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QC Analyst I/II (Microbiology)

Piper Companies

Rockville (MD)

On-site

USD 100,000 - 125,000

Full time

2 days ago
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Job summary

A biotechnology research company in Rockville, MD is seeking a QC Analyst I/II specializing in microbiology. The role involves environmental monitoring, testing, and data analysis in a cGMP setting. Ideal candidates will have relevant experience and a degree in a related field. This position offers a competitive hourly salary and comprehensive benefits.

Benefits

Cigna Medical/Dental/Vision
ADP 401k
PTO
Paid Holidays
Paid sick leave

Qualifications

  • 1+ years of experience with microbiology and/or EM testing in a cGMP environment.
  • Knowledge of GMP/cGMP protocols and SOP writing/revisions preferred.

Responsibilities

  • Perform Environmental Monitoring of Grade C/D Cleanrooms.
  • Conduct bioburden/endotoxin testing on raw materials and drug products.
  • Assist with data trending, analysis, and reporting assignments.

Skills

Microbiology
Environmental Monitoring
Data Trending

Education

BS/BA in Biology
BS/BA in Microbiology
BS/BA in Biotechnology

Job description

Join to apply for the QC Analyst I/II (Microbiology) role at Piper Companies

2 days ago Be among the first 25 applicants

Join to apply for the QC Analyst I/II (Microbiology) role at Piper Companies

Piper Health & Sciences is seeking a QC Analyst I/II, Microbiology to support a biotechnology research company in the Rockville, MD area. This position is 1st shift hours, Monday – Friday.

Responsibilities for the QC Analyst I/II include:

  • Perform Environmental Monitoring of Grade C/D Cleanrooms and aseptic filling isolators, including sampling of viable surfaces, viable air and non-viable particulates in a Phase III/Commercial GMP Manufacturing facility.
  • Conducts routine sampling and testing of Clean Utilities such as Water for Injection and Clean Compressed gasses.
  • Conducts bioburden/endotoxin testing on raw materials, buffers/solutions, in-process and release drug product samples.
  • Provides input on SOP revisions and may assist in the creation and editing of procedures and work instructions.
  • Assists with data trending, analysis, and reporting assignments as needed.

Qualifications for the QC Analyst I/II include:

  • 1+ years of experience with microbiology and/or EM testing in a cGMP environment, preferably within the biotechnology or pharmaceutical industry.
  • BS/BA degree in a relevant field such as Biology, Microbiology, Biotechnology, etc.
  • In depth knowledge of GMP/cGMP protocols and SOP writing/revisions preferred.

Compensation for the QC Analyst I/II includes:

  • Salary range: approximately $35.00 - $40.00 hourly, commensurate with experience
  • Comprehensive Benefits: Cigna Medical/Dental/Vision, ADP 401k, PTO, Paid Holidays, Paid sick leave as required by law

This job is open for applications on 5/16/2025. Applications will be accepted at least 30 days from the posting date.

QC micro, quality control, microbiology, microbiologist, environmental monitoring, em, em testing, aseptic, bioburden, endotoxin, toc, conductivity, data trending, cgmp, gmp, gxp, cleanroom

Seniority level
  • Seniority level
    Entry level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Quality Assurance
  • Industries
    Business Consulting and Services

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