Microbiology Associate I/II

Posted 13 Days Ago
Be an Early Applicant
Durham, NC, USA
In-Office
Entry level
Biotech
The Role
Perform routine microbiology laboratory testing and support for a contract manufacturing biotech facility, including environmental, clean utility, compressed gas, and product testing; execute protocols, document results, troubleshoot, and follow safety and regulatory requirements.
Summary Generated by Built In

The Microbiology Associate will be part of the Microbiology Department responsible for the testing and support for the Microbiology Laboratory in support of a Contract Manufacturing biotechnology facility and Process Development. Responsibilities includes laboratory support, program testing, reporting of results, execution of protocols.


This person is responsible for the aspects of the following programs as directed by management:

  • Environmental Monitoring (Air Viable, Total Air Particulate, Surface Viable)
  • Clean Utility Monitoring (Water Sampling, Bioburden, Conductivity, TOC, Coliform
  • and Nitrates)
  • Compressed Gas Monitoring (Collection, Air Viable, Total Air Particulate, Dragger
  • Tests and specific ID tests)
  • Product Testing (Bioburden, Endotoxin, Host Purity, or Non-Host)
  • Media Release
  • Laboratory Support

Additional Responsibilities:

  • Executes routine Microbial Laboratory work. Utilizes technical discretion in the execution and interpretation of experiments that contribute to program goals.
  • Makes detailed observations and carries out elementary data analysis.
  • Understands monitoring programs and methods and conducts troubleshooting analysis.
  • Working knowledge of sampling equipment and testing instruments.
  • Documentation and technical writing skills.
  • Knowledge of current regulations and scientific literature.
  • Ensures proper labeling, handling, and storage of all chemical and biohazards used in the laboratory. Ensures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe procedures and attends all required safety and health training, including handling hazardous waste

Minimum Requirements:

  • Bachelor’s/Master’s degree in Microbiology, Biology or related technological field of science.
  • BS and 0-3 years of experience or MS and 0-3 years of experience

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

Skills Required

  • Bachelor's or Master's degree in Microbiology, Biology, or related field
  • 0-3 years relevant laboratory experience
  • Experience with environmental monitoring (air viable, total air particulate, surface viable)
  • Experience with clean utility monitoring (water sampling, bioburden, conductivity, TOC, coliforms, nitrates)
  • Compressed gas monitoring experience (collection, air viable, total air particulate, Dragger tests)
  • Product testing experience (bioburden, endotoxin, host purity/non-host)
  • Media release and general laboratory support skills
  • Working knowledge of sampling equipment and testing instruments
  • Documentation and technical writing skills
  • Knowledge of current regulations and scientific literature
  • Adherence to laboratory safety, hazardous waste handling, and completion of required safety training

KBI Biopharma Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about KBI Biopharma and has not been reviewed or approved by KBI Biopharma.

  • Healthcare Strength Health coverage includes medical, dental, and vision with HSA/FSA options, alongside life and disability insurance. Employer-verified listings indicate solid foundational coverage across sites.
  • Leave & Time Off Breadth PTO and paid holidays are provided, with flexible or “unlimited” PTO available in some salaried roles and standard accrual with limited rollover elsewhere. This breadth supports time away options across job families.
  • Parental & Family Support Parental leave is available, with indications of 12 weeks for U.S. employees in recent materials. Maternity and paternity leave are included as part of the package.

KBI Biopharma Insights

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The Company
HQ: Durham, NC
1,282 Employees
Year Founded: 1996

What We Do

KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally. With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs. KBI is proud to be a JSR Life Sciences Company.

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