Science|Biology|Microbiologist,Science,Science|Biology Jobs

Job Description

This position is Second Shift, Tuesday-Saturday

Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.

Essential Duties and Responsibilities:

• Applies GMP/GLP in all areas of responsibility, as appropriate 
• Applies the highest quality standard in all areas of responsibility 
• Demonstrates strong client service skills, communicate effectively, both orally and in writing
• Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration 
• Regular attendance and punctuality 
• Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision 
• Perform/Review preparations of reagents, samples, and standards according to procedures. 
• Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors  
• Read and understand analytical procedures (compendial and client supplied) and internal SOP's
• Use MS Windows applications such as Excel, Word, Outlook email 
• Process data, generate reports, and evaluate data 
• Perform laboratory maintenance and maintain clean workspace
• Commitment to occasional overtime as workload requires 

IN-IDOH-Microbiologist ((phone number removed))
State of Indiana
Title/Role: IN-IDOH-Microbiologist
Region Description:
State of Indiana
Req. Status: Open
No. of Openings: 1
Start Date: 08/03/2026
End Date: 07/30/2027
No New Submittals After: 07/14/2026
Max Submittals by Vendor: 2 Per Opening
Work Arrangement: Onsite
Worksite Address: 550 West 16th St. Indianapolis, IN 46202
CAI Contract Manager (CAI Use Only): Anna Zelko
Workflow Process Designation (CAI Use Only): OOP
Agency Interview Type: In person only

Short Description:
Microbiologist Enteric Lab

Complete Description:
Purpose of Position/Summary:
Incumbent is responsible for coordinating and performing the full range of microbiological examinations and analyses including culture, biochemical tests, EIA, serotyping, PCR, and WGS of clinical specimens for isolation and identification of enteric bacteria including but not limited to Salmonella, E.coli, Shigella, Vibrio, Listeria and Campylobacter. Incumbent will also be responsible for the documentation of all quality control and quality assurance activities according to CLIA regulations. In addition, this position may cross-train in other areas of the lab that may include molecular, microbiological, viral, serological, and other techniques to support routine testing and provide backup capacity.

Essential Duties/Responsibilities:
Incumbent will have in-depth knowledge and ability in the area of microbiology and molecular biology and is able to perform laboratory associated assays or the ability to learn these techniques upon successful completion of proficiency testing. Representative duties include:
• Conducting examinations of samples and/or reference samples for analyses such as but not limited to, molecular detection or isolation and identification of microorganisms/toxins or their antigens/nucleic acids.
• Strictly follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results.
• Extraction of nucleic acids from specimens, isolates, and samples via a variety of manual and automated methods;
•Utilize molecular techniques such as, but not limited to, PCR, sequencing, MALDI-TOF, and WGS;
• Evaluate, interpret, and validate laboratory results and reports findings.
• Maintain laboratory record system of submitted samples and specimens and their possible referral.
• Conduct quality control checks on laboratory methods, materials, and equipment in strict adherence to the laboratory's quality control policies.
• Maintain an inventory of laboratory supplies and order as needed to ensure testing needs are met.
• Assist in preparations of epidemiological and/or statistical reports from data compiled on a daily, weekly, monthly, or annual basis.
• Maintain competency in all trained areas.
• Perform all related work as required.
•Testing personnel responsibilities (493.1495 Standard):
The testing personnel are responsible for specimen processing, test performance and for reporting test results.
(a) Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities.
(b) Each individual performing high complexity testing must—
(1) Follow the laboratory's procedures for specimen handling and
processing, test analyses, reporting and maintaining records of patient
test results;
(2) Maintain records that demonstrate that proficiency testing samples are
tested in the same manner as patient specimens;
(3) Adhere to the laboratory's quality control policies, document all quality
control activities, instrument and procedural calibrations and
maintenance performed;
(4) Follow the laboratory's established policies and procedures whenever
test systems are not within the laboratory's established acceptable levels
of performance;
(5) Be capable of identifying problems that may adversely affect test
performance or reporting of test results and either must correct the
problems or immediately notify the general supervisor, technical
supervisor, clinical consultant, or director;
(6) Document all corrective actions taken when test systems deviate from
the laboratory's established performance specifications; and
(7) Except as specified in paragraph (c) of this section, if qualified under §
493.1489(b)(5), perform high complexity testing only under the onsite,
direct supervision of a general supervisor qualified under § 493.1461.
(c) Exception. For individuals qualified under § 493.1489(b)(5), who were performing
high complexity testing on or before January 19, 1993, the requirements of
paragraph (b)(7) of this section are not effective, provided that all high complexity
testing performed by the individual in the absence of a general supervisor is
reviewed within 24 hours by a general supervisor qualified under § 493.1461.

