Our client, a growing cellular therapeutics facility, is seeking a Quality Specialist to support their growing GMP facility. This individual will be responsible for quality assurance documentation to include batch records, document control, investigations and helping to build out the quality system.
Top Skills Details:
Environmental Monitoring - 1-3 years of experience, while this will only be 30% of the job, they would like someone to come in the door having sampling experience in a GMP regulated environment, whether it be QC or Manufacturing
GMP Experience - need to understand how things are documented, are moving toward using MasterControl for their documentation systems, so any experience with electronic documentation is ideal
Additional Skills & Qualifications:
BS Degree in Biology, Microbiology or other closely related industry
3+ years of industry experience
Environmental monitoring experience
GMP Experience
Experience Level:
Intermediate Level
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