HOURS: Consist of two possible shifts:

Monday - Friday from 7:00 am to 3:30 pm, or Monday - Friday form 10:00 am to 6:30 pm

Some flex in the start and end times may be allowed; weekend work and overtime as required.



• The candidate must have previous quality control microbiology experience. Experience in bioburden testing, membrane filtration, sterility isolator testing, conductivity, total organic carbon or endotoxin assays is preferred

• Basic knowledge of aseptic manufacturing environmental monitoring of Grade A-D Areas.

• SOP review, creation and approval is preferred

• OOS investigations writing is preferred

• Basic knowledge of compliance with all cGMP standards, safety and environmental regulations and company SOPs.

• Data entry of EM sampling results, LIMS, logbooks, and other miscellaneous lab data.

• Interact with Project Teams and cross-functional groups related to site operations
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