Senior QC Microbiologist - GMP/QA Leader

Curia

New Mexico

On-site

USD 85,000 - 115,000

Full time

14 days+
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Benefits offered by this job

Benefits on day 1
Vacation & holidays
Career advancement
Education reimbursement
401K matching
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Job summary

Curia in Albuquerque, NM is seeking a Microbiologist III to join our GMP-quality team supporting product production, environmental monitoring, and product release in a pharmaceutical setting.

This role conducts advanced microbiological testing (endotoxin, sterility, bioburden), trends data, and documents results while applying QA/QC principles and assisting with CAPAs and deviations to uphold patient safety.

Qualifications

  • Bachelor's degree in a science field, preferably microbiology.
  • Minimum 5 years related work experience.
  • GMP/GLP environment experience; pharma cleanrooms preferred.
  • Familiarity with FDA cGMPs (21 CFR 211); ISO standards preferred.
  • Experience validating/qualifying lab microbiology techniques preferred.

Responsibilities

  • Perform microbiological testing (endotoxin, sterility, bioburden) for materials and products.
  • Monitor cleanrooms environmental compliance per USP and EU specs.
  • Review, trend, and report environmental, in-process, raw material, and finished product data.
  • Conduct microbial characterization and send samples for ID.
  • Maintain historical microbiology records and trends.
  • Oversee line clearances, start verifications, and media fill inspections.
  • Serve as SME for sterility and growth-promotion assays for incoming media.
  • Prepare controlled documents: SOPs, protocols, risk assessments.
  • Initiate OOS investigations and recommend CAPAs.

Education

Bachelor's degree in a scientific discipline

Job description

Curia in Albuquerque, NM is seeking a Microbiologist III to join our GMP-quality team supporting product production, environmental monitoring, and product release in a pharmaceutical setting.

This role conducts advanced microbiological testing (endotoxin, sterility, bioburden), trends data, and documents results while applying QA/QC principles and assisting with CAPAs and deviations to uphold patient safety.

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