Associate Director, QC Microbiology

Posted 3 Days Ago
Be an Early Applicant
Durham, NC, USA
In-Office
Expert/Leader
Biotech
The Role
Lead QC microbiology programs including environmental, compressed gas, product testing, media release, and lab support. Oversee method verifications, troubleshooting, data analysis, documentation, regulatory compliance, training, and safety for laboratory operations. Provide technical leadership and may perform testing as needed.
Summary Generated by Built In

JOB SUMMARY

Responsible for overseeing microbiological programs and methods activities for

processes, instruments and equipment. Ensures the effective use of material,

equipment and personnel while developing products and processes at high quality

levels.

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

It is the expectation that this position is required to be onsite full time. Additionally, this position should be in the laboratory at a minimum of 1 hour a day, 3 time per week.

JOB RESPONSIBILITIES

  • Strong understanding of monitoring programs and methods, makes detailed observations and conducts troubleshooting analysis.

  • Strong technical knowledge of programs. Makes detailed observations and carries out advanced data analysis.

  • Execute and review routine Microbial Laboratory work.

  • Utilizes technical discretion in the execution and interpretation of experiments that contribute to program goals.

  • May perform testing when required.

  • Strong documentation and technical writing skills.

  • Familiarity with current regulations and scientific literature.

  • Ensures method verifications and qualification protocols and investigations are performed appropriately. May execute testing when required.

  • Maintains current state of training prior to execution of tasks.

  • Assures proper labeling, handling, and storage of all chemical and biohazards used in the laboratory.

  • Assures 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 of Science degree in a scientific discipline with a minimum of 13 – 15 years of technical management experience; or a Master’s degree with 11 – 14 years or a Doctorate degree in Microbiology study and 9 –12 years related experience and/or equivalent training preferred. Additionally, a minimum of 5 years’ managerial experience.

Also requires a demonstrated track record in the following areas:

  • Attainment of aggressive growth and profit objectives.

  • Strong orientation for Quality and Customer Service.

  • Demonstrated level of respect for individuals.

  • Demonstrated contribution to science in appropriate area.

  • High level of integrity and personal responsibility.

  • Record of Innovation.

  • Strong Collaboration and Team building skills.

Language Ability

  • Ability to read, analyze, and interpret the most complex documents and regulations.

  • Ability to respond effectively to the most sensitive inquiries or complaints.

  • Ability to write speeches and articles using original or innovative techniques or style. Ability to make effective and persuasive speeches and presentations on controversial or complex topics to senior management peer group, employee groups, and/or customers.

Reasoning Ability

  • Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems.

  • Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases.

  • Ability to deal with a variety of abstract and concrete variables.

Math Ability

  • Ability to apply advanced mathematical concepts such as exponents, logarithms, statistical analysis, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity,analysis of variance, correlation techniques, sampling theory and factor analysis.

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 of Science in a scientific discipline with 13-15 years technical management experience; OR Master's with 11-14 years; OR Doctorate in Microbiology with 9-12 years (equivalent training preferred).
  • Minimum of 5 years managerial experience.
  • Onsite full-time presence; in-lab at least one hour per day, three times per week.
  • Experience overseeing Environmental Monitoring, Clean Utility Monitoring, Compressed Gas Monitoring, Product Testing, Media Release, and Laboratory Support programs.
  • Strong technical knowledge, troubleshooting, and advanced data analysis skills.
  • Ability to execute and review routine microbial laboratory work and perform testing when required.
  • Strong documentation and technical writing skills; ability to prepare reports, presentations, and regulatory documents.
  • Familiarity with current regulations and scientific literature relevant to microbiology and QC.
  • Experience with method verifications, qualification protocols, and investigations.
  • Maintains required training and adheres to safety and hazardous waste handling procedures.
  • Demonstrated track record in achieving growth and profit objectives, collaboration, team building, integrity, and innovation.
  • Advanced mathematical, logical, and scientific reasoning abilities (statistics, ANOVA, sampling theory, etc.).

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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