Job Requirements:
Extensive knowledge of the principles, theories and practices of microbiology and related sub- specialties;
• Specialized knowledge of current scientific methods and testing procedures and the ability to apply them when seeking solutions to public health laboratory problems;
• Specialized knowledge of and ability to use a full range of standard technical equipment, complex scientific apparatus, and automated techniques of analysis;
• Extensive knowledge of laboratory safety practices and principles;
• Aware of state and federal laws, rules, regulations, and policies concerning the program area (i.e. CLIA);
• Ability to meet requirements for personnel certification as a technologist pursuant to the Clinical Laboratory Improvement Act (CLIA)
• Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships;
• Ability to satisfactorily participate in proficiency testing programs and recognize QA problems;
• Ability to compile, analyze, evaluate, and prepare laboratory reports.

Difficulty of Work:
Incumbent is engaged in scientific analyses that demand accuracy and demonstrated proficiency in applying laboratory analytical skills to select pertinent guidelines and formulated plans for problem solving. Projects involve many complex variables of great intricacy and the microbiologist is often called upon to analyze and identify unusual specimens/samples. Work requires use of analytical judgment and technical knowledge in order to draw accurate, logical conclusions. Incumbent will also be required to develop and research new testing procedures.

Responsibility:
Incumbent works independently as an expert in the assigned area. Technical and/or detailed instruction is provided only upon request when necessitated by a procedural change and/or special project. Incumbent maintains established safety practices when working with materials that have a chemical hazard or biohazard potential. Reports are reviewed for general technical accuracy; however, tasks are performed independently. Errors in work could adversely affect the health, safety and well being of the incumbent or coworkers.

Personal Work Relationships:
Incumbent works with supervisor and with other State Department of Health staff such as Laboratory Safety Officer and/or external entities (e.g. local health departments, etc.) to devise and implement work procedures and information dissemination. Individual will have contact with employees and the public as a laboratory expert and in the explanation of laboratory procedures and recommendations when appropriate.

Physical Effort:
The required personal protective equipment can be cumbersome and awkward. Extra effort and concentration will be necessary to perform routine laboratory manipulations under these conditions.

Working Conditions:
The incumbent will be performing tests on potentially dangerous specimens. Consequently, safety standards are of primary importance. This position will be required to use all appropriate personal protective equipment in the designated laboratory area. The laboratory space and equipment can experience a dramatic increase in temperature. The incumbent will be required to work in these conditions and maintain a clear thought process during the testing.



Skill Required / Desired Amount of Experience
Must have a Bachelor's degree in Science, preferably biology. Required
Must have 2 years of lab experience. Highly desired 2 Years
Experience in a Molecular Biology lab is preferred. Desired

Job Description

Candidates in this role are responsible for the accurate and efficient execution of microbiological tests including aseptic processing of sterility tests in a cleanroom suite, endotoxin testing, Microbial Limits Testing, Antibiotic Assay, or other microbiology pharmaceutical testing in accordance with established procedures. Candidates Will collect and present data in a well-reasoned and accurate manner and maintain the laboratory environment according to cGMP guidelines.

Responsibilities:

•    Preparing and performing microbiological tests on cosmetics and pharmaceuticals as recommended by current USP, FDA, and AAMI/ISO regulations.
•    Routine Quality Control of laboratory equipment, media, and microorganisms.
•    Provide accurate test results to customers on a timely basis including but not limited to Microbial Limits Testing, Limulus amoebocyte lysate (LAL), Sterility, etc.
•    Record test results accurately and legibly on all documents.
•    Technical report writing including text, tables, graphs, and diagrams.
•    Assist in the training of new Laboratory Technicians.
•    Follow and perform process qualifications and validations for procedures and/or equipment.
•    Maintain control of test samples including logging in, storage, tracking, and disposal.
•    Monitor test status and conditions as described in Work Instructions and Operating Procedures.
•    Routine maintenance of laboratory environment to include cleaning and troubleshooting.
•    Report any deviations and/or nonconformities to Management.
•    Suggest possible preventative and corrective measures to prevent future deviations and nonconformities.
•    Inventory of laboratory supplies to maintain par levels.
•    Gowning and garbing for cleanroom settings.
•    In cooperation with the Laboratory Manager, responsible for the qualification, maintenance, and calibration of critical equipment.
•    Update procedures for improvement to methods.
•    Assist with OOS, NI, CAPA, and Change Control processes in response to Laboratory issues.
•    Other duties as assigned.

