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Quality Control Microbiology Jobs (NOW HIRING)

Guerbet

QC Microbiology Lead

Raleigh, IL

The QC Microbiology Lead role must possess the skills to interact with formulation, filling, validation, engineering, and packaging personnel in support of those functions. The qualified candidate ...

Laboratoire Guerbet

QC Microbiology Lead

Raleigh, IL · On-site

The QC Microbiology Lead role must possess the skills to interact with formulation, filling, validation, engineering, and packaging personnel in support of those functions. The qualified candidate ...

InstantServe LLC

QC Microbiology Analyst

NC · On-site

Job Title: QC Microbiology Analyst Work Location: Durham NC USA 27712 Duration: 6+ Months The day and hours are...M-F, 1st shift, 9-5. Job Description: Description of Responsibilities Position ...

Adecco

QC Microbiology Analyst

Ridgefield, NJ

$38/hr

Micro QC Analyst I Location: Ridgefield, NJ Pay Rate: $ 38.00/hour Position Type: Contract Position Summary We are seeking a detail-oriented Micro QC Analyst I to join a Quality Control Microbiology ...

New

ABL, Inc.

QC Microbiology I

Rockville, MD · On-site

$26 - $34.25/hr

Job Title QC Microbiology I Location Rockville, MD 20850 US (Primary) Job Type Full-time Funding available in current budget 65000 Exemption Type Non-Exempt Career Level Experienced (Non-Manager ...

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Quality Control Microbiology information

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How much do quality control microbiology jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for quality control microbiology in the United States is $30.16, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $32.21 per hour, depending on experience, location, and employer.

What are some common challenges faced by professionals in Quality Control Microbiology and how can they be addressed?

Quality Control Microbiology professionals often encounter challenges such as identifying and controlling contamination, ensuring compliance with strict regulatory standards, and keeping up with evolving testing methodologies. Addressing these issues typically involves rigorous adherence to standard operating procedures, continuous training, and effective communication within cross-functional teams. Staying up-to-date with industry guidelines and maintaining a clean laboratory environment are also crucial for minimizing errors and ensuring product safety.

What is Quality Control Microbiology?

Quality Control Microbiology is a specialized field within quality assurance that focuses on monitoring and ensuring the safety and efficacy of products by detecting and controlling microbial contamination. Professionals in this role test raw materials, in-process samples, and finished products using various microbiological techniques to ensure compliance with regulatory standards. They play a critical role in industries such as pharmaceuticals, food and beverage, and cosmetics to maintain product quality and protect public health.

What are the key skills and qualifications needed to thrive as a Quality Control Microbiology professional, and why are they important?

To thrive as a Quality Control Microbiology professional, you need a strong background in microbiology, laboratory techniques, and an understanding of regulatory standards, often supported by a degree in microbiology or a related field. Familiarity with laboratory information management systems (LIMS), aseptic techniques, and relevant industry certifications like GMP or GLP is commonly required. Attention to detail, strong analytical skills, and effective communication are important soft skills for this role. These competencies ensure accurate testing, compliance with regulations, and the safety and quality of products in pharmaceutical or food industries.

What is the difference between Quality Control Microbiology vs Quality Assurance Microbiology?

AspectQuality Control MicrobiologyQuality Assurance Microbiology
CertificationsMicrobiology or related lab certificationsISO, GMP, or quality management certifications
Work EnvironmentLaboratory testing, sample analysisDocumentation review, process audits
Employer & Industry UsagePharmaceutical, biotech, food industriesPharmaceutical, biotech, food industries
Primary FocusTesting samples for microbial contaminationEnsuring quality processes and compliance

While both roles involve microbiology in quality-related settings, Quality Control Microbiology focuses on testing and analyzing samples for microbial contamination, whereas Quality Assurance Microbiology emphasizes maintaining quality systems, documentation, and compliance to standards. Both are essential in ensuring product safety and quality in regulated industries.

