Overview
On Site
USD 35.00 - 40.00 per hour
Full Time
Skills
Science
Research
Adobe AIR
Manufacturing
Editing
Reporting
Pharmaceutical Industry
Business Analysis
Business Analytics
Biology
Biotechnology
SOP
Writing
Law
Quality Control
Microbiology
Testing
Theory Of Constraints
TOC
Good Manufacturing Practice
GMP
GxP
Job Details
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 1 st 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
#LI-CP1
#LI-ONSITE
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
#LI-CP1
#LI-ONSITE
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