Job Description

In this role, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data in a good manufacturing practices (GMP) microbiology laboratory, including finished products testing, utilities, and environmental monitoring.

Primary Responsibilities

• Perform routine viable and non‑viable Environmental Monitoring of classified cleanroom areas (Grad A-D), including surfaces, air, and equipment.
• Conduct active air, passive air (settle plates), surface sampling, in accordance with site EM programs and GMP requirements.
• Operate and maintain EM instruments (e.g., viable air samplers, particle counters, RODAC plates, isolator/BSC environmental sampling tools).
• Execute aseptic sampling techniques to ensure data integrity and contamination‑free sample collection.
• Perform utility sampling/testing (WFI, purified water, clean steam) and support routine water system monitoring.
• Perform microbiology laboratory testing associated with EM samples, including bioburden, microbial identification, and endotoxin testing.
• Trend, analyze, and interpret EM data; escalate atypical or out‑of‑trend (OOT) results and support investigations.
• Participate in deviation investigations, root cause assessments, and CAPA development related to environmental or microbiological events.
• Maintain accurate documentation of sampling activities in compliance with ALCOA and data‑integrity principles. Inventory management.
• Conduct microbiology finished goods testing and biological indicator (BIs) testing
• Support of sterile operations within the quality control department including utilizing isolator for  sterility testing, conduct method suitability testing, endotoxin, microbial enumeration, media / reagent quality control testing, Experience with testing in clean room environments preferred
• Conduct the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA and data integrity principles
• Partner with internal stakeholders and partners, including Quality, Pipeline, and Operations.
• Perform second scientist review microbiology experiments in line with GMP expectations
• Support internal and external compliance audit activities.
• May need to be flexible with weekday work hours and weekend support as needed

Primary Talent Partners has a new contract opening for an Lab Associate - Microbiologist  with our healthcare client in Round Lake, IL. This is a 12-month contract with a potential for extension.


Pay: $25.00 - $28.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.


Schedule: 1st Shift - 8AM to 5PM Monday to Sunday - Flexible. Saturday and Sunday hours required | Onsite only

Description:
This section focuses on the main purpose of the job in one to four sentences. Primarily support QC Microbiology Laboratory operations at the Manufacturing facility in Round Lake, IL.

This position encompasses biological testing support for pharmaceutical products (biologics and drugs) through all stages of the manufacturing process including incoming raw materials, in-process samples, and finished products and includes facility environmental and critical systems microbiological monitoring.


Essential Duties and Responsibilities:

• This section contains a list of five to eight primary responsibilities of this role that account for the majority of the work. The incumbent will perform other duties assigned.
• Conduct microbial analyses on raw materials, in-process, and finished products, and samples collected from the environmental monitoring programs and manufacturing facility.
• Conduct routine facility environmental monitoring (i.e., surfaces, air, particulate and personnel monitoring) and critical systems monitoring (i.e., water, clean steam, process compressed air and nitrogen).
• Prepare media and reagents used within the laboratory.
• Use laboratory instrumentation (i.e., particle counters, pH meter, SAS, Autoclave) and computer systems (i.e., LIMS) to collect and record data.
• Monitor inventory of supplies, equipment, reagents and media. Order, receive and stock supplies as necessary.
• Maintain a clean, safe and organized laboratory area and perform regular laboratory housekeeping activities.
• Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.
• Maintain data integrity and ensure compliance with company standard operating procedures, FDA, QSR and cGMP regulations.
• Follow, understand and comply with procedures and policies on cGMP’s and safety.
• Contribute to other laboratory tasks and projects as assigned.
• Will work in both Drug Delivery and Penicillin facilities as needed.

Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

• Must not be allergic to Penicillin and Cephalosporin or their related products and minerals.
• Background knowledge in basic Biology and Microbiology principles including aseptic technique is required.
• Proficient in LIMS (laboratory information management systems).
• Ability to handle multiple tasks concurrently, and in a timely fashion. Must be detail oriented, conscientious and have high reading comprehension skills.
• Knowledge of GLP and pharmaceutical aseptic processing cGMP requirements is preferred but not required.
• Demonstrated technical writing skills and knowledge of structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).
• Ability to work independently and as part of a team.
• Self-motivation, adaptability and a positive attitude in a highly dynamic environment.
• Ability to lift up to 50 pounds when required.
• This is a first-shift Thursday-Monday position. Occasional off-shift and vacation work required.

