Interim Microbiology Manager

Spark Recruiting

  • Albuquerque, New Mexico
  • 10 days ago
  • $76 Per Hour
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Skills

  • Asepsisunmatched
  • Biotech and Pharmaceuticalunmatched
  • Change Controlunmatched
  • Corrective Actionunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Qualityunmatched
  • Documentationunmatched
  • Drug Manufacturingunmatched
  • Drug Productsunmatched
  • Environmental Monitoringunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Laboratoryunmatched
  • Laboratory Analysisunmatched
  • Laboratory Managementunmatched
  • Laboratory Operationsunmatched
  • Leadershipunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Microbiologyunmatched
  • Operational Supportunmatched
  • People Managementunmatched
  • Regulationsunmatched
  • Root Cause Analysisunmatched
  • Testingunmatched
  • Time Managementunmatched

Description

Interim Microbiology Manager

Location: Albuquerque, NM

Job Type: Long-Term Contract (2–3 Months with Possible Extension)

Pay: Up to $76.00/hour

Schedule: Full-Time | 100% Onsite

Lead a Critical GMP Microbiology Operation

Our client is seeking an experienced Interim Microbiology Manager to provide immediate leadership for a GMP microbiology laboratory supporting a sterile drug product manufacturing facility in Albuquerque, New Mexico. This is an excellent opportunity for a seasoned microbiology leader who can step into a fast-paced environment, ensure regulatory compliance, and drive laboratory operations while supporting the search for a permanent manager.

Key Responsibilities

  • Lead the day-to-day operations of the GMP microbiology laboratory and supervise laboratory personnel.
  • Oversee environmental monitoring (EM) programs for sterile manufacturing areas.
  • Ensure timely execution and review of bioburden, endotoxin, and sterility testing.
  • Manage laboratory workload, staffing, testing priorities, and turnaround times.
  • Review and support deviations, OOS investigations, CAPAs, change controls, and root cause investigations.
  • Ensure compliance with cGMP, Good Documentation Practices (GDP), data integrity requirements, and company procedures.
  • Support internal and regulatory inspections while maintaining inspection readiness.
  • Partner closely with Quality, Manufacturing, Validation, and Engineering teams.
  • Identify compliance or operational gaps and implement effective corrective actions.
  • Ensure laboratory analysts are fully trained and qualified to perform assigned testing.

Required Qualifications

  • 10+ years of pharmaceutical microbiology experience.
  • 5+ years of leadership or laboratory management experience.
  • Strong experience managing a GMP microbiology laboratory.
  • Hands-on experience in sterile/aseptic pharmaceutical manufacturing.

Extensive knowledge of:

  • Environmental Monitoring (EM)
  • Bioburden Testing
  • Endotoxin Testing
  • Sterility Testing
  • Aseptic Processing
  • Contamination Control
  • EU GMP Annex 1

Experience with:

  • Deviations
  • OOS Investigations
  • CAPAs
  • Change Controls
  • Regulatory Inspection Readiness

Numbers & Facts

LocationAlbuquerque, New Mexico

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