Microbiologist jobs at Mérieux NutriSciences - 533 jobs

About us At Cooper University Health Care , our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees to provide competitive rates and compensation programs. Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement. We also provide attractive working conditions and opportunities for career growth through professional development. Discover why Cooper University Health Care is the employer of choice in South Jersey. Short Description Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget. Work as a team player with all involved in the studies. Experience Required 2+ years research experience. Strong analytical skills. Education Requirements High School Diploma or Equivalent required, Bachelor's degree preferred.

About us At Cooper University Health Care , our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees to provide competitive rates and compensation programs. Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement. We also provide attractive working conditions and opportunities for career growth through professional development. Discover why Cooper University Health Care is the employer of choice in South Jersey. Short Description Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget. Work as a team player with all involved in the studies. Experience Required 2+ years research experience. Strong analytical skills. Education Requirements High School Diploma or Equivalent required, Bachelor's degree preferred.

University Hospitals Fertility Center, part of University Hospitals Cleveland Medical Center, provides comprehensive reproductive care backed by academic research, cutting-edge technology, and compassionate patient-centered service. Our Beachwood location offers state-of-the-art IVF and andrology laboratories, supporting thousands of families each year through advanced reproductive techniques. We here at Peak Recruiter are proud to have partnered with them to locate a new Embryologist III - a senior-level, highly skilled professional - to join their expanding team and contribute to excellence in assisted reproductive technology (ART) outcomes, patient care, and laboratory innovation. Position Summary The Embryologist III plays a key leadership role in all aspects of embryology and IVF laboratory operations. This includes performing complex embryology and micromanipulation procedures, maintaining laboratory quality and compliance standards, assisting with training and mentoring junior staff, and supporting research and development initiatives. The Embryologist III works collaboratively with physicians, nurses, and laboratory personnel to ensure optimal outcomes, patient safety, and adherence to regulatory standards. Key Responsibilities Clinical Laboratory Duties Perform advanced ART procedures, including oocyte retrieval assessment, insemination, ICSI, embryo culture, biopsy, vitrification, and thawing. Assess embryo and gamete quality; prepare detailed documentation in the EMR/LIMS. Execute all aspects of daily embryology workflow with precision and adherence to protocols. Conduct quality control, calibration, and validation of laboratory equipment and consumables. Ensure compliance with CAP, CLIA, FDA, SART, and institutional standards. Maintain meticulous lab records, chain-of-custody documentation, and traceability logs. Leadership & Training Mentor and train junior embryologists, andrology technologists, and trainees. Assist in updating SOPs and protocols to align with best practices and new scientific evidence. Participate in performance review processes and internal audits. Provide on-call and weekend/holiday coverage as part of a rotation schedule. Research & Development Collaborate with the laboratory director and faculty on clinical research, quality improvement, and data analytics projects. Contribute to the introduction and validation of emerging technologies (e.g., time-lapse imaging, AI embryo selection, cryo-optimization). Qualifications Required: Bachelor's degree in biological sciences, clinical laboratory science, or related field. Minimum 5-7 years of experience in human embryology with progressive responsibility. Demonstrated proficiency in ICSI, vitrification, embryo biopsy, and blastocyst culture. Familiarity with CLIA, CAP, and FDA tissue regulations. Strong organizational skills, attention to detail, and ability to multitask in a fast-paced clinical environment. Preferred: Master's or PhD in reproductive biology, embryology, or related discipline. Certification by the American Board of Bioanalysis (ABB) as an Embryology Laboratory Scientist (ELS) or equivalent. Prior experience in an academic or high-volume fertility setting. Experience mentoring or training junior lab staff. Core Competencies Advanced technical proficiency and precision in embryology techniques. Excellent communication, documentation, and collaboration skills. Commitment to patient-centered care and ethical standards. Analytical thinking, adaptability, and innovation. Dedication to continuous learning and scientific advancement. Why Join University Hospitals Fertility Center Work in a nationally recognized fertility program supported by world-class clinicians and researchers. Access to cutting-edge technologies and equipment in a collaborative academic environment. Comprehensive benefits, including health, dental, vision, 403(b), tuition reimbursement, and professional development support. Opportunities to participate in research, publication, and conference presentations.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III) Responsibilities: Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts. Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing. Support cell culture activities and experiments in multiple cell lines, at small and large scales. Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays). Engineer and characterize cell-based systems using synthetic biology tools and techniques. Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity. Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches. Prepare summaries of data and present internally to colleagues and management. Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records. Author scientific reports and data summaries. Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization. Qualifications: Bachelor's or Master's degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. At least 2 years of industry wet lab experience. Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells). Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows) Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment. Strong written and verbal communication skills. Preference will be given to those who display: High throughput screening assay development in an industry setting. High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. First-principles thinking, and an ability to refine one's intuition based on additional data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. High EQ with team-oriented thinking. Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays. Experience with CRISPR-Cas systems and/or gene editing and delivery technologies. Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms). If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III) Responsibilities: Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts. Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing. Support cell culture activities and experiments in multiple cell lines, at small and large scales. Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays). Engineer and characterize cell-based systems using synthetic biology tools and techniques. Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity. Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches. Prepare summaries of data and present internally to colleagues and management. Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records. Author scientific reports and data summaries. Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization. Qualifications: Bachelor's or Master's degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. At least 2 years of industry wet lab experience. Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells). Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows) Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment. Strong written and verbal communication skills. Preference will be given to those who display: High throughput screening assay development in an industry setting. High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. First-principles thinking, and an ability to refine one's intuition based on additional data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. High EQ with team-oriented thinking. Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays. Experience with CRISPR-Cas systems and/or gene editing and delivery technologies. Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms). If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III) Responsibilities: Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts. Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing. Support cell culture activities and experiments in multiple cell lines, at small and large scales. Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays). Engineer and characterize cell-based systems using synthetic biology tools and techniques. Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity. Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches. Prepare summaries of data and present internally to colleagues and management. Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records. Author scientific reports and data summaries. Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization. Qualifications: Bachelor's or Master's degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. At least 2 years of industry wet lab experience. Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells). Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows) Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment. Strong written and verbal communication skills. Preference will be given to those who display: High throughput screening assay development in an industry setting. High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. First-principles thinking, and an ability to refine one's intuition based on additional data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. High EQ with team-oriented thinking. Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays. Experience with CRISPR-Cas systems and/or gene editing and delivery technologies. Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms). If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Amber Bio is a biotechnology company pioneering new gene editing modalities using multi-kilobase edits to reach previously undruggable patient populations. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA editing platform that can correct thousands of bases at once, thereby correcting genetic mutations safely and reversibly. If you are interested in building a new frontier in genetic medicine, we welcome you to apply. Job Description: High-Throughput Screening Research Associate II, III (Biodesigner II, III) Responsibilities: Perform massively parallel reporter assays and high-throughput screens across diverse cellular contexts using cellular and molecular readouts. Develop and execute molecular biology workflows such as vector design and cloning, DNA/RNA extraction, RT-PCR, qPCR, and next-generation sequencing. Support cell culture activities and experiments in multiple cell lines, at small and large scales. Design and execute cell-based assays (AAV/lentiviral transduction, transfection, flow cytometry, immunostaining, and other plate reader assays). Engineer and characterize cell-based systems using synthetic biology tools and techniques. Conduct and troubleshoot experiments, independently and in collaboration with colleagues, to optimize screening throughput, sensitivity, and specificity. Proactively troubleshoot technical issues and recommend potential corrective actions based on personal observations and literature searches. Prepare summaries of data and present internally to colleagues and management. Draft SOPs, follow protocols, diligently document experimental data in lab notebooks, and organize and maintain electronic work records. Author scientific reports and data summaries. Collaborate with cross-functional teams to meet project goals, bridging early discovery with high-throughput screens to nominate and optimize candidates for further characterization. Qualifications: Bachelor's or Master's degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. At least 2 years of industry wet lab experience. Mammalian cell culture experience (culturing, transfecting and transducing cells, and DNA/RNA purification from cells). Molecular biology expertise (vector design and cloning, qPCR, primer and probe design, DNA/RNA extraction workflows) Critical thinker with excellent communication skills who thrives in a multidisciplinary, fast-paced team environment. Strong written and verbal communication skills. Preference will be given to those who display: High throughput screening assay development in an industry setting. High motivation, with a strong work ethic and dedication to generating impact. Attention to detail, with the ability to extract deep insights from data. First-principles thinking, and an ability to refine one's intuition based on additional data. Ability to go from ideation to data in an independent fashion. Long-term personal vision with defined career goals. High EQ with team-oriented thinking. Experience with pooled, high-throughput screens using next-generation sequencing-based readouts, and/or preparing screening plasmid libraries from synthesized oligo arrays. Experience with CRISPR-Cas systems and/or gene editing and delivery technologies. Experience preparing next-generation sequencing libraries (Illumina, PacBio, and/or Nanopore platforms). If you have a passion for advancing gene editing technologies and desire to be part of a pioneering biotech company, we encourage you to apply and join our ambitious team. Please apply directly through LinkedIn. Amber Bio is an equal-opportunity employer and encourages applications from candidates of diverse backgrounds. We value diversity and are committed to creating an inclusive and supportive work environment for all employees.

