Microbiologist II- 236227

job
  • Medix™
Job Summary
Location
Chicago ,IL
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
15 Nov 2024
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Job Description

The Microbiologist II is a key member of the Microbiology and Environmental Monitoring (EM) team, supporting microbiology and EM programs, and ensuring compliance with regulatory standards. This role involves direct interaction with biological non-sterile drug substances and sterile drug product manufacturing processes. Aseptic gowning qualification is required.


Essential Duties & Responsibilities:

  • Conduct environmental monitoring in TPI-controlled and aseptic manufacturing areas.
  • Collect viable (surface, gowning, air) and non-viable (air) particle samples.
  • Incubate viable samples and manage EM isolates, including data entry for trend analysis.
  • Ensure compliance with annual gowning qualifications.
  • Perform routine sanitation, temperature verification for lab refrigerators, and incubators.
  • Monitor water systems (WFI, RO, PW, CS) and submit samples for testing (TOC, conductivity, microbial count, endotoxins).
  • Conduct tests for compressed air (CA) and nitrogen gas (N2) for viable and non-viable particles, oil, and moisture.
  • Execute bacterial endotoxin tests for WFI, CS, IPC, IP, DS, and DP samples.
  • Perform gram staining, growth promotion, bioburden, and microbial limit tests.
  • Visually inspect microbiological, EM samples, and media fill units.
  • Enter data into Excel for trend analysis and review laboratory data.
  • Generate notifications for Out of Specification (OOS) or EM Action/Alert Level deviations, as needed.
  • Lead or support laboratory and manufacturing investigations.
  • Initiate change controls for equipment/instrument qualifications, processes, or document updates.
  • Act as a Contributor for procedure, method, or specification revisions in the Master Control System.
  • Undertake additional tasks as requested by management.


Requirements:

Education:

  • Bachelor’s degree in microbiology, biology, or related field.

Experience:

  • Minimum 3-5 years in a cGMP pharmaceutical manufacturing environment.
  • Knowledge of cGMP regulations (21 CFR 201/211/820).

Special Skills:

  • Strong written and verbal communication.
  • Proficiency with EM equipment (AirIdeal, HACH Met Ones 3440 Series, Lasair III, MiniCapt).
  • Organizational and detail-oriented skills.
  • Time management skills to meet deadlines.
  • Familiarity with Microsoft Excel and Word.

Work Environment & Physical Demands:

  • General Environment: Office and laboratory settings.
  • Aseptic Gowning: Able to work in full aseptic gowning for at least 4 hours weekly.
  • Flexible Hours: Availability to work weekends, holidays, or over 8 hours per day, as required.
  • Exposure: Possible exposure to hazardous chemicals (e.g., disinfectants); requires use of personal protective equipment.
  • Safety Alertness: Required around hazardous equipment and conditions.
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