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QC Microbiology Analyst
- Permanent
- Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Pharmacovigilance Practice (GVP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a QC Microbiology Analyst for a leading biotechnology company located in Philadelphia, PA.
Must be eligible to work in the US.
Job Responsibilities:
Perform daily cGMP quality control laboratory microbiological testing activities
Perform environmental monitoring of the cleanroom areas as scheduled.
Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times.
Perform all activities with respect to cGMP compliance.
Support thorough cGMP investigations for out-of-specification test results.
Support technical problem solving.
Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data.
Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results.
Skills and Requirements:
- Bachelor's degree in Biology, Microbiology or related scientific field is required
- Minimum one (1) year of experience in in a cGMP Quality Control role; experience with cell therapy products is a plus.
- Proficiency in aseptic techniques when executing microbial test methods and environmental monitoring
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) 215-531-6914 or s.briggs@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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