Microbiology QC Scientist II – Onsite, Growth & Impact

Catalent

Saint Petersburg (FL)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Benefits offered by this job

Medical, dental, and vision benefits
Tuition Reimbursement
Competitive PTO and holidays

Job summary

Catalent is seeking a Scientist II in Quality Control - Microbiology in St. Petersburg, FL.

This hands-on laboratory position focuses on microbiological testing of raw materials, in-process materials, finished products, stability, and validation samples, with responsibilities for environmental monitoring and data integrity in a cGMP environment. The role requires a strong microbiology background, excellent technical writing, and ability to work with LIMS.

Qualifications

  • Bachelor or higher degree in microbiology or related life sciences is required.
  • Extensive hands-on microbiology testing experience in regulated labs (pharma/biotech/dietary supplement).
  • Experience with environmental monitoring and trending data.
  • Strong technical writing and ability to review/test records and reports for accuracy.

Responsibilities

  • Perform microbiological testing of raw materials, in-process materials, finished products, stability, and validation samples.
  • Support environmental monitoring programs and data integrity under cGMP.
  • Write and revise SOPs, methods, and technical reports; participate in investigations and CAPAs.
  • Interpret results, review calculations in LIMS, and assist with equipment qualification and safety.

Skills

Microbiology testing
Environmental monitoring
Data integrity
Technical writing

Education

Bachelor of Science in Microbiology or related life science

Tools

LIMS
USP methods

Job description

Catalent is seeking a Scientist II in Quality Control - Microbiology in St. Petersburg, FL.

This hands-on laboratory position focuses on microbiological testing of raw materials, in-process materials, finished products, stability, and validation samples, with responsibilities for environmental monitoring and data integrity in a cGMP environment. The role requires a strong microbiology background, excellent technical writing, and ability to work with LIMS.

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