Certified Group is a leading North American provider of laboratory testing and audit and certification services. The Certified Group of companies includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc. and Micro Quality Labs Inc. The Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, cannabis, nicotine and hemp industries. We are currently looking for a Microbiologist to join our team! ESSENTIAL RESPONSIBILITIES Study the growth, characteristics and effects of bacteria and other microorganisms to better understand their relation to human, plant and animal health. Perform sterility testing Perform API strips & troubleshoot issues and concerns regarding cross-contamination Adapt and understand the procedures from CTFA, AOAC and others as needed. Perform Total Plate Counts, Enrichments, Preservative Effectiveness Testing, raw material testing, bulk testing, water testing and other tests. Perform other duties as assigned. MINIMUM QUALIFICATIONS Must have a B.S. in Microbiology At minimum, 2 years of microbiological testing experience in the cosmetic, nutritional or pharmaceutical industries. Knowledge of current CTFA/PCPC, AOAC and other industry standard methods and procedures. Understanding of pharmaceutical, cosmetic and nutritional microbiology. Understanding and knowledge of the European, United States, Japanese and other Pharmacopeias. Experience performing microbial testing on pharmaceutical, cosmetic and nutritional raw materials, water samples, bulk & finished products. Example of these tests are: Total Plate Count (TPC), Yeast & Mold, Enrichments and Preservative Effectiveness Testing (PET). Computer literate. Be able to work with Microsoft programs, search engines, basic spreadsheets, etc. Able to handle multiple tasks and work in a fast paced environment. Able to adapt to changes to improve company process. May assist in overseeing work performed by Microbiology Technician. Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 4:00 PM to 12:30 AM

Job Description Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Microbiologist to join our growing team! JOB SUMMARY The function of this job is to perform advanced analytical and microbiological testing of food products, ingredients, and environmentals. The position consistently exercises independent judgment and discretion in performing the application and evaluation of approved microbiological techniques and methodologies used in analytical testing, and the interpretation of test results. This role has training and supervisory responsibilities as needed. ESSENTIAL RESPONSIBILITIES Accurately perform and read test results and notify Laboratory Management of deviations Prepare and analyze samples for indicator organisms, pathogens, and chemistries Apply aseptic/microbiological techniques in daily workload Apply independent judgement in the interpretation of qualitative test results Conduct additional testing as needed based upon independent review of test results Accurately perform final determination of special micros and complete final results disposition Communicate results including pathogenic confirmations and maintain a positive relationship with clients Report inventory and expendable supplies/materials needed for testing requirements Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control Assist in quality control duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. Assist with training and research assignments including troubleshooting Independently pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements Assisting in developing and revising Standard Operating Procedures (SOPs) Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends Perform all activities in a neat, safe, hygienic, and efficient manner Share information in an open and timely manner Assist with managing priorities and schedule Responsible for the safety of oneself and others working within their area Responsible for the completion of required training Travel is required and at the discretion of management OTHER DUTIES Perform other duties as assigned As needed from time to time, assist in performing Login Technician, Media Technician, and/or Micro Technician. If assigned, conduct responsibilities of Branch Safety Coordinator outlined in the corporate safety manual and report to the Corporate Safety Officer for assigned duties SUPERVISORY RESPONSIBILITIES This job has no regularly assigned supervisory responsibilities, although the position is expected to train others, and step in to perform supervisory responsibilities when the Sr. Microbiologist, Lead or the Supervisor is not available. MINIMUM QUALIFICATIONS Bachelor's degree in Life Science or related field, microbiology preferred Two or more years of experience in a commercial food-testing or analytical laboratory Or equivalent combination of education and experience Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures Familiar with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures Broad knowledge of concepts, practices, and procedures of a food testing laboratory Ability to travel when necessary KNOWLEDGE, SKILLS, and ABILITIES To perform the job successfully, an individual should demonstrate the following: Computer - Proficient in standard business office software, LIMS, and internet search tools. Customer Service - Responds promptly to customer needs; Responds to requests for service and assistance; Meets commitments. Verbal & Written Communication; Language Skills - Clarity of speech, remaining calm and focused, being polite and making effective presentations to diverse groups. Edits work for correct data, spelling, and grammar. Ability to read and comprehend simple instructions, short correspondence, and memos. Mathematical Skills - Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; Ability to perform financial calculations, compute rate, ratio, and percent and to draw and interpret bar graphs. Analytical, Problem Solving, & Organizational Skills - Gathers and analyzes information skillfully and can efficiently execute on plans/ideas. Ability to deal with problems involving a few concrete variables in standardized situations. Interprets data and test results. Independent Judgement and Discretion - Proficient and confident in exercising independent judgement and discretion on a consistent basis throughout the day in performing the testing, analytical and interpretive responsibilities of the position. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. FSNS complies with its reasonable accommodation obligations under the Americans with Disabilities Act and state law. Regularly required to stand, sit, walk, use hands and arms, talk and hear Lift up to 25 pounds Color vision and depth perception WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens Noise level varies from quiet to loud Temperature varies from hot to cold Interactive and fast-paced team oriented tasks Safety: Required to wear appropriate protective clothing Required to use appropriate protective equipment Responsible for the safety of oneself and others working within their area PROFICIENCY REQUIREMENTS Employees in this role will be evaluated after 90 calendar days from date of hire and annually thereafter based on the following proficiencies: In addition to the responsibilities of this position, maintain competency in duties performed by technicians in other departments (Log-In, Media, Main) to provide assistance when needed Exercise of sound independent judgment and discretion Knowledge of all qualitative, quantitative testing, and confirmations performed Resource for all technicians in Main Lab Proficient in the passing and first approval process and may complete second approvals Excellent aseptic technique and use of the biological hood Understand client specifications Ability to assume the responsibilities and make decisions of the Sr. Microbiologist, Lead, or Supervisor, when they are not available Ensure daily, weekly, and monthly sanitation and QC are complete Help resolve technical issues with machines Proficiency in testing for all path lab analyses on A2LA Scope ( Versed in GLP, FDA, USDA, AOAC, and other method reference sources Manage workload and ensure TAT is met by delegation of work to self and others Assist Technical Manager, as needed All Certified Group employees must be proficient in the following: Ability to multitask and quickly move from one task to the next Ability to complete tasks with accuracy General knowledge of all FSNS safety protocols & general OSHA laboratory safety guidelines Working knowledge of ISO 17025 Quality procedures general to their primary job and area of responsibility Ability to perform laboratory opening and closing procedures Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 8:00AM to 5:00PM

