Overview
On Site
USD 22.00 - 30.00 per hour
Full Time
Skills
Science
Documentation
Regulatory Compliance
Manufacturing
Pharmaceutical Industry
Law
Quality Control
Theory Of Constraints
TOC
GMP
Good Manufacturing Practice
GxP
GDP
ISO 9000
Microbiology
Data Analysis
Biotechnology
Life Sciences
Pharmaceutics
Job Details
Piper Health & Sciences is seeking a QC Technician II to support the quality control microbiology department of a growing biotechnology company in the Columbia, MD area. This role is first shift, Monday - Friday working schedule.
Responsibilities for the QC Technician II include:
Perform routine and in-process environmental monitoring (EM) sampling in a cleanroom environment.
Conduct and monitor environmental parameters including viable sampling, personnel sampling, temperatures, humidity, etc.
Perform bioburden, TOC, conductivity, and endotoxin analysis of water and manufacturing samples.
Properly label and document cleanroom plates, EM data, and logbooks according to Good Documentation Practices (GDP).
Compliance with Good Manufacturing Practices (GMP/cGMP) and guidelines, including proper gowning/PPE and following aseptic protocols.
Qualifications for the QC Technician II include:
2+ years of relevant EM sampling, bioburden, endotoxin, conductivity, and/or TOC analysis within a GxP regulated environment.
Prior experience within the biotechnology or pharmaceutical industry.
Minimum of a High School Diploma/GED is required. Associate's degree or Bachelor's degree in a relevant field is preferred.
Compensation for the QC Technician II includes:
Salary range: approximately $22.00 - $30.00 hourly, commensurate with experience
Comprehensive Benefits: Cigna Medical, Dental, Vision, 401k w/ ADP, PTO. Holidays, Sick leave as required by law
This job opens for applications on 5/2/2025. Applications for this job will be accepted for at least 30 days from the posting date.
QC micro, qc analyst, quality control, em, environmental monitoring, bioburden, endotoxin, toc, conductivity, total organic carbon, gmp, cgmp, gxp, gdp, eqms, clean room, iso 5, iso 8, microbial, microbiology, data analysis, data trending, biotechnology, life sciences, pharmaceutical, biopharmaceutical, biologics
#LI-CP1
#LI-ONSITE
Responsibilities for the QC Technician II include:
Perform routine and in-process environmental monitoring (EM) sampling in a cleanroom environment.
Conduct and monitor environmental parameters including viable sampling, personnel sampling, temperatures, humidity, etc.
Perform bioburden, TOC, conductivity, and endotoxin analysis of water and manufacturing samples.
Properly label and document cleanroom plates, EM data, and logbooks according to Good Documentation Practices (GDP).
Compliance with Good Manufacturing Practices (GMP/cGMP) and guidelines, including proper gowning/PPE and following aseptic protocols.
Qualifications for the QC Technician II include:
2+ years of relevant EM sampling, bioburden, endotoxin, conductivity, and/or TOC analysis within a GxP regulated environment.
Prior experience within the biotechnology or pharmaceutical industry.
Minimum of a High School Diploma/GED is required. Associate's degree or Bachelor's degree in a relevant field is preferred.
Compensation for the QC Technician II includes:
Salary range: approximately $22.00 - $30.00 hourly, commensurate with experience
Comprehensive Benefits: Cigna Medical, Dental, Vision, 401k w/ ADP, PTO. Holidays, Sick leave as required by law
This job opens for applications on 5/2/2025. Applications for this job will be accepted for at least 30 days from the posting date.
QC micro, qc analyst, quality control, em, environmental monitoring, bioburden, endotoxin, toc, conductivity, total organic carbon, gmp, cgmp, gxp, gdp, eqms, clean room, iso 5, iso 8, microbial, microbiology, data analysis, data trending, biotechnology, life sciences, pharmaceutical, biopharmaceutical, biologics
#LI-CP1
#LI-ONSITE
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