Education and/or Experience:
Include the education and experience that is necessary to perform the job satisfactorily.

• Bachelor’s degree in microbiology or biological science with minimum of 2 years experience in a laboratory setting.

Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at (url removed)

#PTPJobs

#LI-PTP

Job Description

This position is Second Shift, Tuesday-Saturday

Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.

Essential Duties and Responsibilities:

• Applies GMP/GLP in all areas of responsibility, as appropriate 
• Applies the highest quality standard in all areas of responsibility 
• Demonstrates strong client service skills, communicate effectively, both orally and in writing
• Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration 
• Regular attendance and punctuality 
• Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision 
• Perform/Review preparations of reagents, samples, and standards according to procedures. 
• Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors  
• Read and understand analytical procedures (compendial and client supplied) and internal SOP's
• Use MS Windows applications such as Excel, Word, Outlook email 
• Process data, generate reports, and evaluate data 
• Perform laboratory maintenance and maintain clean workspace
• Commitment to occasional overtime as workload requires 

Job Description

Candidates in this role are responsible for the accurate and efficient execution of microbiological tests including aseptic processing of sterility tests in a cleanroom suite, endotoxin testing, Microbial Limits Testing, Antibiotic Assay, or other microbiology pharmaceutical testing in accordance with established procedures. Candidates Will collect and present data in a well-reasoned and accurate manner and maintain the laboratory environment according to cGMP guidelines.

Responsibilities:

•    Preparing and performing microbiological tests on cosmetics and pharmaceuticals as recommended by current USP, FDA, and AAMI/ISO regulations.
•    Routine Quality Control of laboratory equipment, media, and microorganisms.
•    Provide accurate test results to customers on a timely basis including but not limited to Microbial Limits Testing, Limulus amoebocyte lysate (LAL), Sterility, etc.
•    Record test results accurately and legibly on all documents.
•    Technical report writing including text, tables, graphs, and diagrams.
•    Assist in the training of new Laboratory Technicians.
•    Follow and perform process qualifications and validations for procedures and/or equipment.
•    Maintain control of test samples including logging in, storage, tracking, and disposal.
•    Monitor test status and conditions as described in Work Instructions and Operating Procedures.
•    Routine maintenance of laboratory environment to include cleaning and troubleshooting.
•    Report any deviations and/or nonconformities to Management.
•    Suggest possible preventative and corrective measures to prevent future deviations and nonconformities.
•    Inventory of laboratory supplies to maintain par levels.
•    Gowning and garbing for cleanroom settings.
•    In cooperation with the Laboratory Manager, responsible for the qualification, maintenance, and calibration of critical equipment.
•    Update procedures for improvement to methods.
•    Assist with OOS, NI, CAPA, and Change Control processes in response to Laboratory issues.
•    Other duties as assigned.

Job Description

***Position is available in various shifts***

Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations

Essential Duties and Responsibilities: 

• Applies GMP/GLP in all areas of responsibility, as appropriate
• Applies the highest quality standard in all areas of responsibility  
• Demonstrates strong client service skills, teamwork, and collaboration
• Proactively plans and multitasks to maximize productivity
• Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
• Performs laboratory operations with good dexterity, good laboratory technique, and high degree of accuracy and precision
• Perform/Review preparations of reagents, samples, and standards according to procedures.
• Document testing, observations, deviations, and results clearly and completely, and in compliance with regulatory requirements - striving to minimize errors
• Understand and perform calculations as required by test methods
• Understand and utilize computers for information access, calculations, and report preparation
• Read and understand analytical procedures (compendial and client supplied) and internal SOP's
• Use MS Windows applications such as Excel, Word, Outlook email
• Process data, generate reports, and evaluate data
• Communicate effectively, both orally and in writing
• Perform laboratory maintenance and ensures good housekeeping with a neat, clean and orderly workspace
• Commitment to occasional overtime as workload requires

Title/Role: IN-IDOH-Microbiologist ((phone number removed))

Req. Status: Open

No. of Openings: 1

Start Date: 09/07/2026

End Date: 12/31/2026

No New Submittals After: 08/19/2026

Work Arrangement: Onsite

Worksite Address: 550 W. 16th Street Indianapolis, IN 46202

CAI Contract Manager (CAI Use Only): Elias Atallah

Agency Interview Type: In person only

Engagement Type: Contract

Short Description:

Incumbent is responsible for coordinating and performing wastewater testing for SARS-CoV-2, Influenza A, Influenza B, RSV, and other pathogens of public health concern.

