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Hired by Matrix, Inc.

Interim Microbiology Manager

Career Insights for Clinical Laboratory Manager

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What they do

A Clinical Laboratory Manager manages laboratory research and procedures for numerous fields such as health, industry, or other natural sciences. Commonly oversees R&D, diagnostic or treatment to allow patients to receive better health outcomes. Responsible for regulatory, health and safety operations during laboratory activities.

$112,961 / year median in New Mexico

+12% projected growth

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Job Description

Interim Microbiology Manager#26-06830 $95-$105 per hour Albuquerque, NM Onsite Job Description
At-a-Glance:
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company. If so, our client is hiring an Interim Microbiology Manager.
Position Type:
Contract Onsite Required Minimum 10 years of experience in pharmaceutical microbiology, including at least 5 years in a leadership or laboratory management role. Strong experience managing a GMP microbiology laboratory. Previous experience in sterile or aseptic drug product manufacturing. Hands-on knowledge of environmental monitoring, bioburden, endotoxin, and sterility testing. Experience managing laboratory analysts, workloads, testing priorities, and operational timelines. Strong knowledge of EU GMP Annex 1, contamination control, aseptic processing, and microbiological controls. Experience with deviations, OOS investigations, CAPAs, change controls, and inspection readiness. Ability to work independently at manager level and start with minimal onboarding. Fluent English and strong communication and leadership skills.
Responsibilities:
Manage daily microbiology laboratory operations and laboratory personnel. Oversee environmental monitoring activities. Ensure timely execution and review of bioburden, endotoxin, and sterility testing. Manage laboratory priorities, workload, staffing, and testing timelines. Review and support deviations, OOS results, investigations, CAPAs, and change controls. Ensure compliance with GMP, Good Documentation Practices, data integrity requirements, and internal procedures. Support inspection readiness and collaborate with Quality, Manufacturing, Validation, and Engineering teams. Identify operational and compliance gaps and implement appropriate corrective actions. Ensure analysts are properly trained and qualified to perform assigned activities. Get in
Touch:
We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Priyanshu at (201) 478-6913 to learn more. #LI-VK1 #HbM6349