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Quality Control Microbiology jobs near you
Infographic showing various Quality Control Microbiology job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $62,737 per year, or $30.2 per hour.
QC Microbiology Analist I, II, III

QC Microbiology Analist I, II, III

Lynkx Staffing LLC

Saddle Brook, NJ • On-site

Full-time

Posted 3 days ago

Job description

Quality Control Microbiology Analytics I, II, III QC Microbiology Analyst I The Quality Control Microbiology Analyst I serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst I will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. This position will report into the Manager of QC Microbiology.
  • Environmental monitoring in controlled environments: Non-viable particulate monitoring; Active viable air monitoring, Personnel monitoring, Surface sampling, Passive air monitoring
  • Equipment monitoring: Ensure equipment is in proper working conditions; Ensure all equipment is properly; maintained/calibrated; Assist with routine laboratory testing; Plate reads and incubations
  • Shipping of test samples and equipment to contract laboratories for testing
  • Complete all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
REQUIREMENTS
  • Associates degree in a science or relevant field required; Minimum 0-2 years of experience or equivalent experience. Environmental monitoring or within the biopharmaceutical industry experience preferred.
  • Proficient with computer software such as; Microsoft Office
  • Strong written and oral communication skills
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
  • Trained in GxP/GDP, Safety
  • The QC Microbiology Analyst I must be able to maintain aseptic behavior within a cleanroom environment for an extended period.
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.
QC Microbiology Analyst II The Quality Control Microbiology Analyst II serves as a support role to clinical and commercial production. Microbiology Analyst II will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. This position will report into the Manager of QC Microbiology.
  • Environmental monitoring in controlled environments; Non-viable particulate monitoring, Active viable air monitoring Personnel monitoring, Surface sampling, Passive air monitoring
  • Equipment monitoring; Ensure equipment is in proper working conditions, Ensure all equipment is properly maintained/calibrated, Program equipment with proper workflows, Assist with routine laboratory testing, Plate reads and incubations
  • Shipping of test samples and equipment to contract laboratories for testing
  • Produce documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
  • Writing/conducting investigations pertaining to environmental monitoring and testing
  • Develop and train QC Microbiology Analyst I personnel on relevant business processes.
REQUIREMENTS
  • BA/BS in a science or relevant field required or equivalent experience; Minimum 2-4 years of experience with environmental monitoring or within the biopharmaceutical industry.
  • GxP/GDP, Safety Trained
  • Proficient with computer software such as; Microsoft Office, MODA/LIMS
  • Familiarity with ISO and EU standards
  • Strong written and oral communication skills
  • Technical training ability
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays, and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
  • The QC Microbiology Analyst II must be able to maintain aseptic behavior within a cleanroom environment for an extended period.
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. QC Microbiology Analyst III The Quality Control Microbiology Analyst III serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst III will coordinate data for batch release, participate in project/client meetings, and author/revise environmental monitoring procedures. Additionally, the QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring.
  • Documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
  • Coordinates data for batch release
  • Participation in project/client meetings and communications, providing scientific and technical expertise
  • Authoring/revising Standard Operating Procedures, Work Instructions, Forms, and Protocols
  • Review of investigations and documentation of non-confirming events and environmental excursions.
  • Apply expertise of compliance requirements to maintain an inspection-ready state.
  • Participate and act as subject matter expert during audits/inspections
  • Develop and train QC Microbiology Analyst II on relevant business processes
  • Processing of purchase orders for outsourced testing and lab supplies
  • Coordinates work orders
REQUIREMENTS
  • BA/BS in a science or relevant field required or equivalent experience; Minimum 5-7 years of experience with environmental monitoring or within the biopharmaceutical industry
  • GxP/GDP Trained
  • Proficient with computer software such as; Microsoft Office, MODA/LIMS, Microsoft Visio (preferred), Netsuite (preferred), Maximo Asset Management System (preferred)
  • Proficient knowledge of ISO and EU standards
  • Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review.
  • Strong written and oral communication skills
  • Strong technical writing skills
  • Technical training experience
  • Must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen.
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
Working Environment
  • While performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens.
  • Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen.
  • Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy.
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays, and as required by the company
  • Must be able to handle the standard/moderate noise of the manufacturing facility
Physical Requirements
  • The QC Microbiology Analyst II must be able to maintain aseptic behavior within a cleanroom environment for an extended period.
  • Must be physically capable to stand; walk; site; bend; stretch; use hands to finger, handle or feel; reach with hands and arms; and talk or hear.
  • Occasionally personal protective equipment may be required including lab coat, latex gloves, safety glasses and/or respirator.
Please note these job descriptions are not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.