Microbiologist I

Tanaq Management Services LLC•Atlanta, GA

3h•Onsite

About The Position

We are seeking a highly motivated Microbiologist I to support ongoing projects within public health and the federal government. The successful candidate will have a strong background in molecular biology, clinical, and laboratory techniques. In addition, the candidate will be able to work independently as well as part of a team. The ideal candidate will also have experience with data analysis and interpretation. The position will involve supporting a variety of laboratory projects, including the development of new vaccines, the study of infectious diseases, molecular epidemiology, and surveillance. The successful candidate will have the opportunity to contribute to important research that is making a difference in the fight against disease. A Microbiologist I is responsible for performing various laboratory-based tasks to support the laboratory. This includes tasks such as sample processing, culturing bacteria, biomolecule isolation, and molecular analyses including PCR, real-time PCR, and whole genome and amplicon sequencing library preparation. The Microbiologist I will also work with the team to develop and implement quality control procedures. This is a fully onsite position at our customer's location in Atlanta, Georgia.

Requirements

Minimum 2-3 years of laboratory experience with molecular biological laboratory procedures and methods.
Experience conducting research that involves preparation and handling of nucleic acid samples, real-time PCR, ELISA, etc.
Extensive knowledge of laboratory principles and standard methods.
Experience analyzing data from scientific projects and programs using appropriate programs (e.g., Excel, BLAST, etc.)
Experience assisting with specimen accessioning, scanning, and uploading documents into the electronic laboratory management system (ELIMS).
Experience writing project reports, research protocols and manuscripts, with the ability to synthesize new research ideas for project research preferred.
Experience performing laboratory work at a biosafety level 2 (BSL-2) or BSL-2-enhanced required.
Proficiency in Microsoft Office suite, including Excel, required.
Strong attention to detail.
Ability to work independently and as part of a team in a fast-paced setting.
Excellent written and verbal communication skills.
Effective organization skills.
Ability to obtain a government clearance.
Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future.
Bachelor’s degree in molecular biology, Microbiology, Life Sciences or closely related field.
Ability to obtain necessary immunizations against vaccine-preventable diseases relevant to laboratory placement, including Hepatitis B, among others.
Ability to obtain respiratory clearance and fit testing may be required.
Prolonged periods of sitting at a desk and working on a computer.
May need to lift 25 pounds regularly.
Must be able to work with hazardous chemicals and potentially infectious biological agents.
Must be physically capable of performing repetitive motions such as pipetting and operating cell counters

Nice To Haves

Experience working in a public health setting, ideally supporting the federal government, preferred.
Experience writing project reports, research protocols and manuscripts, with the ability to synthesize new research ideas for project research preferred.

Responsibilities

Maintain inventories of laboratory equipment and supplies.
Follow standard operating procedures and ensure that all work is completed accurately and efficiently.
Perform aseptic technique, processing, detection, and enumeration of pathogens and associated genes.
Perform conventional and molecular microbiologic techniques for the isolation, identification, and subtyping of pathogens.
Prepare samples for sequencing and metagenomic analysis, including extraction and library prep.
Perform conventional and real-time polymerase chain reaction (PCR) and data analysis.
Meet with SME/project leads at least bi-weekly to discuss testing results and plans.
Assist with preparing written documents, reports, and analyses of various scientific projects and programs by creating drafts, editing, and/or reviewing final products.
Manage incoming specimen processing, inventory, and “chain of custody” requirements as determined by Lab Coordinators.
Prepare written protocols and documents according to QMS guidelines.
Analyze data from scientific projects and programs using appropriate programs (e.g., Excel, BLAST, etc.)
Provide a weekly project update to SME/project leads.
May need to assist with processing clinical samples.