Senior QC Microbiologist – GMP Lab

Curia Aalborg ApS

United States

On-site

USD 85,000 - 120,000

Full time

14 days+

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Benefits offered by this job

Generous benefit options
Paid training, vacation and holidays
Career advancement opportunities
Education reimbursement
401K program with matching

Job summary

Curia Aalborg ApS in Albuquerque, NM is seeking a Microbiologist III to perform advanced microbiology testing and quality activities supporting production, environmental monitoring, and product release in a pharmaceutical manufacturing setting.

The role ensures regulatory compliance by conducting microbiological assays, trend analyses, and accurate documentation, while collaborating across cross-functional teams to drive continuous improvement and uphold patient safety.

Qualifications

  • Bachelor's degree in a scientific discipline and minimum five years related work experience.
  • Minimum of three years industry experience in GMP/GLP environments preferred.
  • Experience with pharmaceutical cleanrooms and FDA cGMPs (21 CFR 211) preferred.
  • Experience with validation/qualification of lab microbiological techniques preferred.
  • Proficient in trend analysis, SOPs, CAPA initiation, and quality documentation.

Responsibilities

  • Perform microbiological testing (endotoxin, sterility, bioburden) for materials and products.
  • Conduct environmental monitoring of cleanrooms in USP/EU contexts.
  • Review and trend results; report environmental and product testing outcomes.
  • Lead OOS investigations and support CAPA effectiveness checks.
  • Maintain documents, SOPs, risk assessments, and controlled records.

Skills

Microbiology knowledge
Regulatory compliance
Documentation

Education

Bachelor's degree in microbiology or related field

Job description

Curia Aalborg ApS in Albuquerque, NM is seeking a Microbiologist III to perform advanced microbiology testing and quality activities supporting production, environmental monitoring, and product release in a pharmaceutical manufacturing setting.

The role ensures regulatory compliance by conducting microbiological assays, trend analyses, and accurate documentation, while collaborating across cross-functional teams to drive continuous improvement and uphold patient safety.

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