A leading biotechnology services provider is seeking a QA Specialist I to assure compliance with GMPs and manage batch record audits. The ideal candidate will have a Bachelor’s in Science and a minimum of 2 years of relevant experience in biotechnology manufacturing. Responsibilities include tracking batch record discrepancies, preparing compliance documentation, and participating in quality meetings. Strong problem-solving and communication skills in both English and Spanish are required. Daily work schedule is Monday to Friday, 8 AM to 5 PM.
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