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Microbiology Technician to join our growing team! JOB SUMMARY Prepare samples for analytical and microbiological testing of nutraceutical products and supplements ingredients, and environmentals. The role is responsible for the application of approved microbiological techniques and methodologies used in analytical testing. ESSENTIAL RESPONSIBILITIES * Assist in microbial challenge testing of new products to determine adequacy of preservation. * Bioburden panel testing, water testing, environmental testing (ie air plates, swabs, conductivity) * Apply aseptic techniques in daily workload. * Inventory and report expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, and trash disposal * Perform quality control monitoring by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Maintain laboratory condition, to include equipment, supplies * Perform all activities in a neat, safe, hygienic, and efficient manner * Prepare media for microbial quality and preservative adequacy testing. * Document media preparation and media control information in appropriate logbooks. * Maintain appropriate notebooks and computer logs required for the department. * Organize the destruction of product discards and assist with special projects. * Share information in an open, and timely manner with Supervisor * Perform other duties as assigned. MINIMUM QUALIFICATIONS: * BS degree in microbiology or related field with 1-2 years of lab experience. * At minimum, 1 or more years of Quality Assurance or Microbiological testing experience in the cosmetic, nutritional, or pharmaceutical industries * Able to handle multiple tasks and work in a fast-paced environment. * Able to adapt to changes to improve company processes. * Able to carry up to 50 pounds. * Able to stand and sit for long periods of time. * Must be able to rotate one weekend day. PHYSICAL DEMANDS * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Occasionally lift and/or move up to 25 pounds. * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off * Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Microbiologist to join our growing team! JOB SUMMARY The function of this job is to perform advanced analytical and microbiological testing of food products, ingredients, and environmentals. The position consistently exercises independent judgment and discretion in performing the application and evaluation of approved microbiological techniques and methodologies used in analytical testing, and the interpretation of test results. This role has training and supervisory responsibilities as needed. ESSENTIAL RESPONSIBILITIES * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Apply independent judgement in the interpretation of qualitative test results * Conduct additional testing as needed based upon independent review of test results * Accurately perform final determination of special micros and complete final results disposition * Communicate results including pathogenic confirmations and maintain a positive relationship with clients * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality control duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Assist with training and research assignments including troubleshooting * Independently pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Assisting in developing and revising Standard Operating Procedures (SOPs) * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assist with managing priorities and schedule * Responsible for the safety of oneself and others working within their area * Responsible for the completion of required training * Travel is required and at the discretion of management OTHER DUTIES * Perform other duties as assigned * As needed from time to time, assist in performing Login Technician, Media Technician, and/or Micro Technician. * If assigned, conduct responsibilities of Branch Safety Coordinator outlined in the corporate safety manual and report to the Corporate Safety Officer for assigned duties SUPERVISORY RESPONSIBILITIES * This job has no regularly assigned supervisory responsibilities, although the position is expected to train others, and step in to perform supervisory responsibilities when the Sr. Microbiologist, Lead or the Supervisor is not available. MINIMUM QUALIFICATIONS * Bachelor's degree in Life Science or related field, microbiology preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiar with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary KNOWLEDGE, SKILLS, and ABILITIES To perform the job successfully, an individual should demonstrate the following: * Computer - Proficient in standard business office software, LIMS, and internet search tools. * Customer Service - Responds promptly to customer needs; Responds to requests for service and assistance; Meets commitments. * Verbal & Written Communication; Language Skills - Clarity of speech, remaining calm and focused, being polite and making effective presentations to diverse groups. Edits work for correct data, spelling, and grammar. Ability to read and comprehend simple instructions, short correspondence, and memos. * Mathematical Skills - Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; Ability to perform financial calculations, compute rate, ratio, and percent and to draw and interpret bar graphs. * Analytical, Problem Solving, & Organizational Skills - Gathers and analyzes information skillfully and can efficiently execute on plans/ideas. Ability to deal with problems involving a few concrete variables in standardized situations. Interprets data and test results. * Independent Judgement and Discretion - Proficient and confident in exercising independent judgement and discretion on a consistent basis throughout the day in performing the testing, analytical and interpretive responsibilities of the position. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. FSNS complies with its reasonable accommodation obligations under the Americans with Disabilities Act and state law. * Regularly required to stand, sit, walk, use hands and arms, talk and hear * Lift up to 25 pounds * Color vision and depth perception WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks Safety: * Required to wear appropriate protective clothing * Required to use appropriate protective equipment * Responsible for the safety of oneself and others working within their area PROFICIENCY REQUIREMENTS Employees in this role will be evaluated after 90 calendar days from date of hire and annually thereafter based on the following proficiencies: * In addition to the responsibilities of this position, maintain competency in duties performed by technicians in other departments (Log-In, Media, Main) to provide assistance when needed * Exercise of sound independent judgment and discretion * Knowledge of all qualitative, quantitative testing, and confirmations performed * Resource for all technicians in Main Lab * Proficient in the passing and first approval process and may complete second approvals * Excellent aseptic technique and use of the biological hood * Understand client specifications * Ability to assume the responsibilities and make decisions of the Sr. Microbiologist, Lead, or Supervisor, when they are not available * Ensure daily, weekly, and monthly sanitation and QC are complete * Help resolve technical issues with machines * Proficiency in testing for all path lab analyses on A2LA Scope ( * Versed in GLP, FDA, USDA, AOAC, and other method reference sources * Manage workload and ensure TAT is met by delegation of work to self and others * Assist Technical Manager, as needed All Certified Group employees must be proficient in the following: * Ability to multitask and quickly move from one task to the next * Ability to complete tasks with accuracy * General knowledge of all FSNS safety protocols & general OSHA laboratory safety guidelines * Working knowledge of ISO 17025 Quality procedures general to their primary job and area of responsibility * Ability to perform laboratory opening and closing procedures Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off * Many positions which qualify for the company bonus program Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Monday through Friday, 8:00AM to 5:00PM