Complete Description:

As the Microbiologist, you are responsible for coordinating and performing tests for SARS-CoV-2 and other targets of public health concern in wastewater and water samples. Duties include sample examination and analyses, recording, interpreting, and result reporting of test results. You are responsible for completing all required Quality Control, compliance with all certification requirements, and maintaining all required safety standards. Work hours are Monday - Friday, 7.5 work hours per day.

A Day in the Life:

The essential functions of this role are as follows:

• Conduct wastewater sample concentration, RNA extraction and PCR molecular testing.

• Maintain laboratory record system of submitted samples.

• Evaluate, interpret, and validate laboratory results.

• Conduct inventory management, purchasing, and quality control checks on laboratory methods, materials, and equipment.

• Assists with preparation of reports from data compiled.

• Participate in evaluation of new products used in environmental laboratory work.

The job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee. Other duties, responsibilities and activities may change or be assigned at any time.

Reasonable accommodations may be made to enable individuals with disabilities to interview and to perform the essential functions of this role.

What You'll Need for Success:

• Four (4) year degree (B.S. or B.A.) in a biological science.

• Experience performing RNA/DNA extraction and PCR testing is required.

• Extensive knowledge of the principles, theories, and practices of molecular testing.

• Specialized knowledge of current molecular scientific methods and testing procedures.

• Specialized knowledge of and ability to use a full range of molecular and standard technical equipment

• Ability to compile, analyze, evaluate, and prepare laboratory reports.

• Extensive knowledge of laboratory safety practices and principles.

• Aware of state and federal laws, rules, regulations, and policies concerning the program area.

• Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships.

• Ability to satisfactorily participate in proficiency testing programs.

Skill Required / Desired Amount of Experience

Candidate must have a BS degree in biological science. Required

Experience performing RNA extraction & qPCR testing is required. Required 1 Years

1 year molecular testing experience preferred. Highly desired

IN-IDOH-Microbiologist ((phone number removed))
State of Indiana
Title/Role: IN-IDOH-Microbiologist
Region Description:
State of Indiana
Req. Status: Open
No. of Openings: 1
Start Date: 08/03/2026
End Date: 07/30/2027
No New Submittals After: 07/14/2026
Max Submittals by Vendor: 2 Per Opening
Work Arrangement: Onsite
Worksite Address: 550 West 16th St. Indianapolis, IN 46202
CAI Contract Manager (CAI Use Only): Anna Zelko
Workflow Process Designation (CAI Use Only): OOP
Agency Interview Type: In person only

Short Description:
Microbiologist Enteric Lab

Complete Description:
Purpose of Position/Summary:
Incumbent is responsible for coordinating and performing the full range of microbiological examinations and analyses including culture, biochemical tests, EIA, serotyping, PCR, and WGS of clinical specimens for isolation and identification of enteric bacteria including but not limited to Salmonella, E.coli, Shigella, Vibrio, Listeria and Campylobacter. Incumbent will also be responsible for the documentation of all quality control and quality assurance activities according to CLIA regulations. In addition, this position may cross-train in other areas of the lab that may include molecular, microbiological, viral, serological, and other techniques to support routine testing and provide backup capacity.

