Delva J. Rodriguez

Background

About Delva J. Rodriguez

Professional experienced in the Pharmaceutical Industry with over 15 years working in Chemical Laboratory, Packaging, Visual Inspection, Parenteral manufacturing and Operations. In depth experience developing SOPs, Change Controls and Manufacturing Investigations. Hands on experience auditing manufacturing areas. Experienced with regulatory agencies, 21 CFR Part 11, cGMPs, OSHA and Lean Manufacturing. Responsible, self-starter highly organized, flexible with proven leadership skills and management/supervisory skills. Capable of managing multiple tasks in a high pressure environment with minimum supervision. Quality and teamwork oriented with excellence interpersonal and communication skills. Ability to influence and motivate others. Computer literate on MS Office, Visio, SAP, TrackWise, MES (Electronic Batch Records), Kronos/ADP, OEE System. Bilingual in English and Spanish.