Full-time Description JOB TITLE: Microbiologist II 2509-18480-MICROII-001 Atlanta, GA, USA ASRT, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients. The successful candidate will be a full-time employee of ASRT, Inc. and will be assigned to the Division of Foodborne, Waterborne, and Environmental Diseases (DFWED), National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), at the CDC, 1600 Clifton Road, Atlanta, GA, to provide scientific and technical support for the EDLB. SCOPE OF WORK The Microbiologist II will provide scientific and laboratory support to the Division of Foodborne, Waterborne and Environmental Diseases (DFWED) in its preparedness and response to foodborne and diarrheal diseases in the United States and abroad. MAJOR DUTIES AND RESPONSIBILITIES Performs laboratory testing of metagenomics and bioinformatics analysis of metagenomics samples to characterize enteric bacteria. Supports data analysis of metagenomics samples. Assists the development and/or validation of molecular approaches, including but not limited to analytical comparisons of next generation sequencing platforms and reagents/chemistries. Assists in crafting new standard operating procedures, technical documents (e.g., analysis aids and troubleshooting guidance) and training materials. Prepares and delivers clear, concise, and accurate reports and presentations for colleagues and collaborators at internal and external meetings. Effectively communicates and coordinates with others regarding work tasks and plans to accomplish unit, team, and branch objectives. Shares work progress and problems encountered with others in a timely manner. Demonstrates an understanding of program goals and objectives through formal communication and collaboration with partner organizations and stakeholders. Supports the development of bioinformatics pipelines for the analysis of large targeted sequencing data sets for the PulseNet surveillance system. Supports the analysis of large targeted amplicon sequencing data sets used in the validation of laboratory and bioinformatic workflows. Supports the creation and revision of SOPs and validation plans for laboratory and bioinformatic workflows. Requirements MINIMUM QUALIFICATIONS Education and Experience: Master's degree, from an accredited academic institution, in a scientific discipline related to the responsibilities of the position. 2-4 years of experience in the genetic and/or bioinformatic analysis of bacterial genetic markers. Required: Previous experience in a similar role. Knowledge of laboratory and safety regulations including CLIA, ISO, and/or OSHA standards. Experience in aseptic techniques and laboratory analysis of samples Experience working with a number of biological organisms and awareness of their handling and storage. Experience working with and adapting/modifying SOPs. Experience working with Microsoft Word, Excel, and PowerPoint for the preparation of memos and reports. Experience with development and management of a complex relational database. Experience working with statistical software such as SAS, R, Stata, or similar software. Experience working with a number of biological organisms and awareness of their handling and storage. Experience working with Laboratory Information Management Systems (LIMS). Immunizations may be required. Desirable: Specific detailed knowledge of quality systems and regulatory requirements, handling of clinical specimens, and aseptic techniques. Experience working with Next Generation Sequencing (NGS) and molecular techniques associated with NGS. Experience scripting in at least one language (Python, R, or shell preferred). Basic statistics training. Familiarity with the following is helpful: UNIX command line bioinformatics tools Use of version control systems and code repositories (e.g., GitHub) Analysis of next-generation sequencing data, including QC, alignment, quantification, or phylogeny tools Language Skills: The candidate must possess excellent oral and written communication skills in English. REQUIREMENT: Must be a United States citizen or permanent resident or have authorization for employment in the United States. SALARY: Commensurate with qualifications and experience. To apply for this position: If you are viewing this position on the ASRT Career page, please click on the "Apply" button. If you are viewing this position on a site other than the ASRT Career page, you may use the "click to apply" link, or you may apply by visiting our Career page and searching for the job title and position number listed at the top of this job posting. To view all of our open positions and to apply to job openings in which you may be interested, please visit our Career page at ******************************** EEO/vets/disabled

Full-time Description JOB TITLE: Microbiologist II 2512-16248-MICRO-01 Atlanta, GA, USA ASRT, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients. The successful candidate will be a full-time employee of ASRT, Inc. and will be assigned to the Meningitis and Vaccine Preventable Diseases (MVPDB), National Center for Immunization and Respiratory Diseases (NCIRD), at the CDC, 1600 Clifton Road, Atlanta, GA, to provide technical support for molecular and serological diagnosis of pertussis and diphtheria. SCOPE OF WORK The Microbiologist II will provide technical support for molecular and serological diagnosis of pertussis and diphtheria. This task will Provide laboratory technical support services for molecular and serologic diagnosis, molecular subtyping including genome-based typing systems, and genomic and proteomic analysis of pertussis and diphtheria etiologic agents. MAJOR DUTIES AND RESPONSIBILITIES Laboratory such as real-time PCR, DNA sequencing, genome-based typing systems and immunologic assays, including conventional and electro chemiluminescent ELISAs, Luminex bead-based assays, western blots, etc. Collaborate on the development and validation of novel diagnostic and molecular typing techniques for Bordetella and Corynebacterium species. Assist in providing support to other areas of the PDL Team (data analysis, specimen management). Perform assays as needed during pertussis and diphtheria outbreak responses or special requests. Collaborate on the development and validation of novel diagnostic assays for Bordetella and Corynebacterium species. Collaborate closely with other epidemiologists/coordinators in other CDC and MVPDB domestic and international programs. Support development and validation of diagnostics tests, molecular typing systems including advanced molecular detection. techniques (genomics, transcriptomes, proteomes), and laboratory diagnosis support during outbreak responses. Since MVPDB, CDC is a global resource for the diagnosis of bacterial meningitis, pertussis and diphtheria and for the taxonomy of the microorganisms involved with these diseases, this project should enhance these important functions. Perform a variety of lab experiments in support of research programs and projects of PDL. Responsibilities will include ability to follow laboratory protocols and conduct microbiological, serological, antibiotic resistance, and molecular biology procedures to accomplish laboratory research goals. Assist in performing domestic and international laboratory training to support surveillance as well as clinical validation of laboratory tests related to the diagnosis of these diseases. Perform inventory management as well as ordering and distribution of panels for proficiency testing if requested. Ensure Compliance with Laboratory Safety procedures and regulations, Quality Management System (QMS) and Clinical Laboratory Improvement Amendments (CLIA) regulations and maintain assigned laboratory areas, equipment and protocols in compliance with local and federal requirements for quality, safety and security. Assist in the accessioning, maintenance and database management of clinical and non-clinical specimens to support studies of vaccines and diagnostics for a range of vaccine preventable diseases including pertussis. Assist in the development and optimization of in vitro assays to measure biological responses to vaccination and infection in human or animal specimens. Maintenance of eukaryotic cell cultures and cell lines; preparation of cell banks and working cell stocks, and cell plates. Receive training for a variety of techniques and participate in research projects. Management and coordination of a variety of special projects (domestic and global) within the branch Participate in collaborative studies, training and QC/QA programs