience)

A leading biotech organization is seeking a Senior Microbiology QC Analyst to support routine and investigational testing, environmental monitoring, data review, and implementation of GMP-compliant lab support systems. This role is hands‑on in the lab and requires strong technical and operational knowledge of microbiological methods.

Key Responsibilities
  • Perform cGMP microbial testing, including endotoxin, bioburden, and environmental monitoring
  • Review raw data, perform peer or technical reviews, and authorize samples
  • Lead and document lab investigations (IA, OOS, AR) with minimal guidance
  • Author, review, and approve SOPs, technical reports, and validation documents
  • Execute and support operational systems such as equipment calibration, data integrity, sample tracking, and LIMS
  • Perform phase‑appropriate method validation and provide data for regulatory filings and inspections
  • Lead and support CAPA and continuous improvement initiatives
Qualifications
  • Bachelor’s degree in Microbiology or a related field
  • 3+ years of experience in a cGMP/GxP environment
  • Hands‑on experience with bioburden, endotoxin, environmental monitoring, and facility qualification
  • Experience authoring and reviewing SOPs and technical documentation
  • Strong organizational and communication skills
  • Self‑motivated with the ability to thrive in a fast‑paced, independent setting
Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance and Research

Industries

Biotechnology Research and Pharmaceutical Manufacturing

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