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Qc Microbiology Analyst Jobs (NOW HIRING)

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 ...

InstantServe LLC

QC Microbiology Analyst

Durham, NC · On-site

$23.25 - $31.25/hr

Quality Control/Testing: I Duration: 5+ Months Location: Durham NC USA 27712 Description of Responsibilities Position Summary The QC Microbiology Analyst 1 role is responsible for microbiological ...

ProKidney

QC Microbiology Analyst 3

Winston Salem, NC · On-site

$22.25 - $29.75/hr

Quality Control (QC) Microbiology Analyst III provides support and execution on ProKidney's Environmental Monitoring and Microbiological testing, maintaining GMP compliance, and mentoring junior ...

Adecco

QC Microbiology Analyst

Ridgefield, NJ · On-site

$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 ...

Bimeda Inc.

QC Microbiology Analyst II

Pomona, CA · On-site

$33 - $36.95/hr

Job Title: QC Microbiology Analyst II Location:Pomona, CA (In-office) Position Type:Full-time Vacancy Status:This position is vacant AI Disclosure in Hiring:We use artificial intelligence to screen ...

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Qc Microbiology Analyst information

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How much do qc microbiology analyst jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for qc microbiology analyst in the United States is $28.25, according to ZipRecruiter salary data. Most workers in this role earn between $23.32 and $31.73 per hour, depending on experience, location, and employer.

What are some common challenges faced by QC Microbiology Analysts in a pharmaceutical environment?

QC Microbiology Analysts often encounter challenges such as strict adherence to Good Manufacturing Practices (GMP), managing time-sensitive sample testing, and ensuring accurate documentation for regulatory compliance. They may also need to troubleshoot unexpected test results or contamination issues, which requires strong problem-solving skills and attention to detail. Collaboration with other departments, such as production and quality assurance, is crucial to address quality concerns and implement corrective actions effectively.

What is the difference between Qc Microbiology Analyst vs Qc Microbiology Technician?

AspectQc Microbiology AnalystQc Microbiology Technician
CredentialsTypically requires a Bachelor's degree in Microbiology or related fieldOften requires a high school diploma or associate degree, with some roles preferring microbiology coursework
Work EnvironmentLaboratory setting, performing analysis, data interpretation, and reportingLaboratory setting, assisting with sample preparation and routine testing
Job ResponsibilitiesAnalyzing microbiological samples, interpreting results, ensuring compliancePreparing samples, conducting routine tests, maintaining lab equipment

The main difference between a Qc Microbiology Analyst and a Qc Microbiology Technician lies in their responsibilities and required education. Analysts typically handle data analysis and reporting, requiring a higher level of education, while technicians focus on sample preparation and routine testing. Both roles are essential in microbiology quality control within manufacturing and pharmaceutical industries.

What are QC Microbiology Analysts?

QC Microbiology Analysts are professionals responsible for testing and analyzing samples to ensure that pharmaceutical, food, or cosmetic products meet established microbiological quality standards. They perform routine laboratory tests, monitor environmental conditions, and document results to detect and prevent microbial contamination. Their work is essential for ensuring product safety and regulatory compliance in industries that require strict hygiene standards.

What are the key skills and qualifications needed to thrive as a QC Microbiology Analyst, and why are they important?

A QC Microbiology Analyst should have a solid background in microbiology, laboratory techniques, and a relevant science degree such as biology or microbiology. Familiarity with aseptic techniques, GMP/GLP compliance, and proficiency in using laboratory equipment like autoclaves and incubators is essential. Attention to detail, strong problem-solving abilities, and effective communication skills help ensure accurate testing and clear documentation. These competencies are vital for maintaining product safety, regulatory compliance, and the reliability of microbiological data in quality control environments.
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Qc Microbiology Analyst jobs near you
Infographic showing various Qc Microbiology Analyst job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 7% Hybrid, and 10% Remote job distribution, with an average salary of $58,768 per year, or $28.3 per hour.
QC Microbiology Analyst II, III

QC Microbiology Analyst II, III

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Posted 7 days ago

Job description

Quality Control Microbiology Analyst II, IIIAllendale, NJ 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
All PositionsWorking 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
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.