designed to promote technology transfer of diagnostic assays and harmonization among laboratories. Collaborate on the development and validation of novel diagnostic and typing techniques for Bordetella species. Assist in providing support to other areas of the pertussis and diphtheria laboratory team (data analysis, specimen management). Perform assays as needed during pertussis outbreak response. Comply CLIA regulations and maintains assigned laboratory areas, equipment and protocols in compliance with local and federal requirements for quality, safety and security. Expert knowledge and ability to perform molecular and immunological methods such as polymerase nucleic acid amplification, ELISA, laboratory databases and specimen managemen.t Liaison between CDC and laboratory supply companies in order to verify delivery of several of equipment Preparation, arrangement and repair for laboratory equipment. Keep accurate reports on contractual renewals for maintenance agreements for laboratory equipment Prepare service contract documents. Review and order lab supplies for the meningitis and pertussis team. Bacterial culture and characterization, antimicrobial susceptibility testing, and bacterial molecular typing techniques such as DNA sequencing and pulsed field gel electrophoresis. The capability of designing experiments independently, developing new assays, and troubleshooting. Familiar with the different bioinformatics software used in the Meningitis Laboratory for data analysis and interpretation useful but not required. Performs laboratory analyses to support efforts described in the statement of work above. Provide support to the CDC EOC for agency response activities when the EOC is activated. Provide support for CDC pandemic activities. Requirements MINIMUM QUALIFICATIONS Education and Experience: Bachelor's degree in microbiology, biology, chemistry, or basic medical science that included at least 20 semester hours in microbiology and other subjects related to the study of microorganisms, and 20 semester hours in the physical and mathematical sciences combining course work in organic chemistry or biochemistry, physics, and college algebra, or their equivalent. Required: Research experience involving the use of molecular and immunological methods such as the preparation and handling of nucleic acid samples, real-time PCR, ELISA, and other standard laboratory methods. Organizational skills demonstrating high attention to detail and the ability to organize and manage multiple priorities. Documentation of daily work with good laboratory practice. Knowledge of biosafety requirements for research being performed. Experience working with Microsoft Office, Access, Excel, and PowerPoint. Strong interpersonal skills required for team work and interaction with people across CDC and with external partners. Desirable: Experience developing real-time PCR or ELISA based in vitro diagnostic assays. Experience writing project reports, research protocols and manuscripts. Ability to synthesize new ideas for project research. Language Skills: The candidate must possess excellent oral and written communication skills in English. REQUIREMENT: Must be a United States citizen or permanent resident or have authorization for employment in the United States. SALARY: Commensurate with qualifications and experience. To apply for this position: If you are viewing this position on the ASRT Career page, please click on the "Apply" button. If you are viewing this position on a site other than the ASRT Career page, you may use the "click to apply" link, or you may apply by visiting our Career page and searching for the job title and position number listed at the top of this job posting. To view all of our open positions and to apply to job openings in which you may be interested, please visit our Career page at ******************************** EEO/VETS/Disabled

Full-time Description JOB TITLE: Microbiologist II 2511-18480-MICROII Atlanta, GA, USA ASRT, Inc. provides scientific, information management, management consulting, bioinformatics, and administrative program support to the Centers for Disease Control and Prevention (CDC) and other Federal and private sector clients. The successful candidate will be a full-time employee of ASRT, Inc. and will be assigned to the Division of Foodborne, Waterborne, and Environmental Diseases (DFWED), National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), at the CDC, 1600 Clifton Road, Atlanta, GA, to provide scientific and technical support for the EDLB. SCOPE OF WORK The Microbiologist II will provide scientific and laboratory support to the Division of Foodborne, Waterborne and Environmental Diseases (DFWED) in its preparedness and response to foodborne and diarrheal diseases in the United States and abroad. MAJOR DUTIES AND RESPONSIBILITIES Tracks, analyzes, troubleshoots, and corrects performance and problems associated with antimicrobial susceptibility, identification, and other related assays. Prepares and updates standard operating procedures for antimicrobial susceptibility and related assays. Co-authors relevant abstracts and peer-reviewed publications related to antimicrobial resistance surveillance and outbreak characterization. Provides consultation, hands-on training and/or competency assessments for antimicrobial susceptibility and related assays with internal and external partners. Develops and maintains documentation and other requirements related to team, branch, and CDC safety and quality programs. Coordinates outbreak characterization and reporting with stakeholders within and outside CDC. Perform antimicrobial susceptibility testing of enteric pathogens, Analyzes, and interprets results to assist in monitoring trends and changes in drug resistance. Effectively communicate and coordinate with others regarding work tasks and plans in order to accomplish antimicrobial susceptibility surveillance and research objectives. Share work progress and problems encountered with others in a timely manner. Demonstrates an understanding of program goals and objectives through formal communication and collaboration with partner organizations and stakeholders Requirements MINIMUM QUALIFICATIONS Education and Experience: Bachelor's degree, from an accredited academic institution, in a scientific discipline related to the responsibilities of the position. Required: Previous experience in a similar role. Knowledge of laboratory and safety regulations including CLIA, ISO, and/or OSHA standards. Experience in aseptic techniques and laboratory analysis of samples Experience working with several biological organisms and awareness of their handling and storage. Experience working with and adapting/modifying SOPs. Experience working with Microsoft Word, Excel, and PowerPoint for the preparation of memos and reports. Experience with the development and management of a complex relational database. Experience working with a number of biological organisms and awareness of their handling and storage. Experience working with Laboratory Information Management Systems (LIMS). Immunizations may be required. Desirable: Specific detailed knowledge of quality systems and regulatory requirements, handling of clinical specimens, and aseptic techniques. Ability to troubleshoot instrument issues or address any aberrant quality control failures. Experience in coordinating with other lab staff in a high-throughput environment. Language Skills: The candidate must possess excellent oral and written communication skills in English. REQUIREMENT: Must be a United States citizen or permanent resident or have authorization for employment in the United States. SALARY: Commensurate with qualifications and experience. To apply for this position: If you are viewing this position on the ASRT Career page, please click on the "Apply" button. If you are viewing this position on a site other than the ASRT Career page, you may use the "click to apply" link, or you may apply by visiting our Career page and searching for the job title and position number listed at the top of this job posting. To view all of our open positions and to apply to job openings in which you may be interested, please visit our Career page at ******************************** EEO/vets/disabled

