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Associate Laboratory Microbiologist Jobs in Rye, NY

Certified Group

Micro Lab Tech

Melville, NY

$19.50 - $25.75/hr

We are currently looking for a Microbiology Technician to join our growing team! JOB SUMMARY ... Associate degree in Life Science or two years of laboratory experience, preferred * Broad knowledge ...

Certified Group

Micro Lab Tech

Melville, NY

$19.50 - $25.75/hr

Certified Laboratories - Provides comprehensive analytical and microbiological testing, primarily ... Associate degree in Life Science or two years of laboratory experience, preferred * Broad knowledge ...

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All JobsAssociate Laboratory Microbiologist JobsAssociate Laboratory Microbiologist Jobs in Rye, NY

Associate Laboratory Microbiologist information

See Rye, NY salary details

$36.6K

$74.9K

$133.5K

How much do associate laboratory microbiologist jobs pay per year?

As of Jun 16, 2026, the average yearly pay for associate laboratory microbiologist in Rye, NY is $74,860.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,600.00 and $87,900.00 per year, depending on experience, location, and employer.

What are Associate Laboratory Microbiologists?

Associate Laboratory Microbiologists are entry- to mid-level professionals who assist in conducting experiments, analyzing samples, and supporting research in microbiology laboratories. Their responsibilities typically include preparing specimens, performing tests to identify microorganisms, recording results, and maintaining laboratory equipment. They work under the supervision of senior microbiologists or laboratory managers, ensuring that all procedures comply with safety and quality standards. This role is essential in industries such as healthcare, pharmaceuticals, food safety, and environmental science.

What are the key skills and qualifications needed to thrive as an Associate Laboratory Microbiologist, and why are they important?

To thrive as an Associate Laboratory Microbiologist, you need a solid understanding of microbiology, aseptic techniques, and laboratory safety, typically supported by a bachelor’s degree in microbiology or a related field. Familiarity with laboratory equipment, molecular testing platforms, and data analysis software such as LIMS is important, and certifications like ASCP may be advantageous. Attention to detail, strong problem-solving skills, and effective communication help you excel in both individual and team settings. These skills and qualities ensure accurate test results, uphold safety standards, and contribute to reliable research or diagnostic outcomes.

What is the difference between Associate Laboratory Microbiologist vs Laboratory Microbiologist?

AspectAssociate Laboratory MicrobiologistLaboratory Microbiologist
Required CredentialsBachelor's degree in microbiology or related field; some roles may require certificationBachelor's degree in microbiology or related field; certification optional
Work EnvironmentResearch labs, healthcare facilities, or industrial settingsResearch labs, healthcare, or public health laboratories
Employer & Industry UsageResearch institutions, biotech companies, government agenciesHospitals, public health labs, research institutions

The main difference between an Associate Laboratory Microbiologist and a Laboratory Microbiologist lies in their roles and responsibilities. The associate role often involves supporting experiments, data collection, and routine testing, while a Laboratory Microbiologist may have more independent responsibilities, including designing experiments and analyzing results. Both roles require similar educational backgrounds, but the associate position is typically an entry-level or supporting role within the microbiology field.

How does an Associate Laboratory Microbiologist typically collaborate with other departments within a research or clinical laboratory?

As an Associate Laboratory Microbiologist, you will frequently interact with colleagues from various departments, such as chemistry, pathology, and quality assurance, to ensure accurate sample testing and data interpretation. Collaboration might involve coordinating on multi-disciplinary projects, troubleshooting unexpected results, or sharing findings that impact broader research objectives. Effective communication and teamwork are essential, as your work often supports or informs the efforts of other scientists, technicians, or healthcare professionals within the organization.
What cities near Rye, NY are hiring for Associate Laboratory Microbiologist jobs? Cities near Rye, NY with the most Associate Laboratory Microbiologist job openings:
Associate Laboratory Microbiologist jobs near you
Infographic showing various Associate Laboratory Microbiologist job openings in Rye, NY as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $74,860 per year, or $36 per hour.

QC Microbiology Analist I, II, III

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Posted 27 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.