Qualifications Summary Highly competent, diligent, and detail-oriented management professional, equipped with extensive experience and expertise focused on various areas of quality improvement, process validation and qualification, manufacturing, risk analysis, as well as implementation of standard procedures and policies within the pharmaceutical industry. Possess solid instrumental analysis skills and expertise in categorizing, prioritizing, and tactical planning equipped with in-depth knowledge of CGMP compliance.

Highlights:

• Management
• Complaints
• CFR Part 11
• High Performance Liquid Chromatography (HPLC)
• FDA
• New Jersey
• MSDS
• Policies and Procedures
• Process Improvement
• Protocol
• CAPA