$10,000.00 SIGN-ON BONUS ELIGIBLE The Laboratory Technologist will demonstrate multiple analytical and judgment skills and knowledge of clinical laboratory science to provide accurate, timely results. The incumbent uses high complexity methods and instrumentation and will work independently in multiple areas of the laboratory. Essential Job Functions * Procure, prepare and process specimen using various approved techniques and procedures. * Perform phlebotomy in accordance with established procedures and in a manner consistent with customer service needs and expectations. * Receive specimens into the LIS, verifies orders, understands priorities and communicates all pertinent information. * Validate test orders, appropriateness of specimen and ensure required documentation is present. * Process and organize specimens using standard precautions, maintaining specimen integrity and identity. * Recognize, resolve and document specimen tracking and integrity issues. * Utilize specimen rejection and irretrievable specimen policies to document specimen issues. * Validate and research unusual reference test orders, arrange proper specimen collection, and ensure that documentation is complete and information effectively communicated. * Package specimens for transport according to regulations and established protocol. * Prepare appropriate quantity of reagents and consumables in accordance with section guidelines; maintains reagents to maximize stability and shelf-life. * Perform preventative and corrective maintenance; anticipate problem situations and take preventative action to avoid delay of patient care. * Maintain supplies at adequate levels to support operations, monitoring utilization and reporting unusual situations to supervisor. * Perform low, moderate and high complexity technical assays, evaluate and interpret results forming conclusions requiring a high level of judgment. * Determine and validate appropriate instrument settings and making adjustments as needed. * Demonstrate competency on all instrumentation and methods in assigned work areas. * Perform laboratory tests in assigned area, using established protocols and with an awareness of accuracy, method sensitivity, specificity, and turn-around-time and cost management. * Assess test methods for procedural validity and testing accuracy, re-evaluating patient data for validity when instrument or methodology malfunctions are suspected. * Perform and document all quality control, maintenance and variances. * Maintain an in-depth knowledge of the test methods and procedures in two or more laboratory sections, and show an understanding of the correlation of patient results to the overall clinical picture. * Identify, investigate and resolve questionable test orders and/or results through correlation of disease state/diagnosis and patient history. * Assess specimen integrity, validity and identification; recognize abnormal, unusual, or problem situations, and correlate patient laboratory results when specimens are suboptimal. * Correlate patient data with other clinical information to assess the possibility of inconsistent orders or results. * Participate in a quality management system to include quality control and assurance of laboratory testing, competency assessment and appropriate utilization of laboratory services. * Compose correlation studies, QC reports, and maintain monthly logs. * Evaluate quality control data to assist the supervisor in the assessment of accuracy, reproducibility and validity of methods. * Participate in section readiness to meet CAP, JCAHO, OSHA and DOH compliance. * Utilize HIS as needed for patient or test order information, and to process supply or work orders. * Utilize functions of LIS to accession, receive, result and monitor functions related to patient testing. * Participate in initial and monthly validation of LIS and instrument interfaces. * Evaluate laboratory data to assess the need for recollection of the specimen. * Correlate patient laboratory results to suspect pathological state, and recognizes the need for follow-up or reflex testing. * Redirect testing to appropriate backup or secondary test methods and seeks to resolve primary testing issues. * Interact with healthcare providers to interpret laboratory results within the framework of medical technology. * Answer inquiries from other healthcare providers concerning test appropriateness, quality, accuracy and procedural requirements. * Assist in the evaluation and development of new methods/instruments. * Recommend process improvements to workflow and assist in implementation of changes to improve operation. * Report and document critical values and read back verifications according to policy. * Adhere to laboratory and section specific Environmental Control Plan. * When appropriate, enter reflex testing codes into LIS to generate billing. * Retain records of instrument printouts and specimens according to policy. * Other duties as assigned. Competency and Experience [Knowledge, Skills and Abilities] Required Qualifications/Experience * Associate of Science or higher-level degree from an accredited institution in chemical, physical, biological or clinical laboratory science, or medical technology, OR, * Equivalent laboratory training and experience meeting the requirements defined by CLIA 88 for individuals performing high complexity testing. * Knowledge of Medical terminology and laboratory information system. * Functional skills in Microsoft Office applications, including Outlook. * Strong leadership ability, good organizational skills, independent and critical thinking skills, sound judgment, and knowledge of legal aspects and liability of nursing practice. * Strong ability to communicate complex and/or controversial topics and concepts to a wide and diverse audience. Preferred Qualifications/Experience * Prior experience within a clinical laboratory. License, Certification & Clearances * ASCP preferred. * Act 33 clearance with renewal. * Act 34 clearance with renewal. * Act 73 FBI Clearance with renewal. Position Type/Expected Hours of Work * Incumbent will be scheduled based on operational need (rotate shifts, standby, on-call, etc.). * Travel may be expected locally between System locations. Equal Employment Opportunity Independence Health and its affiliated companies are Equal Opportunity Employers. It is their policy to prohibit discrimination of any type and to afford equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, marital status, disability, veteran status, or genetic information, or any other classification protected by law. Independence Health and its affiliated companies will comply with all applicable laws and regulations. Disclaimer This job description is not designed to contain a comprehensive listing of all activities, duties or responsibilities that are required of the employee. Moreover, duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Work EnvironmentEffective March 2020 or during pandemic: goggles, face shield and mask are required according to CDC guidelines When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Extreme Heat X X Extreme Cold X X Heights X X Confined Spaces X X Extreme Noise(>85dB) X X Mechanical Hazards X X Use of Vibrating Tools X X Operates Vehicle X Operates Heavy Equipment X Use of Lifting/Transfer Devices X Rotates All Shifts X X 8 Hours Shifts X X 10-12 Hours Shifts X X On-Call X Overtime(+8/hrs/shift; 40/hrs/wk) X X Travel Between Sites X X Direct Patient Care X X Respirator Protective Equipment X X Eye Protection X X Head Protection (hard hat) X Hearing Protection X X Hand Protection X X Feet, Toe Protection X Body Protection X X Latex Exposure X X Solvent Exposure X X Paint (direct use) Exposure X Dust (sanding) Exposure X Ethylene Oxide Exposure X Cytotoxic (Chemo) Exposure X Blood/Body Fluid Exposure X X Chemicals (direct use) Exposure X X Mist Exposure X Wax Stripper (direct use) X Non-Ionizing Radiation Exposure X Ionizing Radiation Exposure X Laser Exposure X X Physical Demands When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Bending (Stooping) X X Sitting X X Walking X X Climbing Stairs X X Climbing Ladders X X Standing X X Kneeling X X Squatting (Crouching) X X Twisting/Turning X X Keyboard/Computer Operation X X Gross Grasp X X Fine Finger Manipulation X X Hand/Arm Coordination X X Pushing/Pulling(lbs. of force) X X Carry X X Transfer/Push/Pull Patients X Seeing Near w/Acuity X X Feeling (Sensation) X X Color Vision X X Hearing Clearly X X Pulling/Pushing Objects Overhead X X Reaching Above Shoulder Level X X Reaching Forward X X Lifting Floor to Knuckle X 25# Lifting Seat Pan to Knuckle X 10# Lifting Knuckle to Shoulder X 10# Lifting Shoulder to Overhead X 10# When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required.

