
About Me
Senior Process Engineer with nearly 6 years of experience in the medical device industry, specializing in process validation, equipment qualification, and regulatory compliance. Proficient in drafting, reviewing, and updating critical documentation, including IQ, OQ, PQ protocols, and validation spreadsheets. Skilled in executing Test Method Validation TMV, Design of Experiments DOE, and ensuring robust process controls to meet quality standards. Adept at cross functional collaboration, driving compliance, and supporting continuous improvement initiatives in highly regulated environments.
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