Quality Assurance Lead
Company Overview >> | (c) 2015 Lyophilization Services of New England |
Biotechnology Quality Professional, experienced in the entire manufacturing process including writing / revising SOPs, Master Batch Record development, GMP training, compounding of drug products, Finished Product inspection and AQL, review and disposition of executed batch records, and deviation/CAPA writing and review. Proven strengths in multi-tasking, identifying and correcting problems, adhering to written procedures (SOPs), and attention to detail. Excellent communication and interpersonal skills. ISO 7 Gown Qualified.
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