$10,000.00 SIGN-ON BONUS ELIGIBLE The Laboratory Technologist will demonstrate multiple analytical and judgment skills and knowledge of clinical laboratory science to provide accurate, timely results. The incumbent uses high complexity methods and instrumentation and will work independently in multiple areas of the laboratory. Essential Job Functions Procure, prepare and process specimen using various approved techniques and procedures. Perform phlebotomy in accordance with established procedures and in a manner consistent with customer service needs and expectations. Receive specimens into the LIS, verifies orders, understands priorities and communicates all pertinent information. Validate test orders, appropriateness of specimen and ensure required documentation is present. Process and organize specimens using standard precautions, maintaining specimen integrity and identity. Recognize, resolve and document specimen tracking and integrity issues. Utilize specimen rejection and irretrievable specimen policies to document specimen issues. Validate and research unusual reference test orders, arrange proper specimen collection, and ensure that documentation is complete and information effectively communicated. Package specimens for transport according to regulations and established protocol. Prepare appropriate quantity of reagents and consumables in accordance with section guidelines; maintains reagents to maximize stability and shelf-life. Perform preventative and corrective maintenance; anticipate problem situations and take preventative action to avoid delay of patient care. Maintain supplies at adequate levels to support operations, monitoring utilization and reporting unusual situations to supervisor. Perform low, moderate and high complexity technical assays, evaluate and interpret results forming conclusions requiring a high level of judgment. Determine and validate appropriate instrument settings and making adjustments as needed. Demonstrate competency on all instrumentation and methods in assigned work areas. Perform laboratory tests in assigned area, using established protocols and with an awareness of accuracy, method sensitivity, specificity, and turn-around-time and cost management. Assess test methods for procedural validity and testing accuracy, re-evaluating patient data for validity when instrument or methodology malfunctions are suspected. Perform and document all quality control, maintenance and variances. Maintain an in-depth knowledge of the test methods and procedures in two or more laboratory sections, and show an understanding of the correlation of patient results to the overall clinical picture. Identify, investigate and resolve questionable test orders and/or results through correlation of disease state/diagnosis and patient history. Assess specimen integrity, validity and identification; recognize abnormal, unusual, or problem situations, and correlate patient laboratory results when specimens are suboptimal. Correlate patient data with other clinical information to assess the possibility of inconsistent orders or results. Participate in a quality management system to include quality control and assurance of laboratory testing, competency assessment and appropriate utilization of laboratory services. Compose correlation studies, QC reports, and maintain monthly logs. Evaluate quality control data to assist the supervisor in the assessment of accuracy, reproducibility and validity of methods. Participate in section readiness to meet CAP, JCAHO, OSHA and DOH compliance. Utilize HIS as needed for patient or test order information, and to process supply or work orders. Utilize functions of LIS to accession, receive, result and monitor functions related to patient testing. Participate in initial and monthly validation of LIS and instrument interfaces. Evaluate laboratory data to assess the need for recollection of the specimen. Correlate patient laboratory results to suspect pathological state, and recognizes the need for follow-up or reflex testing. Redirect testing to appropriate backup or secondary test methods and seeks to resolve primary testing issues. Interact with healthcare providers to interpret laboratory results within the framework of medical technology. Answer inquiries from other healthcare providers concerning test appropriateness, quality, accuracy and procedural requirements. Assist in the evaluation and development of new methods/instruments. Recommend process improvements to workflow and assist in implementation of changes to improve operation. Report and document critical values and read back verifications according to policy. Adhere to laboratory and section specific Environmental Control Plan. When appropriate, enter reflex testing codes into LIS to generate billing. Retain records of instrument printouts and specimens according to policy. Other duties as assigned. Competency and Experience [Knowledge, Skills and Abilities] Required Qualifications/Experience Associate of Science or higher-level degree from an accredited institution in chemical, physical, biological or clinical laboratory science, or medical technology, OR, Equivalent laboratory training and experience meeting the requirements defined by CLIA 88 for individuals performing high complexity testing. Knowledge of Medical terminology and laboratory information system. Functional skills in Microsoft Office applications, including Outlook. Strong leadership ability, good organizational skills, independent and critical thinking skills, sound judgment, and knowledge of legal aspects and liability of nursing practice. Strong ability to communicate complex and/or controversial topics and concepts to a wide and diverse audience. Preferred Qualifications/Experience Prior experience within a clinical laboratory. License, Certification & Clearances ASCP preferred. Act 33 clearance with renewal. Act 34 clearance with renewal. Act 73 FBI Clearance with renewal. Position Type/Expected Hours of Work Incumbent will be scheduled based on operational need (rotate shifts, standby, on-call, etc.). Travel may be expected locally between System locations. Equal Employment Opportunity Independence Health and its affiliated companies are Equal Opportunity Employers. It is their policy to prohibit discrimination of any type and to afford equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, marital status, disability, veteran status, or genetic information, or any other classification protected by law. Independence Health and its affiliated companies will comply with all applicable laws and regulations. Disclaimer This job description is not designed to contain a comprehensive listing of all activities, duties or responsibilities that are required of the employee. Moreover, duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Work EnvironmentEffective March 2020 or during pandemic: goggles, face shield and mask are required according to CDC guidelines When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Extreme Heat X X Extreme Cold X X Heights X X Confined Spaces X X Extreme Noise(>85dB) X X Mechanical Hazards X X Use of Vibrating Tools X X Operates Vehicle X Operates Heavy Equipment X Use of Lifting/Transfer Devices X Rotates All Shifts X X 8 Hours Shifts X X 10-12 Hours Shifts X X On-Call X Overtime(+8/hrs/shift; 40/hrs/wk) X X Travel Between Sites X X Direct Patient Care X X Respirator Protective Equipment X X Eye Protection X X Head Protection (hard hat) X Hearing Protection X X Hand Protection X X Feet, Toe Protection X Body Protection X X Latex Exposure X X Solvent Exposure X X Paint (direct use) Exposure X Dust (sanding) Exposure X Ethylene Oxide Exposure X Cytotoxic (Chemo) Exposure X Blood/Body Fluid Exposure X X Chemicals (direct use) Exposure X X Mist Exposure X Wax Stripper (direct use) X Non-Ionizing Radiation Exposure X Ionizing Radiation Exposure X Laser Exposure X X Physical Demands When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Bending (Stooping) X X Sitting X X Walking X X Climbing Stairs X X Climbing Ladders X X Standing X X Kneeling X X Squatting (Crouching) X X Twisting/Turning X X Keyboard/Computer Operation X X Gross Grasp X X Fine Finger Manipulation X X Hand/Arm Coordination X X Pushing/Pulling(lbs. of force) X X Carry X X Transfer/Push/Pull Patients X Seeing Near w/Acuity X X Feeling (Sensation) X X Color Vision X X Hearing Clearly X X Pulling/Pushing Objects Overhead X X Reaching Above Shoulder Level X X Reaching Forward X X Lifting Floor to Knuckle X 25# Lifting Seat Pan to Knuckle X 10# Lifting Knuckle to Shoulder X 10# Lifting Shoulder to Overhead X 10# When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required.

The Quality Control Microbiologist I is responsible for performing microbiological testing and managing results of incoming raw materials, in-process samples, and final product samples. Review and analyze testing data to ensure internal specifications are met in accordance with standard operating procedures requirements. Ensure testing results are accurate, and results are available in a timely manner. Performs all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Requirements Perform microbiology testing including, but not limited to reading of cultures, gram staining, microbial limit test, cell count and cell viability testing, growth promotion testing, and biochemical testing. Support the environmental monitoring program (EM), Stability Program, and the Dose Audit Program. Perform microbial characterization including subcultures of samples, gram stain, biochemical testing, and final identification using VITEK 2. Conduct testing of clean utilities of the facility, including but not limited to performing TOC, pH, and conductivity testing. Review and analyze test results according to internal standard procedures to ensure proper management, tracking, and disposition of materials and products Responsible for reporting all variances, errors, and deviations to Quality Management. Maintain proper documentation and trend analysis of QC test results. Perform laboratory cleaning and maintenance of equipment. Maintains the laboratory stock of media, reagents and laboratory supplies. Support validations and qualifications that require microbiological testing. Participate in audits and inspections, accreditation, and licensing activities as needed. Supports investigations, complaints, and deviations contributing to the formulation and implementation of corrective actions. Participate in the on-call weekend schedule. Perform other duties as assigned by QC Management. Qualifications Education/Experience: Bachelor's degree in science with at least 0-2 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Associate's degree in science with at least 2 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Required/Preferred Experience: Hands on Environmental Monitoring experience in a regulated GMP environment (cleanroom EM, viable/non-viable monitoring, trend analysis, excursions). Skills: Excellent interpersonal, verbal, and written communication skills required. Must demonstrate excellent organizational and record-keeping skills. Must be detail oriented with the ability to multi-task in a high-pressure environment. Proficient in Microsoft Office. Working conditions Fast pace, lab-oriented work environment. Evening and weekend work may be required. Physical requirements While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. VIVEX Biologics complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.