Essential Duties/Responsibilities:
Incumbent will have in-depth knowledge and ability in the area of microbiology and molecular biology and is able to perform laboratory associated assays or the ability to learn these techniques upon successful completion of proficiency testing. Representative duties include:
• Conducting examinations of samples and/or reference samples for analyses such as but not limited to, molecular detection or isolation and identification of microorganisms/toxins or their antigens/nucleic acids.
• Strictly follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results.
• Extraction of nucleic acids from specimens, isolates, and samples via a variety of manual and automated methods;
•Utilize molecular techniques such as, but not limited to, PCR, sequencing, MALDI-TOF, and WGS;
• Evaluate, interpret, and validate laboratory results and reports findings.
• Maintain laboratory record system of submitted samples and specimens and their possible referral.
• Conduct quality control checks on laboratory methods, materials, and equipment in strict adherence to the laboratory's quality control policies.
• Maintain an inventory of laboratory supplies and order as needed to ensure testing needs are met.
• Assist in preparations of epidemiological and/or statistical reports from data compiled on a daily, weekly, monthly, or annual basis.
• Maintain competency in all trained areas.
• Perform all related work as required.
•Testing personnel responsibilities (493.1495 Standard):
The testing personnel are responsible for specimen processing, test performance and for reporting test results.
(a) Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities.
(b) Each individual performing high complexity testing must—
(1) Follow the laboratory's procedures for specimen handling and
processing, test analyses, reporting and maintaining records of patient
test results;
(2) Maintain records that demonstrate that proficiency testing samples are
tested in the same manner as patient specimens;
(3) Adhere to the laboratory's quality control policies, document all quality
control activities, instrument and procedural calibrations and
maintenance performed;
(4) Follow the laboratory's established policies and procedures whenever
test systems are not within the laboratory's established acceptable levels
of performance;
(5) Be capable of identifying problems that may adversely affect test
performance or reporting of test results and either must correct the
problems or immediately notify the general supervisor, technical
supervisor, clinical consultant, or director;
(6) Document all corrective actions taken when test systems deviate from
the laboratory's established performance specifications; and
(7) Except as specified in paragraph (c) of this section, if qualified under §
493.1489(b)(5), perform high complexity testing only under the onsite,
direct supervision of a general supervisor qualified under § 493.1461.
(c) Exception. For individuals qualified under § 493.1489(b)(5), who were performing
high complexity testing on or before January 19, 1993, the requirements of
paragraph (b)(7) of this section are not effective, provided that all high complexity
testing performed by the individual in the absence of a general supervisor is
reviewed within 24 hours by a general supervisor qualified under § 493.1461.

Job Requirements:
Extensive knowledge of the principles, theories and practices of microbiology and related sub- specialties;
• Specialized knowledge of current scientific methods and testing procedures and the ability to apply them when seeking solutions to public health laboratory problems;
• Specialized knowledge of and ability to use a full range of standard technical equipment, complex scientific apparatus, and automated techniques of analysis;
• Extensive knowledge of laboratory safety practices and principles;
• Aware of state and federal laws, rules, regulations, and policies concerning the program area (i.e. CLIA);
• Ability to meet requirements for personnel certification as a technologist pursuant to the Clinical Laboratory Improvement Act (CLIA)
• Ability to effectively communicate technical information both verbally and in writing and maintain productive working relationships;
• Ability to satisfactorily participate in proficiency testing programs and recognize QA problems;
• Ability to compile, analyze, evaluate, and prepare laboratory reports.

Difficulty of Work:
Incumbent is engaged in scientific analyses that demand accuracy and demonstrated proficiency in applying laboratory analytical skills to select pertinent guidelines and formulated plans for problem solving. Projects involve many complex variables of great intricacy and the microbiologist is often called upon to analyze and identify unusual specimens/samples. Work requires use of analytical judgment and technical knowledge in order to draw accurate, logical conclusions. Incumbent will also be required to develop and research new testing procedures.

Responsibility:
Incumbent works independently as an expert in the assigned area. Technical and/or detailed instruction is provided only upon request when necessitated by a procedural change and/or special project. Incumbent maintains established safety practices when working with materials that have a chemical hazard or biohazard potential. Reports are reviewed for general technical accuracy; however, tasks are performed independently. Errors in work could adversely affect the health, safety and well being of the incumbent or coworkers.

Personal Work Relationships:
Incumbent works with supervisor and with other State Department of Health staff such as Laboratory Safety Officer and/or external entities (e.g. local health departments, etc.) to devise and implement work procedures and information dissemination. Individual will have contact with employees and the public as a laboratory expert and in the explanation of laboratory procedures and recommendations when appropriate.

Physical Effort:
The required personal protective equipment can be cumbersome and awkward. Extra effort and concentration will be necessary to perform routine laboratory manipulations under these conditions.

Working Conditions:
The incumbent will be performing tests on potentially dangerous specimens. Consequently, safety standards are of primary importance. This position will be required to use all appropriate personal protective equipment in the designated laboratory area. The laboratory space and equipment can experience a dramatic increase in temperature. The incumbent will be required to work in these conditions and maintain a clear thought process during the testing.



Skill Required / Desired Amount of Experience
Must have a Bachelor's degree in Science, preferably biology. Required
Must have 2 years of lab experience. Highly desired 2 Years
Experience in a Molecular Biology lab is preferred. Desired