PROFILE Compile an outstanding record of success and significant contributions in the field of QA/QC. Develop an in-depth understanding of pharmaceutical documentation and quality system, been a top performer in high-pressure situations and an excellent problem solver. Have the ability to work well in a project team environment, leader and an asset to any organization. STRENGHTS Complete familiarity with FDA regulations, USP methods and procedures with in-depth knowledge of GLP, cGMP. Experience in a GMP environment, with equipment validation/verification procedures, compliance and company guidelines. Review both production and packaging batch records and system validation as well as investigations and commitments.
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