As a Microbiology Laboratory Technician (MLT) at IDEXX, you will be a key contributor at one of the largest veterinary diagnostic companies in the world. You will perform laboratory testing that helps veterinarians diagnose and treat pets. You will join a fast-paced work environment that encourages teamwork, quality, and offers opportunities for personal growth. This is a full-time role with competitive benefits. Want to see what it is like to work in our lab? Check out these videos from our lab employees talking about working at IDEXX: ****************************** In This Role: * You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. * You will be performing diagnostic tests on blood, urine, fecal or pet biopsy samples that we receive in our lab by the thousands, every day. * You will be responsible for setting up and running lab tests and reading and releasing results according to SOPs (Standard Operating Procedures). * You can expect to specialize in the following area: * Microbiology: Processing clinical samples for the identification of bacteria and fungi using automated and manual methods. What You'll Need to Succeed: * Ideally, you will have experience setting up, running, and reading lab tests, and operating laboratory equipment (microscopes, pipetting and / or clinical diagnostic analyzers). * You have experience with diagnostic microbiology testing. * You have a positive attitude and love to bring that energy into the lab every day to support your colleagues * You are looking forward to working in a team * You concentrate on the details and can work reliably and precisely * You have a great sense of team spirit and responsibility * You possess a High School diploma or equivalent combination of education and experience is required. A 2-, 3- or 4-year degree in a Science-related field is preferred. * It is not required to work in our lab, but if you were a Veterinary Technician (RVT, LVT, CVT) or Medical Laboratory Technician (MLT or MT), this experience and education would be a plus. * Able to meet the physical requirements that go with working in a lab - standing and sitting for extended periods of time, phone & computer use, extended reach, lifting up to 50lb, and specific vision ability - close, color, depth perception, and ability to adjust focus. * This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. What You Can Expect From Us: * Hourly rates targeting $23/hour * Opportunity for annual cash bonus and merit pay increase consideration * Health / Dental / Vision Benefits Day - One * 5% matching 401k * On the job training and career advancement opportunities (experience NOT required) * Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more! * Opportunity to do meaningful work where you positively impact the lives of people and pets all over the world Schedule: * This is a Sunday through Thursday position. Hours on Sunday only are10am-6:30pm; Monday to Thursday the hours are 12:30pm - 9pm. * The shifts and hours may vary slightly depending on business needs. * Reliable and dependable attendance is an essential function of the position. Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. Does this sound like the opportunity for you? Apply today! #LI-SM1

Crete Science Center Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Molecular Microbiologist in 3600 Eagle Nest Dr, Crete, IL 60417 USA. Your mission will be to: Purpose (Objective): The incumbent prepares isolates, RNA and DNA, maintains process documentation to facilitate microbiological and molecular biology analysis procedures and may interpret results for final release. Main activities: ●Performs microbiological tests including gene sequencing, DNA subtyping analysis, MALDI-TOF for identification and real-time PCR methods including non-commercial PCR methods (e.g., open source PCR). ●Perform literature and nucleic acid sequence searches as necessary to investigate and understand results. ●Verifies results before release to the clients. Read and record analysis data to produce a report for the client. Correct any discrepancies that occur. Proactive in contacting industry technical support to troubleshoot results or equipment issues. ●Troubleshooting of data, methods and equipment as required. ●Performs sub-culturing using proper aseptic technique and determines growth conditions for a variety of groups of microorganisms. ●Perform necessary housekeeping duties in a timely manner, keeping the work areas and equipment clean and sanitized. Perform standard maintenance for key pieces of equipment. Perform cleaning protocols for GMP and ISO 17025 laboratory work space. Maintain accurate quality control documentation of analysis procedures.Perform necessary tasks related to quality control parameters for the function being preformed. ●Preparation of reagents, chemical solutions and media as required ●Interact with other department personnel to maintain smooth flow of work. ●Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. ●Support corporate quality and continuous improvement process.Responsibility to support laboratory management in the implementation, maintenance, and improvement of the management system. ●This position has the responsibilities and authority to identify departures from the management system or test procedures and document such observations accordance with the prescribed non-conforming system and notifies the supervisor. ●Adhere to all safety policies. ●Perform other related tasks as needed. YOUR PROFILE Profile: ●Good knowledge of molecular biology and microbiology to accurately perform testing procedures and obtain the correct results. ●Knowledge of growth conditions of a variety of microorganisms is required. ●A basic knowledge of food science is necessary to interpret results. ●A broad knowledge of laboratory safety procedures and policies is necessary to ensure a safe working environment. ●Basic chemistry knowledge is needed to prepare the media to the specification of the sample. ●Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities. Required skills: ●Analytical skills are helpful to complete analysis procedures and determine the concentration of the microorganism. ●Physical dexterity with pipetting is required for pipetting. ●Laboratory skills obtained as a laboratory technician or similar position are essential to perform the necessary analyses. ●Oral and written communication skills are necessary to supervise departmental personnel. ●Organizational and planning skills are useful to schedule testing to ensure that analysis is completed within the specified time period. The incumbent encounters routine difficulties frequently that require the analysis of each situation to determine the cause. Problems can result from incorrect growth conditions and improper technique. Testing procedures require precise measurement and knowledge of microorganisms to be made to avoid problems. The microorganisms do not follow the same pattern continuously and may require testing to be modified by assessment of previous results. The source of the problem will determine the method of solution. Standard procedures and established guidelines provide the needed information to solve testing problems. Coordination of departmental activities with those of other departments is necessary to accomplish accurate analysis of sample. The incumbent recommends action to the supervisor to solve problems using previous knowledge of the position and Standard Operating Procedures. Unique or unusual problems can require the input of the supervisor to determine the optimal solution. Modifications may be unfamiliar to the incumbent and require further research before recommending action. Research can be conducted using written company policies and procedures as well as position precedents. The recommendations will impact the progress of the analysis procedures within the immediate work unit and operating expenses of the procedure. The incumbent receives general supervision. The incumbent works toward specific goals and targets established with the supervisor to provide prompt and accurate service to the client. Results and progress are reviewed on a daily basis. The testing procedure must be completed within an established timeframe to avoid delay in client receiving the results. Repeating the analysis or inaccurate results can strain client relations and increase the cost of the procedure. Compensation: $23/hr Full Time Eligible Benefits Overview: Comprehensive medical, dental, and vision insurance plans. Generous paid time off (PTO) package to support work-life balance following state and local ordinances. Optional 401(k) plan with employer matching contributions. The information above provides a general overview and may vary based on specific job responsibilities, location, or other factors. Details will be clarified during the hiring process. WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button