Microbiologist II

Found in: Resume Library US A2 - 1 week ago


North Liberty Iowa, United States Element Materials Technology Full time
Overview:
Element has a current opening for a Microbiologist II at our North Liberty, IA location. Under general direction, the Microbiologist II performs moderate to highly complex laboratory testing and analysis on bacterial and fungal isolates to provide information to the SENTRY program, new drug development protocols and clinical trial protocols. Utilizes professional skill and judgement to perform a variety of microbiology procedures within the laboratory.

Responsibilities:
May perform highly complex quantitative and qualitative analysis on microbiological isolates for clinical trial and research protocols

Processes incoming bacterial and fungal isolates following safety guidelines and using required PPE, selects and labels appropriate media and properly streaks for isolation

Assesses isolates that are received using professional judgment, knowledge of organism characteristics, MALDI-TOF and biochemical tests to properly identify organisms prior to banking

Performs MALDI-TOF isolate identifications and interprets results

Properly pulls frozen isolates from the bank for SENTRY, drug development protocol testing and clinical trials

Prepares for susceptibility runs by performing purity checks, removing MIC panels from freezers, labeling of panels and tubes, and loosening caps on media tubes

Participates in all aspects of MIC testing including subbing isolates, preparing inoculums, pipetting and running inoculating instruments

Interprets MICs results from broth microdilution, agar dilution, disk diffusion and Etest® methodologies

Participates in new drug development protocols and clinical trial protocols which includes an array of susceptibility testing techniques (Broth microdilution + disks and/or Etest®, agar dilution, time-kills, PAEs, etc.)

Follows GLP rules and guidelines for processing of clinical trial isolates, which includes chain of custody procedures, if part of the clinical trial team

Participates in the overall quality assurance program by performing QC testing and documenting results appropriately

Informs Laboratory Manager and QA department if failures are observed and carries out recommended corrective actions

Provides direction to Laboratory Assistants with regard to processing specimens, susceptibility testing and pulling isolates from the bank

Provides technical direction and oversight to Microbiologist I on complex testing and analysis of microbiological isolates.

Participates in training of Laboratory Assistants and Microbiologist I on testing techniques and interpretation of results, as required

Calibrates, troubleshoots and conducts routine maintenance on laboratory instrumentation

Investigates and resolves problems related to testing procedures

Complies with applicable regulatory and safety requirements of the laboratory

Effectively communicates issues and ideas for efficiencies to the Laboratory Manager

Assists with writing and revising laboratory procedures according to CLSI and regulatory guidelines

Performs routine cleaning and maintenance tasks within the laboratory

Demonstrates professional development

Skills / Qualifications:
Bachelor’s Degree in a laboratory science field from an accredited college or university or an equivalent combination of EDUCATION AND EXPERIENCE is required

Certification by the American Society of Clinical Pathologists or National Certifying Agency is desirable

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Company Overview:
Element is one of the fastest growing testing, inspection and certification businesses in the world. Globally we have more than 9,000 brilliant minds operating from 270 sites across 30 countries. Together we share an ambitious purpose to ‘Make tomorrow safer than today’.

 

When failure in use is not an option, we help customers make certain that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.

 

While we are proud of our global reach, working at Element feels like being part of a smaller company. We empower you to take charge of your career, and reward excellence and integrity with growth and development.

 

Industries across the world depend on our care, attention to detail and the absolute accuracy of our work. The role we have to play in creating a safer world is much bigger than our organization.

Diversity Statement:
At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world’s most trusted testing partner”.

 

All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws.

 

The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c) 

 

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