Ruben Rodriguez Email and Phone Number

Initiated and completed investigations on manufacturing deviations, including the identification of root causes and the corrective and preventive actions related to them. Provided support to selected department metrics. Proposed alternatives or solutions based on data analysis and interpretation. Supported, coordinated and/or participated in process quality improvement projects or initiatives applicable to operations and support or service areas. Performed FMEA on packaging line clearance process. Assessed actual practice vs. SOPs and best industry practices, compliance and process excellence and supports the implementation of best practices.

PROFESSIONAL PROFILETask oriented and committed to results Chemical Engineer with at least 15 years of experience in highly regulated Pharmaceutical environment and Electronic Industry. Expertise in: supervision, conducting and writing manufacturing investigations, tracking commitments, SOP creation and revision, conducting packaging line trials, risk assessments, write protocols, execution and writing protocols reports. Proficient at data analysis and deriving improvements from it. Able to motivate and develop team members. Solid knowledge of productions metrics, cGMP and FDA audits. Outstanding interpersonal and communication skills to communicate across all levels of an organization. Fully bilingual English and Spanish.